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The Journal of Biological Chemistry|April 15, 2000
Cystic fibrosis mutations lead to carboxyl-terminal fragments that highlight an early biogenesis step of the cystic fibrosis transmembrane conductance regulatorM Van Oene, G L Lukacs, J M RommensGenomics|March 15, 2006
Phylogeny, sequence conservation, and functional complementation of the SBDS protein familyG R B Boocock, M R Marit, J M RommensGenomics|February 1, 1989
Chromosomal localization of the human homeo box-containing genes, EN1 and EN2C Logan, H F Willard, J M Rommens, et al.Pflugers Archiv : European Journal of Physiology|February 15, 2002
Non-CFTR chloride channels likely contribute to secretion in the murine small intestineK Gyömörey, E Garami, K Galley, et al.Human Genetics|July 1, 1990
Identification of sequences of chromosome 7 that are expressed in sweat gland epithelial cellsJ Burns, G Melmer, J M Rommens, et al.The American Journal of Physiology|August 1, 1992
Right-angle light scattering to assay basal and regulated plasma membrane Cl- conductancesS Dho, S Chou, X B Chang, et al.Genomics|July 15, 1997
Physical and transcription map in the region 14q24.3: identification of six novel transcriptsA F Roux, J M Rommens, L Read, et al.Nature Genetics|December 1, 1993
The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes geneP C Bull, G R Thomas, J M Rommens, et al.American Journal of Human Genetics|December 1, 1989
Physical localization of two DNA markers closely linked to the cystic fibrosis locus by pulsed-field gel electrophoresisJ M Rommens, S Zengerling-Lentes, B Kerem, et al.Human Molecular Genetics|June 1, 1993
Analysis of CFTR transcripts in nasal epithelial cells and lymphoblasts of a cystic fibrosis patient with 621 + 1G-->T and 711 + 1G-->T mutationsJ Zielenski, D Bozon, D Markiewicz, et al.Pageof 7