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Summary Anatomy Item Literature (6623) Expression Attributions Wiki
XB-ANAT-718

Papers associated with anatomical region (and cftr)

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Estimating the true stability of the prehydrolytic outward-facing state in an ABC protein., Simon MA., Elife. October 2, 2023; 12                   


A single-cell, time-resolved profiling of Xenopus mucociliary epithelium reveals nonhierarchical model of development., Lee J., Sci Adv. April 7, 2023; 9 (14): eadd5745.                                                          


UXT chaperone prevents proteotoxicity by acting as an autophagy adaptor for p62-dependent aggrephagy., Yoon MJ., Nat Commun. March 29, 2021; 12 (1): 1955.                


Structure-activity analysis of a CFTR channel potentiator: Distinct molecular parts underlie dual gating effects., Csanády L., J Gen Physiol. October 1, 2014; 144 (4): 321-36.                    


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.                                              


Conformational changes in the catalytically inactive nucleotide-binding site of CFTR., Csanády L., J Gen Physiol. July 1, 2013; 142 (1): 61-73.                  


Involvement of F1296 and N1303 of CFTR in induced-fit conformational change in response to ATP binding at NBD2., Szollosi A., J Gen Physiol. October 1, 2010; 136 (4): 407-23.                


Strict coupling between CFTR's catalytic cycle and gating of its Cl- ion pore revealed by distributions of open channel burst durations., Csanády L., Proc Natl Acad Sci U S A. January 19, 2010; 107 (3): 1241-6.


Imaging CFTR in its native environment., Schillers H., Pflugers Arch. April 1, 2008; 456 (1): 163-77.


The muscle chloride channel ClC-1 is not directly regulated by intracellular ATP., Zifarelli G., J Gen Physiol. February 1, 2008; 131 (2): 109-16.          


The role of SGK and CFTR in acute adaptation to seawater in Fundulus heteroclitus., Shaw JR., Cell Physiol Biochem. January 1, 2008; 22 (1-4): 69-78.


In vivo phosphorylation of CFTR promotes formation of a nucleotide-binding domain heterodimer., Mense M., EMBO J. October 18, 2006; 25 (20): 4728-39.


Imaging CFTR: a tail to tail dimer with a central pore., Schillers H., Cell Physiol Biochem. January 1, 2004; 14 (1-2): 1-10.


Acute regulation of the SLC26A3 congenital chloride diarrhoea anion exchanger (DRA) expressed in Xenopus oocytes., Chernova MN., J Physiol. May 15, 2003; 549 (Pt 1): 3-19.


A cluster of negative charges at the amino terminal tail of CFTR regulates ATP-dependent channel gating., Fu J., J Physiol. October 15, 2001; 536 (Pt 2): 459-70.


Cysteine substitutions reveal dual functions of the amino-terminal tail in cystic fibrosis transmembrane conductance regulator channel gating., Fu J., J Biol Chem. September 21, 2001; 276 (38): 35660-8.


Anion permeation in Ca(2+)-activated Cl(-) channels., Qu Z., J Gen Physiol. December 1, 2000; 116 (6): 825-44.                          


CFTR chloride channel regulation by an interdomain interaction., Naren AP., Science. October 15, 1999; 286 (5439): 544-8.


Syntaxin 1A inhibits CFTR chloride channels by means of domain-specific protein-protein interactions., Naren AP., Proc Natl Acad Sci U S A. September 1, 1998; 95 (18): 10972-7.


A divergent CFTR homologue: highly regulated salt transport in the euryhaline teleost F. heteroclitus., Singer TD., Am J Physiol. March 1, 1998; 274 (3): C715-23.

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