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Article

Identification and functional analysis of a novel TRPC6 mutation associated with late onset familial focal segmental glomerulosclerosis in Chinese patients

14 Dec 2008

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Share to Chronic Kidney Disease and Diabetes
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 19124028
DOI: 10.1016/j.mrfmmm.2008.11.021

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Related research

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Identification and functional analysis of a novel TRPC6 mutation associated with late onset familial focal segmental glomerulosclerosis in Chinese patientsPMID 19124028Read ↗

Novel gain-of-function mutation of TRPC6 Q134P contributes to late onset focal segmental glomerulosclerosis in a Chinese pedigree.Semantic proximity Read ↗

Screening of ACTN4 and TRPC6 mutations in a Chinese cohort of patients with adult-onset familial focal segmental glomerulosclerosis.Semantic proximity Read ↗

A Mutation in the TRPC6 Cation Channel Causes Familial Focal Segmental GlomerulosclerosisSemantic proximity Read ↗

New TRPC6 gain-of-function mutation in a non-consanguineous Dutch family with late-onset focal segmental glomerulosclerosis.Semantic proximity Read ↗

TRPC6 - a new podocyte gene involved in focal segmental glomerulosclerosis.Semantic proximity Read ↗

TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype.Semantic proximity Read ↗

TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function.Semantic proximity Read ↗

Regulation of TRPC6 ion channels in podocytes - Implications for focal segmental glomerulosclerosis and acquired forms of proteinuric diseases.Semantic proximity Read ↗

TRPC Channels in Proteinuric Kidney DiseasesSemantic proximity Read ↗

TRPC6 gene variants in Turkish children with steroid-resistant nephrotic syndrome.Semantic proximity Read ↗

254C>G: a TRPC6 promoter variation associated with enhanced transcription and steroid-resistant nephrotic syndrome in Chinese children.Semantic proximity Read ↗

Heterozygous missense variant in TRPC6 in a boy with rapidly progressive infantile nephrotic syndrome associated with diffuse mesangial sclerosis.Semantic proximity Read ↗

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