(Q46309756)

21 December 2017

title

Can we generate new hypotheses about Dent's disease from gene analysis of a mouse model? (English)

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21 December 2017

main subject

hypothesis generation

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1

Sandra E Guggino

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21 December 2017

publication date

17 October 2008

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21 December 2017

published in

Experimental Physiology

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21 December 2017

volume

94

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21 December 2017

issue

2

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21 December 2017

page(s)

191-196

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21 December 2017

Regulation of phosphate transport in proximal tubules.

cites work

1 reference

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Transactivation of rat apical sodium-dependent bile acid transporter and increased bile acid transport by 1alpha,25-dihydroxyvitamin D3 via the vitamin D receptor

21 January 2018

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Loss of chloride channel ClC-5 impairs endocytosis by defective trafficking of megalin and cubilin in kidney proximal tubules

21 January 2018

1 reference

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HYPERCALCURIC RICKETS ASSOCIATED WITH RENAL TUBULAR DAMAGE.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.044586

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.044586

Inhibition of Na+-H+ exchange impairs receptor-mediated albumin endocytosis in renal proximal tubule-derived epithelial cells from opossum

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.044586

Mechanisms of disease: what can mouse models tell us about the molecular processes underlying Dent disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.044586

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.044586

Impaired acidification in early endosomes of ClC-5 deficient proximal tubule

21 January 2018

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A common molecular basis for three inherited kidney stone diseases

21 January 2018

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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

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The Chloride Channel ClC-4 Contributes to Endosomal Acidification and Trafficking

21 January 2018

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ClC-5 Cl- -channel disruption impairs endocytosis in a mouse model for Dent's disease.

21 January 2018

1 reference

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Voltage-dependent electrogenic chloride/proton exchange by endosomal CLC proteins

21 January 2018

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

21 January 2018

1 reference

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The ClC-5 knockout mouse model of Dent's disease has renal hypercalciuria and increased bone turnover

21 January 2018

1 reference

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A sperm-specific Na+/H+ exchanger (sNHE) is critical for expression and in vivo bicarbonate regulation of the soluble adenylyl cyclase (sAC)

21 January 2018

1 reference

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A new sperm-specific Na+/H+ exchanger required for sperm motility and fertility

21 January 2018

1 reference

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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

1 reference

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Transcriptional adaptation to Clcn5 knockout in proximal tubules of mouse kidney.

21 January 2018

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X-linked recessive nephrolithiasis with renal failure

21 January 2018

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10.1113/EXPPHYSIOL.2008.044586

21 January 2018

Identifiers

DOI

1 reference

21 December 2017

PubMed ID

18931044

1 reference

21 December 2017