Related references
Note: Only part of the references are listed.Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients
Anja K. Buescher et al.
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Effect of cyclosporin A on proteinuria in the course of glomerulopathy associated with WT1 mutations
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Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis
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COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
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JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2011)
Mutations in INF2 Are a Major Cause of Autosomal Dominant Focal Segmental Glomerulosclerosis
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Variation in genome-wide mutation rates within and between human families
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Immunosuppression and Renal Outcome in Congenital and Pediatric Steroid-Resistant Nephrotic Syndrome
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Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
Elizabeth J. Brown et al.
NATURE GENETICS (2010)
Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans
Giulio Genovese et al.
SCIENCE (2010)
Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis
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AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome
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JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2008)
MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis
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The actin cytoskeleton of kidney podocytes is a direct target of the antiproteinuric effect of cyclosporine A
Christian Faul et al.
NATURE MEDICINE (2008)
Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)
Rasheed Gbadegesin et al.
NEPHROLOGY DIALYSIS TRANSPLANTATION (2008)
Plasma exchange and retransplantation in recurrent nephrosis of patients with congenital nephrotic syndrome of the Finnish type (NPHS1)
Arvi-Matti Kuusniemi et al.
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A familial childhood-onset relapsing nephrotic syndrome
A. Kitamura et al.
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Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome
Rasheed Gbadegesin et al.
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The spectrum of podocytopathies: A unifying view of glomerular diseases
R. C. Wiggins
KIDNEY INTERNATIONAL (2007)
Nephrotic syndrome in the first year of life: Two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2)
Bernward G. Hinkes et al.
PEDIATRICS (2007)
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
Bernward Hinkes et al.
NATURE GENETICS (2006)
Glucocorticoids protect and enhance recovery of cultured murine podocytes via actin filament stabilization
RF Ransom et al.
KIDNEY INTERNATIONAL (2005)
A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis
MP Winn et al.
SCIENCE (2005)
Patients with mutations in NPHS2 (Podocin) do not respond to standard steroid treatment of nephrotic syndrome
RG Ruf et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2004)
NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence
S Weber et al.
KIDNEY INTERNATIONAL (2004)
The potential role of HMG-CoA reductase inhibitors in pediatric nephrotic syndrome
WA Prescott et al.
ANNALS OF PHARMACOTHERAPY (2004)
Human laminin β2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities
M Zenker et al.
HUMAN MOLECULAR GENETICS (2004)
Long-term antiproteinuric and renoprotective efficacy and safety of losartan in children with proteinuria
D Ellis et al.
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Atorvastatin in dyslipidaemia of the nephrotic syndrome
P Valdivielso et al.
NEPHROLOGY (2003)
Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia
CF Boerkoel et al.
NATURE GENETICS (2002)
Time trends and ethnic patterns of childhood nephrotic syndrome in Yorkshire, UK
PA McKinney et al.
PEDIATRIC NEPHROLOGY (2001)
NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
N Boute et al.
NATURE GENETICS (2000)
Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis
JM Kaplan et al.
NATURE GENETICS (2000)