thymine has been researched along with Diabetes Mellitus, Adult-Onset in 19 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "The overall OR (95% CI) of type 2 diabetes was 0." | 2.44 | Association between the T-381C polymorphism of the brain natriuretic peptide gene and risk of type 2 diabetes in human populations. ( Amouyel, P; Arveiler, D; Cottel, D; de Groote, P; Ferrières, J; Groves, CJ; Hattersley, AT; Hitman, GA; McCarthy, MI; Meirhaeghe, A; Sandhu, MS; Walker, M; Wareham, NJ, 2007) |
| "Metabolic syndrome was diagnosed on modified National Cholesterol Education Program Adult Treatment Panel III guidelines, using body mass index (BMI) instead of waist circumference." | 1.33 | Association of mitochondrial deoxyribonucleic acid 16189 variant (T->C transition) with metabolic syndrome in Chinese adults. ( Chen, IY; Chen, JF; Chen, MH; Chen, SD; Eng, HL; Lee, CF; Lin, TK; Liou, CW; Liu, RT; Wang, PW; Wei, YH; Weng, SW, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 18 (94.74) | 29.6817 |
| 2010's | 1 (5.26) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ritt, M | 1 |
| Ott, C | 1 |
| Delles, C | 1 |
| Schneider, MP | 1 |
| Schmieder, RE | 1 |
| Tavridou, A | 1 |
| Arvanitidis, KI | 1 |
| Tiptiri-Kourpeti, A | 1 |
| Petridis, I | 1 |
| Ragia, G | 1 |
| Kyroglou, S | 1 |
| Christakidis, D | 1 |
| Manolopoulos, VG | 1 |
| Yuasa, S | 1 |
| Maruyama, T | 1 |
| Yamamoto, Y | 1 |
| Hirose, H | 1 |
| Kawai, T | 1 |
| Matsunaga-Irie, S | 1 |
| Itoh, H | 1 |
| López, NJ | 1 |
| Valenzuela, CY | 1 |
| Jara, L | 1 |
| Xia, JF | 1 |
| Hu, P | 1 |
| Liang, QL | 1 |
| Zou, TT | 1 |
| Wang, YM | 1 |
| Luo, GA | 1 |
| Doney, A | 1 |
| Fischer, B | 2 |
| Frew, D | 1 |
| Cumming, A | 1 |
| Flavell, DM | 1 |
| World, M | 1 |
| Montgomery, HE | 1 |
| Boyle, D | 1 |
| Morris, A | 1 |
| Palmer, CN | 2 |
| Ohtoshi, K | 1 |
| Yamasaki, Y | 1 |
| Gorogawa, S | 1 |
| Hayaishi-Okano, R | 1 |
| Node, K | 1 |
| Matsuhisa, M | 1 |
| Kajimoto, Y | 1 |
| Hori, M | 1 |
| Malecki, MT | 1 |
| Klupa, T | 1 |
| Wolkow, P | 1 |
| Bochenski, J | 1 |
| Wanic, K | 1 |
| Sieradzki, J | 1 |
| Toye, AA | 1 |
| Moir, L | 1 |
| Hugill, A | 1 |
| Bentley, L | 1 |
| Quarterman, J | 1 |
| Mijat, V | 1 |
| Hough, T | 1 |
| Goldsworthy, M | 1 |
| Haynes, A | 1 |
| Hunter, AJ | 1 |
| Browne, M | 1 |
| Spurr, N | 1 |
| Cox, RD | 1 |
| Doney, AS | 1 |
| Leese, G | 1 |
| Morris, AD | 1 |
| Tavares, V | 1 |
| Hirata, RD | 1 |
| Rodrigues, AC | 1 |
| Monte, O | 1 |
| Salles, JE | 1 |
| Scallissi, N | 1 |
| Speranza, AC | 1 |
| Gomes, S | 1 |
| Hirata, MH | 1 |
| Nakagawa, T | 1 |
| Furuta, H | 1 |
| Sanke, T | 1 |
| Sakagashira, S | 1 |
| Shimomura, H | 1 |
| Shimajiri, Y | 1 |
| Hanabusa, T | 1 |
| Nishi, M | 1 |
| Sasaki, H | 1 |
| Nanjo, K | 1 |
| Weng, SW | 1 |
| Liou, CW | 1 |
| Lin, TK | 1 |
| Wei, YH | 1 |
| Lee, CF | 1 |
| Eng, HL | 1 |
| Chen, SD | 1 |
| Liu, RT | 1 |
| Chen, JF | 1 |
| Chen, IY | 1 |
| Chen, MH | 1 |
| Wang, PW | 1 |
| Dworacka, M | 1 |
| Winiarska, H | 1 |
| Jagodziński, PP | 1 |
| Eroglu, Z | 1 |
| Erdogan, M | 1 |
| Tetik, A | 1 |
| Karadeniz, M | 1 |
| Cetinalp, S | 1 |
| Kosova, B | 1 |
| Gunduz, C | 1 |
| Ozgen, AG | 1 |
| Yilmaz, C | 1 |
| Meirhaeghe, A | 1 |
| Sandhu, MS | 1 |
| McCarthy, MI | 1 |
| de Groote, P | 1 |
| Cottel, D | 1 |
| Arveiler, D | 1 |
| Ferrières, J | 1 |
| Groves, CJ | 1 |
| Hattersley, AT | 1 |
| Hitman, GA | 1 |
| Walker, M | 1 |
| Wareham, NJ | 1 |
| Amouyel, P | 1 |
| Tarnai, I | 1 |
| Csordás, M | 1 |
| Sükei, E | 1 |
| Shemirani, AH | 1 |
| Káplár, M | 1 |
| Góth, L | 1 |
| Yang, T | 1 |
| Lam, CW | 1 |
| Tsang, MW | 1 |
| Tong, SF | 1 |
| Chan, LY | 1 |
| Kam, GY | 1 |
| Poon, PM | 1 |
| Wu, XQ | 1 |
| Pang, CP | 1 |
| Gill-Randall, R | 1 |
| Sherratt, EJ | 1 |
| Thomas, AW | 1 |
| Gagg, JW | 1 |
| Lee, A | 1 |
| Alcolado, JC | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Genetic Based Analysis of Identifying Predictors of Blood Pressure Response in Hypertensive Patients After Renal Denervation[NCT04321044] | 300 participants (Actual) | Interventional | 2019-01-01 | Active, not recruiting | |||
| Prospective Study on Endothelial Function in Subjects With Type 2 Diabetes Mellitus[NCT00905528] | 69 participants (Anticipated) | Observational | 2002-01-31 | Completed | |||
| Genetics of Diabetes Audit and Research in Tayside Scotland (DOLORisk Dundee)[NCT02783469] | 1,915 participants (Actual) | Observational | 2004-10-31 | Completed | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
1 review available for thymine and Diabetes Mellitus, Adult-Onset
| Article | Year |
|---|---|
Association between the T-381C polymorphism of the brain natriuretic peptide gene and risk of type 2 diabetes in human populations.
Topics: Adult; Aged; Animals; Case-Control Studies; Chlorocebus aethiops; COS Cells; Cytosine; Diabetes Mell | 2007 |
18 other studies available for thymine and Diabetes Mellitus, Adult-Onset
| Article | Year |
|---|---|
Impact of the endothelial nitric oxide synthase gene G894T polymorphism on renal endothelial function in patients with type 2 diabetes.
Topics: Alleles; Analysis of Variance; Arginine; Ascorbic Acid; Body Mass Index; Cholesterol, HDL; Diabetes | 2008 |
Impact of the endothelial nitric oxide synthase gene G894T polymorphism on renal endothelial function in patients with type 2 diabetes.
Topics: Alleles; Analysis of Variance; Arginine; Ascorbic Acid; Body Mass Index; Cholesterol, HDL; Diabetes | 2008 |
Impact of the endothelial nitric oxide synthase gene G894T polymorphism on renal endothelial function in patients with type 2 diabetes.
Topics: Alleles; Analysis of Variance; Arginine; Ascorbic Acid; Body Mass Index; Cholesterol, HDL; Diabetes | 2008 |
Impact of the endothelial nitric oxide synthase gene G894T polymorphism on renal endothelial function in patients with type 2 diabetes.
Topics: Alleles; Analysis of Variance; Arginine; Ascorbic Acid; Body Mass Index; Cholesterol, HDL; Diabetes | 2008 |
Thr54 allele of fatty-acid binding protein 2 gene is associated with obesity but not type 2 diabetes mellitus in a Caucasian population.
Topics: Adenine; Amino Acid Substitution; Diabetes Mellitus, Type 2; Fatty Acid-Binding Proteins; Genotype; | 2009 |
MCP-1 gene A-2518G polymorphism and carotid artery atherosclerosis in patients with type 2 diabetes.
Topics: Adenine; Aged; Asian People; Carotid Artery Diseases; Chemokine CCL2; Diabetes Mellitus, Type 2; Dia | 2009 |
Interleukin-1 gene cluster polymorphisms associated with periodontal disease in type 2 diabetes.
Topics: Adult; Age Factors; Aged; Alleles; Case-Control Studies; Chronic Periodontitis; Cytosine; Dental Pla | 2009 |
Correlations of creatine and six related pyrimidine metabolites and diabetic nephropathy in Chinese type 2 diabetic patients.
Topics: Aged; Chromatography, High Pressure Liquid; Creatine; Cytidine; Cytosine; Deoxyuridine; Diabetes Mel | 2010 |
Haplotype analysis of the PPARgamma Pro12Ala and C1431T variants reveals opposing associations with body weight.
Topics: Adult; Alanine; Amino Acid Substitution; Body Mass Index; Body Weight; Cytosine; Diabetes Mellitus, | 2002 |
Association of (-)786T-C mutation of endothelial nitric oxide synthase gene with insulin resistance.
Topics: Adult; Aged; Asian People; Base Sequence; Blood Pressure; Cytidine; Diabetes Mellitus, Type 2; DNA P | 2002 |
Association study of the vitamin D: 1alpha-hydroxylase (CYP1alpha) gene and type 2 diabetes mellitus in a Polish population.
Topics: Cytosine; Diabetes Mellitus; Diabetes Mellitus, Type 2; Genetic Markers; Genotype; Humans; Introns; | 2003 |
A new mouse model of type 2 diabetes, produced by N-ethyl-nitrosourea mutagenesis, is the result of a missense mutation in the glucokinase gene.
Topics: Adenine; Amino Acid Sequence; Amino Acid Substitution; Animals; Chromosome Mapping; Diabetes Mellitu | 2004 |
Cardiovascular risk in type 2 diabetes is associated with variation at the PPARG locus: a Go-DARTS study.
Topics: Age Factors; Alanine; Alleles; Amino Acid Substitution; Cardiovascular Diseases; Cohort Studies; Cyt | 2004 |
Effect of the peroxisome proliferator-activated receptor-gamma C161T polymorphism on lipid profile in Brazilian patients with Type 2 diabetes mellitus.
Topics: Adult; Aged; Base Sequence; Brazil; Case-Control Studies; Cytosine; Diabetes Mellitus, Type 2; Femal | 2005 |
Molecular scanning of the betacellulin gene for mutations in type 2 diabetic patients.
Topics: Aged; Amino Acid Substitution; Base Sequence; Betacellulin; Cysteine; Cytosine; Diabetes Mellitus, T | 2005 |
Association of mitochondrial deoxyribonucleic acid 16189 variant (T->C transition) with metabolic syndrome in Chinese adults.
Topics: Aged; Asian People; Blood Glucose; Case-Control Studies; Cytosine; Diabetes Mellitus, Type 2; DNA, M | 2005 |
Impact of the sulfonylurea receptor 1 (SUR1) exon 16-3c/t polymorphism on acute hyperglycaemia in type 2 diabetic patients.
Topics: Age of Onset; ATP-Binding Cassette Transporters; Body Mass Index; Cytosine; Diabetes Mellitus, Type | 2007 |
The relationship of the methylenetetrahydrofolate reductase C677T gene polymorphism in Turkish type 2 diabetic patients with and without nephropathy.
Topics: Aged; Cytosine; Diabetes Mellitus, Type 2; Diabetic Nephropathies; DNA; DNA Primers; Gene Frequency; | 2007 |
Effect of C111T polymorphism in exon 9 of the catalase gene on blood catalase activity in different types of diabetes mellitus.
Topics: Adult; Catalase; Cytosine; Diabetes Mellitus, Type 1; Diabetes Mellitus, Type 2; Diabetes, Gestation | 2007 |
Novel single nucleotide polymorphisms (3203A>G and 3204C>T) in the 3' end of the mitochondrial 16S rRNA gene.
Topics: 3' Untranslated Regions; Adenine; Base Sequence; Cytosine; Diabetes Mellitus, Type 2; Guanine; Human | 2000 |
Analysis of a polycytosine tract and heteroplasmic length variation in the mitochondrial DNA D-loop of patients with diabetes, MELAS syndrome and race-matched controls.
Topics: Adult; Cytosine; Diabetes Mellitus, Type 2; DNA, Mitochondrial; Genetic Variation; Humans; Leukocyte | 2001 |