(Q79751186)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290294%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

title

A familial childhood-onset relapsing nephrotic syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290294%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

1 reference

Kitamura A

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290294%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Tsukaguchi H

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290294%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Hiramoto R

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290294%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Shono A

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290294%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Doi T

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290294%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Kagami S

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290294%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Iijima K

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290294%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

language of work or name

English

0 references

publication date

7 February 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290294%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290294%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

volume

71

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290294%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

issue

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290294%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

page(s)

946-951

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290294%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/sj.ki.5002110

25 December 2019

exact match

0 references

cites work

Hereditary proteinuria syndromes and mechanisms of proteinuria

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

Lipid rafts and signal transduction

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

Nephrin strands contribute to a porous slit diaphragm scaffold as revealed by electron tomography

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

Clustering-induced tyrosine phosphorylation of nephrin by Src family kinases

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

Fyn binds to and phosphorylates the kidney slit diaphragm component Nephrin

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

SRC-family kinase Fyn phosphorylates the cytoplasmic domain of nephrin and modulates its interaction with podocin

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

Adequate clinical control of congenital nephrotic syndrome by enalapril

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

Monoclonal antibodies to human nephrin.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002110

7 January 2021

Identifiers

DOI

10.1038/SJ.KI.5002110

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290294%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

25 December 2019

0 references

1 reference