Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia.

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Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

@zh-cn

2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia.

@en

Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia.

@nl

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label

Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia.

@en

Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia.

@nl

prefLabel

Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia.

@en

Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia.

@nl

P1476

Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia

@en

P2093

Deborah M Cholon

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

Emanuela Caci

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

Emanuela Pesce

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

Loretta Ferrera

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

Luis Jv Galietta

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

Martina Gentzsch

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

Nancy L Quinney

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

Roberto Ravazzolo

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

Susan E Boyles

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

Valeria Tomati

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P2860

The PDZ-binding chloride channel ClC-3B localizes to the Golgi and associates with cystic fibrosis transmembrane conductance regulator-interacting PDZ proteins

Rescue of ΔF508-CFTR trafficking via a GRASP-dependent unconventional secretion pathway

Rescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770

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

Adapting proteostasis for disease intervention

Degradation of CFTR by the ubiquitin-proteasome pathway

Small-molecule correctors of defective DeltaF508-CFTR cellular processing identified by high-throughput screening.

Rescue of the mutant CFTR chloride channel by pharmacological correctors and low temperature analyzed by gene expression profiling.

Cystic fibrosis transmembrane conductance regulator (CFTR) potentiator VX-770 (ivacaftor) opens the defective channel gate of mutant CFTR in a phosphorylation-dependent but ATP-independent manner.

P31

scholarly article

P356

10.1172/JCI.INSIGHT.98699

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P433

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

P478

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

P50

Nicoletta Pedemonte

Elvira Sondo

Andrea Armirotti

P577

2018-02-08T00:00:00Z

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P698

29415893

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P921

cystic fibrosis

P932

5821210

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