CFTR: Development of high- affinity antibodies and localization in sweat gland
- 27 November 1991
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 181 (1) , 36-43
- https://doi.org/10.1016/s0006-291x(05)81378-6
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2.Molecular and Cellular Biology, 1991
- Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion SelectivityScience, 1991
- Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosisCell, 1990
- Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cellsNature, 1990
- Expression and characterization of the cystic fibrosis transmembrane conductance regulatorNature, 1990
- Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transferCell, 1990
- Cystic fibrosis: a disease in electrolyte transportThe FASEB Journal, 1990
- Abnormal regulation of ion channels in cystic fibrosis epitheliaThe FASEB Journal, 1990
- Identification of the Cystic Fibrosis Gene: Chromosome Walking and JumpingScience, 1989
- Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNAScience, 1989