(Q34185226)

31 July 2017

Intracellular mislocalization of mutant podocin and correction by chemical chaperones (English)

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31 July 2017

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Teiko Ohashi

1

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31 July 2017

Keiko Uchida

2

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31 July 2017

Shinichi Uchida

3

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31 July 2017

Sei Sasaki

4

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31 July 2017

Hiroshi Nihei

5

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31 July 2017

8 March 2003

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Histochemistry and Cell Biology

31 July 2017

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31 July 2017

119

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31 July 2017

3

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31 July 2017

257-264

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https://scigraph.springernature.com/pub.10.1007/s00418-003-0511-x

31 July 2017

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cites work

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

1 reference

12 December 2020

Podocin, a raft-associated component of the glomerular slit diaphragm, interacts with CD2AP and nephrin

1 reference

12 December 2020

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

1 reference

12 December 2020

Interaction with podocin facilitates nephrin signaling

1 reference

12 December 2020

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

1 reference

12 December 2020

A stomatin-like protein necessary for mechanosensation in C. elegans

1 reference

12 December 2020

Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis.

1 reference

12 December 2020

NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele

1 reference

12 December 2020

Defective aquaporin-2 trafficking in nephrogenic diabetes insipidus and correction by chemical chaperones

1 reference

12 December 2020

A stable transfected line of human glomerular epithelial cells

1 reference

12 December 2020

Cytosolic and nuclear aggregation of the amyloid beta-peptide following its expression in the endoplasmic reticulum.

1 reference

12 December 2020

Misfolding of mutant aquaporin-2 water channels in nephrogenic diabetes insipidus

1 reference

12 December 2020

The importance of trimming reactions on asparagine-linked oligosaccharides for protein quality control

1 reference

12 December 2020

Mechanism of protein stabilization by glycerol: preferential hydration in glycerol-water mixtures

1 reference

12 December 2020

Novel mutations in NPHS2 detected in both familial and sporadic steroid-resistant nephrotic syndrome

1 reference

12 December 2020

Formation, isomerisation and reduction of disulphide bonds during protein quality control in the endoplasmic reticulum

1 reference

12 December 2020

Mutations in NPHS2 encoding podocin are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children

1 reference

12 December 2020

Not all in the family: mutations of podocin in sporadic steroid-resistant nephrotic syndrome

1 reference

12 December 2020

Aggregate formation and degradation of overexpressed wild-type and mutant urate oxidase proteins. Quality control of organelle-destined proteins by the endoplasmic reticulum

1 reference

12 December 2020

Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation.

1 reference

12 December 2020

Expression of a mutant ER-retained polytope membrane protein in cultured rat hepatocytes results in Mallory body formation

1 reference

12 December 2020

The biological role of the Alzheimer amyloid precursor protein in epithelial cells

1 reference

12 December 2020

Identification of the phosphorylation site on human erythrocyte band 7 integral membrane protein: implications for a monotopic protein structure.

1 reference

12 December 2020

Co-localization of nephrin, podocin, and the actin cytoskeleton: evidence for a role in podocyte foot process formation

1 reference

12 December 2020

Chemical chaperones correct the mutant phenotype of the delta F508 cystic fibrosis transmembrane conductance regulator protein

1 reference

12 December 2020

10.1007/S00418-003-0511-X

Identifiers

DOI

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1 reference