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Summary Anatomy Item Literature (811) Expression Attributions Wiki
XB-ANAT-1494

Papers associated with duct (and cftr)

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Comparative expression analysis of cysteine-rich intestinal protein family members crip1, 2 and 3 during Xenopus laevis embryogenesis., Hempel A., Int J Dev Biol. January 1, 2014; 58 (10-12): 841-9.                                              


Contribution of casein kinase 2 and spleen tyrosine kinase to CFTR trafficking and protein kinase A-induced activity., Luz S., Mol Cell Biol. November 1, 2011; 31 (22): 4392-404.


SLC26 anion exchangers of guinea pig pancreatic duct: molecular cloning and functional characterization., Stewart AK., Am J Physiol Cell Physiol. August 1, 2011; 301 (2): C289-303.


Mouse cystic fibrosis transmembrane conductance regulator forms cAMP-PKA-regulated apical chloride channels in cortical collecting duct., Lu M., Proc Natl Acad Sci U S A. March 30, 2010; 107 (13): 6082-7.


Metformin treatment of diabetes mellitus increases the risk for pancreatitis in patients bearing the CFTR-mutation S573C., Kongsuphol P., Cell Physiol Biochem. January 1, 2010; 25 (4-5): 389-96.


Inhibition of protein kinase CK2 closes the CFTR Cl channel, but has no effect on the cystic fibrosis mutant deltaF508-CFTR., Treharne KJ., Cell Physiol Biochem. January 1, 2009; 24 (5-6): 347-60.


The Slc26a4 transporter functions as an electroneutral Cl-/I-/HCO3- exchanger: role of Slc26a4 and Slc26a6 in I- and HCO3- secretion and in regulation of CFTR in the parotid duct., Shcheynikov N., J Physiol. August 15, 2008; 586 (16): 3813-24.


Control of epithelial ion transport by Cl- and PDZ proteins., Schreiber R., J Membr Biol. May 15, 2004; 199 (2): 85-98.


ENaC is inhibited by an increase in the intracellular Cl(-) concentration mediated through activation of Cl(-) channels., Kunzelmann K., Pflugers Arch. January 1, 2003; 445 (4): 504-12.


Cystic fibrosis transmembrane conductance regulator-dependent up-regulation of Kir1.1 (ROMK) renal K+ channels by the epithelial sodium channel., Konstas AA., J Biol Chem. July 12, 2002; 277 (28): 25377-84.


Two cystic fibrosis transmembrane conductance regulator mutations have different effects on both pulmonary phenotype and regulation of outwardly rectified chloride currents., Fulmer SB., Proc Natl Acad Sci U S A. July 18, 1995; 92 (15): 6832-6.


Coupled secretion of chloride and mucus in skin of Xenopus laevis: possible role for CFTR., Engelhardt JF., Am J Physiol. August 1, 1994; 267 (2 Pt 1): C491-500.

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