Correction of Defective Protein Kinesis of Human P-glycoprotein Mutants by Substrates and Modulators (Q57976939)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8995353%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

title

Correction of defective protein kinesis of human P-glycoprotein mutants by substrates and modulators (English)

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22 October 2019

1

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22 October 2019

author name string

D M Clarke

series ordinal

2

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22 October 2019

language of work or name

English

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publication date

1 January 1997

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Journal of Biological Chemistry

22 October 2019

published in

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22 October 2019

volume

272

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22 October 2019

issue

2

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22 October 2019

page(s)

709-712

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Misfolding the way to disease

22 October 2019

cites work

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https://api.crossref.org/works/10.1074%2FJBC.272.2.709

Influence of molecular and chemical chaperones on protein folding

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.2.709

Defective protein folding as a basis of human disease

21 January 2018

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Prion diseases and neurodegeneration

21 January 2018

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Normal and abnormal biology of the beta-amyloid precursor protein

21 January 2018

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.2.709

P-glycoprotein. Associations between domains and between domains and molecular chaperones

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.2.709

Mutational Analysis of the Predicted First Transmembrane Segment of Each Homologous Half of Human P-glycoprotein Suggests That They Are Symmetrically Arranged in the Membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.2.709

Biochemistry of multidrug resistance mediated by the multidrug transporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.2.709

Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.2.709

Chemical chaperones correct the mutant phenotype of the delta F508 cystic fibrosis transmembrane conductance regulator protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.2.709

Rapid purification of human P-glycoprotein mutants expressed transiently in HEK 293 cells by nickel-chelate chromatography and characterization of their drug-stimulated ATPase activities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.2.709

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.272.2.709

Alteration of the cystic fibrosis transmembrane conductance regulator folding pathway

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.272.2.709

Degradation of CFTR by the ubiquitin-proteasome pathway

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.272.2.709

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

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.272.2.709

21 January 2018

Identifiers

DOI

10.1074/JBC.272.2.709

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22 October 2019

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