(Q42061054)

15 October 2017

Relevance of the D13 region to the function of the skeletal muscle chloride channel, ClC-1. (English)

1 reference

15 October 2017

2

1 reference

15 October 2017

Hryciw DH

1

1 reference

15 October 2017

Hughes BP

series ordinal

3

1 reference

15 October 2017

Bretag AH

series ordinal

4

1 reference

15 October 2017

language of work or name

English

0 references

publication date

1 February 1998

1 reference

Journal of Biological Chemistry

15 October 2017

4

1 reference

based on heuristic

inferred from page(s)

published in

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15 October 2017

273

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15 October 2017

4304-4307

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15 October 2017

8

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Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytes.

15 October 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4304

Transmembrane topology of a CLC chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4304

Regions involved in the opening of CIC-2 chloride channel by voltage and cell volume

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4304

Reconstitution of functional voltage-gated chloride channels from complementary fragments of CLC-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4304

Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4304

Genomic organization of the human muscle chloride channel CIC-1 and analysis of novel mutations leading to Becker-type myotonia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4304

Molecular basis for decreased muscle chloride conductance in the myotonic goat

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4304

A common molecular basis for three inherited kidney stone diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4304

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4304

Characteristics of skeletal muscle chloride channel C1C-1 and point mutant R304E expressed in Sf-9 insect cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4304

A simple method for quantifying specific mRNAs in small numbers of early mouse embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4304

Concentration and pH dependence of skeletal muscle chloride channel ClC-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4304

pH-dependent interactions of Cd2+ and a carboxylate blocker with the rat C1C-1 chloride channel and its R304E mutant in the Sf-9 insect cell line

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4304

The structure of a domain common to archaebacteria and the homocystinuria disease protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4304

Identification of homer as a homologue of the Wiskott-Aldrich syndrome protein suggests a receptor-binding function for WH1 domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.8.4304

21 January 2018

Identifiers

DOI

10.1074/JBC.273.8.4304

1 reference

15 October 2017

1 reference