(Q34598401)

English

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

scholarly article

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

congenital disorder

0 references

phosphorylation

0 references

author name string

Bradley W McDill

1

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Song-Zhe Li

2

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Paul A Kovach

3

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Li Ding

4

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Feng Chen

5

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

language of work or name

0 references

publication date

25 April 2006

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

103

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

18

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

6952-6957

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Trafficking mechanism of water channel aquaporin-2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

Molecular biology of hereditary diabetes insipidus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

Organization of vesicular trafficking in epithelia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

Molecular mechanisms of membrane polarity in renal epithelial cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

From structure to disease: the evolving tale of aquaporin biology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

Calcineurin is required in urinary tract mesenchyme for the development of the pyeloureteral peristaltic machinery.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

Familial vesicoureteral reflux

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

Animal models of fetal renal disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

Signals transduced by Ca(2+)/calcineurin and NFATc3/c4 pattern the developing vasculature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

Generation and phenotype of mice harboring a nonsense mutation in the V2 vasopressin receptor gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

Molecular and cellular pathophysiology of obstructive nephropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

Protein kinase A phosphorylation is involved in regulated exocytosis of aquaporin-2 in transfected LLC-PK1 cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

Congenital progressive hydronephrosis in mice: a new recessive mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

Hydronephrosis: prevention by restoration of urinary concentrating ability using desamino-8D-arginine vasopressin (DDAVP) in Brattleboro rats

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

7 July 2018

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

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0602087103

21 January 2018

Bidirectional regulation of AQP2 trafficking and recycling: involvement of AQP2-S256 phosphorylation

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0602087103

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0602087103

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0602087103

21 January 2018

PITRESSIN-RESISTANT DIABETES INSIPIDUS AND DIABETES MELLITUS AND BILATERAL HYDRONEPHROSIS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459000

26 October 2018

AQP3, p-AQP2, and AQP2 expression is reduced in polyuric rats with hypercalcemia: prevention by cAMP-PDE inhibitors

1 reference

https://pubmed.ncbi.nlm.nih.gov/16641094

12 December 2020

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inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.0602087103

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

2006PNAS..103.6952M

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

ResearchGate publication ID

0 references

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