Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis.
about
NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated alleleThe carboxyl terminus of Neph family members binds to the PDZ domain protein zonula occludens-1Interaction with podocin facilitates nephrin signalingNephrin and Neph1 co-localize at the podocyte foot process intercellular junction and form cis hetero-oligomersNephrin and CD2AP associate with phosphoinositide 3-OH kinase and stimulate AKT-dependent signalingIdentification of proteins that interact with podocin using the yeast 2-hybrid system.Analysis of mutations in alpha-actinin 4 and podocin genes of patients with chronic renal failure due to sporadic focal segmental glomerulosclerosis.NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review.Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosisExtrarenal effects on the pathogenesis and relapse of idiopathic nephrotic syndrome in Buffalo/Mna ratsManagement of nephrotic syndrome in children.Treatment of steroid-resistant pediatric nephrotic syndrome.NPHS2 mutations account for only 15% of nephrotic syndrome cases.The pediatric nephrotic syndrome spectrum: clinical homogeneity and molecular heterogeneity.Glomerular diseases: genetic causes and future therapeutics.Educational paper: the podocytopathies.The amino acid mutations of the podocin in proteinuria: a meta-analysis.Aicardi-Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?Single-center analysis of early recurrence of nephrotic syndrome following renal transplantation in children.Genetic predisposition for glomerulonephritis-induced glomerulosclerosis in rats is linked to chromosome 1.Proteinuric Kidney Diseases: A Podocyte's Slit Diaphragm and Cytoskeleton Approach
P2860
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P2860
Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis.
description
1995 nî lūn-bûn
@nan
1995 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Mapping a gene (SRN1) to chrom ...... autosomal recessive nephrosis.
@ast
Mapping a gene (SRN1) to chrom ...... autosomal recessive nephrosis.
@en
Mapping a gene
@nl
type
label
Mapping a gene (SRN1) to chrom ...... autosomal recessive nephrosis.
@ast
Mapping a gene (SRN1) to chrom ...... autosomal recessive nephrosis.
@en
Mapping a gene
@nl
prefLabel
Mapping a gene (SRN1) to chrom ...... autosomal recessive nephrosis.
@ast
Mapping a gene (SRN1) to chrom ...... autosomal recessive nephrosis.
@en
Mapping a gene
@nl
P2093
P50
P356
P1476
Mapping a gene (SRN1) to chrom ...... autosomal recessive nephrosis
@en
P2093
P304
P356
10.1093/HMG/4.11.2155
P577
1995-11-01T00:00:00Z