Post-translational disruption of the delta F508 cystic fibrosis transmembrane conductance regulator (CFTR)-molecular chaperone complex with geldanamycin stabilizes delta F508 CFTR in the rabbit reticulocyte lysate. (Q48562819)

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scientific article published in December 2000

Language	Label	Description	Also known as
English	Post-translational disruption of the delta F508 cystic fibrosis transmembrane conductance regulator (CFTR)-molecular chaperone complex with geldanamycin stabilizes delta F508 CFTR in the rabbit reticulocyte lysate.	scientific article published in December 2000

Statements

scholarly article

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/10982807

Post-translational disruption of the delta F508 cystic fibrosis transmembrane conductance regulator (CFTR)-molecular chaperone complex with geldanamycin stabilizes delta F508 CFTR in the rabbit reticulocyte lysate. (English)

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/10982807

cystic fibrosis

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molecular chaperones

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transmembrane protein

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1

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/10982807

author name string

Cuthbert AW

2

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/10982807

language of work or name

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publication date

1 December 2000

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Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/10982807

Journal of Biological Chemistry

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Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/10982807

275

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Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/10982807

48

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Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/10982807

37462-37468

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/10982807

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

1 reference

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Identification of the cystic fibrosis gene: genetic analysis

1 reference

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Generation of cAMP-Activated Chloride Currents by Expression of CFTR

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Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

1 reference

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The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment

1 reference

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

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https://api.crossref.org/works/10.1074%2FJBC.M006278200

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Degradation of CFTR by the ubiquitin-proteasome pathway

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006278200

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Multiple proteolytic systems, including the proteasome, contribute to CFTR processing.

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21 January 2018

Hsp70 family molecular chaperones and mutant insulin receptor: differential binding specificities of BiP and Hsp70/Hsc70 determines accumulation or degradation of insulin receptor

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21 January 2018

The benzoquinone ansamycin 17-allylamino-17-demethoxygeldanamycin binds to HSP90 and shares important biologic activities with geldanamycin

1 reference

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Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells

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21 January 2018

Identifiers

10.1074/JBC.M006278200

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/10982807

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/10982807

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