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American Journal of Respiratory Cell and Molecular Biology|February 3, 2007
VCP/p97 AAA-ATPase does not interact with the endogenous wild-type cystic fibrosis transmembrane conductance regulatorRebecca F Goldstein, Ashutosh Niraj, Todd P Sanderson, et al.The Journal of Biological Chemistry|October 12, 2002
Ablation of internalization signals in the carboxyl-terminal tail of the cystic fibrosis transmembrane conductance regulator enhances cell surface expressionKrisztina Peter, Karoly Varga, Zsuzsa Bebok, et al.The Journal of Biological Chemistry|October 18, 2011
The unfolded protein response (UPR)-activated transcription factor X-box-binding protein 1 (XBP1) induces microRNA-346 expression that targets the human antigen peptide transporter 1 (TAP1) mRNA and governs immune regulatory genesRafal Bartoszewski, Joseph W Brewer, Andras Rab, et al.The Journal of Biological Chemistry|December 13, 2005
Mutations in the amino terminus of the cystic fibrosis transmembrane conductance regulator enhance endocytosisAsta Jurkuvenaite, Karoly Varga, Krzysztof Nowotarski, et al.The New England Journal of Medicine|October 10, 2003
Gentamicin-induced correction of CFTR function in patients with cystic fibrosis and CFTR stop mutationsMichael Wilschanski, Yaacov Yahav, Yasmin Yaacov, et al.The Journal of Biological Chemistry|August 27, 2002
Reactive oxygen nitrogen species decrease cystic fibrosis transmembrane conductance regulator expression and cAMP-mediated Cl- secretion in airway epitheliaZsuzsa Bebok, Karoly Varga, James K Hicks, et al.Journal of Molecular Medicine (Berlin, Germany)|July 23, 2011
Suppression of CFTR premature termination codons and rescue of CFTR protein and function by the synthetic aminoglycoside NB54Steven M Rowe, Peter Sloane, Li Ping Tang, et al.Journal of Molecular Medicine (Berlin, Germany)|August 16, 2023
Pkhd1cyli/cyli mice have altered renal Pkhd1 mRNA processing and hormonally sensitive liver diseaseChaozhe Yang, Naoe Harafuji, Ljubica Caldovic, et al.American Journal of Respiratory Cell and Molecular Biology|March 10, 2007
No detectable improvements in cystic fibrosis transmembrane conductance regulator by nasal aminoglycosides in patients with cystic fibrosis with stop mutationsJohn P Clancy, Steven M Rowe, Zsuzsa Bebok, et al.The Journal of Biological Chemistry|January 1, 2004
Extracellular zinc and ATP restore chloride secretion across cystic fibrosis airway epithelia by triggering calcium entryAkos Zsembery, James A Fortenberry, Lihua Liang, et al.Pageof 4