Decoding F508del misfolding in cystic fibrosis. - Wikidata - awgldk - TriplyDB

Decoding F508del misfolding in cystic fibrosis.

Decoding F508del misfolding in cystic fibrosis.

http://www.wikidata.org/entity/Q33912624

about

Repairing the basic defect in cystic fibrosis - one approach is not enough.A role for the cystic fibrosis transmembrane conductance regulator in the nitric oxide-dependent release of Cl- from acidic organelles in amacrine cells.

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P2860

Decoding F508del misfolding in cystic fibrosis.

http://www.wikidata.org/entity/Q33912624

description

2014 nî lūn-bûn

@nan

2014 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի մայիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Decoding F508del misfolding in cystic fibrosis.

@ast

Decoding F508del misfolding in cystic fibrosis.

@en

type

label

Decoding F508del misfolding in cystic fibrosis.

@ast

Decoding F508del misfolding in cystic fibrosis.

@en

prefLabel

Decoding F508del misfolding in cystic fibrosis.

@ast

Decoding F508del misfolding in cystic fibrosis.

@en

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Decoding F508del misfolding in cystic fibrosis.

@en

P2093

Chenglong Li

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

Xiaodong Robert Wang

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

P275

Creative Commons Attribution

P2860

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

Structure of nucleotide-binding domain 1 of the cystic fibrosis transmembrane conductance regulator

Structure and dynamics of NBD1 from CFTR characterized using crystallography and hydrogen/deuterium exchange mass spectrometry

Structures of a minimal human CFTR first nucleotide-binding domain as a monomer, head-to-tail homodimer, and pathogenic mutant

Requirements for Efficient Correction of ΔF508 CFTR Revealed by Analyses of Evolved Sequences

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

Structural model of ATP-binding proteins associated with cystic fibrosis, multidrug resistance and bacterial transport

Diminished self-chaperoning activity of the DeltaF508 mutant of CFTR results in protein misfolding

Degradation of CFTR by the ubiquitin-proteasome pathway

Interplay between ER exit code and domain conformation in CFTR misprocessing and rescue.

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498-509

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scholarly article

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10.3390/BIOM4020498

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2

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4

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262935630

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24970227

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P921

cystic fibrosis

transport protein

genetic variation

membrane proteins

P932

4101494

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