(Q24294623)

calcium activated cation channel activity

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author name string

Qiang Li

1

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Yan Liu

2

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Wei Zhao

3

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Xing-Zhen Chen

Autosomal dominant polycystic kidney disease

4

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language of work or name

English

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publication date

10 April 2002

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published in

FEBS Letters

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volume

516

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issue

1-3

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page(s)

270-8

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cites work

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PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein

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Identification of PKD2L, a human PKD2-related gene: tissue-specific expression and mapping to chromosome 10q25

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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.

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Mechanism of calcium gating in small-conductance calcium-activated potassium channels.

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Ca2+-sensitive inactivation of L-type Ca2+ channels depends on multiple cytoplasmic amino acid sequences of the alpha1C subunit

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On the molecular basis and regulation of cellular capacitative calcium entry: roles for Trp proteins.

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

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Feedback inhibition of Ca2+ channels by Ca2+ depends on a short sequence of the C terminus that does not include the Ca2+ -binding function of a motif with similarity to Ca2+ -binding domains

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