Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2 (Q36727301)

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scientific article published on August 1, 1991

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English	Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2	scientific article published on August 1, 1991

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scholarly article

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Europe PubMed Central

PMC publication ID

15 August 2017

Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2 (English)

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Europe PubMed Central

PMC publication ID

15 August 2017

transmembrane protein

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cystic fibrosis

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1 reference

10.1128/MCB.11.8.3886-3893.1991

https://api.crossref.org/works/10.1128/MCB.11.8.3886-3893.1991

5 November 2022

Matthew P Anderson

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M. P. Anderson

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5 November 2022

Michael J. Welsh

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5 November 2022

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R. J. Gregory

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5 November 2022

D. P. Rich

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S. H. Cheng

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5 November 2022

D. W. Souza

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S. Paul

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5 November 2022

P. Manavalan

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5 November 2022

A. E. Smith

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5 November 2022

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publication date

1 August 1991

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15 August 2017

full work available at URL

http://mcb.asm.org/cgi/content/abstract/11/8/3886

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5 November 2022

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1712898/?tool=EBI

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5 November 2022

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1712898/pdf/?tool=EBI

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5 November 2022

https://europepmc.org/articles/PMC361177

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5 November 2022

https://europepmc.org/articles/PMC361177?pdf=render

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5 November 2022

https://journals.asm.org/doi/pdf/10.1128/mcb.11.8.3886-3893.1991

1 reference

10.1128/MCB.11.8.3886-3893.1991

https://api.crossref.org/works/10.1128/MCB.11.8.3886-3893.1991

5 November 2022

Molecular and Cellular Biology

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15 August 2017

11

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Europe PubMed Central

PMC publication ID

15 August 2017

8

1 reference

Europe PubMed Central

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15 August 2017

3886-3893

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Distantly related sequences in the alpha- and beta-subunits of ATP synthase, myosin, kinases and other ATP-requiring enzymes and a common nucleotide binding fold

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Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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Rapid and efficient site-specific mutagenesis without phenotypic selection

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Transport of secretory and membrane glycoproteins from the rough endoplasmic reticulum to the Golgi. A rate-limiting step in protein maturation and secretion.

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Regulation of protein export from the endoplasmic reticulum

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Identification of the cystic fibrosis gene: chromosome walking and jumping

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Protein oligomerization in the endoplasmic reticulum

1 reference

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Control of protein exit from the endoplasmic reticulum

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Discrete mutations introduced in the predicted nucleotide-binding sites of the mdr1 gene abolish its ability to confer multidrug resistance

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Identification of the cystic fibrosis gene: genetic analysis

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30 September 2017

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

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30 September 2017

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene

1 reference

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30 September 2017

Protein degradation in the endoplasmic reticulum

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30 September 2017

A mutation in the second nucleotide binding fold of the cystic fibrosis gene.

1 reference

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Structural model of the nucleotide-binding conserved component of periplasmic permeases

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Benign missense variations in the cystic fibrosis gene

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30 September 2017

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

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Screening for non-delta F508 mutations in five exons of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in Italy.

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Abnormal regulation of ion channels in cystic fibrosis epithelia

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Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance

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Generation of cAMP-Activated Chloride Currents by Expression of CFTR

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Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

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A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein

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

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cystic Fibrosis Transmembrane Conductance Regulator: Nucleotide Binding to a Synthetic Peptide

1 reference

https://pubmed.ncbi.nlm.nih.gov/1712898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1128/MCB.11.8.3886

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

10.1128/MCB.11.8.3886-3893.1991

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1712898

5 November 2022

release_bgwvygghfrepjhhog2mnxd7jly

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https://api.fatcat.wiki/v0/release/bgwvygghfrepjhhog2mnxd7jly

24 November 2022

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mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

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