(Q40747347)

23 September 2017

title

Cation channel regulation by COOH-terminal cytoplasmic tail of polycystin-1: mutational and functional analysis (English)

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23 September 2017

David H Vandorpe

1

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23 September 2017

Sabine Wilhelm

2

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23 September 2017

Lianwei Jiang

3

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23 September 2017

Oxana Ibraghimov-Beskrovnaya

4

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23 September 2017

Marina N Chernova

5

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23 September 2017

Alan K Stuart-Tilley

6

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23 September 2017

Seth L Alper

7

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23 September 2017

publication date

28 February 2002

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23 September 2017

published in

Physiological Genomics

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23 September 2017

volume

8

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23 September 2017

issue

2

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23 September 2017

page(s)

87-98

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Molecular genetics and pathogenesis of autosomal dominant polycystic kidney disease

23 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

Cellular activation triggered by the autosomal dominant polycystic kidney disease gene product PKD2

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Mutational analysis within the 3′ region of the PKD1 gene

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

Predicting coiled coils by use of pairwise residue correlations

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

The structure of a PKD domain from polycystin-1: implications for polycystic kidney disease

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

Polycystin-L is a calcium-regulated cation channel permeable to calcium ions

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

Transport function of the naturally occurring pathogenic polycystin-2 mutant, R742X.

21 January 2018

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The TRP ion channel family.

21 January 2018

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Nifedipine blocks Ca2+ store refilling through a pathway not involving L-type Ca2+ channels in rabbit arteriolar smooth muscle

21 January 2018

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Maitotoxin-elicited calcium influx in cultured cells. Effect of calcium-channel blockers

21 January 2018

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Identification of an aspartic residue in the P-loop of the vanilloid receptor that modulates pore properties.

21 January 2018

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Modification of the composition of polycystin-1 multiprotein complexes by calcium and tyrosine phosphorylation

21 January 2018

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Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

Polycystic kidney disease: In danger of being X-rated?

21 January 2018

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Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents

21 January 2018

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Polycystin-1, the PKD1 gene product, is in a complex containing E-cadherin and the catenins

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains

21 January 2018

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Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

Polycystin: in vitro synthesis, in vivo tissue expression, and subcellular localization identifies a large membrane-associated protein

21 January 2018

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The polycystic kidney disease 1 gene product modulates Wnt signaling

21 January 2018

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Predicting coiled coils from protein sequences

21 January 2018

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The sea urchin sperm receptor for egg jelly is a modular protein with extensive homology to the human polycystic kidney disease protein, PKD1.

21 January 2018

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The polycystic kidney disease-1 protein, polycystin-1, binds and activates heterotrimeric G-proteins in vitro.

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

PKD1 interacts with PKD2 through a probable coiled-coil domain

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

The molecular basis of focal cyst formation in human autosomal dominant polycystic kidney disease type I.

21 January 2018

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The 3.2-A crystal structure of the human IgG1 Fc fragment-Fc gammaRIII complex

21 January 2018

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Homo- and heterodimeric interactions between the gene products of PKD1 and PKD2

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

Specific association of the gene product of PKD2 with the TRPC1 channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

The cytoplasmic C-terminal fragment of polycystin-1 regulates a Ca2+-permeable cation channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

Polycystin-2 is a novel cation channel implicated in defective intracellular Ca(2+) homeostasis in polycystic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

Inhibition of CaT1 channel activity by a noncompetitive IP3 antagonist

21 January 2018

1 reference

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The polycystin-1 C-type lectin domain binds carbohydrate in a calcium-dependent manner, and interacts with extracellular matrix proteins in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

Molecular genetics and mechanism of autosomal dominant polycystic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00092.2001

10.1152/PHYSIOLGENOMICS.00092.2001

21 January 2018

Identifiers

DOI

1 reference

23 September 2017

1 reference