cytosine has been researched along with Syndrome in 29 studies
Syndrome: A characteristic symptom complex.
| Excerpt | Relevance | Reference |
|---|---|---|
| " It was the aim of the present study to assess whether the response to aspirin and clopidogrel may be influenced by the 807 C/T polymorphism of the glycoprotein Ia (GpIa) gene in patients with non-ST elevation acute coronary syndrome (NSTE ACS)." | 9.12 | Lack of association between the 807 C/T polymorphism of glycoprotein Ia gene and post-treatment platelet reactivity after aspirin and clopidogrel in patients with acute coronary syndrome. ( Alessi, MC; Bonnet, JL; Camoin, L; Cuisset, T; Frere, C; Juhan-Vague, I; Lambert, M; Morange, PE; Quilici, J; Romero-Barra, M; Saut, N, 2007) |
| " It was the aim of the present study to assess whether the response to aspirin and clopidogrel may be influenced by the 807 C/T polymorphism of the glycoprotein Ia (GpIa) gene in patients with non-ST elevation acute coronary syndrome (NSTE ACS)." | 5.12 | Lack of association between the 807 C/T polymorphism of glycoprotein Ia gene and post-treatment platelet reactivity after aspirin and clopidogrel in patients with acute coronary syndrome. ( Alessi, MC; Bonnet, JL; Camoin, L; Cuisset, T; Frere, C; Juhan-Vague, I; Lambert, M; Morange, PE; Quilici, J; Romero-Barra, M; Saut, N, 2007) |
| " Under immunosuppressive treatment with azathioprine and steroids, the patient developed cytomegalovirus (CMV) enteritis which was triggered by therapy-induced leukopenia." | 3.75 | [A 55-year-old woman with thymoma and hypogammaglobulinemia (Good syndrome), ulcerative colitis, and cytomegalovirus infection]. ( Baba, HA; Gerken, G; Kahraman, A; Maldonado-Lopez, E; Miller, M; Treichel, U, 2009) |
| " Troxacitabine is an anti-leukemic agent which can be associated with palmar-plantar erythrodysesthesia syndrome (PPES)." | 3.71 | Chemotherapy-induced palmar-plantar erythrodysesthesia syndrome--recall following different chemotherapy agents. ( Cortes, JE; Giles, FJ; Hui, YF, 2002) |
| "We have investigated the distribution of DNA methylation in chromosomes and nuclei of normal individuals and ICF (Immunodeficiency, Centromeric instability and Facial abnormalities) syndrome patients, using 5-methylcytosine monoclonal antibody." | 3.69 | Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients. ( Blanquet, V; Bonneau, D; Fischer, A; Herbelin, C; Jeanpierre, M; Miniou, P; Niveleau, A; Sibella, V; Viegas-Péquignot, E, 1994) |
| "APECED is caused by alteration in a single gene, named the autoimmune regulator (AIRE) gene." | 1.32 | Novel compound heterozygous AIRE mutations in a Japanese patient with APECED. ( Asakura, Y; Horikawa, R; Katsumata, N; Kitanaka, S; Sato, U; Tanaka, T, 2004) |
| "All patients had convulsions or loss of consciousness resulting from hypoglycemia at less than 1 year of age." | 1.31 | Novel missense mutations in the glutamate dehydrogenase gene in the congenital hyperinsulinism-hyperammonemia syndrome. ( Hayashi, Y; Kato, H; Miki, Y; Ohura, T; Taki, T; Yanagisawa, M, 2000) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (3.45) | 18.7374 |
| 1990's | 4 (13.79) | 18.2507 |
| 2000's | 20 (68.97) | 29.6817 |
| 2010's | 4 (13.79) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cherkaoui Jaouad, I | 1 |
| El Alloussi, M | 1 |
| Chafai El Alaoui, S | 1 |
| Laarabi, FZ | 1 |
| Lyahyai, J | 1 |
| Sefiani, A | 1 |
| Venza, M | 1 |
| Visalli, M | 1 |
| Venza, I | 1 |
| Torino, C | 1 |
| Tripodo, B | 1 |
| Melita, R | 1 |
| Teti, D | 1 |
| Kahraman, A | 1 |
| Miller, M | 1 |
| Maldonado-Lopez, E | 1 |
| Baba, HA | 1 |
| Treichel, U | 1 |
| Gerken, G | 1 |
| Ali, A | 1 |
| Singh, SK | 1 |
| Raman, R | 1 |
| Pan, S | 1 |
| Xu, LL | 1 |
| Sun, LS | 1 |
| Li, TJ | 1 |
| Keohane, C | 1 |
| Bacon, CL | 1 |
| Moran, B | 1 |
| Irvine, AD | 1 |
| Smith, OP | 1 |
| Descamps, V | 1 |
| Eshghyar, N | 1 |
| Nikbin, B | 1 |
| Amirzargar, A | 1 |
| Dehghani Nazhvani, A | 1 |
| Shakiba, Y | 1 |
| Nichol, K | 1 |
| Pearson, CE | 1 |
| Sato, U | 1 |
| Horikawa, R | 1 |
| Katsumata, N | 1 |
| Asakura, Y | 1 |
| Kitanaka, S | 1 |
| Tanaka, T | 1 |
| Arroyo-Espliguero, R | 1 |
| El-Sharnouby, K | 1 |
| Vázquez-Rey, E | 1 |
| Kalidas, K | 1 |
| Jeffery, S | 1 |
| Kaski, JC | 1 |
| Kellermayer, R | 1 |
| Siitonen, HA | 1 |
| Hadzsiev, K | 1 |
| Kestilä, M | 1 |
| Kosztolányi, G | 1 |
| Anderson, PJ | 1 |
| Netherway, DJ | 1 |
| Cox, TC | 1 |
| Roscioli, T | 1 |
| David, DJ | 1 |
| Vanita, V | 1 |
| Singh, JR | 1 |
| Hejtmancik, JF | 1 |
| Nuernberg, P | 1 |
| Hennies, HC | 1 |
| Singh, D | 1 |
| Sperling, K | 1 |
| Gonzalez-Porras, JR | 1 |
| Martin-Herrero, F | 1 |
| Garcia-Sanz, R | 1 |
| Lopez, ML | 1 |
| Balanzategui, A | 1 |
| Mateos, MV | 1 |
| Pavon, P | 1 |
| Gonzalez, M | 1 |
| Alberca, I | 1 |
| San Miguel, JF | 1 |
| Cuisset, T | 1 |
| Frere, C | 1 |
| Quilici, J | 1 |
| Morange, PE | 1 |
| Saut, N | 1 |
| Romero-Barra, M | 1 |
| Camoin, L | 1 |
| Lambert, M | 1 |
| Juhan-Vague, I | 1 |
| Bonnet, JL | 1 |
| Alessi, MC | 1 |
| Wang, J | 1 |
| Liu, J | 1 |
| Zhang, Q | 1 |
| Meyer-Marcotty, P | 1 |
| Weisschuh, N | 1 |
| Dressler, P | 1 |
| Hartmann, J | 1 |
| Stellzig-Eisenhauer, A | 1 |
| Miniou, P | 1 |
| Jeanpierre, M | 1 |
| Blanquet, V | 1 |
| Sibella, V | 1 |
| Bonneau, D | 1 |
| Herbelin, C | 1 |
| Fischer, A | 1 |
| Niveleau, A | 1 |
| Viegas-Péquignot, E | 1 |
| Inoue, T | 1 |
| Okauchi, Y | 1 |
| Matsuzaki, Y | 1 |
| Kuwajima, K | 1 |
| Kondo, H | 1 |
| Horiuchi, N | 1 |
| Nakao, K | 1 |
| Iwata, M | 1 |
| Yokogoshi, Y | 1 |
| Shintani, Y | 1 |
| Bando, H | 1 |
| Saito, S | 1 |
| Karavellas, MP | 1 |
| Plummer, DJ | 1 |
| Macdonald, JC | 1 |
| Torriani, FJ | 1 |
| Shufelt, CL | 1 |
| Azen, SP | 1 |
| Freeman, WR | 1 |
| Miki, Y | 1 |
| Taki, T | 1 |
| Ohura, T | 1 |
| Kato, H | 1 |
| Yanagisawa, M | 1 |
| Hayashi, Y | 1 |
| Tuck-Muller, CM | 1 |
| Narayan, A | 1 |
| Tsien, F | 1 |
| Smeets, DF | 1 |
| Sawyer, J | 1 |
| Fiala, ES | 1 |
| Sohn, OS | 1 |
| Ehrlich, M | 1 |
| Costello, JF | 1 |
| Plass, C | 1 |
| Bhorade, SM | 1 |
| Sandesara, C | 1 |
| Garrity, ER | 1 |
| Vigneswaran, WT | 1 |
| Norwick, L | 1 |
| Alkan, S | 1 |
| Husain, AN | 1 |
| McCabe, MA | 1 |
| Yeldandi, V | 1 |
| Kosaki, K | 1 |
| Ogata, T | 1 |
| Kosaki, R | 1 |
| Sato, S | 1 |
| Matsuo, N | 1 |
| Hui, YF | 1 |
| Giles, FJ | 1 |
| Cortes, JE | 1 |
| Usala, SJ | 1 |
| Menke, JB | 1 |
| Watson, TL | 1 |
| Bérard, WE | 1 |
| Bradley, C | 1 |
| Bale, AE | 1 |
| Lash, RW | 1 |
| Weintraub, BD | 1 |
| Ozsoylu, S | 1 |
| Hiçsönmez, G | 1 |
2 reviews available for cytosine and Syndrome
| Article | Year |
|---|---|
Identification of a single cytosine base insertion mutation at Arg-597 of the beta subunit of the human epithelial sodium channel in a family with Liddle's disease.
Topics: Adolescent; Adult; Amino Acid Sequence; Amino Acid Substitution; Arginine; Base Sequence; Cytosine; | 1998 |
Methylation matters.
Topics: 5-Methylcytosine; Chromosome Aberrations; CpG Islands; Cytosine; DNA Methylation; DNA Transposable E | 2001 |
1 trial available for cytosine and Syndrome
| Article | Year |
|---|---|
Lack of association between the 807 C/T polymorphism of glycoprotein Ia gene and post-treatment platelet reactivity after aspirin and clopidogrel in patients with acute coronary syndrome.
Topics: Acute Disease; Adenosine Diphosphate; Aged; Aspirin; Blood Platelets; Cell Adhesion Molecules; Clopi | 2007 |
26 other studies available for cytosine and Syndrome
| Article | Year |
|---|---|
Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report.
Topics: Alanine; Amelogenesis Imperfecta; Base Sequence; Child; Codon, Nonsense; Cytosine; Dental Enamel Pro | 2015 |
Altered binding of MYF-5 to FOXE1 promoter in non-syndromic and CHARGE-associated cleft palate.
Topics: 5' Untranslated Regions; Adolescent; Child; Cleft Palate; Consensus Sequence; Cytosine; DNA Mutation | 2009 |
[A 55-year-old woman with thymoma and hypogammaglobulinemia (Good syndrome), ulcerative colitis, and cytomegalovirus infection].
Topics: Agammaglobulinemia; Antiviral Agents; Azathioprine; Cidofovir; Colitis, Ulcerative; Cytomegalovirus | 2009 |
Coding region of IRF6 gene may not be causal for Van der Woude syndrome in cases from India.
Topics: 3' Untranslated Regions; Abnormalities, Multiple; Adenine; Arginine; Cleft Lip; Cleft Palate; Cohort | 2009 |
Identification of known and novel PTCH mutations in both syndromic and non-syndromic keratocystic odontogenic tumors.
Topics: Adolescent; Adult; Amino Acid Sequence; Basal Cell Nevus Syndrome; Chromatography, High Pressure Liq | 2009 |
Drug rash with eosinophilia and systemic symptoms (DRESS) syndrome induced by cidofovir.
Topics: Adenoviridae Infections; Cidofovir; Cytosine; Dermatitis, Exfoliative; Drug Eruptions; Eosinophilia; | 2011 |
Drug reaction with eosinophilia and systemic symptoms (DRESS) induced by cidofovir in a transplant recipient: a misunderstanding of DRESS.
Topics: Antiviral Agents; Cidofovir; Cytosine; Drug Eruptions; Eosinophilia; Humans; Infant; Organ Transplan | 2011 |
Gene polymorphism of interleukin-1 alpha and beta in keratocystic odontogenic tumors.
Topics: Adolescent; Adult; Aged; Alleles; Case-Control Studies; Child; Cytosine; Epithelial Cells; Female; F | 2012 |
CpG methylation modifies the genetic stability of cloned repeat sequences.
Topics: Abnormalities, Multiple; Animals; Cell Line; Centromere; Chlorocebus aethiops; Cloning, Molecular; C | 2002 |
Novel compound heterozygous AIRE mutations in a Japanese patient with APECED.
Topics: Addison Disease; Adult; AIRE Protein; Asian People; Base Sequence; Candidiasis, Chronic Mucocutaneou | 2004 |
CD14 C(-260)T promoter polymorphism and prevalence of acute coronary syndromes.
Topics: Adult; Aged; Aged, 80 and over; Case-Control Studies; Cytosine; Humans; Lipopolysaccharide Receptors | 2005 |
A patient with Rothmund-Thomson syndrome and all features of RAPADILINO.
Topics: Abnormalities, Multiple; Adenosine Triphosphatases; Amino Acid Substitution; Arginine; Bone and Bone | 2005 |
Do Craniosynostosis syndrome phenotypes with both FGFR2 and TWIST mutations have a worse clinical outcome?
Topics: Acrocephalosyndactylia; Adenine; Adolescent; Arginine; Child, Preschool; Craniofacial Dysostosis; Cr | 2006 |
A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family.
Topics: Asian People; Base Sequence; Cataract; Child; Chromosome Mapping; Chromosomes, Human, Pair 21; Corne | 2006 |
Hyperhomocysteinemia is a risk factor of recurrent coronary event in young patients irrespective to the MTHFR C677T polymorphism.
Topics: Acute Disease; Adult; Age Factors; Body Mass Index; Cohort Studies; Coronary Disease; Cytosine; Fema | 2007 |
FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.
Topics: Asian People; Blepharophimosis; Blepharoptosis; Cysteine; Cytosine; Eye Abnormalities; Eyelids; Fork | 2007 |
Morphology of the sella turcica in Axenfeld-Rieger syndrome with PITX2 mutation.
Topics: Adolescent; Cephalometry; Chromosomes, Human, Pair 13; Codon; Cranial Fossa, Posterior; Craniofacial | 2008 |
Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients.
Topics: 5-Methylcytosine; Abnormalities, Multiple; Base Sequence; Case-Control Studies; Centromere; Child; C | 1994 |
Incidence of immune recovery vitritis in cytomegalovirus retinitis patients following institution of successful highly active antiretroviral therapy.
Topics: AIDS-Related Opportunistic Infections; Antiviral Agents; California; Cidofovir; Cohort Studies; Cyto | 1999 |
Novel missense mutations in the glutamate dehydrogenase gene in the congenital hyperinsulinism-hyperammonemia syndrome.
Topics: Adenine; Ammonia; Codon; Cytosine; Female; Glutamate Dehydrogenase; Guanine; Heterozygote; Humans; H | 2000 |
DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients.
Topics: 5-Methylcytosine; Abnormalities, Multiple; Brain; Cell Line; Centromere; Chromosome Aberrations; Chr | 2000 |
Quantification of cytomegalovirus (CMV) viral load by the hybrid capture assay allows for early detection of CMV disease in lung transplant recipients.
Topics: Adult; Antiviral Agents; Cell Culture Techniques; Cidofovir; Cytomegalovirus; Cytomegalovirus Infect | 2001 |
A novel mutation in the FOXL2 gene in a patient with blepharophimosis syndrome: differential role of the polyalanine tract in the development of the ovary and the eyelid.
Topics: Blepharophimosis; Blepharoptosis; Child; Cytosine; DNA Mutational Analysis; DNA Primers; DNA-Binding | 2002 |
Chemotherapy-induced palmar-plantar erythrodysesthesia syndrome--recall following different chemotherapy agents.
Topics: Adult; Antineoplastic Combined Chemotherapy Protocols; Cytosine; Dioxolanes; Erythema; Female; Foot; | 2002 |
A new point mutation in the 3,5,3'-triiodothyronine-binding domain of the c-erbA beta thyroid hormone receptor is tightly linked to generalized thyroid hormone resistance.
Topics: Base Sequence; Binding Sites; Cytosine; Deoxyribonucleases, Type II Site-Specific; Drug Resistance; | 1991 |
A case of erythroleukemia. (di Guglielmo's syndrome).
Topics: Adolescent; Blood Transfusion; Cytosine; Female; Folic Acid; Humans; Leukemia, Erythroblastic, Acute | 1974 |