(Q36577077)

15 August 2017

1 reference

title

Mechanisms of disease: focal segmental glomerulosclerosis (English)

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focal segmental glomerulosclerosis

15 August 2017

1 reference

Alain Meyrier

1

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15 August 2017

1 November 2005

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Nature Clinical Practice Nephrology

15 August 2017

1 reference

15 August 2017

1

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15 August 2017

1

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15 August 2017

44-54

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Cell biology of the glomerular podocyte

15 August 2017

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Caught flat-footed: podocyte damage and the molecular bases of focal glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Pathways to nephron loss starting from glomerular diseases-insights from animal models

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Recurrent nephrotic syndrome in renal allografts.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Focal segmental glomerulosclerosis in nephrotic adults: presentation, prognosis, and response to therapy of the histologic variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Pathologic classification of focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Focal segmental glomerular sclerosis: the cellular lesion

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Increasing incidence of focal-segmental glomerulosclerosis among adult nephropathies: a 20-year renal biopsy study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Idiopathic collapsing focal segmental glomerulosclerosis: a clinicopathologic study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Changing incidence of glomerular diseases in adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Is there really an increase in non-minimal change nephrotic syndrome in children?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Podocyte injury associated glomerulopathies induced by pamidronate

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

HIV-associated nephropathy: Epidemiology, pathogenesis, and treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Association of parvovirus B19 infection with idiopathic collapsing glomerulopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Molecular identification of SV40 infection in human subjects and possible association with kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Glomerular tip lesion: a distinct entity within the minimal change disease/focal segmental glomerulosclerosis spectrum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Pathogenesis of lipoid nephrosis: a disorder of T-cell function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Transmission of glomerular permeability factor from a mother to her child

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Nephrotic plasma alters slit diaphragm-dependent signaling and translocates nephrin, Podocin, and CD2 associated protein in cultured human podocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Sera from patients with collapsing focal segmental glomerulosclerosis increase albumin permeability of isolated glomeruli.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

What determines glomerular capillary permeability?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Apical cell membranes are shed into urine from injured podocytes: a novel phenomenon of podocyte injury

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Signaling at the slit diaphragm

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Podocin and nephrotic syndrome: implications for the clinician.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Molecular basis of the functional podocin-nephrin complex: mutations in the NPHS2 gene disrupt nephrin targeting to lipid raft microdomains

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

No evidence for genotype/phenotype correlation in NPHS1 and NPHS2 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

WT1 proteins: functions in growth and differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

WT1, a multiform protein. Contribution of genetic models to the understanding of its various functions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

The major podocyte protein nephrin is transcriptionally activated by the Wilms' tumor suppressor WT1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

A WT1 exon 1 mutation in a child diagnosed with Denys-Drash syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Congenital diaphragmatic hernia in WAGR syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

The spectrum of systemic involvement in adults presenting with renal lesion and mitochondrial tRNA(Leu) gene mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

Permeability plasma factors in nephrotic syndrome: more than one factor, more than one inhibitor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

E pluribus unum: The riddle of focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Is focal segmental glomerulosclerosis really focal? Distribution of lesions in adults and children

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Induction of renal tubular cell apoptosis in focal segmental glomerulosclerosis: roles of proteinuria and Fas-dependent pathways

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Pathologic classification of focal segmental glomerulosclerosis: a working proposal

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Treatment of primary focal segmental glomerulosclerosis

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Parvovirus B19 DNA in kidney tissue of patients with focal segmental glomerulosclerosis

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Acute cytomegalovirus infection complicated by collapsing glomerulopathy

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Focal segmental glomerulosclerosis associated with nephrotic syndrome in cholesterol atheroembolism: clinicopathological correlations

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Preliminary description of focal segmental glomerulosclerosis in patients with renovascular disease

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Collapsing glomerulopathy in renal allografts: a morphological pattern with diverse clinicopathologic associations

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

De novo collapsing glomerulopathy in renal allografts

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Zonal distribution of glomerular collapse in renal allografts: possible role of vascular changes

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Evolution of nephrotic-associated focal segmental glomerulosclerosis and relation to the glomerular tip lesion

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

The glomerular tip lesion: what does it really mean?

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Effect of plasma protein adsorption on protein excretion in kidney-transplant recipients with recurrent nephrotic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Effect of plasma fractions from patients with focal and segmental glomerulosclerosis on rat proteinuria

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Circulating factor associated with increased glomerular permeability to albumin in recurrent focal segmental glomerulosclerosis

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Glomerular podocytopathy in patients with systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Urinary podocytes in primary focal segmental glomerulosclerosis

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Podocytes undergo phenotypic changes and express macrophagic-associated markers in idiopathic collapsing glomerulopathy

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Differential expression of cyclin-dependent kinase inhibitors in human glomerular disease: role in podocyte proliferation and maturation

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Spectrum of disease in familial focal and segmental glomerulosclerosis

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Clinical spectrum of Denys-Drash and Frasier syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0025

7 January 2021

Identifiers

DOI

10.1038/NCPNEPH0025

1 reference

15 August 2017

1 reference

PubMed ID

16932363