Congenital nephrogenic diabetes insipidus: what can we learn from mouse models? (Q37268479)

19 August 2017

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title

Congenital nephrogenic diabetes insipidus: what can we learn from mouse models? (English)

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nephrogenic diabetes insipidus

19 August 2017

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Michelle Boone

1

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PubMed ID

18790812

19 August 2017

Peter M T Deen

series ordinal

2

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19 August 2017

12 September 2008

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19 August 2017

Experimental Physiology

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19 August 2017

94

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19 August 2017

2

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19 August 2017

186-190

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Hereditary polyuric disorders: new concepts and differential diagnosis.

19 August 2017

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Characterization of an aquaporin-2 water channel gene mutation causing partial nephrogenic diabetes insipidus in a Mexican family: evidence of increased frequency of the mutation in the town of origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Osmoreceptors, osmoreception, and osmoregulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

A novel mechanism in recessive nephrogenic diabetes insipidus: wild-type aquaporin-2 rescues the apical membrane expression of intracellularly retained AQP2-P262L.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Lack of arginine vasopressin-induced phosphorylation of aquaporin-2 mutant AQP2-R254L explains dominant nephrogenic diabetes insipidus

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Water channels encoded by mutant aquaporin-2 genes in nephrogenic diabetes insipidus are impaired in their cellular routing

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Phosphorylation of serine 256 is required for cAMP-dependent regulatory exocytosis of the aquaporin-2 water channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Reversed polarized delivery of an aquaporin-2 mutant causes dominant nephrogenic diabetes insipidus

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

The subcellular localization of an aquaporin-2 tetramer depends on the stoichiometry of phosphorylated and nonphosphorylated monomers

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Missorting of the Aquaporin-2 mutant E258K to multivesicular bodies/lysosomes in dominant NDI is associated with its monoubiquitination and increased phosphorylation by PKC but is due to the loss of E258.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

An impaired routing of wild-type aquaporin-2 after tetramerization with an aquaporin-2 mutant explains dominant nephrogenic diabetes insipidus

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Three families with autosomal dominant nephrogenic diabetes insipidus caused by aquaporin-2 mutations in the C-terminus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Two novel aquaporin-2 mutations responsible for congenital nephrogenic diabetes insipidus in Chinese families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Diabetes insipidus in mice with a mutation in aquaporin-2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Congenital progressive hydronephrosis (cph) is caused by an S256L mutation in aquaporin-2 that affects its phosphorylation and apical membrane accumulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Cell-biologic and functional analyses of five new Aquaporin-2 missense mutations that cause recessive nephrogenic diabetes insipidus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Functionality of aquaporin-2 missense mutants in recessive nephrogenic diabetes insipidus

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Vasopressin increases water permeability of kidney collecting duct by inducing translocation of aquaporin-CD water channels to plasma membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Cellular and subcellular immunolocalization of vasopressin-regulated water channel in rat kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Regulation and dysregulation of aquaporins in water balance disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Cell biological aspects of the vasopressin type-2 receptor and aquaporin 2 water channel in nephrogenic diabetes insipidus

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Severe urinary concentrating defect in renal collecting duct-selective AQP2 conditional-knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Nephrogenic diabetes insipidus in mice caused by deleting COOH-terminal tail of aquaporin-2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Pathogenesis and treatment of autosomal-dominant nephrogenic diabetes insipidus caused by an aquaporin 2 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Defective aquaporin-2 trafficking in nephrogenic diabetes insipidus and correction by chemical chaperones

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

The role of putative phosphorylation sites in the targeting and shuttling of the aquaporin-2 water channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

How does the brain sense osmolality?

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Neonatal mortality in an aquaporin-2 knock-in mouse model of recessive nephrogenic diabetes insipidus

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

Mouse model of inducible nephrogenic diabetes insipidus produced by floxed aquaporin-2 gene deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.043000

10.1113/EXPPHYSIOL.2008.043000

21 January 2018

Identifiers

DOI

1 reference

19 August 2017

1 reference

PubMed ID

18790812