(Q47222434)

English

Identification of two novel mutations in the CLCN5 gene in Japanese patients with familial idiopathic low molecular weight proteinuria (Japanese Dent's disease).

scientific article published in January 2001

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scholarly article

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

Identification of two novel mutations in the CLCN5 gene in Japanese patients with familial idiopathic low molecular weight proteinuria (Japanese Dent's disease). (English)

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

author name string

Takemura T

1

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

Hino S

2

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

Ikeda M

3

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

Okada M

4

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

Igarashi T

5

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

Inatomi J

6

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

Yoshioka K

7

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

publication date

1 January 2001

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

American Journal of Kidney Diseases

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Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

37

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

1

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

138-143

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

Hypercalciuria and nephrocalcinosis in patients with idiopathic low-molecular-weight proteinuria in Japan: is the disease identical to Dent's disease in United Kingdom?

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980067-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5)

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980067-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980067-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A common molecular basis for three inherited kidney stone diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980067-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980067-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980067-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the CLCN5 gene in Japanese patients with familial idiopathic low-molecular-weight proteinuria

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980067-6

7 January 2021

based on heuristic

inferred from DOI database lookup

X-linked hypercalciuric nephrolithiasis: clinical syndromes and chloride channel mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980067-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis)

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980067-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22.

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980067-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical features of X-linked nephrolithiasis in childhood

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980067-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980067-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Membrane receptors for endocytosis in the renal proximal tubule.

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980067-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2801%2980067-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0272-6386(01)80067-6

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/11136179

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