Found: 11
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The ABC protein turned chloride channel whose failure causes cystic fibrosis.
- Published in:
- Nature, 2006, v. 440, n. 7083, p. 477, doi. 10.1038/nature04712
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- Article
A new target for G protein signaling.
- Published in:
- eLife, 2017, p. 1, doi. 10.7554/eLife.31106
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- Article
Asymmetry of movements in CFTR's two ATP sites during pore opening serves their distinct functions.
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- eLife, 2017, p. 1, doi. 10.7554/eLife.29013
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- Article
The proposed channel-enzyme transient receptor potential melastatin 2 does not possess ADP ribose hydrolase activity.
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- eLife, 2016, p. 1, doi. 10.7554/eLife.17600
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- Article
Obligate coupling of CFTR pore opening to tight nucleotide-binding domain dimerization.
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- eLife, 2016, p. 1, doi. 10.7554/eLife.18164
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- Article
The N-terminal transmembrane domain (TMD0) and a cytosolic linker (L0) of sulphonylurea receptor define the unique intrinsic gating of K<sub>ATP</sub> channels.
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- Journal of Physiology, 2006, v. 576, n. 2, p. 379, doi. 10.1113/jphysiol.2006.112748
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- Article
A single active catalytic site is sufficient to promote transport in P-glycoprotein.
- Published in:
- Scientific Reports, 2016, p. 24810, doi. 10.1038/srep24810
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- Article
Molecular pathology of the R117H cystic fibrosis mutation is explained by loss of a hydrogen bond.
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- eLife, 2021, p. 1, doi. 10.7554/eLife.74693
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- Article
Towards personalized medicine for cystic fibrosis patients with rare mutations.
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- Journal of Physiology, 2024, v. 602, n. 2, p. 257, doi. 10.1113/JP286135
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- Article
The twain shall meet: channels, transporters and things between. Meeting on Membrane Transport in Flux: The Ambiguous Interface Between Channels and Pumps.
- Published in:
- EMBO Reports, 2008, v. 9, n. 10, p. 960, doi. 10.1038/embor.2008.172
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- Article
Estimating the true stability of the prehydrolytic outward-facing state in an ABC protein.
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- eLife, 2023, p. 1, doi. 10.7554/eLife.90736
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- Article