An Apical PDZ Protein Anchors the Cystic Fibrosis Transmembrane Conductance Regulator to the Cytoskeleton-Reference-Cited by-同舟云学术

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An Apical PDZ Protein Anchors the Cystic Fibrosis Transmembrane Conductance Regulator to the Cytoskeleton

Published:1998-07 Issue:31 Volume:273 Page:19797-19801
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Short Douglas B.,Trotter Kevin W.,Reczek David,Kreda Silvia M.,Bretscher Anthony,Boucher Richard C.,Stutts M. Jackson,Milgram Sharon L.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference50 articles.

1. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA

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

3. Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

4. CFTR as a cAMP-Dependent Regulator of Sodium Channels

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3. Cystic Fibrosis Modulator Therapies: Bridging Insights from CF to other Membrane Protein Misfolding Diseases;Israel Journal of Chemistry;2024-01-24

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5. Cross‐talk between CFTR and sphingolipids in cystic fibrosis;FEBS Open Bio;2023-06-22

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