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The European Respiratory Journal|June 5, 2004
Genotype/phenotype correlation of the G85E mutation in a large cohort of cystic fibrosis patientsK Decaestecker, E Decaestecker, C Castellani, et al.Pflugers Archiv : European Journal of Physiology|June 22, 2001
The C-terminal part of the R-domain, but not the PDZ binding motif, of CFTR is involved in interaction with Ca(2+)-activated Cl- channelsL Wei, A Vankeerberghen, H Cuppens, et al.Human Molecular Genetics|September 16, 1998
Characterization of 19 disease-associated missense mutations in the regulatory domain of the cystic fibrosis transmembrane conductance regulatorA Vankeerberghen, L Wei, M Jaspers, et al.FEBS Letters|December 16, 1998
Phosphorylation site independent single R-domain mutations affect CFTR channel activityL Wei, A Vankeerberghen, H Cuppens, et al.Biochemistry|November 11, 1999
Functional characterization of the CFTR R domain using CFTR/MDR1 hybrid and deletion constructsA Vankeerberghen, W Lin, M Jaspers, et al.Pflugers Archiv : European Journal of Physiology|October 16, 1999
Capacitance measurements reveal different pathways for the activation of CFTRW M Weber, H Cuppens, J J Cassiman, et al.Clinical Genetics|September 1, 1994
Exclusion of linkage to 14q23-24 in a family with Holt-Oram syndromeJ C Ruiz, E Legius, H Cuppens, et al.Somatic Cell and Molecular Genetics|September 1, 1991
Localization of the gene encoding the alpha 2 subunit of the human VLA-2 receptor to chromosome 5q23-31M Jaspers, P Marynen, M S Aly, et al.Human Molecular Genetics|January 1, 1997
Increased proportion of exon 9 alternatively spliced CFTR transcripts in vas deferens compared with nasal epithelial cellsH Teng, M Jorissen, H Van Poppel, et al.Pflugers Archiv : European Journal of Physiology|November 11, 1999
Interaction between calcium-activated chloride channels and the cystic fibrosis transmembrane conductance regulatorL Wei, A Vankeerberghen, H Cuppens, et al.Pageof 5