Christine E Bear


Ontology type: schema:Person     


Person Info

NAME

Christine E

SURNAME

Bear

Publications in SciGraph latest 50 shown

  • 2018-12 Activity of a novel antimicrobial peptide against Pseudomonas aeruginosa biofilms in SCIENTIFIC REPORTS
  • 2017-12 Phenotypic profiling of CFTR modulators in patient-derived respiratory epithelia in NPJ GENOMIC MEDICINE
  • 2017-01 Current insights into the role of PKA phosphorylation in CFTR channel activity and the pharmacological rescue of cystic fibrosis disease-causing mutants in CELLULAR AND MOLECULAR LIFE SCIENCES
  • 2015-08 Directed differentiation of cholangiocytes from human pluripotent stem cells in NATURE BIOTECHNOLOGY
  • 2015-08 The cystic fibrosis transmembrane conductance regulator is an extracellular chloride sensor in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2015-03 Efficient generation of functional CFTR-expressing airway epithelial cells from human pluripotent stem cells in NATURE PROTOCOLS
  • 2014-08 Genetic, cell biological, and clinical interrogation of the CFTR mutation c.3700 A>G (p.Ile1234Val) informs strategies for future medical intervention in GENETICS IN MEDICINE
  • 2012-09 Directed differentiation of human pluripotent stem cells into mature airway epithelia expressing functional CFTR protein in NATURE BIOTECHNOLOGY
  • 2010-07 ClC transporters: discoveries and challenges in defining the mechanisms underlying function and regulation of ClC-5 in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2006-03 Role of intramolecular and intermolecular interactions in ClC channel and transporter function in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2002-11 Epithelial Cell Chloride Channel Activity Correlates with Improved Airway Function in Cystic Fibrosis Patients with the Major Mutant: Delta F508: Commentary on the article by Sermet-Gaudelus <i>et al.</i> on page 628 in PEDIATRIC RESEARCH
  • 2002-10-29 Epithelial cell chloride channel activity correlates with improved airway function in cystic fibrosis patients with the major mutant: Delta F508. in PEDIATRIC RESEARCH
  • 2002-03-04 Studies of the Molecular Basis for Cystic Fibrosis Using Purified Reconstituted CFTR Protein in CYSTIC FIBROSIS METHODS AND PROTOCOLS
  • 2001-11 Non-CFTR chloride channels likely contribute to secretion in the murine small intestine in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2000-12 Amelioration of Intestinal Disease Severity in Cystic Fibrosis Mice Is Associated with Improved Chloride Secretory Capacity in PEDIATRIC RESEARCH
  • 1999-02 ClC-2 Activation Modulates Regulatory Volume Decrease in THE JOURNAL OF MEMBRANE BIOLOGY
  • 1997-10 Coupling of ATP Hydrolysis with Channel Gating by Purified, Reconstituted CFTR in JOURNAL OF BIOENERGETICS AND BIOMEMBRANES
  • 1996-05 Erratum: Modulation of disease severity in cystic f ibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor in NATURE GENETICS
  • 1996-03 Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor in NATURE GENETICS
  • 1993-04 The cystic fibrosis mutation (ΔF508) does not influence the chloride channel activity of CFTR in NATURE GENETICS
  • 1991 Regulation of Ion Conductance in Human Skin Fibroblasts in THE IDENTIFICATION OF THE CF (CYSTIC FIBROSIS) GENE
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