Compounds > histidine
Page last updated: 2024-08-17

histidine and Genetic Predisposition

histidine has been researched along with Genetic Predisposition in 69 studies

Research

Studies (69)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's44 (63.77)29.6817
2010's24 (34.78)24.3611
2020's1 (1.45)2.80

Authors

AuthorsStudies
Liu, JL; Msafiri Makene, A1
Chen, QY; Fu, DJ; Li, J; Liu, ZM; Mao, TT; Peng, YJ; She, WT1
Chang, CW; Cohn, DE; Cosgrove, CM; Dama, P; Gillespie, JL; Goodfellow, PJ; Mutch, DG; O'Hern, MJ; Rush, CM; Selvendiran, K; Shakya, R; Smith, B; Song, JW; Stein, ME; Walker, CJ; Zingarelli, RA1
Gomes, J; Padhi, AK1
Alechine, E; Caputo, M; Corach, D; Irisarri, M; Micheli, FE; Pellene, LA; Perandones, C; Roca, CU1
Abdi, Z; Adamson, G; Barnes, J; Beck, JA; Blair, M; Campbell, T; Clegg, SL; Collinge, J; Crutch, SJ; Druyeh, R; Fox, NC; Gambetti, P; Guerreiro, RJ; Harper, L; Kenny, J; Kretzschmar, H; Leung, KK; Lowe, J; Mahoney, CJ; Mead, S; Nicholas, JM; Ponto, C; Rohrer, JD; Rossor, MN; Rowe, JB; Schott, JM; Slattery, CF; Uphill, J; Warren, JD; Zerr, I1
Agúndez, JA; Alonso-Navarro, H; Annesi, G; Berg, D; Brighina, L; Clarimon, J; Coria, F; Ezquerra, M; García-Martin, E; Gironell, A; Jiménez-Jiménez, FJ; Krüger, R; Lin, JJ; Lorenzo, E; Lorenzo-Betancor, O; Marti, MJ; Mielke, C; Ortega-Cubero, S; Pastor, MA; Pastor, P; Ross, OA; Sharma, M; Wszolek, ZK; Wurster, I; Yueh, KC1
Bacares, R; Figueiredo, J; Melo, S; Ruggeri, J; Seruca, R; Shah, MA; Simões-Correia, J; Somar, J; Xiao, A; Zhang, L1
Ehmen, C; Horstmann, RD; Meyer, CG; Owusu-Dabo, E; Reiling, N; Ruge, G; Thye, T1
Amador, MA; de Almeida Ferreira, J; de Mello, WA; Ferreira, DL; Maestri, A; Santos, SE; Sortica, VA; Sousa, RC1
Fuhs, SR; Hunter, T; Li, Z; Panda, S; Skolnik, EY; Srivastava, S; Vaeth, M1
Abad Gonzalez, E; Carija, A; Carloni, P; Fernández, CO; Foguel, D; Fonseca-Ornelas, L; Gerhardt, E; Lopes da Fonseca, T; Masaracchia, C; Milosevic, I; Outeiro, TF; Pinho, R; Rossetti, G; Sant'Anna, R; Szegö, ÉM; Ventura, S; Villar-Piqué, A; Zweckstetter, M1
Clish, CB; Coresh, J; Fox, CS; Gerszten, RE; Hwang, SJ; Larson, MG; Levy, D; Li, M; McMahon, GM; O'Donnell, CJ; Rhee, EP; Tin, A; Yang, Q; Young, JH1
Borggraefe, I; Fischer, H; Garavaglia, B; Gasser, T; Grundmann, K; Kamm, C; Klein, C; Kullmann, S; Kupsch, A; Lobsien, E; Nardocci, N; Schrader, C; Sharma, M1
Feng, JB; Li, LH; Li, WX; Li, XP; Pan, HF; Ye, DQ; Yuan, H1
Inoue, N; Kasahara, M; Miyaishi, A; Osawa, K; Osawa, Y; Shimada, E; Tabuchi, Y; Takahashi, J; Tanaka, K; Tsutou, A; Yamamoto, M; Yoshida, K1
Ankarali, HC; Basar, MM; Gunel-Ozcan, A; Kisa, U1
Averbukh, E; Axer-Siegel, R; Banin, E; Chowers, I; Cohen, Y; Goldenberg-Cohen, N; Hemo, I; Lederman, M; Lichtinger, A; Meir, T; Pollack, A; Vicuna-Kojchen, J; Weinstein, O1
Bonifati, V; Farrer, MJ; Ferreira, JJ; Griffith, A; Haugarvoll, K; Kachergus, J; Latsoudis, H; Lin, CH; Plaitakis, A; Ross, OA; Sampaio, C; Spanaki, C; Wu, RM; Zabetian, CP1
Acutis, PL; Agrimi, U; Bona, C; Caramelli, M; Casalinuovo, F; Casalone, C; Colussi, S; Di Sarno, A; Lorenzetti, R; Maniaci, MG; Maurella, C; Mazza, M; Nonno, R; Ru, G; Troiano, P; Vaccari, G; Zuccon, F1
Chen, Y; Fang, Y; He, Z; Peng, B; Shen, Y; Wu, L; Xu, Q1
Bertolacini, CD; Ribeiro-Bicudo, LA; Richieri-Costa, A1
Donglan, S; Na, W; Rongmiao, Z; Yan, L; Yanan, D; Zhifeng, C1
Berhane, N; Hosseini, SA; Kler, R; Kuttiat, V; Mehedi, SA; Sobti, RC; Wanchu, A1
Abicht, A; Christen, HJ; Durmus, H; Hietala, M; Krabetz, K; Lochmüller, H; Müller, JS; Pihko, H; Rodolico, C; Schara, U; Schreiber, G; Talim, B; Topaloglu, H; Voss, W1
Amano, A; Ezekwudo, D; Kamat, A; Panchanathan, R; Selvaraj, P; Shashidharamurthy, R; Zhang, F; Zhu, C1
Chibani, JB; Daimi, H; Denden, S; Hassine, M; Khelil, AH; Knani, J; Lakhdar, R; Leban, N; Lefranc, G1
Huang, B; Mai, R; Zhang, G1
Bahman, I; Bhatia, KP; Brüggemann, N; Erogullari, A; Kaiser, FJ; Klein, C; Lohmann, K; Najmabadi, H; Osmanovic, A; Ramirez, A; Schneider, SA; Shafa, MA; Shafiee, K; Winkler, S1
Burgunder, JM; Chen, Y; Huang, R; Shang, HF; Song, W1
Hans, VM; Mehta, DS1
Breman, C; Delanghe, J; Gahutu, JB; Masaisa, F; Mukiibi, J; Philippé, J1
Ando, F; Hibi, T; Kato, K; Nakashima, T; Nishio, N; Otake, H; Shimokata, H; Sone, M; Sugiura, S; Tagaya, M; Teranishi, M; Uchida, Y; Yoshida, T1
Bauer, M; Borte, M; Gräbsch, C; Heinrich, J; Herbarth, O; Illig, T; Klopp, N; Krämer, U; Lehmann, I; Röder, S; Schaaf, B; Schlink, U; von Berg, A1
Boonsuwan, T; Kitkumthorn, N; Mutirangura, A; Yanatatsaneejit, P1
Lin, CS; Su, T; Suzui, M; Wang, L; Weinstein, IB; Xing, WQ1
Ammar, N; Amouri, R; Barisić, N; Ceuterick, C; De Jonghe, P; Hentati, F; Martin, JJ; Merlini, L; Nelis, E; Timmerman, V1
Maurer, P; Nitsche, DP; Paulsson, M; Spitznagel, L; Zaucke, F1
Chen, ZF; Guo, W; Jin, X; Kuang, G; Li, Y; Wang, N; Wang, R; Wang, SJ; Wei, LZ; Wen, DG; Zhang, JH1
Murashima, YL; Nakagawa, Y; Nakano, K; Tanaka, K; Watanabe, Y; Yawata, I1
Abe, H; Asaoka, R; Fujimaki, T; Fukuchi, T; Funayama, T; Hotta, Y; Ideta, H; Ishikawa, K; Iwata, T; Kanamoto, T; Kimura, I; Kudoh, J; Kurosaka, D; Mashima, Y; Mishima, H; Murakami, A; Nakamoto, K; Ohtake, Y; Shimada, N; Shimizu, N; Suzuki, K; Tanihara, H; Tanino, T; Yasuda, N1
Balasubramanian, SP; Bhattacharyya, NP; Cox, A; Healey, CS; MacPherson, G; Meuth, M; Pharoah, PD; Ponder, BA; Reed, MW; Teare, MD1
Beaulieu, JM; Burch, LH; Caron, MG; Gainetdinov, RR; Krishnan, KR; Schwartz, DA; Sotnikova, TD; Williams, RB; Zhang, X1
Brosnan, MJ; Dominiczak, AF; Graham, D; Hamilton, CA; Hanlon, N; Lee, WK; Mathers, J; McBride, MW; McLellan, LI; Miller, WH; Polke, JM1
Abel, KJ; Edwards, AO; Farrer, LA; Manning, A; Panhuysen, C; Ritter, R1
Barnstable, C; Bracken, MB; Chew, EY; Ferris, FL; Haynes, C; Henning, AK; Hoh, J; Klein, RJ; Mane, SM; Mayne, ST; Ott, J; Sackler, RS; SanGiovanni, JP; Tsai, JY; Zeiss, C1
Daiger, SP1
Aschauer, HN; Basile, VS; Cavallaro, R; Chong, SA; Heresco-Levy, U; Kennedy, JL; Lerer, B; Macciardi, F; Meltzer, HY; Scharfetter, J; Segman, RH; Strous, R; Tan, EC; Verga, M1
Bermejo, JL; Bugert, P; Burwinkel, B; Frank, B; Hemminki, K; Klaes, R; Schmutzler, RK; Wappenschmidt, B1
Heils, A; Hempelmann, A; Lenzen, KP; Lorenz, S; Sander, T1
Bhatnagar, P; Brahmachari, SK; Chauhan, C; Gupta, S; Jain, S; Janardhan Reddy, YC; Kubendran, S; Kukreti, R; Tripathi, S1
Abraham, SC; Adams, LA; Angulo, P; Brandhagen, D; Torgerson, H1
Bergen, AA; de Jong, PT; Despriet, DD; Hofman, A; Kardys, I; Klaver, CC; Oostra, BA; Uitterlinden, AG; Van Duijn, CM; Witteman, JC1
Fingert, JH; Grassi, MA; Kawase, K; Mullins, RF; Ritch, R; Roos, BR; Scheetz, TE; Shire, AM; Stone, EM; West, SK1
Joshi, MB; Rajshekher, GP; Reddy, AG; Singh, L; Thangaraj, K; Vanniarajan, A1
Latsoudis, H; Plaitakis, A; Spanaki, C1
Dorak, MT1
Njajou, OT; Sinke, RJ; Sutedja, NA; Van den Berg, LH; Van der Linden, MW; Van der Schouw, YT; Van Duijn, CM; Van Vught, PW; Veldink, JH; Wokke, JH1
Böcker, U; Haas, SL; Ruether, A; Schreiber, S; Singer, MV1
DeWan, A; Hoh, J; Iwata, T; Minami, M; Mizota, A; Obazawa, M; Okamoto, H; Saito, Y; Sakamoto, R; Takagi, I; Tanaka, M; Yoshida, T; Zhang, H1
Asaka, T; Hirohata, M; Komai, K; Motozaki, Y; Ono, K; Yamada, M1
Casali, C; Di Lorenzo, C; Di Lorenzo, G; Ghiotto, N; Grieco, GS; Guaschino, E; Nappi, G; Perrotta, A; Pierelli, F; Rengo, C; Sances, G; Santorelli, FM; Siracusano, A; Troisi, A1
Altshuler, D; Bell, DW; Daly, MB; Freedman, ML; Garber, JE; Godwin, AK; Haber, DA; Haiman, CA; Harris, PL; Haserlat, SM; Henderson, BE; Kim, SH; Le Marchand, L; Niendorf, KB; Olopade, OI; Schiripo, TA; Sgroi, DC; Smith, MR; Wahrer, DC1
Andersson, ME; Andreasen, N; Blennow, K; Bogdanovic, N; Gustafson, DR; Landgren, S; Minthon, L; Palmér, MS; Skoog, I; Thelle, DS; Wallin, A; Zetterberg, H; Zetterberg, M1
Abderrahim, H; Abelson, AK; Alarcón-Riquelme, ME; Barizzone, N; Barrizzone, N; D'Alfonso, S; Danieli, MG; González-Escribano, MF; Gunnarsson, I; Gutierrez, C; Jönsen, A; Junker, P; Kozyrev, SV; Laustrup, H; Linga Reddy, MV; Martin, J; Pons-Estel, BA; Sanchez, E; Sturfelt, G; Suarez, A; Svenungsson, E; Truedsson, L; Witte, T; Wojcik, J; Zaghlool, A1
Kühn, KU; Maier, W; Mössner, R; Quednow, BB; Schuhmacher, A; Schwab, SG; Wagner, M1
Amarenco, P; Arveiler, D; Cambien, F; Elbaz, A; Evans, A; Gariepy, J; Grandchamp, B; Hetet, G; Kee, F; Morrison, C; Nicaud, V; Simon, A1
Borrego, N; Corbella, J; Gené, M; Gómez-Catalán, J; Piqué, E; To-Figueras, J1
Beutler, E; Felitti, V; Gelbart, T; Ho, NJ; Waalen, J1

Reviews

4 review(s) available for histidine and Genetic Predisposition

ArticleYear
Meta analysis on the association between FcgammaRIIa-R/H131 polymorphisms and systemic lupus erythematosus.
    Molecular biology reports, 2009, Volume: 36, Issue:5

    Topics: Arginine; Ethnicity; Genetic Predisposition to Disease; Histidine; Humans; Lupus Erythematosus, Systemic; Lupus Nephritis; Odds Ratio; Polymorphism, Single Nucleotide; Publication Bias; Receptors, IgG; Regression Analysis

2009
ADH1B Arg47His polymorphism is associated with esophageal cancer risk in high-incidence Asian population: evidence from a meta-analysis.
    PloS one, 2010, Oct-27, Volume: 5, Issue:10

    Topics: Alcohol Dehydrogenase; Alcohol Drinking; Arginine; Asia; Carcinoma, Squamous Cell; Case-Control Studies; Epistasis, Genetic; Esophageal Neoplasms; Genetic Predisposition to Disease; Histidine; Humans; Incidence; Polymorphism, Genetic

2010
Combined analysis of 635 patients confirms an age-related association of the serotonin 2A receptor gene with tardive dyskinesia and specificity for the non-orofacial subtype.
    The international journal of neuropsychopharmacology, 2005, Volume: 8, Issue:3

    Topics: Adult; Aged; Aging; Analysis of Variance; Chi-Square Distribution; Dyskinesia, Drug-Induced; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Histidine; Humans; International Cooperation; Logistic Models; Male; Middle Aged; Mutation; Polymorphism, Genetic; Receptor, Serotonin, 5-HT2A; Tryptophan

2005
Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus.
    Nature genetics, 2008, Volume: 40, Issue:2

    Topics: Adaptor Proteins, Signal Transducing; Alleles; Alternative Splicing; Amino Acid Motifs; Amino Acid Sequence; Amino Acid Substitution; Ankyrin Repeat; B-Lymphocytes; Case-Control Studies; Chromosomes, Human; Cohort Studies; DNA, Complementary; Exons; Gene Deletion; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genome, Human; Haplotypes; Histidine; Humans; Introns; Linkage Disequilibrium; Logistic Models; Lupus Erythematosus, Systemic; Membrane Proteins; Molecular Sequence Data; Physical Chromosome Mapping; Polymorphism, Single Nucleotide; Protein Isoforms; Protein Structure, Tertiary; Sequence Analysis, DNA; Sweden

2008

Other Studies

65 other study(ies) available for histidine and Genetic Predisposition

ArticleYear
Association between CARD14 gene polymorphisms and psoriasis vulgaris in Hainan Han population based on exon sequencing: A case-control study.
    Medicine, 2022, Oct-07, Volume: 101, Issue:40

    Topics: Aspartic Acid; CARD Signaling Adaptor Proteins; Case-Control Studies; Exons; Gene Frequency; Genetic Predisposition to Disease; Genome-Wide Association Study; Guanylate Cyclase; Histidine; Humans; Membrane Proteins; Polymorphism, Single Nucleotide; Psoriasis

2022
A novel gene mutation of Runx2 in cleidocranial dysplasia.
    Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban, 2017, Volume: 37, Issue:5

    Topics: Adult; Amino Acid Substitution; Cleidocranial Dysplasia; Core Binding Factor Alpha 1 Subunit; Exons; Female; Genetic Predisposition to Disease; Histidine; Humans; Mutation, Missense; Pedigree; Sequence Analysis, DNA; Tryptophan

2017
MAX Mutations in Endometrial Cancer: Clinicopathologic Associations and Recurrent MAX p.His28Arg Functional Characterization.
    Journal of the National Cancer Institute, 2018, 05-01, Volume: 110, Issue:5

    Topics: Aged; Aged, 80 and over; Amino Acid Substitution; Animals; Animals, Outbred Strains; Arginine; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors; Carcinoma, Endometrioid; Cells, Cultured; Codon, Nonsense; Endometrial Neoplasms; Female; Genetic Association Studies; Genetic Predisposition to Disease; HEK293 Cells; Histidine; Humans; Mice; Mice, Nude; Middle Aged; Neoplasm Invasiveness; Neovascularization, Pathologic

2018
A molecular dynamics based investigation reveals the role of rare Ribonuclease 4 variants in amyotrophic lateral sclerosis susceptibility.
    Mutation research, 2019, Volume: 813

    Topics: Amino Acid Sequence; Amyotrophic Lateral Sclerosis; Catalysis; Cell Nucleus; Crystallography, X-Ray; Genetic Predisposition to Disease; Histidine; Humans; Molecular Dynamics Simulation; Mutation, Missense; Protein Conformation; Protein Transport; Ribonucleases; Sequence Homology, Amino Acid

2019
Analysis of D216H polymorphism in Argentinean patients with primary dystonia.
    Journal of neurogenetics, 2013, Volume: 27, Issue:1-2

    Topics: Adolescent; Adult; Age of Onset; Argentina; Aspartic Acid; Child; Dystonic Disorders; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Histidine; Humans; Male; Middle Aged; Molecular Chaperones; Polymorphism, Single Nucleotide; Young Adult

2013
R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia.
    Alzheimer's & dementia : the journal of the Alzheimer's Association, 2014, Volume: 10, Issue:6

    Topics: Aged; Aged, 80 and over; Alzheimer Disease; Arginine; Brain; Cohort Studies; Creutzfeldt-Jakob Syndrome; Exons; Female; Frontotemporal Dementia; Genetic Predisposition to Disease; Genetic Variation; Genome-Wide Association Study; Genotype; Histidine; Humans; Male; Membrane Glycoproteins; Middle Aged; Phenotype; Receptors, Immunologic; Risk Factors

2014
TREM2 R47H variant and risk of essential tremor: a cross-sectional international multicenter study.
    Parkinsonism & related disorders, 2015, Volume: 21, Issue:3

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Arginine; Cross-Sectional Studies; DNA Mutational Analysis; Essential Tremor; Female; Genetic Predisposition to Disease; Genotype; Germany; Histidine; Humans; International Cooperation; Italy; Male; Membrane Glycoproteins; Middle Aged; North America; Receptors, Immunologic; Risk Factors; Spain; Taiwan; Young Adult

2015
The germline CDH1 c.48 G>C substitution contributes to cancer predisposition through generation of a pro-invasive mutation.
    Mutation research, 2014, Volume: 770

    Topics: Amino Acid Substitution; Animals; Antigens, CD; Cadherins; CHO Cells; Cricetinae; Cricetulus; Female; Genetic Predisposition to Disease; Germ-Line Mutation; Glutamic Acid; Histidine; Humans; Neoplasm Invasiveness; Pedigree; Stomach Neoplasms; Young Adult

2014
TLR1 Variant H305L Associated with Protection from Pulmonary Tuberculosis.
    PloS one, 2016, Volume: 11, Issue:5

    Topics: Amino Acid Substitution; Case-Control Studies; Disease Resistance; Gene Frequency; Genes, Recessive; Genetic Association Studies; Genetic Predisposition to Disease; Ghana; Histidine; Humans; Leucine; Polymorphism, Single Nucleotide; Toll-Like Receptor 1; Tuberculosis, Pulmonary

2016
The His131Arg substitution in the FCGR2A gene (rs1801274) is not associated with the severity of influenza A(H1N1)pdm09 infection.
    BMC research notes, 2016, Jun-07, Volume: 9

    Topics: Adolescent; Adult; Alleles; Amino Acid Substitution; Arginine; Child; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Histidine; Host-Pathogen Interactions; Humans; Influenza A Virus, H1N1 Subtype; Influenza, Human; Logistic Models; Male; Middle Aged; Polymorphism, Single Nucleotide; Receptors, IgG; Severity of Illness Index; Young Adult

2016
Identification of PGAM5 as a Mammalian Protein Histidine Phosphatase that Plays a Central Role to Negatively Regulate CD4(+) T Cells.
    Molecular cell, 2016, 08-04, Volume: 63, Issue:3

    Topics: Animals; Calcium Signaling; CD4-Positive T-Lymphocytes; Cytokines; Genetic Predisposition to Disease; Graft vs Host Disease; HEK293 Cells; Hematopoietic Stem Cell Transplantation; Histidine; Humans; Inflammation Mediators; Intermediate-Conductance Calcium-Activated Potassium Channels; Jurkat Cells; Lymphocyte Activation; Mice, Inbred BALB C; Mice, Inbred C57BL; Mice, Knockout; Mitochondrial Proteins; Nucleoside-Diphosphate Kinase; Phenotype; Phosphoprotein Phosphatases; Phosphorylation; Receptors, Antigen, T-Cell; RNA Interference; Time Factors; Transfection

2016
Environmental and genetic factors support the dissociation between α-synuclein aggregation and toxicity.
    Proceedings of the National Academy of Sciences of the United States of America, 2016, 10-18, Volume: 113, Issue:42

    Topics: alpha-Synuclein; Amino Acid Substitution; Animals; Cells, Cultured; Copper; Environment; Genetic Predisposition to Disease; Histidine; Humans; Inclusion Bodies; Kinetics; Mutation; Neurons; Phosphorylation; Protein Aggregates; Protein Aggregation, Pathological; Protein Conformation, alpha-Helical; Rats

2016
Urinary metabolites along with common and rare genetic variations are associated with incident chronic kidney disease.
    Kidney international, 2017, Volume: 91, Issue:6

    Topics: Aged; Amino Acid Transport Systems, Basic; Amino Acids; Biomarkers; Case-Control Studies; Chi-Square Distribution; Female; Genetic Predisposition to Disease; Glycine; Histidine; Humans; Incidence; Logistic Models; Lysine; Male; Mass Spectrometry; Massachusetts; Metabolomics; Middle Aged; Odds Ratio; Oligonucleotide Array Sequence Analysis; omega-N-Methylarginine; Phenotype; Polymorphism, Single Nucleotide; Proportional Hazards Models; Prospective Studies; Protective Factors; Renal Insufficiency, Chronic; Risk Assessment; Risk Factors; Urinalysis

2017
Susceptibility to DYT1 dystonia in European patients is modified by the D216H polymorphism.
    Neurology, 2008, Jun-03, Volume: 70, Issue:23

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Aspartic Acid; Child; Dystonia; Genetic Predisposition to Disease; Histidine; Humans; Middle Aged; Molecular Chaperones; Polymorphism, Single Nucleotide; White People

2008
Association of MUTYH Gln324His and APEX1 Asp148Glu with colorectal cancer and smoking in a Japanese population.
    Journal of experimental & clinical cancer research : CR, 2008, Sep-30, Volume: 27

    Topics: Aged; Asian People; Aspartic Acid; Case-Control Studies; Colorectal Neoplasms; DNA Glycosylases; DNA-(Apurinic or Apyrimidinic Site) Lyase; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutamine; Histidine; Humans; Male; Middle Aged; Polymorphism, Genetic; Smoking

2008
Hereditary haemochromatosis gene (HFE) H63D mutation shows an association with abnormal sperm motility.
    Molecular biology reports, 2009, Volume: 36, Issue:7

    Topics: Adolescent; Adult; Age Distribution; Amino Acid Substitution; Aspartic Acid; Genetic Predisposition to Disease; Genotype; Hemochromatosis Protein; Histidine; Histocompatibility Antigens Class I; Humans; Infertility, Male; Male; Membrane Proteins; Mutation; Sperm Motility

2009
Association of complement factor H Y402H polymorphism with phenotype of neovascular age related macular degeneration in Israel.
    Molecular vision, 2008, Volume: 14

    Topics: Aged; Choroidal Neovascularization; Complement Factor H; Female; Gene Frequency; Genetic Predisposition to Disease; Histidine; Humans; Israel; Macular Degeneration; Male; Phenotype; Photochemotherapy; Polymorphism, Single Nucleotide; Tyrosine

2008
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.
    Parkinsonism & related disorders, 2009, Volume: 15, Issue:6

    Topics: Adult; Arginine; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Haplotypes; Histidine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Parkinsonian Disorders; Polymorphism, Single Nucleotide; Protein Serine-Threonine Kinases

2009
Histidine at codon 154 of the prion protein gene is a risk factor for Nor98 scrapie in goats.
    The Journal of general virology, 2008, Volume: 89, Issue:Pt 12

    Topics: Animals; Case-Control Studies; Codon; Genetic Predisposition to Disease; Genotype; Goat Diseases; Goats; Histidine; Mutation; Polymorphism, Genetic; Prions; Risk Factors; Scrapie

2008
A novel mutation of the nicotinic acetylcholine receptor gene CHRNA4 in sporadic nocturnal frontal lobe epilepsy.
    Epilepsy research, 2009, Volume: 83, Issue:2-3

    Topics: Adolescent; Adult; Arginine; Child; Child, Preschool; DNA Mutational Analysis; Electroencephalography; Epilepsy, Frontal Lobe; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Histidine; Humans; Infant; Male; Mutation, Missense; Receptors, Nicotinic; Young Adult

2009
Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly.
    Brain & development, 2010, Volume: 32, Issue:3

    Topics: DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glutamine; Hedgehog Proteins; Histidine; Holoprosencephaly; Humans; Magnetic Resonance Imaging; Male; Mutation

2010
Polymorphisms of XRCC1 gene and risk of gastric cardiac adenocarcinoma.
    Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus, 2009, Volume: 22, Issue:5

    Topics: Adenine; Adenocarcinoma; Adult; Aged; Arginine; Cardia; Case-Control Studies; Codon; Cytosine; DNA Repair; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Haplotypes; Histidine; Humans; Linkage Disequilibrium; Male; Middle Aged; Polymorphism, Single Nucleotide; Risk Factors; Smoking; Stomach Neoplasms; Thymine; Tryptophan; X-ray Repair Cross Complementing Protein 1

2009
Association and impact of XPG Asp 1104 His gene polymorphism in HIV 1 disease progression to AIDS among north Indian HIV seropositive individuals.
    Molecular biology reports, 2010, Volume: 37, Issue:1

    Topics: Acquired Immunodeficiency Syndrome; Adolescent; Adult; Amino Acid Substitution; Aspartic Acid; Case-Control Studies; Disease Progression; DNA-Binding Proteins; Endonucleases; Female; Gene Frequency; Genetic Predisposition to Disease; Histidine; HIV Seropositivity; HIV-1; Humans; India; Male; Marital Status; Middle Aged; Nuclear Proteins; Polymorphism, Single Nucleotide; Spouses; Transcription Factors; Young Adult

2010
Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations.
    European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2010, Volume: 14, Issue:4

    Topics: Arginine; Choline O-Acetyltransferase; Electric Stimulation; Electroencephalography; Enzyme Inhibitors; Female; Genetic Predisposition to Disease; Genetic Testing; Glycine; Histidine; Humans; Longitudinal Studies; Magnetic Resonance Imaging; Male; Muscle, Skeletal; Mutation; Myasthenic Syndromes, Congenital; Receptor Protein-Tyrosine Kinases; Receptors, Cholinergic

2010
Dynamics of the interaction of human IgG subtype immune complexes with cells expressing R and H allelic forms of a low-affinity Fc gamma receptor CD32A.
    Journal of immunology (Baltimore, Md. : 1950), 2009, Dec-15, Volume: 183, Issue:12

    Topics: Alleles; Animals; Antigen-Antibody Complex; Arginine; Autoimmune Diseases; Bacterial Infections; Binding, Competitive; Cell Line; Cell Membrane; CHO Cells; Cricetinae; Cricetulus; Dimerization; Genetic Predisposition to Disease; Histidine; Humans; Immunoglobulin G; Ligands; Polymorphism, Genetic; Protein Binding; Receptors, IgG; Recombinant Fusion Proteins

2009
Microsomal epoxide hydrolase gene polymorphisms and susceptibility to chronic obstructive pulmonary disease in the Tunisian population.
    Genetic testing and molecular biomarkers, 2010, Volume: 14, Issue:6

    Topics: Aged; Alleles; Epoxide Hydrolases; Exons; Female; Genetic Predisposition to Disease; Histidine; Humans; Male; Middle Aged; Polymorphism, Genetic; Pulmonary Disease, Chronic Obstructive; Smoking; Tunisia

2010
Homozygous THAP1 mutations as cause of early-onset generalized dystonia.
    Movement disorders : official journal of the Movement Disorder Society, 2011, Volume: 26, Issue:5

    Topics: Adult; Apoptosis Regulatory Proteins; Carcinoma; Cell Line, Tumor; Consanguinity; DNA-Binding Proteins; Dystonia; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Histidine; Homozygote; Humans; Iran; Leucine; Male; Middle Aged; Mutation; Nuclear Proteins; Pedigree

2011
Assessment of D216H DYT1 polymorphism in a Chinese primary dystonia patient cohort.
    European journal of neurology, 2012, Volume: 19, Issue:6

    Topics: Adult; Aged; Asian People; Asparagine; Dystonic Disorders; Female; Follow-Up Studies; Genetic Association Studies; Genetic Predisposition to Disease; Histidine; Humans; Male; Middle Aged; Molecular Chaperones; Polymorphism, Single Nucleotide; Young Adult

2012
Genetic polymorphism of Fcγ-receptors IIa, IIIa and IIIb in South Indian patients with generalized aggressive periodontitis.
    Journal of oral science, 2011, Volume: 53, Issue:4

    Topics: Adult; Aggressive Periodontitis; Amino Acid Substitution; Analysis of Variance; Arginine; Case-Control Studies; Chi-Square Distribution; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; GPI-Linked Proteins; Histidine; Humans; India; Isoantigens; Male; Mouth Mucosa; Odds Ratio; Periodontal Index; Phenylalanine; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Receptors, IgG; Risk Factors; Valine; White People; Young Adult

2011
Ferroportin (SLC40A1) Q248H mutation is associated with lower circulating serum hepcidin levels in Rwandese HIV-positive women.
    Annals of hematology, 2012, Volume: 91, Issue:6

    Topics: Adolescent; Adult; Amino Acid Substitution; Antimicrobial Cationic Peptides; Cation Transport Proteins; Cross-Sectional Studies; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Glutamine; Hepcidins; Histidine; HIV Infections; HIV Seropositivity; HIV-1; Humans; Middle Aged; Mutation, Missense; Osmolar Concentration; Rwanda; Young Adult

2012
Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes.
    Gene, 2012, May-10, Volume: 499, Issue:1

    Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Case-Control Studies; Complement Factor H; Diabetes Complications; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Hearing Loss, Sensorineural; Hearing Loss, Sudden; Histidine; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Tyrosine; Young Adult

2012
Genetic association between obstructive bronchitis and enzymes of oxidative stress.
    Metabolism: clinical and experimental, 2012, Volume: 61, Issue:12

    Topics: Adult; Arginine; Aryldialkylphosphatase; Bronchitis; Catechol O-Methyltransferase; Chi-Square Distribution; Child; Cohort Studies; Epoxide Hydrolases; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Germany; Histidine; Humans; Leucine; Lung Diseases, Obstructive; Male; Methionine; NAD(P)H Dehydrogenase (Quinone); Oxidative Stress; Polymorphism, Single Nucleotide; Pregnancy; Pregnancy Complications; Prenatal Exposure Delayed Effects; Proline; Prospective Studies; Risk Factors; Serine; Smoking; Valine

2012
XRCC1 gene polymorphisms and risk of ameloblastoma.
    Archives of oral biology, 2013, Volume: 58, Issue:6

    Topics: Adenine; Adult; Ameloblastoma; Arginine; Codon; DNA Repair; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glycine; Guanine; Haplotypes; Histidine; Humans; Male; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors; Sequence Analysis, DNA; Thailand; Thymine; Tryptophan; X-ray Repair Cross Complementing Protein 1

2013
Deletion of histidine triad nucleotide-binding protein 1/PKC-interacting protein in mice enhances cell growth and carcinogenesis.
    Proceedings of the National Academy of Sciences of the United States of America, 2003, Jun-24, Volume: 100, Issue:13

    Topics: Animals; Benzylamines; Carcinogens; Carcinoma, Squamous Cell; Cells, Cultured; Gene Deletion; Gene Expression Regulation, Neoplastic; Genes, Tumor Suppressor; Genetic Predisposition to Disease; Genetic Vectors; Genotype; Histidine; Immunoblotting; Mice; Mice, Transgenic; Models, Genetic; Nerve Tissue Proteins; Papilloma; Phenotype; Protein Kinase C; Recombination, Genetic; Time Factors

2003
Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease.
    Neuromuscular disorders : NMD, 2003, Volume: 13, Issue:9

    Topics: Alleles; Arginine; Charcot-Marie-Tooth Disease; Cysteine; Demyelinating Diseases; DNA Mutational Analysis; Electrophysiology; Family Health; Female; Genetic Predisposition to Disease; Glycine; Histidine; Humans; Male; Microscopy, Electron; Mutation; Nerve Tissue Proteins; Neural Conduction; Pedigree; Peripheral Nerves; Sequence Analysis, DNA; Tryptophan

2003
Characterization of a pseudoachondroplasia-associated mutation (His587-->Arg) in the C-terminal, collagen-binding domain of cartilage oligomeric matrix protein (COMP).
    The Biochemical journal, 2004, Jan-15, Volume: 377, Issue:Pt 2

    Topics: Arginine; Binding Sites; Cartilage Oligomeric Matrix Protein; Cell Line; Collagen; Extracellular Matrix Proteins; Genetic Predisposition to Disease; Glycoproteins; Histidine; Humans; Matrilin Proteins; Mutation; Osteochondrodysplasias; Protein Conformation; Protein Structure, Tertiary

2004
Epoxide hydrolase Tyr113His polymorphism is not associated with susceptibility to esophageal squamous cell carcinoma in population of North China.
    World journal of gastroenterology, 2003, Volume: 9, Issue:12

    Topics: Adult; Amino Acid Substitution; Base Sequence; Carcinoma, Squamous Cell; China; DNA Primers; Epoxide Hydrolases; Esophageal Neoplasms; Female; Genetic Predisposition to Disease; Histidine; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Reference Values; Smoking; Tyrosine

2003
Role of histaminergic neurons in development of epileptic seizures in EL mice.
    Brain research. Molecular brain research, 2004, Dec-06, Volume: 132, Issue:1

    Topics: Animals; Brain; Disease Models, Animal; Drug Therapy, Combination; Enzyme Inhibitors; Epilepsy; Epilepsy, Temporal Lobe; Female; Genetic Predisposition to Disease; Histamine; Histamine H1 Antagonists; Histamine N-Methyltransferase; Histidine; Histidine Decarboxylase; Male; Mice; Mice, Neurologic Mutants; Neurons; Pyrimethamine; Receptors, Histamine H3; Up-Regulation

2004
Variants in optineurin gene and their association with tumor necrosis factor-alpha polymorphisms in Japanese patients with glaucoma.
    Investigative ophthalmology & visual science, 2004, Volume: 45, Issue:12

    Topics: Adult; Aging; Alleles; Asian People; Aspartic Acid; Cell Cycle Proteins; Chromatography, High Pressure Liquid; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glaucoma, Open-Angle; Heterozygote; Histidine; Humans; Intraocular Pressure; Male; Membrane Transport Proteins; Middle Aged; Mutation; Polymorphism, Genetic; Threonine; Transcription Factor TFIIIA; Tumor Necrosis Factor-alpha; Visual Fields

2004
Association of a common variant of the CASP8 gene with reduced risk of breast cancer.
    Journal of the National Cancer Institute, 2004, Dec-15, Volume: 96, Issue:24

    Topics: Aspartic Acid; Breast Neoplasms; Case-Control Studies; Caspase 10; Caspase 8; Caspases; England; Female; Genetic Predisposition to Disease; Genetic Variation; Heterozygote; Histidine; Homozygote; Humans; Odds Ratio; Polymorphism, Single Nucleotide; Receptors, TNF-Related Apoptosis-Inducing Ligand; Receptors, Tumor Necrosis Factor

2004
Loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression.
    Neuron, 2005, Jan-06, Volume: 45, Issue:1

    Topics: Adult; Amino Acid Sequence; Amino Acid Substitution; Animals; Arginine; Bipolar Disorder; Brain; Depressive Disorder, Major; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Histidine; Humans; Male; Mice; Middle Aged; Molecular Sequence Data; Mutation; PC12 Cells; Polymorphism, Single Nucleotide; Rats; Serotonin; Tryptophan Hydroxylase

2005
Reduction of Gstm1 expression in the stroke-prone spontaneously hypertension rat contributes to increased oxidative stress.
    Hypertension (Dallas, Tex. : 1979), 2005, Volume: 45, Issue:4

    Topics: Amino Acid Sequence; Animals; Aorta; Arginine; Blotting, Western; Computer Systems; Genetic Predisposition to Disease; Glutathione Transferase; Histidine; Hypertension; Immunohistochemistry; Kidney; Molecular Sequence Data; Oxidative Stress; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Rats; Rats, Inbred SHR; Rats, Inbred WKY; Stroke; Superoxides

2005
Complement factor H polymorphism and age-related macular degeneration.
    Science (New York, N.Y.), 2005, Apr-15, Volume: 308, Issue:5720

    Topics: Aged; Alleles; Amino Acid Substitution; Case-Control Studies; Chromosomes, Human, Pair 1; Complement Activation; Complement Factor H; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Haplotypes; Histidine; Homozygote; Humans; Linkage Disequilibrium; Macular Degeneration; Male; Middle Aged; Multigene Family; Polymorphism, Single Nucleotide; Risk Factors; Tyrosine

2005
Complement factor H polymorphism in age-related macular degeneration.
    Science (New York, N.Y.), 2005, Apr-15, Volume: 308, Issue:5720

    Topics: Aged; Aged, 80 and over; Aging; Alleles; Amino Acid Substitution; Case-Control Studies; Choroid; Chromosomes, Human, Pair 1; Complement Factor H; Complement Membrane Attack Complex; Exons; Female; Genetic Markers; Genetic Predisposition to Disease; Genotype; Haplotypes; Histidine; Humans; Immunity, Innate; Introns; Linkage Disequilibrium; Macular Degeneration; Male; Oligonucleotide Array Sequence Analysis; Pigment Epithelium of Eye; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Risk Factors; Smoking

2005
Genetics. Was the Human Genome Project worth the effort?
    Science (New York, N.Y.), 2005, Apr-15, Volume: 308, Issue:5720

    Topics: Alleles; Amino Acid Substitution; ATP-Binding Cassette Transporters; Case-Control Studies; Chromosome Mapping; Chromosomes, Human, Pair 1; Complement Factor H; Complement System Proteins; Genetic Markers; Genetic Predisposition to Disease; Genetic Variation; Haplotypes; Histidine; Human Genome Project; Humans; Immunity, Innate; Macular Degeneration; Mutation; Oligonucleotide Array Sequence Analysis; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Retrospective Studies; Risk Factors

2005
Re: Association of a common variant of the CASP8 gene with reduced risk of breast cancer.
    Journal of the National Cancer Institute, 2005, Jul-06, Volume: 97, Issue:13

    Topics: Adult; Aged; Aged, 80 and over; Aspartic Acid; Breast Neoplasms; Case-Control Studies; Caspase 8; Caspases; Cohort Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Germany; Histidine; Humans; Middle Aged; Odds Ratio; Risk Assessment; Risk Factors

2005
Association analysis of the Arg220His variation of the human gene encoding the GABA delta subunit with idiopathic generalized epilepsy.
    Epilepsy research, 2005, Volume: 65, Issue:1-2

    Topics: Arginine; Case-Control Studies; Chi-Square Distribution; DNA Mutational Analysis; Epilepsy, Generalized; Exons; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Histidine; Humans; Male; Polymorphism, Genetic; Receptors, GABA-A; Retrospective Studies

2005
Association of DRD2 gene variant with schizophrenia.
    Neuroscience letters, 2006, Jan-09, Volume: 392, Issue:1-2

    Topics: Adolescent; Adult; Age of Onset; Case-Control Studies; Chi-Square Distribution; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Histidine; Humans; Male; Polymorphism, Genetic; Psychiatric Status Rating Scales; Receptors, Dopamine D2; Schizophrenia; Valine

2006
The effect of the metabolic syndrome, hepatic steatosis and steatohepatitis on liver fibrosis in hereditary hemochromatosis.
    Liver international : official journal of the International Association for the Study of the Liver, 2006, Volume: 26, Issue:3

    Topics: Adult; Aged; Aspartic Acid; Cysteine; Fatty Liver; Female; Genetic Predisposition to Disease; Glucose Intolerance; Hemochromatosis; Hepatitis; Heterozygote; Histidine; Homozygote; Humans; Iron Overload; Liver Cirrhosis; Male; Metabolic Syndrome; Middle Aged; Multivariate Analysis; Predictive Value of Tests; Prospective Studies; Risk Factors; Tyrosine

2006
A common polymorphism in the complement factor H gene is associated with increased risk of myocardial infarction: the Rotterdam Study.
    Journal of the American College of Cardiology, 2006, Apr-18, Volume: 47, Issue:8

    Topics: Aged; Cholesterol; Complement Factor H; Diabetes Complications; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Histidine; Homozygote; Humans; Incidence; Male; Middle Aged; Myocardial Infarction; Polymorphism, Genetic; Proportional Hazards Models; Risk Factors; Smoking; Tyrosine

2006
Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His.
    Human mutation, 2006, Volume: 27, Issue:9

    Topics: Aged; Alleles; Amino Acid Substitution; Complement Factor H; Computational Biology; Gene Frequency; Genetic Predisposition to Disease; Haplotypes; Histidine; Humans; Linkage Disequilibrium; Macular Degeneration; Middle Aged; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Racial Groups; Risk Factors; Tyrosine; White People

2006
Novel mitochondrial mutation in the ND4 gene associated with Leigh syndrome.
    Acta neurologica Scandinavica, 2006, Volume: 114, Issue:5

    Topics: Amino Acid Sequence; Amino Acid Substitution; Basal Ganglia; Basal Ganglia Diseases; DNA Mutational Analysis; DNA, Mitochondrial; Electron Transport Complex I; Female; Genetic Predisposition to Disease; Histidine; Humans; Infant; Leigh Disease; Magnetic Resonance Imaging; Molecular Sequence Data; Mutation, Missense; Protein Subunits; Tyrosine

2006
LRRK2 mutations on Crete: R1441H associated with PD evolving to PSP.
    Neurology, 2006, Oct-24, Volume: 67, Issue:8

    Topics: Age of Onset; Aged; Aged, 80 and over; Arginine; Cohort Studies; Dementia; Disease Progression; Female; Genetic Predisposition to Disease; Greece; Histidine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Mutation; Parkinson Disease; Pedigree; Protein Serine-Threonine Kinases; Supranuclear Palsy, Progressive

2006
HFE H63D variant and leukemia susceptibility.
    Leukemia & lymphoma, 2006, Volume: 47, Issue:11

    Topics: Aspartic Acid; Genetic Predisposition to Disease; Histidine; Humans; Leukemia; Mutation

2006
The association between H63D mutations in HFE and amyotrophic lateral sclerosis in a Dutch population.
    Archives of neurology, 2007, Volume: 64, Issue:1

    Topics: Adult; Aged; Aged, 80 and over; Amyotrophic Lateral Sclerosis; Asparagine; Confidence Intervals; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Hemochromatosis Protein; Histidine; Histocompatibility Antigens Class I; Humans; Male; Membrane Proteins; Middle Aged; Mutation; Netherlands; Odds Ratio; Retrospective Studies

2007
Functional P2X7 receptor polymorphisms (His155Tyr, Arg307Gln, Glu496Ala) in patients with Crohn's disease.
    Scandinavian journal of immunology, 2007, Volume: 65, Issue:2

    Topics: Alanine; Amino Acid Substitution; Arginine; Case-Control Studies; Crohn Disease; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Histidine; Humans; Male; Polymorphism, Single Nucleotide; Receptors, Purinergic P2; Receptors, Purinergic P2X7; Tyrosine

2007
HTRA1 promoter polymorphism predisposes Japanese to age-related macular degeneration.
    Molecular vision, 2007, Apr-04, Volume: 13

    Topics: Aged; Aged, 80 and over; Alleles; Asian People; Cohort Studies; Complement Factor H; Conserved Sequence; Female; Gene Dosage; Genes, Recessive; Genetic Predisposition to Disease; Genotype; High-Temperature Requirement A Serine Peptidase 1; Histidine; Humans; Linkage Disequilibrium; Macular Degeneration; Male; Middle Aged; Odds Ratio; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Serine Endopeptidases; Tyrosine

2007
Hereditary inclusion body myopathy with a novel mutation in the GNE gene associated with proximal leg weakness and necrotizing myopathy.
    European journal of neurology, 2007, Volume: 14, Issue:9

    Topics: Adult; Creatine Kinase; Genetic Predisposition to Disease; Histidine; Humans; Leg; Male; Multienzyme Complexes; Mutation; Myelitis, Transverse; Myositis, Inclusion Body; Proline

2007
The wolframin His611Arg polymorphism influences medication overuse headache.
    Neuroscience letters, 2007, Sep-13, Volume: 424, Issue:3

    Topics: Adult; Arginine; Case-Control Studies; DNA Mutational Analysis; Drug-Related Side Effects and Adverse Reactions; Female; Genetic Predisposition to Disease; Headache; Histidine; Humans; Male; Membrane Proteins; Middle Aged; Multivariate Analysis; Polymorphism, Genetic

2007
Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts.
    International journal of cancer, 2007, Dec-15, Volume: 121, Issue:12

    Topics: Adult; Age of Onset; Aged; Asian People; Black or African American; Breast Neoplasms; Case-Control Studies; Checkpoint Kinase 2; DNA Mutational Analysis; DNA, Complementary; Female; Gene Frequency; Genetic Predisposition to Disease; Germ-Line Mutation; Hawaii; Hispanic or Latino; Histidine; Humans; Isoleucine; Leucine; Male; Middle Aged; Mutation; Mutation, Missense; Predictive Value of Tests; Proline; Prostatic Neoplasms; Protein Serine-Threonine Kinases; Risk Assessment; Risk Factors; Threonine; Tyrosine; United States; White People

2007
Association of complement factor H Y402H gene polymorphism with Alzheimer's disease.
    American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2008, Sep-05, Volume: 147B, Issue:6

    Topics: Aged; Aged, 80 and over; Alzheimer Disease; Amyloid beta-Peptides; Apolipoprotein E4; Case-Control Studies; Cohort Studies; Comorbidity; Complement Factor H; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Histidine; Humans; Macular Degeneration; Male; Middle Aged; Polymorphism, Single Nucleotide; tau Proteins; Tyrosine

2008
Sensorimotor gating of schizophrenia patients is influenced by 5-HT2A receptor polymorphisms.
    Biological psychiatry, 2008, Sep-01, Volume: 64, Issue:5

    Topics: Acoustic Stimulation; Adolescent; Adult; Aged; Analysis of Variance; Female; Gait Disorders, Neurologic; Gene Frequency; Genetic Predisposition to Disease; Genotype; Habituation, Psychophysiologic; Histidine; Humans; Inhibition, Psychological; Male; Middle Aged; Polymorphism, Genetic; Psychiatric Status Rating Scales; Receptor, Serotonin, 5-HT2A; Reflex, Startle; Schizophrenia; Tyrosine

2008
Association studies between haemochromatosis gene mutations and the risk of cardiovascular diseases.
    European journal of clinical investigation, 2001, Volume: 31, Issue:5

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Arteriosclerosis; Aspartic Acid; Brain Infarction; Cardiovascular Diseases; Case-Control Studies; Cysteine; Female; France; Genetic Predisposition to Disease; Genotype; Hemochromatosis; Hemochromatosis Protein; Histidine; Histocompatibility Antigens Class I; HLA Antigens; Humans; Male; Membrane Proteins; Middle Aged; Mutation; Myocardial Infarction; Northern Ireland; Polymorphism, Genetic; Prevalence; Prospective Studies; Tyrosine; Ultrasonography; United Kingdom

2001
Lung cancer susceptibility in relation to combined polymorphisms of microsomal epoxide hydrolase and glutathione S-transferase P1.
    Cancer letters, 2001, Nov-28, Volume: 173, Issue:2

    Topics: Adult; Aged; Aged, 80 and over; Epoxide Hydrolases; Exons; Female; Genetic Predisposition to Disease; Genotype; Glutathione Transferase; Histidine; Homozygote; Humans; Lung Neoplasms; Male; Microsomes; Middle Aged; Odds Ratio; Phenotype; Polymorphism, Genetic; Protein Isoforms; Smoking; Tyrosine

2001
Prevalence of hemochromatosis-related symptoms among individuals with mutations in the HFE gene.
    Mayo Clinic proceedings, 2002, Volume: 77, Issue:6

    Topics: Adult; Aged; Aspartic Acid; Case-Control Studies; Cysteine; Double-Blind Method; Female; Ferritins; Genetic Predisposition to Disease; Genetic Testing; Genotype; Hemochromatosis; Hispanic or Latino; Histidine; Homozygote; Humans; Male; Middle Aged; Mutation; Prevalence; Surveys and Questionnaires; Transferrin; Tyrosine; United States; White People

2002