Literature DB >> 18255011

Examining diabetic nephropathy through the lens of mouse genetics.

Matthew D Breyer1, Elena Tchekneva, Zhonghua Qi, Takamune Takahashi, Agnes B Fogo, Raymond C Harris.   

Abstract

Although diabetic nephropathy occurs in only a minority of patients with diabetes, it is the major cause of end-stage renal disease in the United States. Hyperglycemia and hypertension are important factors predisposing patients to diabetic nephropathy, but accumulating evidence points to critical genetic factors predisposing only a subset of patients with diabetes to nephropathy. It has been challenging to define the genes conferring risk for nephropathy in human populations. Comparative genomics using the robust genetic reagents available in laboratory mice should provide a complementary approach to defining genes that may predispose to diabetic nephropathy in mice and humans. This article reviews new studies to identify genetic risk factors for diabetic nephropathy and the unique approaches that may be used to elucidate the genetic pathogenesis of this disorder in mice.

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Year:  2007        PMID: 18255011     DOI: 10.1007/s11892-007-0078-3

Source DB:  PubMed          Journal:  Curr Diab Rep        ISSN: 1534-4827            Impact factor:   4.810


  67 in total

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2.  Familial clustering of diabetic kidney disease. Evidence for genetic susceptibility to diabetic nephropathy.

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Review 6.  Glucose, glycation, and RAGE: implications for amplification of cellular dysfunction in diabetic nephropathy.

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Journal:  J Am Soc Nephrol       Date:  2003-05       Impact factor: 10.121

7.  Retinopathy and nephropathy in patients with type 1 diabetes four years after a trial of intensive therapy.

Authors:  John M Lachin; Saul Genuth; Patricia Cleary; Matthew D Davis; David M Nathan
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8.  Deficiency of endothelial nitric-oxide synthase confers susceptibility to diabetic nephropathy in nephropathy-resistant inbred mice.

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Review 9.  ENU mutagenesis in the mouse: application to human genetic disease.

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3.  Evaluation of renal hypoxia in diabetic mice by BOLD MRI.

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