Cystic fibrosis transmembrane conductance regulator (CFTR) functionality is dependent on coatomer protein I (COPI).

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Functional Rescue of F508del-CFTR Using Small Molecule Correctors Cystic fibrosis transmembrane conductance regulator trafficking is mediated by the COPI coat in epithelial cells.A hierarchical coherent-gene-group model for brain development.

P2860

Q38051325-FE42783F-B927-4A33-9164-BE8872477C2A Q40068817-B57E2984-6D53-4003-8A0D-9B6AA360B68D Q46046510-FA3F367D-7D26-4C2E-928F-DDB19F953A36

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Cystic fibrosis transmembrane conductance regulator (CFTR) functionality is dependent on coatomer protein I (COPI).

Item

http://www.wikidata.org/entity/Q40153875

description

2007 nî lūn-bûn

@nan

2007年の論文

@ja

2007年論文

@yue

2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

@wuu

2007年论文

@zh

2007年论文

@zh-cn

name

Cystic fibrosis transmembrane ...... on coatomer protein I (COPI).

@en

type

Item

label

Cystic fibrosis transmembrane ...... on coatomer protein I (COPI).

@en

prefLabel

Cystic fibrosis transmembrane ...... on coatomer protein I (COPI).

@en

P1476

Cystic fibrosis transmembrane ...... on coatomer protein I (COPI).

@en

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Igor Tsigelny

http://www.w3.org/2001/XMLSchema#string

Jason X-J Yuan

http://www.w3.org/2001/XMLSchema#string

Oleksandr Platoshyn

http://www.w3.org/2001/XMLSchema#string

Olga Safrina

http://www.w3.org/2001/XMLSchema#string

Steven H Keller

http://www.w3.org/2001/XMLSchema#string

Ying Yu

http://www.w3.org/2001/XMLSchema#string

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Perturbation of Hsp90 interaction with nascent CFTR prevents its maturation and accelerates its degradation by the proteasome

The cochaperone HspBP1 inhibits the CHIP ubiquitin ligase and stimulates the maturation of the cystic fibrosis transmembrane conductance regulator

Hsp70 chaperones: cellular functions and molecular mechanism

A single binding site for dilysine retrieval motifs and p23 within the gamma subunit of coatomer

Gamma-COP appendage domain - structure and function

The alpha- and beta'-COP WD40 domains mediate cargo-selective interactions with distinct di-lysine motifs.

Coatomer is essential for retrieval of dilysine-tagged proteins to the endoplasmic reticulum.

Duplication of genes encoding non-clathrin coat protein gamma-COP in vertebrate, insect and plant evolution

Visualization of ER-to-Golgi transport in living cells reveals a sequential mode of action for COPII and COPI

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433-444

http://www.w3.org/2001/XMLSchema#string

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scholarly article

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10.1042/BC20060114

http://www.w3.org/2001/XMLSchema#string

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http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2007-08-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

6418299

http://www.w3.org/2001/XMLSchema#string

P698

17388782

http://www.w3.org/2001/XMLSchema#string

P921

cystic fibrosis

transmembrane protein

Cystic fibrosis transmembrane conductance regulator (CFTR) functionality is dependent on coatomer protein I (COPI).

about

P2860

P2860

Cystic fibrosis transmembrane conductance regulator (CFTR) functionality is dependent on coatomer protein I (COPI).

description

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type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P921