99 related articles for article (PubMed ID: 10383081)
1. Association between AGT T235 variant and microalbuminuria in Canadian Oji-Cree with type 2 diabetes mellitus.
Hegele RA; Harris SB; Hanley AJ; Zinman B
Clin Biochem; 1999 Apr; 32(3):201-5. PubMed ID: 10383081
[TBL] [Abstract][Full Text] [Related]
2. -6A promoter variant of angiotensinogen and blood pressure variation in Canadian Oji-Cree.
Hegele RA; Harris SB; Hanley AJ; Sun F; Connelly PW; Zinman B
J Hum Genet; 1998; 43(1):37-41. PubMed ID: 9609996
[TBL] [Abstract][Full Text] [Related]
3. Association between AGT codon 235 polymorphism and variation in serum concentrations of creatinine and urea in Canadian Oji-Cree.
Hegele RA; Harris SB; Hanley AJ; Zinman B
Clin Genet; 1999 Jun; 55(6):438-43. PubMed ID: 10450860
[TBL] [Abstract][Full Text] [Related]
4. Angiotensinogen gene T235 variant: a marker for the development of persistent microalbuminuria in children and adolescents with type 1 diabetes mellitus.
Gallego PH; Shephard N; Bulsara MK; van Bockxmeer FM; Powell BL; Beilby JP; Arscott G; Le Page M; Palmer LJ; Davis EA; Jones TW; Choong CS
J Diabetes Complications; 2008; 22(3):191-8. PubMed ID: 18413222
[TBL] [Abstract][Full Text] [Related]
5. Association of the angiotensinogen M235T and angiotensin-converting enzyme insertion/deletion gene polymorphisms in Turkish type 2 diabetic patients with and without nephropathy.
Eroglu Z; Cetinkalp S; Erdogan M; Kosova B; Karadeniz M; Kutukculer A; Gunduz C; Tetik A; Topcuoglu N; Ozgen AG; Tuzun M
J Diabetes Complications; 2008; 22(3):186-90. PubMed ID: 18413162
[TBL] [Abstract][Full Text] [Related]
6. The hepatic nuclear factor-1alpha G319S variant is associated with early-onset type 2 diabetes in Canadian Oji-Cree.
Hegele RA; Cao H; Harris SB; Hanley AJ; Zinman B
J Clin Endocrinol Metab; 1999 Mar; 84(3):1077-82. PubMed ID: 10084598
[TBL] [Abstract][Full Text] [Related]
7. NAT2 polymorphism associated with plasma glucose concentration in Canadian Oji-Cree.
Hegele RA; Kwan K; Harris SB; Hanley AJ; Zinman B; Cao H
Pharmacogenetics; 2000 Apr; 10(3):233-8. PubMed ID: 10803679
[TBL] [Abstract][Full Text] [Related]
8. The private hepatocyte nuclear factor-1alpha G319S variant is associated with plasma lipoprotein variation in Canadian Oji-Cree.
Hegele RA; Cao H; Harris SB; Hanley AJ; Zinman B; Connelly PW
Arterioscler Thromb Vasc Biol; 2000 Jan; 20(1):217-22. PubMed ID: 10634821
[TBL] [Abstract][Full Text] [Related]
9. Study of the polymorphism of angiotensinogen, anigiotensin-converting enzyme and angiotensin receptor in type II diabetes with end-stage renal disease in Taiwan.
Chang HR; Cheng CH; Shu KH; Chen CH; Lian JD; Wu MY
J Chin Med Assoc; 2003 Jan; 66(1):51-6. PubMed ID: 12728975
[TBL] [Abstract][Full Text] [Related]
10. Clinical and genetic associations with hypertriglyceridemic waist in a Canadian aboriginal population.
Pollex RL; Hanley AJ; Zinman B; Harris SB; Hegele RA
Int J Obes (Lond); 2006 Mar; 30(3):484-91. PubMed ID: 16276364
[TBL] [Abstract][Full Text] [Related]
11. Association of the angiotensinogen M235T and APO E gene polymorphisms in Turkish type 2 diabetic patients with and without nephropathy.
Reis KA; Ebinç FA; Koç E; Demirci H; Erten Y; Güz G; Derici UB; Bali M; Söylemezoğlu O; Arınsoy T; Sindel S
Ren Fail; 2011; 33(5):469-74. PubMed ID: 21500980
[TBL] [Abstract][Full Text] [Related]
12. Angiotensinogen M235T polymorphism is associated with plasma angiotensinogen and cardiovascular disease.
Winkelmann BR; Russ AP; Nauck M; Klein B; Böhm BO; Maier V; Zotz R; Matheis G; Wolf A; Wieland H; Gross W; Galton DJ; März W
Am Heart J; 1999 Apr; 137(4 Pt 1):698-705. PubMed ID: 10097233
[TBL] [Abstract][Full Text] [Related]
13. Renin-angiotensin-aldosterone system genotypes and haplotypes affect the susceptibility to nephropathy in type 2 diabetes patients.
Mtiraoui N; Ezzidi I; Turki A; Chaieb M; Mahjoub T; Almawi WY
J Renin Angiotensin Aldosterone Syst; 2011 Dec; 12(4):572-80. PubMed ID: 21421655
[TBL] [Abstract][Full Text] [Related]
14. [Relationships of angiotensinogen gene M235T variant with diabetic nephropathy in Chinese type 2 diabetes mellitus].
Wang J; Zhu X; Yang L; Zhou W; Li H; Fu H; Zhu L; Yuan S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):299-302. PubMed ID: 10514536
[TBL] [Abstract][Full Text] [Related]
15. Albuminuria and the renin-angiotensin system gene polymorphisms in type-2-diabetic and in normoglycemic hypertensive Chinese.
Thomas GN; Critchley JA; Tomlinson B; Lee ZS; Young RP; Cockran CS; Chan JC
Clin Nephrol; 2001 Jan; 55(1):7-15. PubMed ID: 11200871
[TBL] [Abstract][Full Text] [Related]
16. Polymorphism in the angiotensin converting enzyme but not in the angiotensinogen gene is associated with hypertension and type 2 diabetes: the Skaraborg Hypertension and diabetes project.
Bengtsson K; Orho-Melander M; Lindblad U; Melander O; Bøg-Hansen E; Ranstam J; Råstam L; Groop L
J Hypertens; 1999 Nov; 17(11):1569-75. PubMed ID: 10608470
[TBL] [Abstract][Full Text] [Related]
17. Association analyses of the polymorphisms of angiotensin-converting enzyme and angiotensinogen genes with diabetic nephropathy in Japanese non-insulin-dependent diabetics.
Ohno T; Kawazu S; Tomono S
Metabolism; 1996 Feb; 45(2):218-22. PubMed ID: 8596493
[TBL] [Abstract][Full Text] [Related]
18. Metabolic syndrome in aboriginal Canadians: prevalence and genetic associations.
Pollex RL; Hanley AJ; Zinman B; Harris SB; Khan HM; Hegele RA
Atherosclerosis; 2006 Jan; 184(1):121-9. PubMed ID: 15869758
[TBL] [Abstract][Full Text] [Related]
19. Genetic polymorphisms of the renin-angiotensin system and complications of insulin-dependent diabetes mellitus.
van Ittersum FJ; de Man AM; Thijssen S; de Knijff P; Slagboom E; Smulders Y; Tarnow L; Donker AJ; Bilo HJ; Stehouwer CD
Nephrol Dial Transplant; 2000 Jul; 15(7):1000-7. PubMed ID: 10862638
[TBL] [Abstract][Full Text] [Related]
20. Angiotensinogen and angiotensin-I converting enzyme gene polymorphisms and the risk of coronary artery disease in Chinese.
Ko YL; Ko YS; Wang SM; Chu PH; Teng MS; Cheng NJ; Chen WJ; Hsu TS; Kuo CT; Chiang CW; Lee YS
Hum Genet; 1997 Aug; 100(2):210-4. PubMed ID: 9254851
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]