PRKCSH/80K-H, the protein mutated in polycystic liver disease, protects polycystin-2/TRPP2 against HERP-mediated degradation (Q24321394)

Polycystin 2, transient receptor potential cation channel

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Transient receptor potential cation channel subfamily V member 1

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phosphoprotein binding

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Polycystic kidney disease 2

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polycystic liver disease

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inferred from title

author

Albrecht Kramer-Zucker

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object named as

Albrecht Kramer-Zucker

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author name string

Hongyu Gao

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Yan Wang

2

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Tomasz Wegierski

3

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Kassiani Skouloudaki

4

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Michael Pütz

5

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Xiao Fu

6

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Christina Engel

7

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Christopher Boehlke

8

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Hongquan Peng

9

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E Wolfgang Kuehn

10

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Emily Kim

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Gerd Walz

Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease

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language of work or name

English

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publication date

1 January 2010

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published in

Human Molecular Genetics

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volume

19

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issue

1

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page(s)

16-24

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cites work

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https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

Mutations in PRKCSH cause isolated autosomal dominant polycystic liver disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

Mutations in SEC63 cause autosomal dominant polycystic liver disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

Polycystic liver disease is a disorder of cotranslational protein processing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

Endoplasmic reticulum glucosidase II is composed of a catalytic subunit, conserved from yeast to mammals, and a tightly bound noncatalytic HDEL-containing subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

N-glycan processing in ER quality control

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

Identification of p90, a prominent tyrosine-phosphorylated protein in fibroblast growth factor-stimulated cells, as 80K-H.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

Molecular identity and cellular distribution of advanced glycation endproduct receptors: relationship of p60 to OST-48 and p90 to 80K-H membrane proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

Elevated 80K-H protein in breast cancer: a role for FGF-1 stimulation of 80K-H.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

Mediators of endoplasmic reticulum stress-induced apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

Trafficking of TRPP2 by PACS proteins represents a novel mechanism of ion channel regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

Polycystin-2 is regulated by endoplasmic reticulum-associated degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

A genetic screen in zebrafish identifies cilia genes as a principal cause of cystic kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

Autosomal dominant polycystic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

The subcellular localization of TRPP2 modulates its function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

80K-H as a new Ca2+ sensor regulating the activity of the epithelial Ca2+ channel transient receptor potential cation channel V5 (TRPV5).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

The primary cilium as the cell's antenna: signaling at a sensory organelle

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

Cilia and developmental signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

Molecular characterization of hepatocystin, the protein that is defective in autosomal dominant polycystic liver disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

The HECT ubiquitin ligase AIP4 regulates the cell surface expression of select TRP channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

TRPP2 channels regulate apoptosis through the Ca2+ concentration in the endoplasmic reticulum

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

Immunolocalization of vacuolar system-associated protein-60 (VASAP-60).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

7 January 2021

inferred from DOI database lookup

Polycystic kidney disease

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https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

7 January 2021

inferred from DOI database lookup

OS-9 regulates the transit and polyubiquitination of TRPV4 in the endoplasmic reticulum

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP463

7 January 2021