cytosine has been researched along with Syndrome in 29 studies
Syndrome: A characteristic symptom complex.
Excerpt | Relevance | Reference |
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" 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 |
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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 |
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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 |
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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 |
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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 |