Her primary areas of investigation include Cystic fibrosis transmembrane conductance regulator, Cell biology, Chloride channel, Cystic fibrosis and Biochemistry. Her Cystic fibrosis transmembrane conductance regulator study combines topics from a wide range of disciplines, such as Secretion, Mutant protein and Molecular biology. Her biological study spans a wide range of topics, including Biophysics, Endoplasmic reticulum and Chinese hamster ovary cell.
Her work deals with themes such as Cell culture, Gene expression, Induced pluripotent stem cell, Directed differentiation and Flux, which intersect with Cell biology. Her Chloride channel research incorporates themes from Congenic, Disease, Ion channel, Endomembrane system and Endosome. Her Cystic fibrosis research is multidisciplinary, relying on both Mutation, Transfection, Function and Phosphorylation.
Her primary scientific interests are in Cystic fibrosis transmembrane conductance regulator, Cell biology, Cystic fibrosis, Biochemistry and Chloride channel. Christine E. Bear does research in Cystic fibrosis transmembrane conductance regulator, focusing on Chloride channel activity specifically. Her Cell biology course of study focuses on Transporter and Function.
Her studies in Cystic fibrosis integrate themes in fields like Mutation and Immunology, Potentiator. As part of the same scientific family, Christine E. Bear usually focuses on Biochemistry, concentrating on Biophysics and intersecting with Intracellular, Membrane, Lipid bilayer and Adenine nucleotide. Her work investigates the relationship between Chloride channel and topics such as Molecular biology that intersect with problems in Transmembrane protein.
The scientist’s investigation covers issues in Cystic fibrosis, Cystic fibrosis transmembrane conductance regulator, Cell biology, Mutant and Mutation. The study incorporates disciplines such as Cancer research, CRISPR, Bioinformatics, Induced pluripotent stem cell and Drug in addition to Cystic fibrosis. Her Cystic fibrosis transmembrane conductance regulator study incorporates themes from HEK 293 cells, Chloride channel, Molecular biology and Phosphorylation.
Her Cell biology study combines topics in areas such as Cell, Cell type, Cell culture, Mutant protein and Anion channel activity. Her Mutant research includes elements of Nonsense mutation, Potentiator and Transmembrane protein. Her Mutation research includes themes of In silico, Transfection, Small molecule and Drug discovery.
Her main research concerns Cystic fibrosis, Cystic fibrosis transmembrane conductance regulator, Cell biology, Mutant and Mutation. Her Cystic fibrosis research is multidisciplinary, incorporating elements of Cancer research, Lung and Microbiology. Her biological study spans a wide range of topics, including HEK 293 cells and Mutant protein.
Her study in the field of Progenitor cell is also linked to topics like Population. Her work deals with themes such as Protein kinase A, Phosphorylation, Calcium signaling, Chloride channel and Calmodulin, which intersect with Mutant. Her Mutation research is multidisciplinary, relying on both In silico, Small molecule and Bioinformatics.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)
Christine E. Bear;Canhui Li;Norbert Kartner;Robert J. Bridges.
Cell (1992)
Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance
Norbert Kartner;John W. Hanrahan;Tim J. Jensen;A. Leonard Naismith.
Cell (1991)
Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor
Richard Rozmahel;Michael Wilschanski;Angabin Matin;Suzanne Plyte.
Nature Genetics (1996)
Directed differentiation of human pluripotent stem cells into mature airway epithelia expressing functional CFTR protein.
Amy P Wong;Christine E Bear;Stephanie Chin;Peter Pasceri.
Nature Biotechnology (2012)
ATPase Activity of the Cystic Fibrosis Transmembrane Conductance Regulator
Canhui Li;Mohabir Ramjeesingh;Wei Wang;Elizabeth Garami.
Journal of Biological Chemistry (1996)
The delta F508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane. Determination of functional half-lives on transfected cells.
Gergely L. Lukacs;Xiu Bao Chang;Christine Bear;Norbert Kartner.
Journal of Biological Chemistry (1993)
Cystic fibrosis transmembrane conductance regulator (CFTR) potentiator VX-770 (ivacaftor) opens the defective channel gate of mutant CFTR in a phosphorylation-dependent but ATP-independent manner.
Paul D.W. Eckford;Canhui Li;Mohabir Ramjeesingh;Christine E. Bear.
Journal of Biological Chemistry (2012)
Cl- channel activity in Xenopus oocytes expressing the cystic fibrosis gene.
C E Bear;F Duguay;A L Naismith;N Kartner.
Journal of Biological Chemistry (1991)
The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR.
Canhui Li;Mohabir Ramjeesingh;Evangelica Reyes;Tim Jensen.
Nature Genetics (1993)
Directed differentiation of cholangiocytes from human pluripotent stem cells
Mina Ogawa;Shinichiro Ogawa;Christine E Bear;Saumel Ahmadi.
Nature Biotechnology (2015)
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