Christopher R. Marino

Author

University of Tennessee Health Science Center

Also Known As

C MARINO, C Marino, C R Marino, C. Marino, C. R. Marino, C.R. Marino, Christopher Marino, Christopher R Marino, Christopher R. Marino

Publications

3.4K

Citations

H-Index

Concepts

All Affiliations

University of Tennessee Health Science Center Yale University Erasmus University Rotterdam The University of Texas Southwestern Medical Center University of Miami

About

Christopher R. Marino is an author at University of Tennessee Health Science Center specializing in medicine, cell biology, and molecular physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	17	2.4K
2	Natural Sciences	6	6	521
3	Biochemistry	4	4	303
4	Health Sciences	1	1	200
5	Biology	1	1	99

Christopher R. Marino

Publications

3.2K

Citations

H-Index

Page 1

	Year	Citations
Submucosal glands are the predominant site of CFTR expression in the human bronchus John F. Engelhardt, James R. Yankaskas, Stephen A. Ernst, Nature Genetics Predominant SitePulmonary CirculationPhysiologyPathologyPulmonary Physiology	1992	649
Dynamic Association of Proteasomal Machinery with the Centrosome W. Christian Wigley, Rosalind P. Fabunmi, Min Goo Lee, The Journal of Cell Biology	1999	513
Localization of the cystic fibrosis transmembrane conductance regulator in pancreas. Christopher R. Marino, Lisa M. Matovcik, Fred S. Gorelick, Journal of Clinical Investigation Protein SecretionImmunocytochemical TechniqueImmunologyPathologyCytoskeleton	1991	305
Expansion of Pdx1-expressing pancreatic epithelium and islet neogenesis in transgenic mice overexpressing transforming growth factor α Si Young Song, Maureen Gannon, M. Kay Washington, Gastroenterology Developmental BiologyTissue DevelopmentPancreatic CancerGrowth Factor αCell Proliferation	1999	200
Slc26a6 regulates CFTR activity in vivo to determine pancreatic duct HCO3− secretion: relevance to cystic fibrosis Youxue Wang, Abigail A. Soyombo, Nikolay Shcheynikov, The EMBO Journal Cftr ActivityFibrosisMolecular PhysiologySignal TransductionPancreatic Cancer	2006	158
Immuno and functional characterization of CFTR in submandibular and pancreatic acinar and duct cells Weizhong Zeng, Min Goo Lee, Ming Yan, American Journal of Physiology-Cell Physiology Protein SecretionCystic Fibrosis ResultsLaboratory ImmunologyImmunologyPathology	1997	157
Regulation of Cl−/ HCO3−Exchange by Cystic Fibrosis Transmembrane Conductance Regulator Expressed in NIH 3T3 and HEK 293 Cells Min Goo Lee, W. Christian Wigley, Weizhong Zeng, Journal of Biological Chemistry Protein SecretionMolecular BiologyCellular PhysiologyNih 3T3Membrane Transport	1999	146
A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo. Pim J. French, J. Hikke van Doorninck, Ronald H. Peters, Journal of Clinical Investigation Molecular BiologyTemperature-sensitive Processing DefectDelta F508 MutationCellular PhysiologyMembrane Transport	1996	139
A unique subset of rat and human intestinal villus cells express the cystic fibrosis transmembrane conductance regulator Nadia A. Ameen, Thomas Ardito, Michael Kashgarian, Gastroenterology Molecular PhysiologyPhysiologyUnique SubsetIntercellular CommunicationDigestive Tract	1995	107
The ΔF508 mutation shortens the biochemical half-life of plasma membrane CFTR in polarized epithelial cells Ghanshyam D. Heda, Mridul Tanwani, Christopher R. Marino American Journal of Physiology-Cell Physiology	2001	106

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