Christine Bear

Affiliations: 
Biochemistry University of Toronto, Toronto, ON, Canada 
Area:
Cell Biology, Physiology Biology, Pharmacology, Biochemistry
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"Christine Bear"
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Publications

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Birimberg-Schwartz L, Ip W, Bartlett C, et al. (2023) Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis. Life Science Alliance. 6
Xia S, Di Paola M, Jones NL, et al. (2022) A Fluorescence-based Assay of Membrane Potential for High-throughput Functional Study of Two Endogenous Ion Channels in Two Epithelial Cell Lines. Journal of Visualized Experiments : Jove
Lim SH, Snider J, Birimberg-Schwartz L, et al. (2022) CFTR interactome mapping using the mammalian membrane two-hybrid high-throughput screening system. Molecular Systems Biology. 18: e10629
Xia S, Bozóky Z, Di Paola M, et al. (2021) High-Throughput Functional Analysis of CFTR and Other Apically Localized Proteins in iPSC-Derived Human Intestinal Organoids. Cells. 10
Derichs N, Taylor-Cousar JL, Davies JC, et al. (2021) Riociguat for the treatment of Phe508del homozygous adults with cystic fibrosis. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
Laselva O, Qureshi Z, Zeng ZW, et al. (2021) Identification of binding sites for ivacaftor on the cystic fibrosis transmembrane conductance regulator. Iscience. 24: 102542
Laselva O, Ardelean MC, Bear CE. (2021) Phenotyping Rare CFTR Mutations Reveal Functional Expression Defects Restored by TRIKAFTA. Journal of Personalized Medicine. 11
Laselva O, McCormack J, Bartlett C, et al. (2020) Preclinical Studies of a Rare CF-Causing Mutation in the Second Nucleotide Binding Domain (c.3700A>G) Show Robust Functional Rescue in Primary Nasal Cultures by Novel CFTR Modulators. Journal of Personalized Medicine. 10
Laselva O, Bartlett C, Popa A, et al. (2020) Emerging preclinical modulators developed for F508del-CFTR have the potential to be effective for ORKAMBI resistant processing mutants. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
Erwood S, Laselva O, Bily TMI, et al. (2020) Allele-Specific Prevention of Nonsense-Mediated Decay in Cystic Fibrosis Using Homology-Independent Genome Editing. Molecular Therapy. Methods & Clinical Development. 17: 1118-1128
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