(Q37956193)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22083641%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

title

ClC-5 mutations associated with Dent's disease: a major role of the dimer interface (English)

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16 January 2020

1

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16 January 2020

Jacques Teulon

6

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16 January 2020

author name string

Teddy Grand

2

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16 January 2020

Johanna Burgos

3

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16 January 2020

Wendy González

4

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16 January 2020

Francisco V Sepúlveda

5

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16 January 2020

publication date

15 November 2011

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16 January 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22083641%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

volume

463

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16 January 2020

issue

2

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16 January 2020

page(s)

247-256

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https://scigraph.springernature.com/pub.10.1007/s00424-011-1052-0

16 January 2020

exact match

0 references

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Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease

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21 January 2018

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21 January 2018

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21 January 2018

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Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis

21 January 2018

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Novel CLCN5 mutations in patients with Dent's disease result in altered ion currents or impaired exchanger processing

21 January 2018

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Heterogeneity in the processing of CLCN5 mutants related to Dent disease.

21 January 2018

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21 January 2018

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ClC-5, the chloride channel mutated in Dent's disease, colocalizes with the proton pump in endocytotically active kidney cells

21 January 2018

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21 January 2018

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Cofilin interacts with ClC-5 and regulates albumin uptake in proximal tubule cell lines.

21 January 2018

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Nedd4-2 functionally interacts with ClC-5: involvement in constitutive albumin endocytosis in proximal tubule cells

21 January 2018

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Regulation of albumin endocytosis by PSD95/Dlg/ZO-1 (PDZ) scaffolds. Interaction of Na+-H+ exchange regulatory factor-2 with ClC-5.

21 January 2018

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ClC-5: a chloride channel with multiple roles in renal tubular albumin uptake.

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Coexpression of complementary fragments of ClC-5 and restoration of chloride channel function in a Dent's disease mutation.

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Functional characterization of a novel missense CLCN5 mutation causing alterations in proximal tubular endocytic machinery in Dent's disease.

21 January 2018

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21 January 2018

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Mice lacking renal chloride channel, CLC-5, are a model for Dent's disease, a nephrolithiasis disorder associated with defective receptor-mediated endocytosis.

21 January 2018

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ClC-5: role in endocytosis in the proximal tubule.

21 January 2018

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Lysosomal degradation of endocytosed proteins depends on the chloride transport protein ClC-7.

21 January 2018

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ATP induces conformational changes in the carboxyl-terminal region of ClC-5

21 January 2018

1 reference

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Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

21 January 2018

1 reference

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Modeling study of human renal chloride channel (hCLC-5) mutations suggests a structural-functional relationship.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00424-011-1052-0

Mutational analysis of CLC-5, cofilin and CLC-4 in patients with Dent's disease

21 January 2018

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Determinants of anion-proton coupling in mammalian endosomal CLC proteins

21 January 2018

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21 January 2018

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Intracellular regulation of human ClC-5 by adenine nucleotides

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-1052-0

Characterization of renal chloride channel (CLCN5) mutations in Dent's disease

21 January 2018

1 reference

12 December 2020

Mutations in CLCN5 chloride channel in Japanese patients with low molecular weight proteinuria

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12 December 2020

Cellular and subcellular immunolocalization of ClC-5 channel in mouse kidney: colocalization with H+-ATPase

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12 December 2020

Dent's disease; a familial proximal renal tubular syndrome with low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance.

1 reference

12 December 2020

10.1007/S00424-011-1052-0

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22083641%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference