Genetics of childhood steroid-sensitive nephrotic syndrome (Q38911915)

7 September 2017

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title

Genetics of childhood steroid-sensitive nephrotic syndrome (English)

1 reference

7 September 2017

Alana M Karp

1

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7 September 2017

Rasheed A Gbadegesin

series ordinal

2

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7 September 2017

publication date

29 July 2016

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7 September 2017

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The Genetics of Nephrotic Syndrome

7 September 2017

cites work

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Permeability factors in idiopathic nephrotic syndrome: historical perspectives and lessons for the future

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HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome

1 October 2018

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A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome

1 October 2018

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Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

1 October 2018

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Mutations in EMP2 cause childhood-onset nephrotic syndrome

1 October 2018

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Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndrome

1 October 2018

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HLA-DQA1 and PLA2R1 polymorphisms and risk of idiopathic membranous nephropathy.

1 October 2018

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Familial steroid-sensitive idiopathic nephrotic syndrome: seven cases from three families in China

1 October 2018

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Serum suPAR in patients with FSGS: trash or treasure?

1 October 2018

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Treatment of steroid-sensitive nephrotic syndrome: new guidelines from KDIGO.

1 October 2018

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Genetically distinct subsets within ANCA-associated vasculitis

1 October 2018

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New developments in steroid-resistant nephrotic syndrome

1 October 2018

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Rituximab targets podocytes in recurrent focal segmental glomerulosclerosis

1 October 2018

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Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy

1 October 2018

1 reference

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Podocyte-secreted angiopoietin-like-4 mediates proteinuria in glucocorticoid-sensitive nephrotic syndrome

1 October 2018

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Circulating Permeability Factors in Idiopathic Nephrotic Syndrome and Focal Segmental Glomerulosclerosis

1 October 2018

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Association of trypanolytic ApoL1 variants with kidney disease in African Americans

1 October 2018

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Failure of regulation results in an amplified oxidation burst by neutrophils in children with primary nephrotic syndrome

1 October 2018

1 reference

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Urinary CD80 is elevated in minimal change disease but not in focal segmental glomerulosclerosis

1 October 2018

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M-type phospholipase A2 receptor as target antigen in idiopathic membranous nephropathy

1 October 2018

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

1 October 2018

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Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome.

1 October 2018

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

1 October 2018

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High incidence of initial and late steroid resistance in childhood nephrotic syndrome

1 October 2018

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Altered activity of plasma hemopexin in patients with minimal change disease in relapse

1 October 2018

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

1 October 2018

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Role of the immune system in the pathogenesis of idiopathic nephrotic syndrome

1 October 2018

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Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS).

1 October 2018

1 reference

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Vascular permeability factors in steroid-sensitive nephrotic syndrome and focal segmental glomerulosclerosis.

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5276801

Nephrotic syndrome in childhood.

1 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5276801

Identification of the first gene locus (SSNS1) for steroid-sensitive nephrotic syndrome on chromosome 2p.

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5276801

Clinical and genetic evaluation of familial steroid-responsive nephrotic syndrome in childhood.

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5276801

Circulating mediators of proteinuria in idiopathic minimal lesion nephrotic syndrome

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5276801

Interleukin-8 alters glomerular heparan sulfate glycosaminoglycan chain size and charge in rats

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5276801

Changing patterns in the histopathology of idiopathic nephrotic syndrome in children

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5276801

Association of DQB1*0302 alloantigens in Japanese pediatric patients with steroid-sensitive nephrotic syndrome

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5276801

Long-term outcome of primary nephrotic syndrome

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5276801

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

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5276801

High incidence of minimal change nephrotic syndrome in Asians

1 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5276801

HLA extended haplotypes in steroid-sensitive nephrotic syndrome of childhood

1 October 2018

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Treatment of diabetic nephropathy with angiotensin II blockers

1 October 2018

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Familial steroid-responsive nephrotic syndrome and HLA antigens in Bengali children

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Major histocompatibility complex class II antigens in steroid-sensitive nephrotic syndrome in Chinese children

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12 December 2020

The significance of caveolae in the glomeruli in glomerular disease

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Genes encoding the beta-chains of HLA-DR7 and HLA-DQw2 define major susceptibility determinants for idiopathic nephrotic syndrome

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The increase of memory T cell subsets in children with idiopathic nephrotic syndrome

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Minimal-change glomerular nephritis. Normal kidneys in an abnormal environment?

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The familial nephrotic syndrome. II. A clinicopathological study

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Increased urinary protein excretion in the rat produced by serum from a patient with recurrent focal glomerular sclerosis after renal transplantation

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HLA‐DQB1 allele associates with idiopathic nephrotic syndrome in Japanese children

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HLA class II associations with idiopathic nephrotic syndrome in children

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HLA-DR, -DQB typing of steroid-sensitive idiopathic nephrotic syndrome children in Taiwan

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Familial steroid-sensitive nephrotic syndrome in Southern Israel: clinical and genetic observations

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

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Expression of vascular endothelial growth factor and its receptors in rats with protein-overload nephrosis

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HLA-DQ gene polymorphism in primary IgA nephropathy in three European populations

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12 December 2020

Primary nephrotic syndrome in children: clinical significance of histopathologic variants of minimal change and of diffuse mesangial hypercellularity. A Report of the International Study of Kidney Disease in Children

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Resolution of recurrent focal segmental glomerulosclerosis after retransplantation

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Steroid-sensitive nephrotic syndrome in two families

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T-cell subsets, interleukin-2 receptor expression and production of interleukin-2 in minimal change nephrotic syndrome

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Familial nephropathy and multiple exostoses with exostosin-1 (EXT1) gene mutation

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Tumor necrosis factor-alpha blocking agent as a treatment for nephrotic syndrome

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A familial childhood-onset relapsing nephrotic syndrome

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10.1007/S00467-016-3456-8

Identifiers

DOI

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Dimensions Publication ID

1018896214

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PMC publication ID

5276801

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1 reference