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Find link is a tool written by Edward Betts.searching for Cystic fibrosis transmembrane conductance regulator 38 found (427 total)
alternate case: cystic fibrosis transmembrane conductance regulator
Co-chaperone
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co-chaperone, Aha1, is essential to the proper folding of cystic fibrosis transmembrane conductance regulator (CFTR). Other examples of co-chaperone's role inMir-384 microRNA precursor family (203 words) [view diff] exact match in snippet view article find links to article
2011). "MicroRNA regulation of expression of the cystic fibrosis transmembrane conductance regulator gene". The Biochemical Journal. 438 (1): 25–32. doi:10Ductal cells (1,792 words) [view diff] exact match in snippet view article find links to article
ducts as well as many other secretory epithelia. Cystic fibrosis transmembrane conductance regulator (CFTR) is the mutated gene and is essential to chlorideJue Chen (scientist) (1,717 words) [view diff] exact match in snippet view article
the thousands of ABC transporters, one member, the cystic fibrosis transmembrane conductance regulator (CFTR), has evolved to function as an ATP-gated ionChannel-conductance-controlling ATPase (210 words) [view diff] exact match in snippet view article find links to article
"Membrane insertion, processing, and topology of cystic fibrosis transmembrane conductance regulator (CFTR) in microsomal membranes". Mol. Membr. BiolMIR494 (684 words) [view diff] case mismatch in snippet view article find links to article
"Synergistic post-transcriptional regulation of the Cystic Fibrosis Transmembrane conductance Regulator (CFTR) by miR-101 and miR-494 specific binding".LMTK2 (813 words) [view diff] exact match in snippet view article find links to article
transmembrane Ser/Thr kinase KPI-2 reveals reactivity with cystic fibrosis transmembrane conductance regulator and phosphorylase". Molecular & Cellular ProteomicsSodium bicarbonate cotransporter 3 (518 words) [view diff] exact match in snippet view article find links to article
S2CID 4457223. Park M, Ko SB, Choi JY, et al. (2003). "The cystic fibrosis transmembrane conductance regulator interacts with and regulates the activity of theMicroRNA 138-1 (712 words) [view diff] exact match in snippet view article find links to article
and biosynthesis of wild-type and DeltaF508 mutant cystic fibrosis transmembrane conductance regulator". Proc. Natl. Acad. Sci. U.S.A. 109 (33): 13362–7MicroRNA 138-1 (712 words) [view diff] exact match in snippet view article find links to article
and biosynthesis of wild-type and DeltaF508 mutant cystic fibrosis transmembrane conductance regulator". Proc. Natl. Acad. Sci. U.S.A. 109 (33): 13362–7Cystic Fibrosis Foundation (957 words) [view diff] exact match in snippet view article find links to article
Sionna Therapeutics, for the development of a new cystic fibrosis transmembrane conductance regulator (CFTR) modulators, a type of therapy that treatsRNF5 (907 words) [view diff] exact match in snippet view article find links to article
"Sequential quality-control checkpoints triage misfolded cystic fibrosis transmembrane conductance regulator". Cell. 126 (3): 571–82. doi:10.1016/j.cell.2006Sec61 alpha 1 (672 words) [view diff] exact match in snippet view article find links to article
King SA, et al. (1998). "The mechanism underlying cystic fibrosis transmembrane conductance regulator transport from the endoplasmic reticulum to the proteasomeRCP9 (786 words) [view diff] exact match in snippet view article find links to article
gene-related peptide responsiveness to oocytes by using a cystic fibrosis transmembrane conductance regulator assay". Proc Natl Acad Sci U S A. 93 (8): 3455–60STX8 (1,287 words) [view diff] exact match in snippet view article find links to article
A (Apr 2004). "Syntaxin 8 impairs trafficking of cystic fibrosis transmembrane conductance regulator (CFTR) and inhibits its channel activity". JournalMYO5B (982 words) [view diff] exact match in snippet view article find links to article
2007). "Myosin Vb is required for trafficking of the cystic fibrosis transmembrane conductance regulator in Rab11a-specific apical recycling endosomes inDNAJB6 (1,270 words) [view diff] exact match in snippet view article find links to article
is required for the in vivo stabilization of the cystic fibrosis transmembrane conductance regulator by Hsp70". The Biochemical Journal. 366 (Pt 3): 797–806Uterine epithelium (1,667 words) [view diff] exact match in snippet view article find links to article
expression of epithelial Na+ channel subunits and cystic fibrosis transmembrane conductance regulator in mouse endometrium by a low sodium diet. Cell biologyChemical chaperone (1,382 words) [view diff] exact match in snippet view article find links to article
resulting from a failure to maintain the level of cystic fibrosis transmembrane conductance regulator (CFTR), which functions as a chloride channel inPRKAA2 (969 words) [view diff] exact match in snippet view article find links to article
gating by AMP-activated protein kinase modulates cystic fibrosis transmembrane conductance regulator activity in lung submucosal cells". J. Biol. ChemSLC23A2 (886 words) [view diff] exact match in snippet view article find links to article
Schwarzer C, Illek B (2004). "Vitamin C controls the cystic fibrosis transmembrane conductance regulator chloride channel". Proc. Natl. Acad. Sci. U.S.A.Tara Matise (1,055 words) [view diff] exact match in snippet view article find links to article
Her contribution to the identification of the cystic fibrosis transmembrane conductance regulator (CFTR) gene was honored by the Cystic Fibrosis FoundationSEC61B (905 words) [view diff] exact match in snippet view article find links to article
King SA, et al. (1998). "The mechanism underlying cystic fibrosis transmembrane conductance regulator transport from the endoplasmic reticulum to the proteasomePRKG1 (1,307 words) [view diff] exact match in snippet view article find links to article
P, Nairn AC (Jun 1992). "Phosphorylation of the cystic fibrosis transmembrane conductance regulator". The Journal of Biological Chemistry. 267 (18):STUB1 (1,473 words) [view diff] exact match in snippet view article find links to article
ubiquitin ligase and stimulates the maturation of the cystic fibrosis transmembrane conductance regulator". Molecular Biology of the Cell. 15 (9): 4003–10P2RY1 (1,102 words) [view diff] exact match in snippet view article find links to article
the beta2-adrenergic receptor, P2Y1 receptor and cystic fibrosis transmembrane conductance regulator determines binding to the Na+/H+ exchanger regulatoryProtein kinase, AMP-activated, alpha 1 (1,257 words) [view diff] exact match in snippet view article find links to article
Raghuram V, Kemp BE, et al. (2000). "Inhibition of cystic fibrosis transmembrane conductance regulator by novel interaction with the metabolic sensor AMP-activatedVAPA (1,892 words) [view diff] case mismatch in snippet view article find links to article
"VAMP-associated Proteins (VAP) as Receptors That Couple Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Proteostasis with Lipid Homeostasis". TheSeliciclib (1,512 words) [view diff] exact match in snippet view article find links to article
affinity activators of wild type, G551D, and F508del cystic fibrosis transmembrane conductance regulator chloride channels". J Pharmacol Exp Ther. 319 (1):Jean-Pierre Lecocq (1,763 words) [view diff] case mismatch in snippet view article find links to article
Lecocq and R.G. Crystal In vivo Transfer of the Human Cystic Fibrosis Transmembrane Conductance Regulator Gene to Airway Epithelium Cell, 68, 143-155 (1992)Calnexin (2,214 words) [view diff] exact match in snippet view article find links to article
chaperone calnexin (p88, IP90) in the biogenesis of the cystic fibrosis transmembrane conductance regulator". The Journal of Biological Chemistry. 269 (17):Derlin-1 (2,259 words) [view diff] exact match in snippet view article find links to article
"Derlin-1 promotes the efficient degradation of the cystic fibrosis transmembrane conductance regulator (CFTR) and CFTR folding mutants". The Journal ofYAP1 (3,445 words) [view diff] exact match in snippet view article find links to article
NHE-RF-PDZ1 domain matches the C-terminal sequence of cystic fibrosis transmembrane conductance regulator (CFTR)". FEBS Letters. 427 (1): 103–8. Bibcode:1998FEBSLBeta-2 adrenergic receptor (3,420 words) [view diff] exact match in snippet view article find links to article
the beta2-adrenergic receptor, P2Y1 receptor and cystic fibrosis transmembrane conductance regulator determines binding to the Na+/H+ exchanger regulatoryRNA editing (7,435 words) [view diff] exact match in snippet view article find links to article
(November 2013). "Correction of mutations within the cystic fibrosis transmembrane conductance regulator by site-directed RNA editing". Proceedings of theOrganoid (8,995 words) [view diff] exact match in snippet view article find links to article
disease that is caused by gene mutations of the cystic fibrosis transmembrane conductance regulator gene that encodes an epithelial ion channel necessaryCRISPR gene editing (19,890 words) [view diff] exact match in snippet view article find links to article
(November 2013). "Correction of mutations within the cystic fibrosis transmembrane conductance regulator by site-directed RNA editing". Proceedings of theDevelopmental bioelectricity (17,264 words) [view diff] exact match in snippet view article find links to article
PMID 25683120. Uzun, S; Gökçe, S.; Wagner, K. (2005). "Cystic fibrosis transmembrane conductance regulator gene mutations in infertile males with congenital