Studies of the molecular basis for cystic fibrosis using purified reconstituted CFTR protein

scientific article published on January 2002

Studies of the molecular basis for cystic fibrosis using purified reconstituted CFTR protein is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1385/1-59259-187-6:143
P698PubMed publication ID11917519

P2093author name stringCanhui Li
Christine E Bear
Mohabir Ramjeesingh
Ilana Kogan
P921main subjectcystic fibrosisQ178194
P304page(s)143-157
P577publication date2002-01-01
P1433published inMethods in Molecular MedicineQ15764356
P1476titleStudies of the molecular basis for cystic fibrosis using purified reconstituted CFTR protein
P478volume70

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cites work (P2860)
Q24322612ACF7 regulates cytoskeletal-focal adhesion dynamics and migration and has ATPase activity
Q28489019ATP-driven self-assembly of a morphogenetic protein in Bacillus subtilis
Q39756358CFTR directly mediates nucleotide-regulated glutathione flux.
Q92344344Cholesterol Interaction Directly Enhances Intrinsic Activity of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)
Q38976933Current insights into the role of PKA phosphorylation in CFTR channel activity and the pharmacological rescue of cystic fibrosis disease-causing mutants
Q34033437Cystic fibrosis transmembrane conductance regulator (CFTR) potentiator VX-770 (ivacaftor) opens the defective channel gate of mutant CFTR in a phosphorylation-dependent but ATP-independent manner
Q41819157Cystic fibrosis transmembrane conductance regulator: the NBF1+R (nucleotide-binding fold 1 and regulatory domain) segment acting alone catalyses a Co2+/Mn2+/Mg2+-ATPase activity markedly inhibited by both Cd2+ and the transition-state analogue ortho
Q42010061Nucleotides bind to the C-terminus of ClC-5.
Q38787827Specific stabilization of CFTR by phosphatidylserine

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