Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD - Wikidata - wikimedia - TriplyDB

Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD

Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD

http://www.wikidata.org/entity/Q34021318

about

Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans Association of trypanolytic ApoL1 variants with kidney disease in African Americans Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene Genome-wide association studies of chronic kidney disease: what have we learned?Developments in renal pharmacogenomics and applications in chronic kidney disease A genome-wide association search for type 2 diabetes genes in African Americans Worldwide distribution of the MYH9 kidney disease susceptibility alleles and haplotypes: evidence of historical selection in Africa A genome-wide association study for diabetic nephropathy genes in African Americans Analysis of coding variants identified from exome sequencing resources for association with diabetic and non-diabetic nephropathy in African Americans Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.Genetics of focal segmental glomerulosclerosis and human immunodeficiency virus-associated collapsing glomerulopathy: the role of MYH9 genetic variation.Is collapsing C1q nephropathy another MYH9-associated kidney disease? A case report.Reappraisal of the impact of race on survival in patients on dialysis.Essential hypertension and risk of nephropathy: a reappraisal.Potential effects of MYH9-associated nephropathy on dialysis and kidney transplant outcomes.Hereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations.Genetic basis of nondiabetic end-stage renal disease The non-muscle Myosin heavy chain 9 gene (MYH9) is not associated with lupus nephritis in African Americans The association of the MYH9 gene and kidney outcomes in American Indians: the Strong Heart Family Study The spectrum of MYH9-associated nephropathy The population genetics of chronic kidney disease: insights from the MYH9-APOL1 locus.Chronic kidney disease prediction is an inexact science: The concept of "progressors" and "nonprogressors"APOL1 risk variants, race, and progression of chronic kidney disease Coincident idiopathic focal segmental glomerulosclerosis collapsing variant and diabetic nephropathy in an African American homozygous for MYH9 risk variants 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.APOL1 null alleles from a rural village in India do not correlate with glomerulosclerosis.Recent developments in HIV-related kidney disease.Genetic susceptibility to idiopathic membranous nephropathy in high-prevalence Area, Taiwan MYH9 genetic variants associated with glomerular disease: what is the role for genetic testing?The MYH9/APOL1 region and chronic kidney disease in European-Americans.Susceptibility gene search for nephropathy and related traits in Mexican-Americans.Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA.Apolipoprotein L1 nephropathy risk variants associate with HDL subfraction concentration in African Americans.African origins and chronic kidney disease susceptibility in the human immunodeficiency virus era.Population-based risk assessment of APOL1 on renal disease.Target organ damage in African American hypertension: role of APOL1.Effect of Genetic African Ancestry on eGFR and Kidney Disease.Genome-wide association of BMI in African Americans.Implication of European-derived adiposity loci in African Americans.

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P2860

Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD

http://www.wikidata.org/entity/Q34021318

description

2009 nî lūn-bûn

@nan

2009 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հունիսին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Non-muscle myosin heavy chain ...... betes mellitus-associated ESRD

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Non-muscle myosin heavy chain ...... betes mellitus-associated ESRD

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Non-muscle myosin heavy chain ...... betes mellitus-associated ESRD

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type

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Non-muscle myosin heavy chain ...... betes mellitus-associated ESRD

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Non-muscle myosin heavy chain ...... betes mellitus-associated ESRD

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Non-muscle myosin heavy chain ...... betes mellitus-associated ESRD

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Non-muscle myosin heavy chain ...... betes mellitus-associated ESRD

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Non-muscle myosin heavy chain ...... betes mellitus-associated ESRD

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Non-muscle myosin heavy chain ...... betes mellitus-associated ESRD

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P1433

Nephrology Dialysis Transplantation

P1476

Non-muscle myosin heavy chain ...... betes mellitus-associated ESRD

@en

P2093

Anthony J Bleyer

http://www.w3.org/2001/XMLSchema#string

Barry I Freedman

http://www.w3.org/2001/XMLSchema#string

Carl D Langefeld

http://www.w3.org/2001/XMLSchema#string

Cheryl A Winkler

http://www.w3.org/2001/XMLSchema#string

Donald W Bowden

http://www.w3.org/2001/XMLSchema#string

George W Nelson

http://www.w3.org/2001/XMLSchema#string

Jasmin Divers

http://www.w3.org/2001/XMLSchema#string

Mary E Comeau

http://www.w3.org/2001/XMLSchema#string

Meredith A Bostrom

http://www.w3.org/2001/XMLSchema#string

Pamela J Hicks

http://www.w3.org/2001/XMLSchema#string

P2860

A note on exact tests of Hardy-Weinberg equilibrium

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis

MYH9 is associated with nondiabetic end-stage renal disease in African Americans

Haploview: analysis and visualization of LD and haplotype maps

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.

Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene.

Estimation of individual admixture: analytical and study design considerations.

The Family Investigation of Nephropathy and Diabetes (FIND): design and methods.

Molecular genetic approaches for studying the etiology of diabetic nephropathy.

Familial clustering of chronic kidney disease.

P304

3366-3371

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scholarly article

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10.1093/NDT/GFP316

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P407

P433

11

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P478

24

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Jeffrey B. Kopp

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2009-06-30T00:00:00Z

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26331372

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19567477

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P921

type-2 diabetes

P932

2910323

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