A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.
about
PodocytesGenes and podocytes - new insights into mechanisms of podocytopathyTranslating genetic findings in hereditary nephrotic syndrome: the missing loopsIn vivo Modeling Implicates APOL1 in Nephropathy: Evidence for Dominant Negative Effects and Epistasis under Anemic StressClinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1.Focal segmental glomerulosclerosis: molecular genetics and targeted therapiesWnt/β-catenin signalling and podocyte dysfunction in proteinuric kidney disease.The Genetics of Nephrotic Syndrome.Dysregulation of WTI (-KTS) is Associated with the Kidney-Specific Effects of the LMX1B R246Q Mutation.Whole exome sequencing: a state-of-the-art approach for defining (and exploring!) genetic landscapes in pediatric nephrology.Genetic mutational testing of Chinese children with familial hematuria with biopsy‑proven FSGS.Hereditary Podocytopathies in Adults: The Next Generation.Clinical Aspects of WT1 and the Kidney.Clinical and pathological phenotype of genetic causes of focal segmental glomerulosclerosis in adults.Zebrafish as a Model for Drug Screening in Genetic Kidney Diseases.Genetic Testing for Steroid-Resistant-Nephrotic Syndrome in an Outbred Population
P2860
Q26766118-A4CB2152-495A-4756-AE20-0849F4790960Q26866422-659BB733-6977-46F6-8AC5-375821584E7CQ28088653-4E1BFDEB-1E46-4114-96D9-CD305018F8ADQ28546164-D7C29EA2-3788-4BD1-B610-D2289F6AD0EFQ35576147-0F411CF2-E9A6-4269-8CE2-B7A7B6456925Q35686453-4094564D-D76B-428C-BADC-80E3885FBF05Q36908181-D0A9EE9E-747C-4846-A49B-67802B35CCE7Q37032671-26704C7B-49AE-447A-95DD-5400BD91FA53Q37563312-4E2C6542-F74F-41F3-B87D-60E3A1F0129BQ38703307-3DEB7617-CCEE-4B47-AF67-AAE569044DADQ47401355-2F9B0D98-2CEF-4A15-B30D-E78269872254Q47861655-FE66E8F4-855E-4C29-A35D-4123D42C4862Q50498732-F2CF89EC-9765-4872-969C-AE5108E0C010Q54985317-ABEE531F-71B5-4920-AE0F-F144419E0BC2Q55689509-ECF56049-8E37-45D9-8921-885A75DF1672Q58580692-3A79CDBD-D612-4A9E-A74D-E9E8C6F3610C
P2860
A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.
description
2014 nî lūn-bûn
@nan
2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.
@ast
A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.
@en
type
label
A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.
@ast
A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.
@en
prefLabel
A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.
@ast
A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.
@en
P2093
P2860
P356
P1476
A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.
@en
P2093
Alison Homstad
Andrew F Malone
Andrey Shaw
David N Howell
Edwin C Oh
Gentzon Hall
Guanghong Wu
Jason Eckel
Liming Wang
Michelle P Winn
P2860
P304
P356
10.1681/ASN.2013101053
P577
2014-08-21T00:00:00Z