Zobrazeno 1 - 4
of 4
pro vyhledávání: '"L S, Ostedgaard"'
Autor:
J, Marshall, S, Fang, L S, Ostedgaard, C R, O'Riordan, D, Ferrara, J F, Amara, H, Hoppe, R K, Scheule, M J, Welsh, A E, Smith
Publikováno v:
The Journal of biological chemistry. 269(4)
We have generated several clones of Chinese hamster ovary, mouse epitheloid C127, and pig kidney epithelial LLCPK1 cells producing high levels of functional recombinant human cystic fibrosis transmembrane conductance regulator (CFTR). Processing of C
Publikováno v:
Journal of cell science. Supplement. 17
The cystic fibrosis transmembrane conductance regulator (CFTR) is mutated in patients with cystic fibrosis (CF). The most common CF-associated mutation is deletion of phenylalanine at residue 508, CFTR delta F508. When expressed in heterologous cells
Autor:
L S, Ostedgaard, M J, Welsh
Publikováno v:
The Journal of biological chemistry. 267(36)
We have investigated several purification strategies for the cystic fibrosis transmembrane regulator (CFTR) based on its structural similarity to other proteins of the traffic ATPase/ABC transporter family. Recombinant CFTR expressed in heterologous
Publikováno v:
The Journal of biological chemistry. 267(14)
Membrane vesicles, prepared from mouse NIH-3T3 fibroblasts and Chinese hamster ovary cells expressing high levels of cystic fibrosis transmembrane conductance regulator (CFTR), were fused with Mueller-Rudin planar lipid bilayers. Upon addition of the