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searching for Cystic fibrosis transmembrane conductance regulator 38 found (427 total)

alternate case: cystic fibrosis transmembrane conductance regulator

Co-chaperone (777 words) [view diff] exact match in snippet view article find links to article

co-chaperone, Aha1, is essential to the proper folding of cystic fibrosis transmembrane conductance regulator (CFTR). Other examples of co-chaperone's role in
Mir-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:10
Ductal 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 chloride
Jue 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 ion
Channel-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. Biol
MIR494 (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 Proteomics
Sodium 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 the
MicroRNA 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): 13362–7
MicroRNA 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): 13362–7
Cystic 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 treats
RNF5 (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.2006
Sec61 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 proteasome
RCP9 (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): 3455–60
STX8 (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". Journal
MYO5B (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 in
DNAJB6 (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): 797–806
Uterine 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 biology
Chemical 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 in
PRKAA2 (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. Chem
SLC23A2 (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 Foundation
SEC61B (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 proteasome
PRKG1 (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): 4003–10
P2RY1 (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 regulatory
Protein 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-activated
VAPA (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". The
Seliciclib (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 of
YAP1 (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:1998FEBSL
Beta-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 regulatory
RNA 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 the
Organoid (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 necessary
CRISPR 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 the
Developmental 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