Page last updated: 2024-10-17

cytosine and Syndrome

cytosine has been researched along with Syndrome in 29 studies

Syndrome: A characteristic symptom complex.

Research Excerpts

ExcerptRelevanceReference
" 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)."9.12Lack 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)."5.12Lack 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)."3.71Chemotherapy-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."3.69Abnormal 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."1.32Novel 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."1.31Novel 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)

Research

Studies (29)

TimeframeStudies, this research(%)All Research%
pre-19901 (3.45)18.7374
1990's4 (13.79)18.2507
2000's20 (68.97)29.6817
2010's4 (13.79)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cherkaoui Jaouad, I1
El Alloussi, M1
Chafai El Alaoui, S1
Laarabi, FZ1
Lyahyai, J1
Sefiani, A1
Venza, M1
Visalli, M1
Venza, I1
Torino, C1
Tripodo, B1
Melita, R1
Teti, D1
Kahraman, A1
Miller, M1
Maldonado-Lopez, E1
Baba, HA1
Treichel, U1
Gerken, G1
Ali, A1
Singh, SK1
Raman, R1
Pan, S1
Xu, LL1
Sun, LS1
Li, TJ1
Keohane, C1
Bacon, CL1
Moran, B1
Irvine, AD1
Smith, OP1
Descamps, V1
Eshghyar, N1
Nikbin, B1
Amirzargar, A1
Dehghani Nazhvani, A1
Shakiba, Y1
Nichol, K1
Pearson, CE1
Sato, U1
Horikawa, R1
Katsumata, N1
Asakura, Y1
Kitanaka, S1
Tanaka, T1
Arroyo-Espliguero, R1
El-Sharnouby, K1
Vázquez-Rey, E1
Kalidas, K1
Jeffery, S1
Kaski, JC1
Kellermayer, R1
Siitonen, HA1
Hadzsiev, K1
Kestilä, M1
Kosztolányi, G1
Anderson, PJ1
Netherway, DJ1
Cox, TC1
Roscioli, T1
David, DJ1
Vanita, V1
Singh, JR1
Hejtmancik, JF1
Nuernberg, P1
Hennies, HC1
Singh, D1
Sperling, K1
Gonzalez-Porras, JR1
Martin-Herrero, F1
Garcia-Sanz, R1
Lopez, ML1
Balanzategui, A1
Mateos, MV1
Pavon, P1
Gonzalez, M1
Alberca, I1
San Miguel, JF1
Cuisset, T1
Frere, C1
Quilici, J1
Morange, PE1
Saut, N1
Romero-Barra, M1
Camoin, L1
Lambert, M1
Juhan-Vague, I1
Bonnet, JL1
Alessi, MC1
Wang, J1
Liu, J1
Zhang, Q1
Meyer-Marcotty, P1
Weisschuh, N1
Dressler, P1
Hartmann, J1
Stellzig-Eisenhauer, A1
Miniou, P1
Jeanpierre, M1
Blanquet, V1
Sibella, V1
Bonneau, D1
Herbelin, C1
Fischer, A1
Niveleau, A1
Viegas-Péquignot, E1
Inoue, T1
Okauchi, Y1
Matsuzaki, Y1
Kuwajima, K1
Kondo, H1
Horiuchi, N1
Nakao, K1
Iwata, M1
Yokogoshi, Y1
Shintani, Y1
Bando, H1
Saito, S1
Karavellas, MP1
Plummer, DJ1
Macdonald, JC1
Torriani, FJ1
Shufelt, CL1
Azen, SP1
Freeman, WR1
Miki, Y1
Taki, T1
Ohura, T1
Kato, H1
Yanagisawa, M1
Hayashi, Y1
Tuck-Muller, CM1
Narayan, A1
Tsien, F1
Smeets, DF1
Sawyer, J1
Fiala, ES1
Sohn, OS1
Ehrlich, M1
Costello, JF1
Plass, C1
Bhorade, SM1
Sandesara, C1
Garrity, ER1
Vigneswaran, WT1
Norwick, L1
Alkan, S1
Husain, AN1
McCabe, MA1
Yeldandi, V1
Kosaki, K1
Ogata, T1
Kosaki, R1
Sato, S1
Matsuo, N1
Hui, YF1
Giles, FJ1
Cortes, JE1
Usala, SJ1
Menke, JB1
Watson, TL1
Bérard, WE1
Bradley, C1
Bale, AE1
Lash, RW1
Weintraub, BD1
Ozsoylu, S1
Hiçsönmez, G1

Reviews

2 reviews available for cytosine and Syndrome

ArticleYear
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.
    European journal of endocrinology, 1998, Volume: 138, Issue:6

    Topics: Adolescent; Adult; Amino Acid Sequence; Amino Acid Substitution; Arginine; Base Sequence; Cytosine;

1998
Methylation matters.
    Journal of medical genetics, 2001, Volume: 38, Issue:5

    Topics: 5-Methylcytosine; Chromosome Aberrations; CpG Islands; Cytosine; DNA Methylation; DNA Transposable E

2001

Trials

1 trial available for cytosine and Syndrome

ArticleYear
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.
    Thrombosis and haemostasis, 2007, Volume: 97, Issue:2

    Topics: Acute Disease; Adenosine Diphosphate; Aged; Aspirin; Blood Platelets; Cell Adhesion Molecules; Clopi

2007

Other Studies

26 other studies available for cytosine and Syndrome

ArticleYear
Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report.
    BMC oral health, 2015, Jan-30, Volume: 15

    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.
    Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2009, Volume: 38, Issue:1

    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].
    Medizinische Klinik (Munich, Germany : 1983), 2009, Feb-15, Volume: 104, Issue:2

    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.
    The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2009, Volume: 46, Issue:5

    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.
    International journal of oral science, 2009, Volume: 1, Issue:1

    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.
    Pediatric transplantation, 2011, Volume: 15, Issue:1

    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.
    Pediatric transplantation, 2011, Volume: 15, Issue:4

    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.
    Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2012, Volume: 41, Issue:9

    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.
    Genome research, 2002, Volume: 12, Issue:8

    Topics: Abnormalities, Multiple; Animals; Cell Line; Centromere; Chlorocebus aethiops; Cloning, Molecular; C

2002
Novel compound heterozygous AIRE mutations in a Japanese patient with APECED.
    Journal of pediatric endocrinology & metabolism : JPEM, 2004, Volume: 17, Issue:6

    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.
    International journal of cardiology, 2005, Feb-15, Volume: 98, Issue:2

    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.
    Archives of dermatology, 2005, Volume: 141, Issue:5

    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?
    The Journal of craniofacial surgery, 2006, Volume: 17, Issue:1

    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.
    Molecular vision, 2006, May-22, Volume: 12

    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.
    Thrombosis research, 2007, Volume: 119, Issue:6

    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.
    Molecular vision, 2007, Jan-26, Volume: 13

    Topics: Asian People; Blepharophimosis; Blepharoptosis; Cysteine; Cytosine; Eye Abnormalities; Eyelids; Fork

2007
Morphology of the sella turcica in Axenfeld-Rieger syndrome with PITX2 mutation.
    Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2008, Volume: 37, Issue:8

    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.
    Human molecular genetics, 1994, Volume: 3, Issue:12

    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.
    The Journal of infectious diseases, 1999, Volume: 179, Issue:3

    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.
    The Journal of pediatrics, 2000, Volume: 136, Issue:1

    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.
    Cytogenetics and cell genetics, 2000, Volume: 89, Issue:1-2

    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.
    The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation, 2001, Volume: 20, Issue:9

    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.
    Ophthalmic genetics, 2002, Volume: 23, Issue:1

    Topics: Blepharophimosis; Blepharoptosis; Child; Cytosine; DNA Mutational Analysis; DNA Primers; DNA-Binding

2002
Chemotherapy-induced palmar-plantar erythrodysesthesia syndrome--recall following different chemotherapy agents.
    Investigational new drugs, 2002, Volume: 20, Issue:1

    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.
    The Journal of clinical endocrinology and metabolism, 1991, Volume: 72, Issue:1

    Topics: Base Sequence; Binding Sites; Cytosine; Deoxyribonucleases, Type II Site-Specific; Drug Resistance;

1991
A case of erythroleukemia. (di Guglielmo's syndrome).
    The Turkish journal of pediatrics, 1974, Volume: 26, Issue:2

    Topics: Adolescent; Blood Transfusion; Cytosine; Female; Folic Acid; Humans; Leukemia, Erythroblastic, Acute

1974