thymine has been researched along with Symptom Cluster in 19 studies
| 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) |
| "In contrast, Cockayne syndrome (CS) patients exhibit severe developmental and neurological defects, in addition to photosensitivity." | 1.33 | Host cell reactivation of plasmids containing oxidative DNA lesions is defective in Cockayne syndrome but normal in UV-sensitive syndrome fibroblasts. ( Hanawalt, PC; Spivak, G, 2006) |
| "Familial macrothrombocytopenias are a group of rare autosomal dominant platelet disorders including many syndromes in particular the May-Hegglin anomaly." | 1.33 | [The MYH9 syndrome: report of a new case with a new mutation of the MYH9 gene]. ( Bardet, V; Berda-Haddad, Y; Bernit, E; Camoin, L; Difeo, A; Ebbo, M; Favier, R; Harle, JR; Heudier, P; Kaplanski, G; Mazodier, K; Schleinitz, N; Veit, V, 2006) |
| "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 | 0 (0.00) | 18.7374 |
| 1990's | 1 (5.26) | 18.2507 |
| 2000's | 16 (84.21) | 29.6817 |
| 2010's | 2 (10.53) | 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 |
| Ali, A | 1 |
| Singh, SK | 1 |
| Raman, R | 1 |
| Pan, S | 1 |
| Xu, LL | 1 |
| Sun, LS | 1 |
| Li, TJ | 1 |
| Eshghyar, N | 1 |
| Nikbin, B | 1 |
| Amirzargar, A | 1 |
| Dehghani Nazhvani, A | 1 |
| Shakiba, Y | 1 |
| Arroyo-Espliguero, R | 1 |
| El-Sharnouby, K | 1 |
| Vázquez-Rey, E | 1 |
| Kalidas, K | 1 |
| Jeffery, S | 1 |
| Kaski, JC | 1 |
| Wong, K | 1 |
| Barbin, Y | 1 |
| Chakrabarti, S | 1 |
| Adams, P | 1 |
| Kellermayer, R | 1 |
| Siitonen, HA | 1 |
| Hadzsiev, K | 1 |
| Kestilä, M | 1 |
| Kosztolányi, G | 1 |
| Spivak, G | 1 |
| Hanawalt, PC | 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 |
| Schleinitz, N | 1 |
| Favier, R | 1 |
| Mazodier, K | 1 |
| Difeo, A | 1 |
| Ebbo, M | 1 |
| Veit, V | 1 |
| Berda-Haddad, Y | 1 |
| Bernit, E | 1 |
| Heudier, P | 1 |
| Kaplanski, G | 1 |
| Camoin, L | 2 |
| Bardet, V | 1 |
| Harle, JR | 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 |
| Matsuzawa, N | 1 |
| Shimozato, K | 1 |
| Natsume, N | 1 |
| Niikawa, N | 1 |
| Yoshiura, K | 1 |
| Cuisset, T | 1 |
| Frere, C | 1 |
| Quilici, J | 1 |
| Morange, PE | 1 |
| Saut, N | 1 |
| Romero-Barra, M | 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 |
| Seller, A | 1 |
| Kennedy, CR | 1 |
| Temple, IK | 1 |
| Brown, GK | 1 |
| Miki, Y | 1 |
| Taki, T | 1 |
| Ohura, T | 1 |
| Kato, H | 1 |
| Yanagisawa, M | 1 |
| Hayashi, Y | 1 |
| Sztriha, L | 1 |
| Frossard, P | 1 |
| Hofstra, RM | 1 |
| Verlind, E | 1 |
| Nork, M | 1 |
1 trial available for thymine and Symptom Cluster
| 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 |
18 other studies available for thymine and Symptom Cluster
| 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 |
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 |
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 |
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 point mutation in the iron-responsive element of the L-ferritin in a family with hereditary hyperferritinemia cataract syndrome.
Topics: Adult; Cataract; Female; Ferritins; Genes, Dominant; Guanine; Heterozygote; Humans; Iron-Regulatory | 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 |
Host cell reactivation of plasmids containing oxidative DNA lesions is defective in Cockayne syndrome but normal in UV-sensitive syndrome fibroblasts.
Topics: beta-Galactosidase; Cell Survival; Cells, Cultured; Cockayne Syndrome; DNA Damage; DNA Repair; DNA, | 2006 |
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 |
[The MYH9 syndrome: report of a new case with a new mutation of the MYH9 gene].
Topics: Adenine; Adolescent; Exons; Female; Humans; Molecular Motor Proteins; Myosin Heavy Chains; Point Mut | 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 |
A novel missense mutation in Van der Woude syndrome: usefulness of fingernail DNA for genetic analysis.
Topics: Adenine; Chromosomes, Human, Pair 1; Cleft Lip; Cleft Palate; DNA; Exons; Female; Genetic Linkage; H | 2006 |
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 |
Leigh syndrome resulting from de novo mutation at position 8993 of mitochondrial DNA.
Topics: DNA, Mitochondrial; Fatal Outcome; Guanine; Humans; Infant, Newborn; Leigh Disease; Male; Point Muta | 1997 |
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 |
Novel missense mutation in the L1 gene in a child with corpus callosum agenesis, retardation, adducted thumbs, spastic paraparesis, and hydrocephalus.
Topics: Agenesis of Corpus Callosum; Child; Guanine; Humans; Hydrocephalus; Intellectual Disability; Leukocy | 2000 |