116 related articles for article (PubMed ID: 25730040)
1. MYH9 gene polymorphisms may be associated with cerebrovascular blood flow in patients with type 2 diabetes.
Ling C; Cai CY; Chang BC; Shi WT; Wei FJ; Yu P; Chen LM; Li WD
Genet Mol Res; 2015 Feb; 14(1):1008-16. PubMed ID: 25730040
[TBL] [Abstract][Full Text] [Related]
2. Association between
Zhao H; Ma L; Yan M; Wang Y; Zhao T; Zhang H; Liu P; Liu Y; Li P
J Diabetes Res; 2018; 2018():5068578. PubMed ID: 29862302
[TBL] [Abstract][Full Text] [Related]
3. Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans.
Cooke JN; Bostrom MA; Hicks PJ; Ng MC; Hellwege JN; Comeau ME; Divers J; Langefeld CD; Freedman BI; Bowden DW
Nephrol Dial Transplant; 2012 Apr; 27(4):1505-11. PubMed ID: 21968013
[TBL] [Abstract][Full Text] [Related]
4. Association of MYH9 Polymorphisms with Hypertension in Patients with Chronic Kidney Disease in China.
Liu L; Wang C; Mi Y; Liu D; Li L; Fan J; Nan L; Jia N; Du Y
Kidney Blood Press Res; 2016; 41(6):956-965. PubMed ID: 27924804
[TBL] [Abstract][Full Text] [Related]
5. Association between a MYH9 polymorphism (rs3752462) and renal function in the Spanish RENASTUR cohort.
Tavira B; Coto E; Gómez J; Tranche S; Miguélez K; Ortega F; Díez B; Sánchez E; Marín R; Arenas J; Alvarez V
Gene; 2013 May; 520(1):73-6. PubMed ID: 23470845
[TBL] [Abstract][Full Text] [Related]
6. Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD.
Freedman BI; Hicks PJ; Bostrom MA; Comeau ME; Divers J; Bleyer AJ; Kopp JB; Winkler CA; Nelson GW; Langefeld CD; Bowden DW
Nephrol Dial Transplant; 2009 Nov; 24(11):3366-71. PubMed ID: 19567477
[TBL] [Abstract][Full Text] [Related]
7. The association of the MYH9 gene and kidney outcomes in American Indians: the Strong Heart Family Study.
Franceschini N; Voruganti VS; Haack K; Almasy L; Laston S; Goring HH; Umans JG; Lee ET; Best LG; Fabsitz RR; MacCluer JW; Howard BV; North KE; Cole SA
Hum Genet; 2010 Mar; 127(3):295-301. PubMed ID: 19921264
[TBL] [Abstract][Full Text] [Related]
8. Functional Effects of SNPs in MYH9 and Risks of Nonsyndromic Orofacial Clefts.
Wang Y; Li D; Xu Y; Ma L; Lu Y; Wang Z; Wang L; Zhang W; Pan Y
J Dent Res; 2018 Apr; 97(4):388-394. PubMed ID: 29207917
[TBL] [Abstract][Full Text] [Related]
9. Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans.
Freedman BI; Hicks PJ; Bostrom MA; Cunningham ME; Liu Y; Divers J; Kopp JB; Winkler CA; Nelson GW; Langefeld CD; Bowden DW
Kidney Int; 2009 Apr; 75(7):736-45. PubMed ID: 19177153
[TBL] [Abstract][Full Text] [Related]
10. MYH9 and APOL1 are both associated with sickle cell disease nephropathy.
Ashley-Koch AE; Okocha EC; Garrett ME; Soldano K; De Castro LM; Jonassaint JC; Orringer EP; Eckman JR; Telen MJ
Br J Haematol; 2011 Nov; 155(3):386-94. PubMed ID: 21910715
[TBL] [Abstract][Full Text] [Related]
11. Polymorphisms in the non-muscle myosin heavy chain gene (MYH9) are associated with lower glomerular filtration rate in mixed ancestry diabetic subjects from South Africa.
Matsha TE; Masconi K; Yako YY; Hassan MS; Macharia M; Erasmus RT; Kengne AP
PLoS One; 2012; 7(12):e52529. PubMed ID: 23285077
[TBL] [Abstract][Full Text] [Related]
12. Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with the progression of IgA nephropathy in Chinese.
Cheng W; Zhou X; Zhu L; Shi S; Lv J; Liu L; Zhang H
Nephrol Dial Transplant; 2011 Aug; 26(8):2544-9. PubMed ID: 21245129
[TBL] [Abstract][Full Text] [Related]
13. African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans.
Behar DM; Rosset S; Tzur S; Selig S; Yudkovsky G; Bercovici S; Kopp JB; Winkler CA; Nelson GW; Wasser WG; Skorecki K
Hum Mol Genet; 2010 May; 19(9):1816-27. PubMed ID: 20144966
[TBL] [Abstract][Full Text] [Related]
14. Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.
Tzur S; Rosset S; Shemer R; Yudkovsky G; Selig S; Tarekegn A; Bekele E; Bradman N; Wasser WG; Behar DM; Skorecki K
Hum Genet; 2010 Sep; 128(3):345-50. PubMed ID: 20635188
[TBL] [Abstract][Full Text] [Related]
15. Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study.
Freedman BI; Kopp JB; Winkler CA; Nelson GW; Rao DC; Eckfeldt JH; Leppert MF; Hicks PJ; Divers J; Langefeld CD; Hunt SC
Am J Nephrol; 2009; 29(6):626-32. PubMed ID: 19153477
[TBL] [Abstract][Full Text] [Related]
16. MYH9 and APOL1 gene polymorphisms and the risk of CKD in patients with lupus nephritis from an admixture population.
Colares VS; Titan SM; Pereira Ada C; Malafronte P; Cardena MM; Santos S; Santos PC; Fridman C; Barros RT; Woronik V
PLoS One; 2014; 9(3):e87716. PubMed ID: 24658608
[TBL] [Abstract][Full Text] [Related]
17. The MYH9/APOL1 region and chronic kidney disease in European-Americans.
O'Seaghdha CM; Parekh RS; Hwang SJ; Li M; Köttgen A; Coresh J; Yang Q; Fox CS; Kao WH
Hum Mol Genet; 2011 Jun; 20(12):2450-6. PubMed ID: 21429915
[TBL] [Abstract][Full Text] [Related]
18. Association of single nucleotide polymorphisms in TCF2 with type 2 diabetes susceptibility in a Han Chinese population.
Zhang X; Qiao H; Zhao Y; Wang X; Sun H; Liu A; Xu L; Sun D; Jin Y; Yu Y; Meng X; Bai J; Chen F; Fu S
PLoS One; 2012; 7(12):e52938. PubMed ID: 23300827
[TBL] [Abstract][Full Text] [Related]
19. Evaluation of candidate nephropathy susceptibility genes in a genome-wide association study of African American diabetic kidney disease.
Palmer ND; Ng MC; Hicks PJ; Mudgal P; Langefeld CD; Freedman BI; Bowden DW
PLoS One; 2014; 9(2):e88273. PubMed ID: 24551085
[TBL] [Abstract][Full Text] [Related]
20. Impact of diabetes-related gene polymorphisms on the clinical characteristics of type 2 diabetes Chinese Han population.
Li J; Wei J; Xu P; Yan M; Li J; Chen Z; Jin T
Oncotarget; 2016 Dec; 7(51):85464-85471. PubMed ID: 27863428
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]