TRPC6 gene promoter polymorphisms in steroid resistant nephrotic syndrome children.

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TRPC6 gene promoter polymorphisms in steroid resistant nephrotic syndrome children.

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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2015年學術文章

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TRPC6 gene promoter polymorphisms in steroid resistant nephrotic syndrome children.

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TRPC6 gene promoter polymorphisms in steroid resistant nephrotic syndrome children.

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TRPC6 gene promoter polymorphisms in steroid resistant nephrotic syndrome children.

@en

TRPC6 gene promoter polymorphisms in steroid resistant nephrotic syndrome children.

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TRPC6 gene promoter polymorphisms in steroid resistant nephrotic syndrome children.

@en

TRPC6 gene promoter polymorphisms in steroid resistant nephrotic syndrome children.

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P1476

TRPC6 gene promoter polymorphisms in steroid resistant nephrotic syndrome children.

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P2093

Elumalai Ramprasad

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Kempanahalli Basappa Mahesh Kumar

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Lakkakula Vks Bhaskar

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Periasamy Soundararajan

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Senguttuvan Prabha

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P2860

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

Haploview: analysis and visualization of LD and haplotype maps

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis

TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function

CD2AP localizes to the slit diaphragm and binds to nephrin via a novel C-terminal domain.

A novel TRPC6 mutation that causes childhood FSGS.

A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis.

TRPC6 single nucleotide polymorphisms and progression of idiopathic membranous nephropathy

Hereditary proteinuria syndromes and mechanisms of proteinuria.

P304

52-56

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P31

scholarly article

P433

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

P478

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P577

2015-02-23T00:00:00Z

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P698

28197477

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P932

5297484

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