Cystic Fibrosis as a Disease of Misprocessing of the Cystic Fibrosis Transmembrane Conductance Regulator Glycoprotein-Reference-Cited by-同舟云学术

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Cystic Fibrosis as a Disease of Misprocessing of the Cystic Fibrosis Transmembrane Conductance Regulator Glycoprotein

Published:1999-06 Issue:6 Volume:64 Page:1499-1504
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Riordan John R.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference39 articles.

1. ATP-sensitive potassium channels, sulfonylurea receptors and persistent hyperinvulinemic hypoglycemia of infancy;Agular-Bryan;Diabetes Rev,1996

2. Cargo selection by the COPII budding machinery during export from the ER;Aridor;J Cell Biol,1998

3. Chemical chaperones correct the mutant phenotype of the delta F508 cystic fibrosis transmembrane conductance regulator protein;Brown;Cell Stress Chaperones,1996

4. Missense mutation R1066C in the second transmembrane domain of CFTR causes a severe cystic fibrosis phenotype: study of 19 heterozygous and 2 homozygous patients;Casals;Hum Mutat,1997

5. ATPase activity of purified multidrug resistance-associated protein;Chang;J Biol Chem,1997

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3. 4PBA Restores Signaling of a Cysteine-substituted Mutant BMPR2 Receptor Found in Patients with Pulmonary Arterial Hypertension;American Journal of Respiratory Cell and Molecular Biology;2020-08

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5. Cystic Fibrosis;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2020

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