Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
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Mutations in PAX2 associate with adult-onset FSGSMutations in the gene that encodes the F-actin binding protein anillin cause FSGSDisruption of PTPRO causes childhood-onset nephrotic syndromeAn actin-dependent step in mitochondrial fission mediated by the ER-associated formin INF2COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.PodocytesGenetic causes of focal segmental glomerulosclerosis: implications for clinical practiceCell biology and pathology of podocytesGenes and podocytes - new insights into mechanisms of podocytopathyPodocyte endocytosis in the regulation of the glomerular filtration barrierFormins at a glanceThe Impact of Histologic Variants on FSGS OutcomesCalcium regulates podocyte actin dynamics.Pathogenesis of Focal Segmental GlomerulosclerosisBiochemical and Cellular Determinants of Renal Glomerular ElasticityRevisiting the Phylogeny of the Animal Formins: Two New Subtypes, Relationships with Multiple Wing Hairs Proteins, and a Lost Human ForminAn mDia1-INF2 formin activation cascade facilitated by IQGAP1 regulates stable microtubules in migrating cells.Podocyte biology and pathogenesis of kidney diseaseThe myosin passenger protein Smy1 controls actin cable structure and dynamics by acting as a formin damperInducible podocyte injury and proteinuria in transgenic zebrafish.INF2 promotes the formation of detyrosinated microtubules necessary for centrosome reorientation in T cellsMYO1E mutations and childhood familial focal segmental glomerulosclerosis.LMX1B is essential for the maintenance of differentiated podocytes in adult kidneys.Podocyte-associated talin1 is critical for glomerular filtration barrier maintenance.Calcium-mediated actin reset (CaAR) mediates acute cell adaptationsGenetic testing in steroid-resistant nephrotic syndrome: when and how?Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal Disease.A molecular profile of focal segmental glomerulosclerosis from formalin-fixed, paraffin-embedded tissue.Podocyte-specific overexpression of wild type or mutant trpc6 in mice is sufficient to cause glomerular disease.Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndrome.Exome sequencing and in vitro studies identified podocalyxin as a candidate gene for focal and segmental glomerulosclerosis.Actin-depolymerizing factor cofilin-1 is necessary in maintaining mature podocyte architectureHereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations.Prkdc participates in mitochondrial genome maintenance and prevents Adriamycin-induced nephropathy in mice.Splice variant-specific cellular function of the formin INF2 in maintenance of Golgi architecture.Visualization of cytoskeletal dynamics in podocytes using adenoviral vectors.INF2-mediated severing through actin filament encirclement and disruption.Novel roles for actin in mitochondrial fissionThe primary glomerulonephritides: a systems biology approach.Exploring the genetic basis of early-onset chronic kidney disease.
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P2860
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
@ast
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
@en
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
@en-gb
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
@nl
type
label
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
@ast
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
@en
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
@en-gb
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
@nl
prefLabel
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
@ast
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
@en
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
@en-gb
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
@nl
P2093
P2860
P3181
P356
P1433
P1476
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
@en
P2093
Andrea L Uscinski
Daniel J Becker
Elizabeth J Brown
Hiroyasu Tsukaguchi
Johannes S Schlöndorff
Martin R Pollak
Stephen J Tonna
P2507
P2860
P2888
P3181
P356
10.1038/NG.505
P407
P577
2010-01-01T00:00:00Z
P5875
P6179
1044676559