(Q47301037)

13 January 2018

title

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

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13 January 2018

author name string

Akuta N

1

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13 January 2018

Lloyd SE

2

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13 January 2018

Igarashi T

3

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13 January 2018

Shiraga H

4

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13 January 2018

Matsuyama T

5

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13 January 2018

Yokoro S

6

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13 January 2018

Cox JP

7

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13 January 2018

Thakker RV

8

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13 January 2018

language of work or name

English

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publication date

1 October 1997

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13 January 2018

published in

Kidney International

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13 January 2018

volume

52

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13 January 2018

issue

4

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13 January 2018

page(s)

911-916

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13 January 2018

https://scigraph.springernature.com/pub.10.1038/ki.1997.412

exact match

0 references

cites work

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/10.1038%2FKI.1997.412

7 January 2021

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/10.1038%2FKI.1997.412

7 January 2021

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/10.1038%2FKI.1997.412

7 January 2021

Properties of voltage-gated chloride channels of the ClC gene family

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.412

7 January 2021

ClC-6 and ClC-7 are two novel broadly expressed members of the CLC chloride channel family

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.412

7 January 2021

A common molecular basis for three inherited kidney stone diseases

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.412

7 January 2021

Cloning and functional expression of rat CLC-5, a chloride channel related to kidney disease

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.412

7 January 2021

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/10.1038%2FKI.1997.412

7 January 2021

X-linked recessive nephrolithiasis with renal failure

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.412

7 January 2021

Genetic mapping in the Xp11.2 region of a new form of X-linked hypophosphatemic rickets

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.412

7 January 2021

Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.412

7 January 2021

Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.412

7 January 2021

A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.412

7 January 2021

Gating of the voltage-dependent chloride channel CIC-0 by the permeant anion.

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.412

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.412

7 January 2021

CpNpG methylation in mammalian cells

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.412

7 January 2021

Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.412

7 January 2021

Identifiers

DOI

10.1038/KI.1997.412

1 reference

13 January 2018

PubMed ID

9328929

1 reference

13 January 2018