(Q38025336)

27 August 2017

New developments in steroid-resistant nephrotic syndrome (English)

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27 August 2017

1

Moin A Saleem

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27 August 2017

11 July 2012

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27 August 2017

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27 August 2017

28

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27 August 2017

5

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27 August 2017

699-709

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https://scigraph.springernature.com/pub.10.1007/s00467-012-2239-0

27 August 2017

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cites work

Disease recurrence in paediatric renal transplantation

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

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/10.1007%2FS00467-012-2239-0

CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Nephrin mutations can cause childhood-onset steroid-resistant nephrotic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Nck adaptor proteins link nephrin to the actin cytoskeleton of kidney podocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

The podocyte cytoskeleton--key to a functioning glomerulus in health and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Activation of RhoA in podocytes induces focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

A high-powered view of the filtration barrier

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Modification of kidney barrier function by the urokinase receptor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Podocyte migration during nephrotic syndrome requires a coordinated interplay between cathepsin L and alpha3 integrin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Proteinuria: an enzymatic disease of the podocyte?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Synaptopodin orchestrates actin organization and cell motility via regulation of RhoA signalling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Antagonistic regulation of actin dynamics and cell motility by TRPC5 and TRPC6 channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

The molecular and functional phenotype of glomerular podocytes reveals key features of contractile smooth muscle cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Functional distinctions in cytosolic calcium regulation between cells of the glomerular filtration barrier

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Rearrangements of the cytoskeleton and cell contacts induce process formation during differentiation of conditionally immortalized mouse podocyte cell lines.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Glucocorticoids protect and enhance recovery of cultured murine podocytes via actin filament stabilization

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

The actin cytoskeleton of kidney podocytes is a direct target of the antiproteinuric effect of cyclosporine A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Rituximab targets podocytes in recurrent focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Interferon-beta reduces proteinuria in experimental glomerulonephritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Mutation in the key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria and is rescued by N-acetylmannosamine

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Circulating urokinase receptor as a cause of focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

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/10.1007%2FS00467-012-2239-0

Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Hemopexin induces nephrin-dependent reorganization of the actin cytoskeleton in podocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Donor splice-site mutations in WT1 are responsible for Frasier syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

MYO1E mutations and childhood familial focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

A case of mitochondrial cytopathy with a typical point mutation for MELAS, presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Focal segmental glomerulosclerosis in patients with mandibuloacral dysplasia owing to ZMPSTE24 deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Disruption of PTPRO causes childhood-onset nephrotic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Common variation in GPC5 is associated with acquired nephrotic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2239-0

Nephrin-signature molecule of the glomerular podocyte?

21 January 2018

1 reference

12 December 2020

Mitochondrial DNA mutations in focal segmental glomerulosclerosis lesions

1 reference

12 December 2020

Congenital nephrotic syndrome: a novel phenotype of type I carbohydrate-deficient glycoprotein syndrome

1 reference

12 December 2020

Short-term efficacy of rituximab versus tacrolimus in steroid-dependent nephrotic syndrome

1 reference

12 December 2020

Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis

1 reference

12 December 2020

A conditionally immortalized human podocyte cell line demonstrating nephrin and podocin expression.

1 reference

12 December 2020

Genetics in clinical practice: nephrotic and proteinuric syndromes

1 reference

12 December 2020

Glomerular podocytes contain neuron-like functional synaptic vesicles

1 reference

12 December 2020

Induction of TRPC6 channel in acquired forms of proteinuric kidney disease

1 reference

12 December 2020

suPAR: the molecular crystal ball

1 reference

12 December 2020

Idiopathic nephrotic syndrome in New Zealand children, demographic, clinical features, initial management and outcome after twelve-month follow-up: results of a three-year national surveillance study

1 reference

12 December 2020

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

1 reference

12 December 2020

Early coenzyme Q10 supplementation in primary coenzyme Q10 deficiency

1 reference

12 December 2020

The bioactivity of plasma factors in focal segmental glomerulosclerosis

1 reference

12 December 2020

Congenital nephrotic syndrome in mice lacking CD2-associated protein

1 reference

12 December 2020

Rituximab in steroid-dependent idiopathic nephrotic syndrome in childhood--follow-up after CD19 recovery

1 reference

12 December 2020

10.1007/S00467-012-2239-0

Identifiers

DOI

1 reference

PubMed ID

22782578

Dimensions Publication ID

27 August 2017

0 references

1 reference

PubMed ID

22782578