Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology.
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COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.Opportunities and Challenges of Genotyping Patients With Nephrotic Syndrome in the Genomic EraMutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndromeBiallelic Mutations in Nuclear Pore Complex Subunit NUP107 Cause Early-Childhood-Onset Steroid-Resistant Nephrotic SyndromeMYO1E mutations and childhood familial focal segmental glomerulosclerosis.Angiotensin II has acute effects on TRPC6 channels in podocytes of freshly isolated glomeruli.Genetic kidney diseases.Hereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations.High Steroid Sensitivity among Children with Nephrotic Syndrome in Southwestern Nigeria.The glomerulus--a view from the outside--the podocyte.A comparative transcriptome analysis identifying FGF23 regulated genes in the kidney of a mouse CKD model.A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGSA novel TRPC6 mutation in a family with podocytopathy and clinical variability.Heterogeneous genetic alterations in sporadic nephrotic syndrome associate with resistance to immunosuppressionCRB2 mutations produce a phenotype resembling congenital nephrosis, Finnish type, with cerebral ventriculomegaly and raised alpha-fetoprotein.Myo1e impairment results in actin reorganization, podocyte dysfunction, and proteinuria in zebrafish and cultured podocytesAlpha-actinin-4 and CLP36 protein deficiencies contribute to podocyte defects in multiple human glomerulopathies.Nephrotic syndrome in children: from bench to treatmentRenal Lipotoxicity-Associated Inflammation and Insulin Resistance Affects Actin Cytoskeleton Organization in PodocytesSingle-channel Analysis and Calcium Imaging in the Podocytes of the Freshly Isolated GlomeruliARB protects podocytes from HIV-1 nephropathy independently of podocyte AT1.Diagnosing FSGS without kidney biopsy - a novel INF2-mutation in a family with ESRD of unknown originBackground strain and the differential susceptibility of podocyte-specific deletion of Myh9 on murine models of experimental glomerulosclerosis and HIV nephropathyMutational analysis in podocin-associated hereditary nephrotic syndrome in Polish patients: founder effect in the Kashubian populationLMX1B mutations cause hereditary FSGS without extrarenal involvementKeap1 inhibition attenuates glomerulosclerosis.Genetics of hereditary nephrotic syndrome: a clinical review.MicroRNAs in kidney development: lessons from the frog.Glomerular basement membrane composition and the filtration barrier.Podocyte-specific deletion of Myh9 encoding nonmuscle myosin heavy chain 2A predisposes mice to glomerulopathy.Organogenesis of the kidney glomerulus: focus on the glomerular basement membrane.Glomerular disease in 2011: New clues to environmental influences in glomerular disease.Childhood nephrotic syndrome--current and future therapies.New developments in steroid-resistant nephrotic syndrome.Genetics and the nephron.Podocyte Purinergic P2X4 Channels Are Mechanotransducers That Mediate Cytoskeletal Disorganization.Metabolism and homeostasis in the kidney: metabolic regulation through insulin signaling in the kidney.Immunohistochemical and electronmicroscopic features of mesenchymal-to-epithelial transition in human developing, postnatal and nephrotic podocytes.N-wasp is required for stabilization of podocyte foot processes.The amino acid mutations of the podocin in proteinuria: a meta-analysis.
P2860
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P2860
Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on October 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology.
@en
Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology.
@nl
type
label
Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology.
@en
Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology.
@nl
prefLabel
Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology.
@en
Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology.
@nl
P356
P1476
Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology.
@en
P2093
Eduardo Machuca
Geneviève Benoit
P304
P356
10.1093/HMG/DDP328
P577
2009-10-01T00:00:00Z