(Q36891913)

16 August 2017

1 reference

title

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

1 reference

16 August 2017

1

Sandra E Guggino

1 reference

16 August 2017

publication date

1 August 2007

1 reference

Nature Clinical Practice Nephrology

16 August 2017

published in

1 reference

16 August 2017

volume

3

1 reference

16 August 2017

issue

8

1 reference

16 August 2017

page(s)

449-455

1 reference

The ClC-5 chloride channel knock-out mouse - an animal model for Dent's disease.

16 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

HYPERCALCURIC RICKETS ASSOCIATED WITH RENAL TUBULAR DAMAGE.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

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%2FNCPNEPH0541

7 January 2021

Recent advances in understanding the clinical and genetic heterogeneity of Dent's disease.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

Role of ClC-5 in the pathogenesis of hypercalciuria: recent insights from transgenic mouse models.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

X-linked recessive nephrolithiasis with renal failure

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

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%2FNCPNEPH0541

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%2FNCPNEPH0541

7 January 2021

A common molecular basis for three inherited kidney stone diseases

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

Dent Disease with mutations in OCRL1

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

Novel OCRL1 mutations in patients with the phenotype of Dent disease.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

The CLC chloride channel family

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

Chloride channels cough up

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

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/10.1038%2FNCPNEPH0541

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

Tissue distribution and subcellular localization of the ClC-5 chloride channel in rat intestinal cells

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

Membrane receptors for endocytosis in the renal proximal tubule.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

High citrate diet delays progression of renal insufficiency in the ClC-5 knockout mouse model of Dent's disease

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

Diet-dependent hypercalciuria in transgenic mice with reduced CLC5 chloride channel expression.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

Kidney-specific upregulation of vitamin D3 target genes in ClC-5 KO mice.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

Genetic disorders of renal electrolyte transport

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

Alkali citrate prophylaxis in idiopathic recurrent calcium oxalate urolithiasis--a prospective randomized study

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

Megalin and cubilin: multifunctional endocytic receptors

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0541

7 January 2021

Identifiers

DOI

10.1038/NCPNEPH0541

1 reference

16 August 2017

1 reference