Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with the progression of IgA nephropathy in Chinese.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association - 1 Aug 2011

Cheng Wenrong, Zhou Xujie, Zhu Li, Shi Sufang, Lv Jicheng, Liu Lijun, Zhang Hong

Abstract excerpt

BACKGROUND: IgA nephropathy (IgAN) is the leading cause of end-stage renal disease (ESRD) in China considering different compositions of ESRD causes in different ethnicities. A recent genome-wide association study (GWAS) indicated that the MYH9 gene was significantly associated with non-diabetic ESRD in African-Americans and also influenced kidney function in Europeans. Thus, in the present study, we aim to...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Asian People
Share to Disease Progression

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glomerular Filtration Rate

Share to Glomerulonephritis, IGA

Share to Molecular Motor Proteins

Share to Myosin Heavy Chains

Share to Neoplasm Grading

Share to Polymorphism, Restriction Fragment Length

Source

Identifiers

PMID: 21245129
DOI: 10.1093/ndt/gfq768

Genes

MYH9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with the progression of IgA nephropathy in Chinese.PMID 21245129Read ↗

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

The spectrum of MYH9-associated nephropathy.Semantic proximity Read ↗

Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study.Semantic proximity Read ↗

Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans.Semantic proximity Read ↗

Association between a MYH9 polymorphism (rs3752462) and renal function in the Spanish RENASTUR cohort.Semantic proximity Read ↗

Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.Semantic proximity Read ↗

Association of MYH9 Polymorphisms with Hypertension in Patients with Chronic Kidney Disease in China.Semantic proximity Read ↗

The Potential Impact of MYH9 (rs3752462) and ELMO1 (rs741301) Genetic Variants on the Risk of Nephrotic Syndrome Incidence.Semantic proximity Read ↗

Potential effects of MYH9-associated nephropathy on dialysis and kidney transplant outcomes.Semantic proximity Read ↗

The potential impact of MYH9 gene (rs3752462) and ELMO1 (rs741301) variants on the risk of Nephrotic syndrome incidenceSemantic proximity Read ↗

Effect of donor non-muscle myosin heavy chain (MYH9) gene polymorphisms on clinically relevant kidney allograft dysfunction.Semantic proximity Read ↗

MYH9 is associated with nondiabetic end-stage renal disease in African Americans.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.