Rescuing ΔF508 CFTR with trimethylangelicin, a dual-acting corrector and potentiator.

about

CFTR and lung homeostasis.Hallmarks of therapeutic management of the cystic fibrosis functional landscape.CFTR is a tumor suppressor gene in murine and human intestinal cancer Ion channels of the lung and their role in disease pathogenesis.Molecular basis of cystic fibrosis: from bench to bedside

P2860

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P2860

Rescuing ΔF508 CFTR with trimethylangelicin, a dual-acting corrector and potentiator.

Item

http://www.wikidata.org/entity/Q44455766

description

2014 nî lūn-bûn

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2014年の論文

@ja

2014年学术文章

@wuu

2014年学术文章

@zh

2014年学术文章

@zh-cn

2014年学术文章

@zh-hans

2014年学术文章

@zh-my

2014年学术文章

@zh-sg

2014年學術文章

@yue

2014年學術文章

@zh-hant

name

Rescuing ΔF508 CFTR with trimethylangelicin, a dual-acting corrector and potentiator.

@en

Rescuing ΔF508 CFTR with trimethylangelicin, a dual-acting corrector and potentiator.

@nl

type

Item

label

Rescuing ΔF508 CFTR with trimethylangelicin, a dual-acting corrector and potentiator.

@en

Rescuing ΔF508 CFTR with trimethylangelicin, a dual-acting corrector and potentiator.

@nl

prefLabel

Rescuing ΔF508 CFTR with trimethylangelicin, a dual-acting corrector and potentiator.

@en

Rescuing ΔF508 CFTR with trimethylangelicin, a dual-acting corrector and potentiator.

@nl

P1476

Rescuing ΔF508 CFTR with trimethylangelicin, a dual-acting corrector and potentiator

@en

P2093

James F Collawn

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

Sadis Matalon

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

P2860

Identification of the cystic fibrosis gene: chromosome walking and jumping

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

Cystic fibrosis

A functional CFTR assay using primary cystic fibrosis intestinal organoids

Degradation of CFTR by the ubiquitin-proteasome pathway

Design and synthesis of a hybrid potentiator-corrector agonist of the cystic fibrosis mutant protein DeltaF508-CFTR

Conformational and temperature-sensitive stability defects of the delta F508 cystic fibrosis transmembrane conductance regulator in post-endoplasmic reticulum compartments.

Modulation of endocytic trafficking and apical stability of CFTR in primary human airway epithelial cultures

Identification of synergistic combinations of F508del cystic fibrosis transmembrane conductance regulator (CFTR) modulators.

P304

L431-4

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P31

scholarly article

editorial

P356

10.1152/AJPLUNG.00177.2014

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P433

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

P478

307

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P50

Karl Fu

Rafal Bartoszewski

P577

2014-07-25T00:00:00Z

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P5875

264623595

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P698

25063802

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P932

4166784

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

Rescuing ΔF508 CFTR with trimethylangelicin, a dual-acting corrector and potentiator.

about

P2860

P2860

Rescuing ΔF508 CFTR with trimethylangelicin, a dual-acting corrector and potentiator.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932