Back to search

Article

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

2009-01-01

Abstract excerpt

No abstract is available from the source.

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
26744409-bca5-5a01-b302-6eee08af6085
DOI
10.1016/s0084-3873(09)79367-8
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
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 AmericansDOI 10.1016/s0084-3873(09)79367-8
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.Semantic proximity
Hypertension-associated kidney disease: perhaps no more.Semantic proximity
The spectrum of MYH9-associated nephropathy.Semantic proximity
Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study.Semantic proximity
Potential effects of MYH9-associated nephropathy on dialysis and kidney transplant outcomes.Semantic proximity
The association of the MYH9 gene and kidney outcomes in American Indians: the Strong Heart Family Study.Semantic proximity
MYH9 is associated with nondiabetic end-stage renal disease in African Americans.Semantic proximity
Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD.Semantic proximity
Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.Semantic proximity
Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans.Semantic proximity
KIDNEY DISEASE GENETICS AND THE IMPORTANCE OF DIVERSITY IN PRECISION MEDICINE.Semantic proximity
Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans.Semantic proximity
Select a neighboring publication to make it the new centre.