isomethyleugenol has been researched along with Genetic Predisposition in 97 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 5 (5.15) | 18.2507 |
| 2000's | 18 (18.56) | 29.6817 |
| 2010's | 53 (54.64) | 24.3611 |
| 2020's | 21 (21.65) | 2.80 |
| Authors | Studies |
|---|---|
| Boughanem, H; Crujeiras, AB; de Luque, V; Macias-Gonzalez, M; Ruiz-Limon, P; Tinahones, FJ | 1 |
| Kumar, VC; Pai, R | 1 |
| Blumberg, B; Joloya, EM; Mohajer, N; Seo, J; Shioda, T | 1 |
| Aránega, A; Dueñas, Á; Franco, D; García-López, V; Garcia-Martínez, V; García-Padilla, C; López-Sánchez, C | 1 |
| Gowri, P; Mahesh Kumar, S; Sathish, P; Sundaresan, P | 1 |
| Chong, Y; Feng, F; Ma, X; Ren, Q; Zhu, H | 1 |
| Li, HM; Li, R; Li, XM; Tan, Z; Wang, GS; Xiang, N; Zhang, TP | 1 |
| Guo, C; Han, M; Hu, D; Hu, F; Huang, S; Li, Q; Li, Y; Liu, D; Qie, R; Qin, P; Tian, G; Wu, X; Zhang, M; Zhang, Y; Zhao, Y; Zhou, Q | 1 |
| Chandra, GB; M K, S; Manrai, M; Mishra, Y; Misra, P; Mukherjee, B; Negi, R; S V, A; Singh, A; Singh, MU; Singh, R | 1 |
| Bijak, M; Grębowski, R; Saluk, J; Szemraj, J; Wigner, P | 1 |
| Chen, H; Chen, X; Jia, Z; Jiang, Y; Lv, H; Lv, W; Sun, C; Tang, G; Tao, J; Wei, S; Xu, J; Zhang, M | 1 |
| Amengual, JE; Gonzalez, Y; Liu, Y | 1 |
| Chu, H; Du, M; Fu, Z; Gu, D; Li, S; Meng, Y; Wang, M; Wu, Y; Xu, K; Zhang, Z; Zhu, L | 1 |
| Bąk, M; Bruckmann, A; Dock-Bregeon, AC; Fischer, U; Grauer, E; Hasler, D; Heizinger, L; Kalb, R; Kunstmann, E; Lehmann, G; Li, ZT; Liu, MF; Meduri, R; Meister, G; Merkl, R; Sement, FM; Wang, X; Zavolan, M | 1 |
| Ali, AT; Hodgkinson, A; Idaghdour, Y | 1 |
| Asou, N; Benoukraf, T; Matsumura, T; Matsuoka, M; Muddineni, SSNA; Nakamura-Ishizu, A; Okuda, T; Osato, M; Sian, S; Suda, T; Tan, DQ; Tirado-Magallanes, R; Tokunaga, K; Wang, CQ | 1 |
| Hayashi, T; Kato, Y; Nagai, M; Nakamura, M; Sano, A; Sasaki, N; Tomiyasu, A; Tomiyasu, Y; Ueno, SI; Umehara, H; Yokotsuka-Ishida, S | 1 |
| Choi, YJ; Hur, S; Jung, Y; Kang, BS; Kim, M; Lee, S; Liu, J | 1 |
| Ribatti, D | 1 |
| Bik Multanowski, M; Czogała, M; Czogała, W; Hałubiec, P; Kowalczyk, W; Miklusiak, K; Skoczeń, S; Strojny, W; Tomasik, P; Wątor, G; Wędrychowicz, A; Wójcik, M; Wołkow, P; Łazarczyk, A | 1 |
| Bartenhagen, C; Bäumer, N; Berdel, WE; Cui, C; Dugas, M; Farouq, D; Garcia-Cuellar, MP; Gerloff, D; Göllner, S; Hébert, J; Hüttelmaier, S; Klein, HU; Köhn, M; Liu, Y; Maciejewski, JP; Misiak, D; Müller-Tidow, C; Oellerich, T; Pabst, C; Pauli, C; Przychodzen, B; Regev, A; Rohde, C; Sauvageau, G; Schwartz, S; Seliger, B; Serve, H; Slany, R; Taketo, MM; Zhou, F | 1 |
| Dai, XL; Jin, MH; Liu, GC; Mi, NN; Ren, XY; Wang, J; Wang, SQ; Zhang, J | 1 |
| Briand, N; Cahyani, I; Collas, P; Moskaug, JØ; Oldenburg, A; Shah, A; Sørensen, AL | 1 |
| Adams, DJ; Basheer, F; Bashford-Rogers, R; Burrows, N; Chan, WI; Clipson, A; Du, MQ; Erdem, A; Fitzgibbon, J; Foerster, S; Gallipoli, P; Giotopoulos, G; Hodson, D; Horton, SJ; Huntly, BJP; Laurenti, E; Maxwell, P; Okosun, J; Osaki, H; Petrunkina Harrison, A; Rashid, M; Sasca, D; Sheppard, O; Smith, KG; Sustic, T; Sybirna, A; Vohra, S; Wright, P; Yiangou, L; Yun, H; Zhao, W | 1 |
| Li, L; Li, Y; Lv, H; Pi, J; Sun, G; Wang, H; Xu, Y; Zhu, J | 1 |
| Hu, W; Lin, X; Zhang, H; Zhao, N | 1 |
| Chen, YX; Fang, JY; Fu, LN; Tan, J | 1 |
| Ahmed, A; Ahsan, H; Finnell, RH; Gamble, MV; Graziano, JH; Hall, MN; Ilievski, V; Islam, T; Kibriya, MG; Levy, D; Liu, X; Navas-Acien, A; Niedzwiecki, MM; Parvez, F; Siddique, AB; Slavkovich, V; Zhu, H | 1 |
| Ao, PL; Chen, WJ; Hsueh, YM; Huang, CY; Lin, YC; Pu, YS; Shiue, HS; Su, CT | 1 |
| Kaneko, S; Li, X | 1 |
| Abdollahi, S; Anvar, Z; Banaei, M; Dastgheib, SA; Gharesi-Fard, B; Jahromi, BN; Moein-Vaziri, N; Poorang, S; Tabei, SMB | 1 |
| Banerjee, HN; Kahan, W; Kumar, V; Verma, M | 1 |
| Kang, C; Kim, MY; Lee, SW; Park, DY | 1 |
| Adams, PD; Birse, RT; Bodmer, R; Dall'Agnese, A; Diop, SB; Guida, MC; Mai, A; Puri, PL; Toto, PC | 1 |
| Barco, A; Scandaglia, M | 1 |
| Cieśla, M; Darmochwał-Kolarz, D; Kolarz, B; Majdan, M | 1 |
| Bojin, FM; Cristea, MI; Gruia, AT; Ivan, A; Lam, D; Margineanu, F; Oprean, C; Paunescu, V; Saffery, R; Tatu, CA; Telea, A | 1 |
| Chen, F; Fu, Y; Shi, J; Stemmer, P; Sun, J; Thakur, C; Zhang, Q | 1 |
| Jadavji, NM; Murray, LK | 1 |
| Antonelli, R; Cowden, J; Sams, R; Shao, K; Thomas, DJ | 1 |
| Sakata-Yanagimoto, M | 1 |
| Ozanne, SE | 1 |
| Nachman, PH; Pendergraft, WF | 1 |
| Auclair-Perrossier, J; Blanché, H; Bodo, S; Bourdeaut, F; Brems, H; Brugières, L; Buhard, O; Buisine, MP; Cabaret, O; Caron, O; Chalastanis, A; Cohen-Haguenauer, O; Colas, C; Collura, A; Coulet, F; Duval, A; Entz-Werle, N; Fedhila, F; Fléjou, JF; Frébourg, T; Gauthier-Villars, M; Gerdes, AM; Goldberg, Y; Grandjouan, S; Guilloux, A; Hamelin, R; Ilencikova, D; Kinzel, M; Knappe, UJ; Lafitte, P; Lavoine, N; Leclerc, J; Leis, A; Lejeune, S; Malka, D; Mathieu-Dramard, M; Mortemousque, I; Muleris, M; Parfait, B; Ruiz-Ponte, C; Sheridan, E; Soubrier, F; Svrcek, M; Tinat, J; Vasen, H; Verloes, A; Vidaud, D; Wafaa, B; Wang, Q; Wimmer, K | 1 |
| Elalaf, H; Hineno, S; Ikeya, M; Jin, Y; Kato, T; Kobayashi, Y; Matsuda, S; Matsunaga, K; Nagata, S; Okamoto, T; Tamaki, S; Toguchida, J; Watanabe, M; Woltjen, K | 1 |
| Amin, SG; Belinsky, SA; Collins, LB; Crowell, RE; Desai, D; Gilliland, FD; Jauregui, AR; Juri, DE; Leng, S; Lin, Y; Liu, Y; Picchi, MA; Stidley, CA; Swenberg, JA; Tellez, CS; Thomas, CL; Wathelet, MG; Wu, G; Zhang, X | 1 |
| Balakrishnan, P; Cole, SA; Franceschini, N; Francesconi, KA; Gilliland, F; Goessler, W; Gribble, MO; Haack, K; Laston, SL; Navas-Acien, A; North, KE; Tellez-Plaza, M; Thomas, DC; Umans, JG; Voruganti, VS | 1 |
| Chen, WJ; Hsueh, YM; Huang, CY; Lin, YC; Pu, YS; Shiue, HS | 1 |
| Agusa, T; Binh Minh, T; Fujihara, J; Hung Viet, P; Iwata, H; Kunito, T; Minh Tue, N; Takahashi, S; Takeshita, H; Tanabe, S; Thi Kim Trang, P; Thi Mai Lan, V | 1 |
| Anttila, V; Bulik-Sullivan, B; Daly, MJ; Day, FR; Farh, K; Finucane, HK; Gusev, A; Lindstrom, S; Loh, PR; Neale, BM; Okada, Y; Patterson, N; Perry, JR; Price, AL; Purcell, S; Raychaudhuri, S; Reshef, Y; Ripke, S; Stahl, E; Trynka, G; Xu, H; Zang, C | 1 |
| Allard, DE; Conley, B; Cook, KD; Davenport, ML; Fry, RC; Magnuson, T; Rager, JE; Shpargel, KB; Starmer, J; Su, MA; Whitfield-Larry, F; Whitmire, JK | 1 |
| Bovée, JV; Briaire-de Bruijn, I; Cleton-Jansen, AM; Cleven, AH; Höcker, S; Szuhai, K | 1 |
| Aslani, S; Jamshidi, AR; Karami, J; Mahmoudi, M; Malekshahi, Z; Nicknam, MH | 1 |
| Feng, F; Li, S; Li, Y; Ren, Q; Xiao, Y; Zhang, J; Zheng, G; Zhu, L; Zhu, X | 1 |
| Cebrián, ME; Hernández-Alcaraz, C; Hernández-Ramírez, RU; López-Carrillo, L; Pineda-Belmontes, CP | 1 |
| Fan, Y; Fang, J; Han, S; He, X; Heng, D; Liu, W; Peng, B; Wang, Z; Xu, J; Yu, F; Zhang, Y | 1 |
| Datta, M; Kesharwani, D; Poddar, S | 1 |
| Araki, Y; Mimura, T | 1 |
| De Luca, V; Dhoot, R; Kennedy, JL; Viggiano, E; Wong, AH | 1 |
| Baud, P; Courtet, P; Deutsch, S; Guillaume, S; Guipponi, M; Jollant, F; Kohler, K; La Harpe, R; Laforge, T; Le Gal, F; Malafosse, A; Perroud, N; Petit, B; Vessaz, M | 1 |
| Bryant, SC; Garrity-Park, MM; Loftus, EV; Sandborn, WJ; Smyrk, TC | 2 |
| Niwa, T; Shimazu, T; Takeshima, H; Ushijima, T; Yamashita, S | 1 |
| Bai, CH; Chen, CJ; Chung, CJ; Hsueh, YM; Huang, YK; Huang, YL; Yang, MH | 1 |
| Naumov, AV; Razvodovskiĭ, IuE | 1 |
| Gadalla, SM; Greene, MH; Korde, L; Mirabello, L; Savage, SA | 1 |
| Yano, K | 1 |
| Hitchins, MP | 1 |
| Chung, CJ; Hsueh, YM; Huang, CY; Pu, YS; Su, CT | 1 |
| Akan, P; Beck, S; Bell, CG; Deloukas, P; Down, TA; Finer, S; Frayling, TM; Hattersley, AT; Hitman, GA; Lindgren, CM; McCarthy, MI; Mill, J; Morison, IM; Pidsley, R; Prokopenko, I; Rakyan, VK; Stupka, E; Teschendorff, AE; Wilson, GA | 1 |
| Garrity-Park, M; Loftus, EV; Sandborn, WJ; Smyrk, TC | 1 |
| Boidin, D; Buisine, MP; Crépin, M; Dieu, MC; Escande, F; Lejeune, S; Manouvrier, S; Mathieu, M; Morin, G; Porchet, N | 1 |
| Badner, JA; Barrett, TB; Berrettini, WH; Bloss, CS; Byerley, W; Chen, C; Cheng, L; Coryell, W; Cox, NJ; Craig, DW; Edenberg, HJ; Foroud, T; Gamazon, ER; Gershon, ES; Greenwood, TA; Hipolito, M; Kelsoe, JR; Koller, DL; Lawson, WB; Liu, C; Mahon, PB; McInnis, MG; McKinney, R; McMahon, FJ; Nievergelt, CM; Nurnberger, JI; Nwulia, EA; Potash, JB; Rice, J; Scheftner, WA; Schork, NJ; Schulze, TG; Shilling, PD; Smith, EN; Szelinger, S; Zandi, PP; Zhang, C; Zhang, D; Zhang, P; Zöllner, S | 1 |
| Altamura, C; Arosio, B; Bastias Candia, S; Bergamaschini, L; Bulbarelli, A; Candeletti, S; D'Addario, C; Dell'Osso, B; Galimberti, D; Gussago, C; Lonati, E; MacCarrone, M; Mari, D; Mastronardi, L; Romualdi, P; Scarpini, E | 1 |
| Chen, CJ; Chen, JW; Huang, YL; Li, WF; Sun, CW; Wang, SL; Wang, YH | 1 |
| Cascella, N; Colantuoni, C; Eaton, W; Goldman, D; Han, F; Ji, H; Kano, S; Lee, Y; Rapoport, J; Sawa, A; Takayanagi, Y; Wilson, A; Yuan, Q; Zhou, Z | 1 |
| Croul, S; Dubuc, AM; Eberhart, CG; Hawkins, C; Hielscher, T; Jones, DT; Jones, SJ; Kool, M; Korshunov, A; Marra, MA; Mendez-Lago, M; Morrissy, AS; Northcott, PA; Peacock, J; Pfister, SM; Ramaswamy, V; Remke, M; Rolider, A; Rutka, JT; Shih, D; Taylor, MD; Unterberger, A; Vibhakar, R; Wang, X; Weiss, WA; Witt, H; Zhan, SH | 1 |
| Bertelsen, RJ; Carlsen, KC; Carlsen, KH; Gervin, K; Granum, B; Hjorthaug, HS; Lyle, R; Mowinckel, P; Munthe-Kaas, MC; Torjussen, TM; Undlien, DE | 1 |
| Bahr, GM; Blanot, D; Girardin, SE; Magalhaes, JG; Philpott, D; Rubino, SJ | 1 |
| Alexander, J; Paulsen, JE; Steffensen, IL | 1 |
| Canfield, M; Finnell, RH; Hendricks, K; Lammer, EJ; Shaw, GM; Suarez, L; Wicker, NJ; Zhu, H | 1 |
| Favier, A; Galan, P; Guilland, JC; Hercberg, S; Potier de Courcy, G | 1 |
| Chan, MW; Chu, ES; Leung, WK; To, KF | 1 |
| Blom, HJ; den Heijer, M; Finnell, RH; Shaw, GM | 1 |
| Bates, MN; Biggs, ML; Hopenhayn, C; Kalman, D; Moore, LE; Rey, OA; Shipp, M; Smith, AH; Steinmaus, C; Wiencke, JK; Zheng, S | 1 |
| Amiel, J; Bourdeaut, F; Brugieres, L; Chompret, A; de Pontual, L; Delattre, O; Etchevers, H; Janoueix-Lerosey, I; Lyonnet, S; Minard, V; Munnich, A; Thomas, S; Trochet, D; Valteau, D | 1 |
| Dobrovic, A; Krypuy, M; Loughrey, MB; Snell, C; Wong, EM | 1 |
| Glavac, D; Korosec, B; Ravnik-Glavac, M; Volavsek, M | 1 |
| Berns, A; de Wind, N; Dekker, M; Radman, M; te Riele, H | 1 |
| Kunkel, TA; Umar, A | 1 |
| Ainsworth, P; Andrews, J; Chakraborty, P; Lopes, E; Mancini, D; Rodenhiser, D; Singh, S | 1 |
| Cattaneo, M; Lecchi, A; Lombardi, R; Zighetti, ML | 1 |
| Law, MR; Wald, NJ | 1 |
| Rozen, R | 1 |
| Emi, M; Nagai, H | 1 |
| Cara Terribas, CJ; González Guijarro, L | 1 |
25 review(s) available for isomethyleugenol and Genetic Predisposition
| Article | Year |
|---|---|
Genes of the month: H3.3 histone genes: H3F3A and H3F3B.
Topics: Acetylation; Animals; Chromatin Assembly and Disassembly; DNA Methylation; Genetic Predisposition to Disease; Histones; Humans; Methylation; Mutation; Neoplasms; Neurodevelopmental Disorders; Protein Processing, Post-Translational | 2021 |
Epigenetic Transgenerational Inheritance of the Effects of Obesogen Exposure.
Topics: Animals; Chromatin; DNA Methylation; Endocrine Disruptors; Environmental Exposure; Epigenesis, Genetic; Female; Genetic Predisposition to Disease; Histones; Humans; Inheritance Patterns; Male; Methylation; Obesity; Phenotype | 2021 |
Molecular Mechanisms of lncRNAs in the Dependent Regulation of Cancer and Their Potential Therapeutic Use.
Topics: Animals; Biomarkers, Tumor; Carcinogenesis; Disease Management; Disease Susceptibility; DNA Methylation; Epigenesis, Genetic; Gene Expression Regulation, Neoplastic; Genetic Engineering; Genetic Predisposition to Disease; Genetic Therapy; Histones; Humans; Methylation; Molecular Targeted Therapy; Neoplasms; Oncogenes; Protein Processing, Post-Translational; RNA Processing, Post-Transcriptional; RNA, Long Noncoding | 2022 |
Effect of 12-week of aerobic exercise on hormones and lipid profile status in adolescent girls with polycystic ovary syndrome: A study during COVID-19.
Topics: Actin Cytoskeleton; Actins; Adaptor Proteins, Signal Transducing; Adenocarcinoma; Adenosine Triphosphate; Adsorption; Adult; Africa, Eastern; Aged; Air Pollutants; Air Pollution; Air Pollution, Indoor; Alcohol Drinking; Allergens; Alzheimer Disease; Amyotrophic Lateral Sclerosis; Animals; Anti-Bacterial Agents; Antibodies; Antibodies, Immobilized; Antigen Presentation; Antigens, CD; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Antioxidants; Apoptosis; Aptamers, Nucleotide; Asthma; Asthma, Exercise-Induced; Atrophy; Autophagy; Azoospermia; Bacillus cereus; Bacterial Infections; Beclin-1; Bile Duct Neoplasms; Bile Ducts, Intrahepatic; Biofouling; Biological Monitoring; Biomarkers; Biomarkers, Tumor; Biosensing Techniques; Blastocyst; Bone Neoplasms; Bone Regeneration; Bronchoconstriction; Burkitt Lymphoma; C9orf72 Protein; Campylobacter; Campylobacter Infections; Campylobacter jejuni; Carcinogenesis; Carcinoma, Hepatocellular; Carcinoma, Pancreatic Ductal; Carcinoma, Squamous Cell; Cardiomyopathies; Caregivers; Carmine; Case-Control Studies; Catalysis; Cattle; Cause of Death; CCAAT-Enhancer-Binding Protein-alpha; CD8-Positive T-Lymphocytes; Cefepime; Cell Differentiation; Cell Line, Tumor; Cell Nucleus; Cell Transdifferentiation; Chelating Agents; Chemical and Drug Induced Liver Injury, Chronic; Chemoradiotherapy, Adjuvant; Child; Child, Preschool; China; Chlorquinaldol; Cholangiocarcinoma; Cholera; Chromatin; Clinical Trials as Topic; Cognitive Dysfunction; Cohort Studies; Colonic Neoplasms; Colorectal Neoplasms; Colorimetry; Cooking; Coordination Complexes; COVID-19; Creatinine; CRISPR-Cas Systems; Critical Care; Critical Illness; Cross-Sectional Studies; Cryopreservation; Cryoprotective Agents; Cysteine; Cytokines; Device Removal; Diet; Diet, High-Fat; Diet, Mediterranean; Dietary Supplements; Dimethyl Sulfoxide; Dipeptides; Disease Models, Animal; Dithiothreitol; DNA; DNA Repeat Expansion; DNA, Bacterial; DNA, Complementary; Dopamine; Electrochemical Techniques; Electrodes; Endocannabinoids; Environmental Exposure; Environmental Monitoring; Environmental Pollutants; Enzyme-Linked Immunosorbent Assay; Erlotinib Hydrochloride; Escherichia coli; Escherichia coli O157; Esophageal Neoplasms; Esophagitis, Peptic; Ethylene Glycol; Europium; Exanthema; Fallopian Tubes; Feces; Female; Fertilization in Vitro; Fluoresceins; Fluorescent Dyes; Follicle Stimulating Hormone; Follow-Up Studies; Food Microbiology; Forced Expiratory Volume; Forkhead Transcription Factors; Frontotemporal Dementia; G-Quadruplexes; Galactose; Gastroenteritis; Gastrointestinal Diseases; Gastrointestinal Microbiome; Gastrointestinal Neoplasms; Gastrointestinal Tract; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genital Neoplasms, Female; Genome-Wide Association Study; Genome, Viral; Genomics; Genotype; Glucose; Glutathione; Glycerol; Gold; Graphite; GTPase-Activating Proteins; Heat-Shock Proteins; Heme Oxygenase-1; Hepacivirus; Hepatitis C; Hepatocytes; Histamine; Histocompatibility Antigens Class II; Hoarseness; Hospice and Palliative Care Nursing; Humans; Hydrogen; Hydrogen Peroxide; Hydrogen Sulfide; Hydroxybenzoates; Hydroxyl Radical; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Hyperthermia, Induced; Hysteroscopy; Immunoassay; Indigo Carmine; Inflammation; Inflammatory Bowel Diseases; Insulin Resistance; Intensive Care Units; Interleukin-11; Interleukin-6; Interleukins; Iodine Radioisotopes; Iran; Iridium; Islets of Langerhans; Kinetics; Lactation; Lactobacillus; Lactobacillus plantarum; Lamins; Latin America; Lead; Lectins; Leukopenia; Ligands; Limit of Detection; Lipopolysaccharides; Lipoprotein Lipase; Liver; Liver Cirrhosis; Liver Neoplasms; Lolium; Luminescent Measurements; Luminol; Lung; Luteinizing Hormone; Macrophages; Magnetic Phenomena; Magnetic Resonance Imaging; Male; Malnutrition; Maltose; Manganese Compounds; Maternal Nutritional Physiological Phenomena; Melatonin; Metabolic Engineering; Metal Nanoparticles; Metallocenes; Metaplasia; Methicillin-Resistant Staphylococcus aureus; Methylation; Mevalonic Acid; Mexico; Mice; Mice, Inbred C57BL; Mice, Transgenic; Microbial Sensitivity Tests; Microbiota; MicroRNAs; Milk; Mitomycin; Molecular Diagnostic Techniques; Molecular Docking Simulation; Monte Carlo Method; Moringa oleifera; Multiple Sclerosis; Muscle Strength; Muscle, Skeletal; Nanocomposites; Nanotubes, Carbon; Neoadjuvant Therapy; Neoplasms; Neurodegenerative Diseases; Neurotransmitter Agents; NF-E2-Related Factor 2; Nickel; Nitrogen Dioxide; Non-alcoholic Fatty Liver Disease; Nucleic Acid Amplification Techniques; Nucleic Acid Hybridization; Nucleocapsid Proteins; Nutritional Status; Obesity; Osteogenesis; Osteosarcoma; Oxidation-Reduction; Oxides; Oxygen; Oxyquinoline; Pain; Palliative Care; Pancreatic Neoplasms; Pandemics; Particulate Matter; Peroxidase; Peroxidases; Phagocytosis; Phaseolus; Photothermal Therapy; Point-of-Care Systems; Polyethyleneimine; Polymers; Polymorphism, Single Nucleotide; Polysomnography; Postoperative Complications; Pregnancy; Pregnant Women; Prenatal Exposure Delayed Effects; Prevalence; Printing, Three-Dimensional; Probability; Probiotics; Prognosis; Prophages; Prospective Studies; Proteomics; Proto-Oncogene Proteins; Pseudomonas aeruginosa; Pseudomonas putida; Pulmonary Disease, Chronic Obstructive; Pulmonary Embolism; Pyridines; Pyrroles; Quality of Life; Quinolones; Rabbits; Rats; Rats, Sprague-Dawley; Reactive Oxygen Species; Real-Time Polymerase Chain Reaction; Receptors, Histamine; Receptors, Histamine H2; Recombinases; Rectal Neoplasms; Reperfusion Injury; Respiration; Respiratory Function Tests; Respiratory Rate; Respiratory Sounds; Retrospective Studies; rho GTP-Binding Proteins; Risk Assessment; Risk Factors; RNA; RNA, Messenger; RNA, Ribosomal, 16S; Robotic Surgical Procedures; Running; Rural Population; Saccharomyces cerevisiae; Salpingectomy; Sarcopenia; SARS-CoV-2; Seeds; Semen; Sensitivity and Specificity; Sepsis; Shock, Septic; Signal Transduction; Silicon Dioxide; Silver; Sirtuin 1; Skin Neoplasms; Sleep Apnea, Obstructive; Soil; Spain; Spectrum Analysis, Raman; Sperm Retrieval; Spermatozoa; Spirometry; Staphylococcus aureus; STAT3 Transcription Factor; Stereoisomerism; Sterilization, Tubal; Stroke Volume; Sulfadiazine; Sulfites; Superoxide Dismutase; Surface Plasmon Resonance; tau Proteins; Testis; Testosterone; Thioredoxin-Disulfide Reductase; Thyroid Neoplasms; Thyroidectomy; Trans-Activators; Transcription Factor AP-1; Treatment Outcome; Triazoles; Triclosan; Trifluridine; Tumor Microenvironment; Tumor Necrosis Factor-alpha; United States; Uracil; Vagina; Vegetables; Ventricular Function, Left; Ventricular Pressure; Vibrio cholerae; Vietnam; Virulence; Vital Capacity; Vitrification; Walking; Water; Water Pollutants, Radioactive; Whole Genome Sequencing; Wind; YAP-Signaling Proteins; Zeolites; Zinc Oxide | 2023 |
Chromatin-Remodeled State in Lymphoma.
Topics: Acetylation; Animals; Chromatin; Chromatin Assembly and Disassembly; Disease Management; Disease Susceptibility; Epigenesis, Genetic; Gene Expression Regulation, Neoplastic; Genetic Predisposition to Disease; Histones; Humans; Lymphoma; Methylation | 2019 |
Epigenetics and Its Ethical Implications.
Topics: Diabetes Mellitus, Type 2; Epigenesis, Genetic; Gene Expression Regulation; Genetic Predisposition to Disease; Germ Cells; Histones; Humans; Methylation; Neoplasms; Neurodegenerative Diseases; Obesity; Phenotype | 2021 |
Contribution of spurious transcription to intellectual disability disorders.
Topics: Chromatin; Chromatin Assembly and Disassembly; DNA Methylation; Ectopic Gene Expression; Epigenesis, Genetic; Genetic Association Studies; Genetic Predisposition to Disease; Genomic Instability; Histones; Humans; Intellectual Disability; Methylation; Mutation; Neurons; Transcription, Genetic | 2019 |
New discoveries of mdig in the epigenetic regulation of cancers.
Topics: Animals; Biomarkers, Tumor; Cell Cycle; Dioxygenases; DNA Methylation; Epigenesis, Genetic; Gene Expression Regulation, Neoplastic; Genetic Association Studies; Genetic Predisposition to Disease; Histone Demethylases; Histones; Humans; Methylation; Neoplasms; Neoplastic Stem Cells; Nuclear Proteins; Prognosis | 2019 |
The role of one-carbon metabolism and homocysteine in Parkinson's disease onset, pathology and mechanisms.
Topics: Animals; Diet; Folic Acid; Genetic Predisposition to Disease; Homocysteine; Humans; Levodopa; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Nutritional Status; One-Carbon Group Transferases; Parkinson Disease; Polymorphism, Genetic; Vitamin B Complex | 2019 |
AS3MT, GSTO, and PNP polymorphisms: impact on arsenic methylation and implications for disease susceptibility.
Topics: Arsenic; Genetic Predisposition to Disease; Genotype; Glutathione Transferase; Humans; Methylation; Methyltransferases; Purine-Nucleoside Phosphorylase | 2014 |
[TET2 dysregulation in hematologic malignancies].
Topics: Azacitidine; Cytosine; Decitabine; Dioxygenases; DNA-Binding Proteins; Enzyme Inhibitors; Epigenesis, Genetic; Genetic Predisposition to Disease; Hematologic Neoplasms; Humans; Methylation; Molecular Targeted Therapy; Multigene Family; Mutation; Neoplasm Proteins; Proto-Oncogene Proteins | 2014 |
Epigenetic signatures of obesity.
Topics: Animals; Carbohydrates; Chromatin; Chromosomal Proteins, Non-Histone; Diet; Disease Models, Animal; Drosophila melanogaster; Drosophila Proteins; Epigenesis, Genetic; Female; Genetic Predisposition to Disease; Humans; Male; Methylation; Mice; Obesity; Spermatozoa; Transcription, Genetic; Triglycerides | 2015 |
Recent pathogenetic advances in ANCA-associated vasculitis.
Topics: Alleles; Animals; Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis; Antibodies, Antineutrophil Cytoplasmic; Autoantigens; Biomarkers; Disease Models, Animal; Epigenesis, Genetic; Ethnicity; Forecasting; Genetic Predisposition to Disease; Genome-Wide Association Study; Histones; Humans; Jumonji Domain-Containing Histone Demethylases; Lymphocyte Subsets; Methylation; Myeloblastin; Peroxidase; Phenotype; Polymorphism, Single Nucleotide; Protein Processing, Post-Translational | 2015 |
[Relationship between Arsenic (+3 Oxidation State) Methyltransferase Genetic Polymorphisms and Methylation Capacity of Inorganic Arsenic].
Topics: Arsenic; Arsenic Poisoning; Arsenicals; Cells, Cultured; Genetic Predisposition to Disease; Genotype; Hepatocytes; Humans; Methylation; Methyltransferases; Polymorphism, Single Nucleotide; Urinary Bladder Neoplasms | 2015 |
Epigenetic alterations underlying autoimmune diseases.
Topics: Acetylation; Autoimmune Diseases; DNA Methylation; Environment; Epigenesis, Genetic; Gene Expression Regulation; Gene-Environment Interaction; Genetic Predisposition to Disease; Histones; Humans; Methylation; MicroRNAs | 2016 |
Interplay between the miRNome and the epigenetic machinery: Implications in health and disease.
Topics: Animals; DNA Methylation; Epigenesis, Genetic; Genetic Predisposition to Disease; Histones; Humans; Methylation; MicroRNAs; RNA Stability; RNA, Messenger; Transcription, Genetic | 2017 |
The Histone Modification Code in the Pathogenesis of Autoimmune Diseases.
Topics: Animals; Arthritis, Rheumatoid; Autoantibodies; Autoimmune Diseases; Autoimmunity; Catalysis; Chromatin; Diabetes Mellitus, Type 1; DNA; DNA Methylation; Epigenesis, Genetic; Genetic Predisposition to Disease; Histone Code; Histones; Humans; Inflammation; Lupus Erythematosus, Systemic; Methylation; Phenotype; Phosphorylation | 2017 |
[The role of methylation processes in etiology and pathogenesis of schizophrenia].
Topics: DNA; Genetic Predisposition to Disease; Homocysteine; Humans; Methylation; Receptors, Dopamine; Schizophrenia | 2009 |
Inheritance of epigenetic aberrations (constitutional epimutations) in cancer susceptibility.
Topics: Adaptor Proteins, Signal Transducing; Agouti Signaling Protein; alpha-Thalassemia; Animals; Biomarkers, Tumor; Colorectal Neoplasms, Hereditary Nonpolyposis; DNA Mismatch Repair; Epigenesis, Genetic; Female; Gene Silencing; Genes, Tumor Suppressor; Genetic Predisposition to Disease; Humans; Linaria; Male; Methylation; Mice; MicroRNAs; MutL Protein Homolog 1; MutS Homolog 2 Protein; Neoplasms; Nuclear Proteins; Polymorphism, Single Nucleotide | 2010 |
[Hyperhomocysteinemia: an independent risk factor or a simple marker of vascular disease?. 1. Basic data].
Topics: Animals; Arteriosclerosis; Biomarkers; Cystathionine beta-Synthase; Folic Acid Deficiency; Genetic Predisposition to Disease; Homocysteine; Homocystinuria; Humans; Hyperhomocysteinemia; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Models, Biological; Nitric Oxide; Oxidative Stress; Oxidoreductases Acting on CH-NH Group Donors; Rats; Risk Factors; S-Adenosylmethionine; Signal Transduction; Thrombophilia; Vascular Diseases; Vasodilation; Vitamin B 6 Deficiency | 2003 |
Neural tube defects and folate: case far from closed.
Topics: Animals; Central Nervous System; Folic Acid; Folic Acid Deficiency; Genetic Predisposition to Disease; Homocysteine; Humans; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Neural Tube Defects | 2006 |
DNA-replication fidelity, mismatch repair and genome instability in cancer cells.
Topics: Base Sequence; Colorectal Neoplasms, Hereditary Nonpolyposis; DNA Repair; DNA Replication; DNA-Directed DNA Polymerase; Escherichia coli; Genetic Predisposition to Disease; Humans; Methylation; Microsatellite Repeats; Molecular Sequence Data; Mutation; Neoplasms | 1996 |
Homocysteine and ischaemic heart disease.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Case-Control Studies; Cohort Studies; Comorbidity; Cystathionine beta-Synthase; Female; Folic Acid; Genetic Predisposition to Disease; Homocysteine; Humans; Hyperhomocysteinemia; Male; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Myocardial Ischemia; Odds Ratio; Oxidoreductases Acting on CH-NH Group Donors; Retrospective Studies | 1999 |
Genetic modulation of homocysteinemia.
Topics: Amino Acid Substitution; Cardiovascular Diseases; Cystathionine beta-Synthase; Cysteine; Folic Acid; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Homocysteine; Homocystinuria; Humans; Hyperhomocysteinemia; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Methyltransferases; Mutation, Missense; Oxidoreductases Acting on CH-NH Group Donors; Point Mutation; Polymorphism, Genetic; Sulfur; Tetrahydrofolates | 2000 |
[Cancer predisposing and disease gene isolation by large scale genomic sequencing].
Topics: Carrier Proteins; Chromosome Mapping; Chromosomes, Human, Pair 4; Cloning, Molecular; Gene Deletion; Genetic Predisposition to Disease; Humans; Intracellular Signaling Peptides and Proteins; Keratoderma, Palmoplantar; Liver Neoplasms; Methylation; Microsatellite Repeats; Polymorphism, Single Nucleotide; Repressor Proteins; Sequence Analysis, DNA; Suppressor of Cytokine Signaling 1 Protein; Suppressor of Cytokine Signaling Proteins | 2001 |
1 trial(s) available for isomethyleugenol and Genetic Predisposition
| Article | Year |
|---|---|
Effect of 12-week of aerobic exercise on hormones and lipid profile status in adolescent girls with polycystic ovary syndrome: A study during COVID-19.
Topics: Actin Cytoskeleton; Actins; Adaptor Proteins, Signal Transducing; Adenocarcinoma; Adenosine Triphosphate; Adsorption; Adult; Africa, Eastern; Aged; Air Pollutants; Air Pollution; Air Pollution, Indoor; Alcohol Drinking; Allergens; Alzheimer Disease; Amyotrophic Lateral Sclerosis; Animals; Anti-Bacterial Agents; Antibodies; Antibodies, Immobilized; Antigen Presentation; Antigens, CD; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Antioxidants; Apoptosis; Aptamers, Nucleotide; Asthma; Asthma, Exercise-Induced; Atrophy; Autophagy; Azoospermia; Bacillus cereus; Bacterial Infections; Beclin-1; Bile Duct Neoplasms; Bile Ducts, Intrahepatic; Biofouling; Biological Monitoring; Biomarkers; Biomarkers, Tumor; Biosensing Techniques; Blastocyst; Bone Neoplasms; Bone Regeneration; Bronchoconstriction; Burkitt Lymphoma; C9orf72 Protein; Campylobacter; Campylobacter Infections; Campylobacter jejuni; Carcinogenesis; Carcinoma, Hepatocellular; Carcinoma, Pancreatic Ductal; Carcinoma, Squamous Cell; Cardiomyopathies; Caregivers; Carmine; Case-Control Studies; Catalysis; Cattle; Cause of Death; CCAAT-Enhancer-Binding Protein-alpha; CD8-Positive T-Lymphocytes; Cefepime; Cell Differentiation; Cell Line, Tumor; Cell Nucleus; Cell Transdifferentiation; Chelating Agents; Chemical and Drug Induced Liver Injury, Chronic; Chemoradiotherapy, Adjuvant; Child; Child, Preschool; China; Chlorquinaldol; Cholangiocarcinoma; Cholera; Chromatin; Clinical Trials as Topic; Cognitive Dysfunction; Cohort Studies; Colonic Neoplasms; Colorectal Neoplasms; Colorimetry; Cooking; Coordination Complexes; COVID-19; Creatinine; CRISPR-Cas Systems; Critical Care; Critical Illness; Cross-Sectional Studies; Cryopreservation; Cryoprotective Agents; Cysteine; Cytokines; Device Removal; Diet; Diet, High-Fat; Diet, Mediterranean; Dietary Supplements; Dimethyl Sulfoxide; Dipeptides; Disease Models, Animal; Dithiothreitol; DNA; DNA Repeat Expansion; DNA, Bacterial; DNA, Complementary; Dopamine; Electrochemical Techniques; Electrodes; Endocannabinoids; Environmental Exposure; Environmental Monitoring; Environmental Pollutants; Enzyme-Linked Immunosorbent Assay; Erlotinib Hydrochloride; Escherichia coli; Escherichia coli O157; Esophageal Neoplasms; Esophagitis, Peptic; Ethylene Glycol; Europium; Exanthema; Fallopian Tubes; Feces; Female; Fertilization in Vitro; Fluoresceins; Fluorescent Dyes; Follicle Stimulating Hormone; Follow-Up Studies; Food Microbiology; Forced Expiratory Volume; Forkhead Transcription Factors; Frontotemporal Dementia; G-Quadruplexes; Galactose; Gastroenteritis; Gastrointestinal Diseases; Gastrointestinal Microbiome; Gastrointestinal Neoplasms; Gastrointestinal Tract; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genital Neoplasms, Female; Genome-Wide Association Study; Genome, Viral; Genomics; Genotype; Glucose; Glutathione; Glycerol; Gold; Graphite; GTPase-Activating Proteins; Heat-Shock Proteins; Heme Oxygenase-1; Hepacivirus; Hepatitis C; Hepatocytes; Histamine; Histocompatibility Antigens Class II; Hoarseness; Hospice and Palliative Care Nursing; Humans; Hydrogen; Hydrogen Peroxide; Hydrogen Sulfide; Hydroxybenzoates; Hydroxyl Radical; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Hyperthermia, Induced; Hysteroscopy; Immunoassay; Indigo Carmine; Inflammation; Inflammatory Bowel Diseases; Insulin Resistance; Intensive Care Units; Interleukin-11; Interleukin-6; Interleukins; Iodine Radioisotopes; Iran; Iridium; Islets of Langerhans; Kinetics; Lactation; Lactobacillus; Lactobacillus plantarum; Lamins; Latin America; Lead; Lectins; Leukopenia; Ligands; Limit of Detection; Lipopolysaccharides; Lipoprotein Lipase; Liver; Liver Cirrhosis; Liver Neoplasms; Lolium; Luminescent Measurements; Luminol; Lung; Luteinizing Hormone; Macrophages; Magnetic Phenomena; Magnetic Resonance Imaging; Male; Malnutrition; Maltose; Manganese Compounds; Maternal Nutritional Physiological Phenomena; Melatonin; Metabolic Engineering; Metal Nanoparticles; Metallocenes; Metaplasia; Methicillin-Resistant Staphylococcus aureus; Methylation; Mevalonic Acid; Mexico; Mice; Mice, Inbred C57BL; Mice, Transgenic; Microbial Sensitivity Tests; Microbiota; MicroRNAs; Milk; Mitomycin; Molecular Diagnostic Techniques; Molecular Docking Simulation; Monte Carlo Method; Moringa oleifera; Multiple Sclerosis; Muscle Strength; Muscle, Skeletal; Nanocomposites; Nanotubes, Carbon; Neoadjuvant Therapy; Neoplasms; Neurodegenerative Diseases; Neurotransmitter Agents; NF-E2-Related Factor 2; Nickel; Nitrogen Dioxide; Non-alcoholic Fatty Liver Disease; Nucleic Acid Amplification Techniques; Nucleic Acid Hybridization; Nucleocapsid Proteins; Nutritional Status; Obesity; Osteogenesis; Osteosarcoma; Oxidation-Reduction; Oxides; Oxygen; Oxyquinoline; Pain; Palliative Care; Pancreatic Neoplasms; Pandemics; Particulate Matter; Peroxidase; Peroxidases; Phagocytosis; Phaseolus; Photothermal Therapy; Point-of-Care Systems; Polyethyleneimine; Polymers; Polymorphism, Single Nucleotide; Polysomnography; Postoperative Complications; Pregnancy; Pregnant Women; Prenatal Exposure Delayed Effects; Prevalence; Printing, Three-Dimensional; Probability; Probiotics; Prognosis; Prophages; Prospective Studies; Proteomics; Proto-Oncogene Proteins; Pseudomonas aeruginosa; Pseudomonas putida; Pulmonary Disease, Chronic Obstructive; Pulmonary Embolism; Pyridines; Pyrroles; Quality of Life; Quinolones; Rabbits; Rats; Rats, Sprague-Dawley; Reactive Oxygen Species; Real-Time Polymerase Chain Reaction; Receptors, Histamine; Receptors, Histamine H2; Recombinases; Rectal Neoplasms; Reperfusion Injury; Respiration; Respiratory Function Tests; Respiratory Rate; Respiratory Sounds; Retrospective Studies; rho GTP-Binding Proteins; Risk Assessment; Risk Factors; RNA; RNA, Messenger; RNA, Ribosomal, 16S; Robotic Surgical Procedures; Running; Rural Population; Saccharomyces cerevisiae; Salpingectomy; Sarcopenia; SARS-CoV-2; Seeds; Semen; Sensitivity and Specificity; Sepsis; Shock, Septic; Signal Transduction; Silicon Dioxide; Silver; Sirtuin 1; Skin Neoplasms; Sleep Apnea, Obstructive; Soil; Spain; Spectrum Analysis, Raman; Sperm Retrieval; Spermatozoa; Spirometry; Staphylococcus aureus; STAT3 Transcription Factor; Stereoisomerism; Sterilization, Tubal; Stroke Volume; Sulfadiazine; Sulfites; Superoxide Dismutase; Surface Plasmon Resonance; tau Proteins; Testis; Testosterone; Thioredoxin-Disulfide Reductase; Thyroid Neoplasms; Thyroidectomy; Trans-Activators; Transcription Factor AP-1; Treatment Outcome; Triazoles; Triclosan; Trifluridine; Tumor Microenvironment; Tumor Necrosis Factor-alpha; United States; Uracil; Vagina; Vegetables; Ventricular Function, Left; Ventricular Pressure; Vibrio cholerae; Vietnam; Virulence; Vital Capacity; Vitrification; Walking; Water; Water Pollutants, Radioactive; Whole Genome Sequencing; Wind; YAP-Signaling Proteins; Zeolites; Zinc Oxide | 2023 |
72 other study(ies) available for isomethyleugenol and Genetic Predisposition
| Article | Year |
|---|---|
25-Hydroxyvitamin D status is associated with interleukin-6 methylation in adipose tissue from patients with colorectal cancer.
Topics: Case-Control Studies; Colorectal Neoplasms; Epigenesis, Genetic; Female; Genetic Predisposition to Disease; Humans; Interleukin-6; Intra-Abdominal Fat; Male; Methylation; Middle Aged; Spain; Survival Analysis; Vitamin D | 2021 |
Mutation profile of neurodegenerative mitochondriopathy - LHON in Southern India.
Topics: Adolescent; Adult; Asian People; Child; Child, Preschool; DNA, Mitochondrial; Female; Genes, Mitochondrial; Genetic Predisposition to Disease; Genome, Mitochondrial; Humans; India; Male; Methylation; Middle Aged; Mitochondria; Mutation; Neurodegenerative Diseases; Optic Atrophy, Hereditary, Leber; Pedigree; Phylogeny; Young Adult | 2022 |
Interaction between the HIF-1α gene rs1957757 polymorphism and CpG island methylation in the promoter region is associated with the risk of anti-tuberculosis drug-induced liver injury in humans: A case-control study.
Topics: Antitubercular Agents; Case-Control Studies; Chemical and Drug Induced Liver Injury; CpG Islands; DNA Methylation; Genetic Predisposition to Disease; Humans; Hypoxia-Inducible Factor 1, alpha Subunit; Methylation; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Tuberculosis | 2022 |
The Contribution of Genetic Variation and Aberrant Methylation of Aryl Hydrocarbon Receptor Signaling Pathway Genes to Rheumatoid Arthritis.
Topics: Arthritis, Rheumatoid; Aryl Hydrocarbon Receptor Nuclear Translocator; Basic Helix-Loop-Helix Transcription Factors; Genetic Predisposition to Disease; Humans; Methylation; Polymorphism, Single Nucleotide; Receptors, Aryl Hydrocarbon; Repressor Proteins; Signal Transduction | 2022 |
Integrated analysis of probability of type 2 diabetes mellitus with polymorphisms and methylation of SLC30A8 gene: a nested case-control study.
Topics: Case-Control Studies; China; Cohort Studies; Diabetes Mellitus, Type 2; Genetic Predisposition to Disease; Genotype; Humans; Hypertension; Hypertriglyceridemia; Methylation; Polymorphism, Single Nucleotide; Probability; Zinc Transporter 8 | 2022 |
Association of promoter methylation status of NRF2 and PNPLA3 genes in alcoholic liver disease.
Topics: End Stage Liver Disease; Ethanol; Genetic Predisposition to Disease; Humans; Liver; Liver Diseases, Alcoholic; Methylation; NF-E2-Related Factor 2; Polymorphism, Single Nucleotide; Severity of Illness Index | 2022 |
Variability, Expression, and Methylation of
Topics: Case-Control Studies; Genetic Predisposition to Disease; Humans; Inflammation; Interleukin-6; Interleukin-8; Methylation; Polymorphism, Single Nucleotide; Urinary Bladder Neoplasms; Urologic Diseases | 2023 |
Epigenome-wide methylation haplotype association analysis identified HLA-DRB1, HLA-DRB5 and HLA-DQB1 as risk factors for rheumatoid arthritis.
Topics: Alleles; Arthritis, Rheumatoid; Case-Control Studies; Epigenome; Genetic Predisposition to Disease; Haplotypes; HLA-DQ beta-Chains; HLA-DRB1 Chains; HLA-DRB5 Chains; Humans; Methylation; Risk Factors | 2023 |
Genetic variants in m6A modification genes are associated with colorectal cancer risk.
Topics: Adenosine; Aged; Case-Control Studies; Cell Line, Tumor; Colorectal Neoplasms; Endonucleases; Female; Gene Expression Regulation, Neoplastic; Genetic Predisposition to Disease; Humans; Male; Methylation; Middle Aged; Polymorphism, Single Nucleotide; RNA Processing, Post-Transcriptional; RNA, Messenger | 2020 |
The Alazami Syndrome-Associated Protein LARP7 Guides U6 Small Nuclear RNA Modification and Contributes to Splicing Robustness.
Topics: Alternative Splicing; Binding Sites; Cell Line, Tumor; Child; Child, Preschool; Conserved Sequence; Developmental Disabilities; Female; Genetic Predisposition to Disease; HEK293 Cells; Humans; Male; Methylation; Middle Aged; Mutation; Nucleic Acid Conformation; Protein Binding; Protein Interaction Domains and Motifs; Ribonucleoproteins; RNA, Small Nuclear; Spliceosomes | 2020 |
Analysis of mitochondrial m1A/G RNA modification reveals links to nuclear genetic variants and associated disease processes.
Topics: Adenosine; ATP-Dependent Proteases; Cell Nucleus; Databases, Genetic; Genetic Predisposition to Disease; Genome-Wide Association Study; Guanine; Humans; Methylation; Mitochondria; Mitochondrial Proteins; Mutation, Missense; Phenotype; Polymorphism, Single Nucleotide; Quantitative Trait Loci; Ribonuclease P; RNA Processing, Post-Transcriptional; RNA-Seq; RNA, Mitochondrial; tRNA Methyltransferases | 2020 |
Hematopoietic stem cells acquire survival advantage by loss of RUNX1 methylation identified in familial leukemia.
Topics: Animals; Apoptosis; Cell Survival; Core Binding Factor Alpha 2 Subunit; Family; Female; Genetic Predisposition to Disease; Genotype; Hematopoietic Stem Cells; Humans; Leukemia; Leukemia, Myeloid, Acute; Male; Methylation; Methyltransferases; Mice; Mice, Inbred C57BL; Mice, Transgenic; Middle Aged; Mutation, Missense; Myelodysplastic Syndromes; Pedigree; Protein Processing, Post-Translational | 2020 |
Positional cloning and comprehensive mutation analysis identified a novel KDM2B mutation in a Japanese family with minor malformations, intellectual disability, and schizophrenia.
Topics: Cloning, Molecular; DNA Mutational Analysis; Exome; Exome Sequencing; F-Box Proteins; Female; Genetic Linkage; Genetic Predisposition to Disease; Haplotypes; Histone Demethylases; Histones; Humans; Intellectual Disability; Japan; Jumonji Domain-Containing Histone Demethylases; Male; Marfan Syndrome; Methylation; Mutation; Pedigree; Schizophrenia | 2021 |
Peripheral blood
Topics: BRCA1 Protein; BRCA2 Protein; Carcinoma, Ovarian Epithelial; Female; Genetic Predisposition to Disease; Germ-Line Mutation; Humans; Methylation; Ovarian Neoplasms | 2021 |
Methylation and Expression of
Topics: Adiposity; Adolescent; Alpha-Ketoglutarate-Dependent Dioxygenase FTO; Anthropometry; Blood Glucose; Blood Pressure; Child; DNA-Binding Proteins; Epigenomics; Female; Gene Expression; Genetic Predisposition to Disease; Glucose; Humans; Insulin Resistance; Leukocytes, Mononuclear; Lipid Metabolism; Lipids; Logistic Models; Male; Methylation; Pediatric Obesity; Transcriptome; Waist Circumference | 2021 |
AML1-ETO requires enhanced C/D box snoRNA/RNP formation to induce self-renewal and leukaemia.
Topics: Animals; Cell Proliferation; Cell Self Renewal; Cell Transformation, Neoplastic; Co-Repressor Proteins; Core Binding Factor Alpha 2 Subunit; DEAD-box RNA Helicases; Gene Expression Regulation, Leukemic; Genetic Predisposition to Disease; HEK293 Cells; HL-60 Cells; Humans; K562 Cells; Leukemia; Methylation; Mice, Inbred C57BL; Mice, Knockout; Myeloid-Lymphoid Leukemia Protein; Oncogene Proteins, Fusion; Phenotype; Protein Interaction Maps; Proto-Oncogene Proteins c-myc; Repressor Proteins; Ribonucleoproteins; RNA, Ribosomal; RNA, Small Nucleolar; RUNX1 Translocation Partner 1 Protein; Signal Transduction; Time Factors; Transcription Factors; U937 Cells | 2017 |
An Inframe Trinucleotide Deletion in MTRR Exon 1 is Associated with the Risk of Spina Bifida.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adult; Amino Acid Sequence; Cells, Cultured; Exons; Female; Ferredoxin-NADP Reductase; Folic Acid; Genetic Predisposition to Disease; Genotype; Homocysteine; Humans; Hyperhomocysteinemia; Infant, Newborn; Methylation; Models, Molecular; Pregnancy; Pregnancy Complications; Protein Conformation; Recombinant Proteins; Sequence Alignment; Sequence Deletion; Spinal Dysraphism; Young Adult | 2017 |
A lipodystrophy-causing lamin A mutant alters conformation and epigenetic regulation of the anti-adipogenic
Topics: Acetylation; Adipocytes; Adipogenesis; Cells, Cultured; Chromatin; Chromatin Assembly and Disassembly; Epigenesis, Genetic; Fibroblasts; Genetic Predisposition to Disease; Histones; Humans; Lamin Type A; Lipodystrophy, Familial Partial; Methylation; MicroRNAs; Mutation; Nucleic Acid Conformation; Phenotype; Promoter Regions, Genetic; Stem Cells; Structure-Activity Relationship; Up-Regulation | 2017 |
Early loss of Crebbp confers malignant stem cell properties on lymphoid progenitors.
Topics: Acetylation; Animals; Cell Proliferation; Cell Self Renewal; Cell Transformation, Neoplastic; Cells, Cultured; CREB-Binding Protein; DNA Damage; Epigenesis, Genetic; Gene Expression Regulation, Neoplastic; Genetic Predisposition to Disease; Histones; Lymphangiogenesis; Lymphoid Progenitor Cells; Lymphoma; Lymphopoiesis; Methylation; Mice; Mice, Inbred C57BL; Mice, Knockout; Mutation; Neoplastic Stem Cells; Phenotype; Signal Transduction; Time Factors; Transcription, Genetic; Tumor Suppressor Protein p53 | 2017 |
Effects of Nrf2 deficiency on arsenic metabolism in mice.
Topics: Animals; Arsenic Poisoning; Arsenites; Biotransformation; Gene Expression Regulation, Enzymologic; Genetic Predisposition to Disease; Glutathione Transferase; Liver; Methylation; Mice, Inbred C57BL; Mice, Knockout; NF-E2-Related Factor 2; Oxidative Stress; Phenotype; RNA, Messenger; Sodium Compounds; Time Factors | 2017 |
ATP Binding Cassette Subfamily A Member 2 (ABCA2) Expression and Methylation are Associated with Alzheimer's Disease.
Topics: Alzheimer Disease; Amyloid beta-Protein Precursor; ATP-Binding Cassette Transporters; Cognitive Dysfunction; CpG Islands; Databases, Genetic; Epigenesis, Genetic; Genetic Predisposition to Disease; Humans; Huntington Disease; Methylation; RNA, Messenger; Tissue Array Analysis; Up-Regulation | 2017 |
Genetic variants in the histone methylation and acetylation pathway and their risks in eight types of cancers.
Topics: Acetylation; Genetic Predisposition to Disease; Genetic Variation; Germ-Line Mutation; Histones; Humans; Methylation; Neoplasms; Polymorphism, Single Nucleotide; Signal Transduction | 2018 |
Serum homocysteine, arsenic methylation, and arsenic-induced skin lesion incidence in Bangladesh: A one-carbon metabolism candidate gene study.
Topics: Arsenic; Arsenicals; Bangladesh; Case-Control Studies; Genetic Predisposition to Disease; Homocysteine; Humans; Methylation; Polymorphism, Single Nucleotide; Skin Diseases | 2018 |
Polymorphisms of Arsenic (+3 Oxidation State) Methyltransferase and Arsenic Methylation Capacity Affect the Risk of Bladder Cancer.
Topics: Arsenic; Case-Control Studies; Female; Genetic Predisposition to Disease; Haplotypes; Humans; Logistic Models; Male; Methylation; Methyltransferases; Middle Aged; Polymorphism, Single Nucleotide; Risk; Sociological Factors; Urinary Bladder Neoplasms | 2018 |
X chromosome protects against bladder cancer in females via a
Topics: Animals; Cell Transformation, Neoplastic; Cyclin-Dependent Kinase Inhibitor p21; Disease Models, Animal; Disease Progression; Epigenesis, Genetic; Female; Gene Expression Regulation, Neoplastic; Genes, X-Linked; Genetic Predisposition to Disease; Gonadal Steroid Hormones; Histone Demethylases; Methylation; Mice; Mice, Knockout; Mutation; Prognosis; Sex Chromosomes; Sex Factors; Tumor Suppressor Protein p53; Tumor Suppressor Proteins; Urinary Bladder Neoplasms; X Chromosome | 2018 |
The Impact of Methylenetetrahydrofolate Reductase (MTHFR) Sperm Methylation and Variants on Semen Parameters and the Chance of Recurrent Pregnancy Loss in the Couple.
Topics: Abortion, Habitual; Adult; Female; Genetic Predisposition to Disease; Humans; Male; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Polymorphism, Single Nucleotide; Pregnancy; Semen Analysis; Spermatozoa | 2018 |
Methylation and MicroRNA Profiling to Understand Racial Disparities of Prostate Cancer.
Topics: Biomarkers, Tumor; Cell Transformation, Neoplastic; DNA Methylation; Epigenesis, Genetic; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Genetic Predisposition to Disease; High-Throughput Nucleotide Sequencing; Humans; Incidence; Male; Methylation; MicroRNAs; Neoplasms; Population Groups; Prevalence; Risk Factors | 2018 |
Synergistic triad epistasis of epigenetic H3K27me modifier genes, EZH2, KDM6A, and KDM6B, in gastric cancer susceptibility.
Topics: Adult; Aged; Aged, 80 and over; Biomarkers, Tumor; Case-Control Studies; Enhancer of Zeste Homolog 2 Protein; Epigenesis, Genetic; Epistasis, Genetic; Female; Follow-Up Studies; Gene Expression Regulation, Neoplastic; Genes, Modifier; Genetic Predisposition to Disease; Histone Demethylases; Histones; Humans; Jumonji Domain-Containing Histone Demethylases; Male; Methylation; Middle Aged; Nuclear Proteins; Polymorphism, Single Nucleotide; Prognosis; Retrospective Studies; Stomach Neoplasms | 2019 |
Intergenerational inheritance of high fat diet-induced cardiac lipotoxicity in Drosophila.
Topics: Animals; Animals, Genetically Modified; Cardiomyopathies; Diet, High-Fat; Disease Models, Animal; Drosophila; Drosophila Proteins; Female; Genetic Predisposition to Disease; Histones; Humans; Lipase; Lipid Metabolism; Male; Methylation; Myocardium; Obesity; Positive Transcriptional Elongation Factor B; Triglycerides | 2019 |
IRF5 promoter methylation as a new potential marker of rheumatoid arthritis.
Topics: Adult; Aged; Arthritis, Rheumatoid; Biomarkers; Case-Control Studies; Female; Genetic Predisposition to Disease; Genotype; Humans; Interferon Regulatory Factors; Male; Methylation; Middle Aged; Polymorphism, Single Nucleotide; Virulence Factors | 2019 |
Differential methylation pattern of xenobiotic metabolizing genes and susceptibility to Balkan endemic nephropathy, in a cohort of Romanian patients.
Topics: Aged; Aged, 80 and over; Arylamine N-Acetyltransferase; Balkan Nephropathy; Cohort Studies; Cytochrome P-450 CYP1A1; Cytochrome P-450 CYP1A2; Female; Genetic Predisposition to Disease; Glutathione Transferase; Humans; Isoenzymes; Male; Methylation; Middle Aged; NAD(P)H Dehydrogenase (Quinone); Pilot Projects; Renal Insufficiency, Chronic; Romania; Xenobiotics | 2020 |
Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents.
Topics: Adaptor Proteins, Signal Transducing; Adenosine Triphosphatases; Adult; Antineoplastic Agents, Alkylating; Biomarkers, Tumor; Brain Neoplasms; Caco-2 Cells; Case-Control Studies; Colorectal Neoplasms; Colorectal Neoplasms, Hereditary Nonpolyposis; DNA Mutational Analysis; DNA Repair Enzymes; DNA-Binding Proteins; Drug Resistance, Neoplasm; Female; Genetic Predisposition to Disease; Genetic Testing; Germ-Line Mutation; HCT116 Cells; Heredity; Humans; Lymphocytes; Male; Methylation; Microsatellite Instability; Mismatch Repair Endonuclease PMS2; Multiplex Polymerase Chain Reaction; MutL Protein Homolog 1; MutS Homolog 2 Protein; Neoplastic Syndromes, Hereditary; Nuclear Proteins; Phenotype; Predictive Value of Tests; Reproducibility of Results; Transfection; Young Adult | 2015 |
Mutant IDH1 Dysregulates the Differentiation of Mesenchymal Stem Cells in Association with Gene-Specific Histone Modifications to Cartilage- and Bone-Related Genes.
Topics: Bone Neoplasms; Cell Differentiation; Cells, Cultured; Chondrosarcoma; Enchondromatosis; Epigenesis, Genetic; Gene Expression Regulation, Neoplastic; Genetic Association Studies; Genetic Predisposition to Disease; Histones; Humans; Isocitrate Dehydrogenase; Mesenchymal Stem Cells; Methylation; Mutation, Missense; Osteosarcoma; Protein Processing, Post-Translational | 2015 |
Implication of a Chromosome 15q15.2 Locus in Regulating UBR1 and Predisposing Smokers to MGMT Methylation in Lung.
Topics: Base Sequence; Chromosomes, Human, Pair 15; DNA Methylation; DNA Modification Methylases; DNA Repair Enzymes; Epithelial Cells; Female; Gene Expression Regulation; Genetic Predisposition to Disease; Genome-Wide Association Study; Guanine; Humans; Longitudinal Studies; Lung Neoplasms; Male; Methylation; Methylnitrosourea; Molecular Sequence Data; Polymorphism, Single Nucleotide; Smoking; Tumor Suppressor Proteins; Ubiquitin-Protein Ligases | 2015 |
Linkage Analysis of Urine Arsenic Species Patterns in the Strong Heart Family Study.
Topics: Adult; Arizona; Arsenic Poisoning; Arsenicals; Biomarkers; Biotransformation; Cohort Studies; Female; Genetic Linkage; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; Linkage Disequilibrium; Logistic Models; Male; Methylation; Methyltransferases; Microsatellite Repeats; Midwestern United States; Polymorphism, Single Nucleotide; Principal Component Analysis; Toxicokinetics | 2015 |
Polymorphisms of human 8-oxoguanine DNA glycosylase 1 and 8-hydroxydeoxyguanosine increase susceptibility to arsenic methylation capacity-related urothelial carcinoma.
Topics: 8-Hydroxy-2'-Deoxyguanosine; Arsenic; Carcinogens, Environmental; Carcinoma; Case-Control Studies; Data Interpretation, Statistical; Deoxyguanosine; DNA Glycosylases; Genetic Predisposition to Disease; Genotype; Humans; Methylation; Polymorphism, Single Nucleotide; Risk Factors; Urologic Neoplasms | 2016 |
Partitioning heritability by functional annotation using genome-wide association summary statistics.
Topics: Algorithms; Computer Simulation; Disease; Female; Gene Frequency; Genetic Predisposition to Disease; Genome-Wide Association Study; Histones; Humans; Inheritance Patterns; Lysine; Male; Methylation; Models, Genetic; Polymorphism, Single Nucleotide | 2015 |
T Follicular Helper Cell-Dependent Clearance of a Persistent Virus Infection Requires T Cell Expression of the Histone Demethylase UTX.
Topics: Animals; Antibodies, Viral; Cell Differentiation; Female; Gene Dosage; Gene Expression Regulation; Genetic Predisposition to Disease; Histone Demethylases; Histones; Humans; Immunologic Memory; Interleukin-6 Receptor alpha Subunit; Lymphocyte Cooperation; Lymphocytic Choriomeningitis; Lymphocytic choriomeningitis virus; Methylation; Mice; Models, Immunological; Nuclear Proteins; Otitis Media; Protein Processing, Post-Translational; Receptors, CXCR5; Species Specificity; T-Lymphocyte Subsets; T-Lymphocytes, Helper-Inducer; Transcription, Genetic; Turner Syndrome; Viremia; Virulence; X Chromosome Inactivation | 2015 |
Mutation Analysis of H3F3A and H3F3B as a Diagnostic Tool for Giant Cell Tumor of Bone and Chondroblastoma.
Topics: Adolescent; Adult; Aged; Biomarkers, Tumor; Biopsy; Bone Neoplasms; Chondroblastoma; Diagnosis, Differential; DNA Helicases; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Giant Cell Tumor of Bone; Histones; Humans; Immunohistochemistry; Isocitrate Dehydrogenase; Male; Methylation; Middle Aged; Mutation; Nuclear Proteins; Phenotype; Predictive Value of Tests; Tissue Array Analysis; X-linked Nuclear Protein; Young Adult | 2015 |
Correlation of CpG Island Methylation of the Cytochrome P450 2E1/2D6 Genes with Liver Injury Induced by Anti-Tuberculosis Drugs: A Nested Case-Control Study.
Topics: Adult; Aged; Antitubercular Agents; Asian People; Case-Control Studies; Chemical and Drug Induced Liver Injury; CpG Islands; Cytochrome P-450 CYP2D6; Cytochrome P-450 CYP2E1; DNA Methylation; Female; Genetic Predisposition to Disease; Humans; Male; Methylation; Middle Aged; Odds Ratio; Polymorphism, Genetic; Risk; Tuberculosis; Young Adult | 2016 |
Genetic polymorphisms of PPAR gamma, arsenic methylation capacity and breast cancer risk in Mexican women.
Topics: Adult; Aged; Arsenic; Arsenicals; Breast Neoplasms; Carrier Proteins; Case-Control Studies; Chromatography, High Pressure Liquid; Environmental Exposure; Female; Genetic Predisposition to Disease; Humans; Mass Spectrometry; Methylation; Middle Aged; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; PPAR gamma; Risk; RNA-Binding Proteins; Young Adult | 2016 |
Decreased Methylation Level of H3K27me3 Increases Seizure Susceptibility.
Topics: Animals; Cell Line; Cells, Cultured; Female; Genetic Predisposition to Disease; Hyperthermia, Induced; Jumonji Domain-Containing Histone Demethylases; Male; Methylation; Rats; Rats, Sprague-Dawley; Seizures | 2017 |
Methylation and QTDT analysis of the 5-HT2A receptor 102C allele: analysis of suicidality in major psychosis.
Topics: Adult; Alleles; Bipolar Disorder; Female; Genetic Predisposition to Disease; Humans; Leukocytes; Male; Methylation; Polymerase Chain Reaction; Polymorphism, Genetic; Prefrontal Cortex; Psychotic Disorders; Quantitative Trait, Heritable; Receptor, Serotonin, 5-HT2A; Schizophrenia; Schizophrenic Psychology; Suicide | 2009 |
Genetic and epigenetic analysis of SSAT gene dysregulation in suicidal behavior.
Topics: Acetyltransferases; Adolescent; Adult; Aged; Aged, 80 and over; Down-Regulation; Female; Gene Expression Regulation; Genetic Predisposition to Disease; Humans; Male; Methylation; Middle Aged; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Prefrontal Cortex; Promoter Regions, Genetic; RNA, Messenger; Self-Injurious Behavior; Suicide; Young Adult | 2009 |
MHC Class II alleles in ulcerative colitis-associated colorectal cancer.
Topics: Adult; Aged; Aged, 80 and over; Case-Control Studies; Colitis, Ulcerative; Colorectal Neoplasms; Female; Gene Frequency; Genes, MHC Class II; Genetic Predisposition to Disease; Genotype; HLA-DQ Antigens; HLA-DR Antigens; HLA-DR1 Antigen; HLA-DR7 Antigen; Humans; Immunohistochemistry; Logistic Models; Male; Methylation; Middle Aged; Nuclear Proteins; Polymerase Chain Reaction; Risk; Trans-Activators | 2009 |
The presence of RNA polymerase II, active or stalled, predicts epigenetic fate of promoter CpG islands.
Topics: Cell Line; Cell Line, Tumor; Chromatin Immunoprecipitation; CpG Islands; DNA Methylation; Female; Genetic Predisposition to Disease; Histones; Humans; Lysine; Male; Methylation; Oligonucleotide Array Sequence Analysis; Promoter Regions, Genetic; Prostatic Neoplasms; Protein Binding; RNA Polymerase II; Transcription, Genetic | 2009 |
Polymorphisms in arsenic metabolism genes, urinary arsenic methylation profile and cancer.
Topics: Arsenic; Arsenic Poisoning; Chromatography, High Pressure Liquid; Female; Genetic Predisposition to Disease; Humans; Incidence; Male; Methylation; Neoplasms; Polymorphism, Single Nucleotide; Taiwan; Water Pollutants, Chemical | 2009 |
Methylation status of genes in non-neoplastic mucosa from patients with ulcerative colitis-associated colorectal cancer.
Topics: Adaptor Proteins, Signal Transducing; Adult; Aged; Aged, 80 and over; Biomarkers, Tumor; Case-Control Studies; Chi-Square Distribution; Colitis, Ulcerative; Colorectal Neoplasms; Core Binding Factor Alpha 3 Subunit; Cyclooxygenase 2; Disease Progression; Female; Genetic Predisposition to Disease; Humans; Intestinal Mucosa; Logistic Models; Male; Methylation; Middle Aged; Nerve Tissue Proteins; Polymerase Chain Reaction; Precancerous Conditions; Risk Factors | 2010 |
LINE-1 methylation is inherited in familial testicular cancer kindreds.
Topics: Adult; Base Sequence; DNA; DNA Methylation; DNA Primers; Family; Genetic Predisposition to Disease; Humans; Lithiasis; Long Interspersed Nucleotide Elements; Male; Methylation; Middle Aged; Polymerase Chain Reaction; Risk Assessment; Testicular Neoplasms | 2010 |
Gene expression correlation analysis predicts involvement of high- and low-confidence risk genes in different stages of prostate carcinogenesis.
Topics: DNA Methylation; Genetic Predisposition to Disease; Histones; Humans; Male; Metaplasia; Methylation; Neoplasm Staging; Oligonucleotide Array Sequence Analysis; Prostate; Prostatic Neoplasms; Receptors, Androgen; Receptors, Estrogen; Risk Assessment; Stem Cells | 2010 |
Gene polymorphisms of glutathione S-transferase omega 1 and 2, urinary arsenic methylation profile and urothelial carcinoma.
Topics: Arsenic; Arsenicals; Carcinoma; Environmental Pollutants; Female; Genetic Predisposition to Disease; Glutathione Transferase; Humans; Male; Methylation; Middle Aged; Polymorphism, Single Nucleotide; Risk Assessment; Urologic Neoplasms; Urothelium | 2011 |
Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus.
Topics: Adult; Algorithms; Animals; Base Sequence; Bayes Theorem; CpG Islands; Diabetes Mellitus, Type 2; DNA Methylation; Epigenomics; Evolution, Molecular; Female; Gene Expression Profiling; Gene Frequency; Genetic Predisposition to Disease; Genotype; Haplotypes; Histones; Humans; Methylation; Obesity; Oligonucleotide Array Sequence Analysis; Polymorphism, Single Nucleotide; Sequence Analysis, DNA | 2010 |
Myeloperoxidase immunohistochemistry as a measure of disease activity in ulcerative colitis: association with ulcerative colitis-colorectal cancer, tumor necrosis factor polymorphism and RUNX3 methylation.
Topics: Adult; Aged; Aged, 80 and over; Case-Control Studies; Colitis, Ulcerative; Colorectal Neoplasms; Core Binding Factor Alpha 3 Subunit; Female; Genetic Predisposition to Disease; Humans; Immunohistochemistry; Male; Methylation; Middle Aged; Peroxidase; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Risk; Severity of Illness Index; Tumor Necrosis Factor-alpha | 2012 |
Evidence of constitutional MLH1 epimutation associated to transgenerational inheritance of cancer susceptibility.
Topics: Adaptor Proteins, Signal Transducing; Adult; Aged; Child; Cohort Studies; Colorectal Neoplasms, Hereditary Nonpolyposis; DNA Mismatch Repair; Epigenesis, Genetic; Female; Genetic Predisposition to Disease; Genetic Testing; Germ-Line Mutation; Heredity; Heterozygote; Humans; Male; Methylation; Middle Aged; MutL Protein Homolog 1; MutS Homolog 2 Protein; Nuclear Proteins; Pedigree; Proto-Oncogene Proteins B-raf; Sequence Analysis, DNA | 2012 |
Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants.
Topics: Bipolar Disorder; Cerebellum; DNA Methylation; Gene Expression Regulation; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; Methylation; Polymorphism, Single Nucleotide; Quantitative Trait Loci | 2013 |
Pin1 contribution to Alzheimer's disease: transcriptional and epigenetic mechanisms in patients with late-onset Alzheimer's disease.
Topics: Aged; Aged, 80 and over; Alzheimer Disease; Analysis of Variance; Apolipoprotein E4; Case-Control Studies; Epigenesis, Genetic; Female; Genetic Predisposition to Disease; Humans; Italy; Leukocytes, Mononuclear; Male; Methylation; NIMA-Interacting Peptidylprolyl Isomerase; Peptidylprolyl Isomerase; Phosphorylation; Promoter Regions, Genetic; Serine | 2012 |
Arsenic methylation, GSTO1 polymorphisms, and metabolic syndrome in an arseniasis endemic area of southwestern Taiwan.
Topics: Adult; Arsenic; Arsenic Poisoning; Asian People; Endemic Diseases; Female; Genetic Predisposition to Disease; Glutathione Transferase; Humans; Logistic Models; Male; Metabolic Syndrome; Methylation; Methyltransferases; Middle Aged; Polymorphism, Genetic; Taiwan | 2012 |
Genome-wide profiling of multiple histone methylations in olfactory cells: further implications for cellular susceptibility to oxidative stress in schizophrenia.
Topics: Case-Control Studies; Epigenesis, Genetic; Female; Gene Expression Profiling; Genetic Predisposition to Disease; Genome-Wide Association Study; Histones; Humans; Male; Methylation; Olfactory Mucosa; Oxidative Stress; Schizophrenia; Signal Transduction; Tissue Array Analysis | 2013 |
Aberrant patterns of H3K4 and H3K27 histone lysine methylation occur across subgroups in medulloblastoma.
Topics: Base Sequence; Cerebellar Neoplasms; Cohort Studies; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Genome; Histone Demethylases; Histone Methyltransferases; Histone-Lysine N-Methyltransferase; Humans; Lysine; Male; Medulloblastoma; Methylation; Mutation; Neoplasm Proteins; Nuclear Proteins; Polymorphism, Single Nucleotide | 2013 |
Pet keeping and tobacco exposure influence CD14 methylation in childhood.
Topics: Allergens; Animals; Asthma; Cats; Child; Child, Preschool; Dogs; Epigenomics; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Humans; Hypersensitivity, Immediate; Lipopolysaccharide Receptors; Male; Methylation; Pets; Tobacco Smoke Pollution | 2012 |
Identification of a synthetic muramyl peptide derivative with enhanced Nod2 stimulatory capacity.
Topics: Acetylmuramyl-Alanyl-Isoglutamine; Animals; Crohn Disease; Dendritic Cells; Enzyme Activation; Genetic Predisposition to Disease; HEK293 Cells; Humans; Interleukin-6; Macrophages; Methylation; Mice; Mice, Inbred C57BL; Mice, Knockout; Mutation; Nod2 Signaling Adaptor Protein; Polymorphism, Genetic; Protein Engineering; Signal Transduction; Transgenes | 2013 |
The food mutagen 2-amino-9H-pyrido[2,3-b]indole (AalphaC) but not its methylated form (MeAalphaC) increases intestinal tumorigenesis in neonatally exposed multiple intestinal neoplasia mice.
Topics: Animals; Animals, Newborn; Carbolines; Female; Food; Genes, APC; Genetic Predisposition to Disease; Intestinal Neoplasms; Male; Methylation; Mice; Mice, Inbred C57BL; Mutagens | 2002 |
Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Female; Ferredoxin-NADP Reductase; Genetic Predisposition to Disease; Genotype; Humans; Infant, Newborn; Male; Methylation; Neural Tube Defects; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length | 2003 |
Quantitative detection of methylated SOCS-1 , a tumor suppressor gene, by a modified protocol of quantitative real time methylation-specific PCR using SYBR green and its use in early gastric cancer detection.
Topics: Adult; Benzothiazoles; Biomarkers, Tumor; Diamines; DNA Methylation; Female; Genes, Tumor Suppressor; Genetic Predisposition to Disease; Genetic Testing; Humans; Intracellular Signaling Peptides and Proteins; Male; Methylation; Middle Aged; Organic Chemicals; Polymerase Chain Reaction; Quinolines; Repressor Proteins; Reproducibility of Results; Sensitivity and Specificity; Stomach Neoplasms; Suppressor of Cytokine Signaling 1 Protein; Suppressor of Cytokine Signaling Proteins | 2004 |
Genetic polymorphisms in MTHFR 677 and 1298, GSTM1 and T1, and metabolism of arsenic.
Topics: Adult; Aged; Aged, 80 and over; Argentina; Arsenic; Arsenicals; Case-Control Studies; Environmental Monitoring; Environmental Pollutants; Epidemiological Monitoring; Female; Genetic Predisposition to Disease; Glutathione Transferase; Humans; Male; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Polymorphism, Genetic; Urinary Bladder Neoplasms | 2007 |
Methylation-associated PHOX2B gene silencing is a rare event in human neuroblastoma.
Topics: Cell Line, Tumor; DNA Mutational Analysis; Female; Gene Frequency; Gene Silencing; Genetic Predisposition to Disease; Homeodomain Proteins; Humans; Loss of Heterozygosity; Male; Methylation; Neuroblastoma; Pedigree; Transcription Factors | 2007 |
BRCA1 promoter methylation in peripheral blood DNA of mutation negative familial breast cancer patients with a BRCA1 tumour phenotype.
Topics: Adult; Alleles; BRCA1 Protein; Breast Neoplasms; Disease Susceptibility; DNA; Female; Genetic Predisposition to Disease; Humans; Methylation; Middle Aged; Mutation; Phenotype; Promoter Regions, Genetic | 2008 |
Alterations in genes encoding sarcoplasmic-endoplasmic reticulum Ca(2+) pumps in association with head and neck squamous cell carcinoma.
Topics: Base Sequence; Carcinoma, Squamous Cell; Genetic Predisposition to Disease; Genetic Variation; Germ-Line Mutation; Head and Neck Neoplasms; Humans; Methylation; Molecular Sequence Data; Promoter Regions, Genetic; Sarcoplasmic Reticulum Calcium-Transporting ATPases | 2008 |
Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer.
Topics: Animals; Base Composition; Base Sequence; Chimera; DNA; DNA Repair; DNA-Binding Proteins; Fungal Proteins; Genetic Predisposition to Disease; Lymphoma; Methylation; Methylnitronitrosoguanidine; Mice; Mice, Mutant Strains; Molecular Sequence Data; Mutagenesis; MutS Homolog 2 Protein; Oligodeoxyribonucleotides; Polymerase Chain Reaction; Recombination, Genetic; Stem Cells | 1995 |
Heterogenous point mutations in the BRCA1 breast cancer susceptibility gene occur in high frequency at the site of homonucleotide tracts, short repeats and methylatable CpG/CpNpG motifs.
Topics: Base Composition; Base Sequence; BRCA1 Protein; Breast Neoplasms; CpG Islands; DNA Transposable Elements; Female; Genetic Predisposition to Disease; Humans; Methylation; Microsatellite Repeats; Molecular Sequence Data; Mutagenesis; Mutation; Neoplasm Proteins; Oligodeoxyribonucleotides; Point Mutation; Sequence Deletion; Transcription Factors; Trinucleotide Repeats | 1996 |
Is the oral methionine loading test insensitive to the remethylation pathway of homocysteine?
Topics: Artifacts; Folic Acid Deficiency; Genetic Predisposition to Disease; Genotype; Homocysteine; Humans; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Oxidoreductases Acting on CH-NH Group Donors; Point Mutation; Reproducibility of Results; Risk Factors; Thrombophilia | 1999 |
[Hypomethylation and multiple sclerosis, the susceptibility factor?].
Topics: Autoimmune Diseases; Azathioprine; Genetic Predisposition to Disease; Humans; Immunosuppressive Agents; Inflammatory Bowel Diseases; Methylation; Methyltransferases; Multiple Sclerosis; Phenotype; Polymorphism, Genetic; Purines; Spain | 2002 |