John E. Mickle
Johns Hopkins University(US)Johns Hopkins Medicine(US)
Publications by Year
Research Areas
Neonatal Respiratory Health Research, Cystic Fibrosis Research Advances, Tracheal and airway disorders, Neuroscience and Neuropharmacology Research, Advanced Sensor and Energy Harvesting Materials
Most-Cited Works
- → A mutation in CFTR produces different phenotypes depending on chromosomal background(1993)441 cited
- → A PDZ-interacting domain in CFTR is an apical membrane polarization signal(1999)274 cited
- → A Golgi-associated PDZ Domain Protein Modulates Cystic Fibrosis Transmembrane Regulator Plasma Membrane Expression(2002)234 cited
- → The PDZ-interacting Domain of Cystic Fibrosis Transmembrane Conductance Regulator Is Required for Functional Expression in the Apical Plasma Membrane(2000)148 cited
- → GENOTYPE-PHENOTYPE RELATIONSHIPS IN CYSTIC FIBROSIS(2000)141 cited
- → Immunology: Congenital unilateral absence of the vas deferens: a heterogeneous disorder with two distinct subpopulations based upon aetiology and mutational status of the cystic fibrosis gene(1995)131 cited
- → A mutation in the cystic fibrosis transmembrane conductance regulator gene associated with elevated sweat chloride concentrations in the absence of cystic fibrosis(1998)96 cited
- → A PDZ-binding motif is essential but not sufficient to localize the C terminus of CFTR to the apical membrane(2001)91 cited
- → CLINICAL IMPLICATIONS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR MUTATIONS(1998)73 cited
- → Pulmonary Function and Clinical Observations in Men With Congenital Bilateral Absence of the Vas Deferens(1996)52 cited