C. Marino

发表

Submucosal glands are the predominant site of CFTR expression in the human bronchus

James M. Wilson, Yiping Yang, J. Yankaskas, 1992, Nature Genetics.

Regulation of Cl−/ HCO3 −Exchange by Cystic Fibrosis Transmembrane Conductance Regulator Expressed in NIH 3T3 and HEK 293 Cells*

M. G. Lee, Min Goo Lee, S. Muallem, 1999, The Journal of Biological Chemistry.

CFTR channel insertion to the apical surface in rat duodenal villus epithelial cells is upregulated by VIP in vivo.

C. Marino, J. Isenberg, N. Ameen, 1999, Journal of cell science.

Slc26a6 regulates CFTR activity in vivo to determine pancreatic duct HCO3− secretion: relevance to cystic fibrosis

S. Muallem, P. Thomas, C. Marino, 2006, The EMBO journal.

Antibodies to an epitope on synapsin I detect a protein associated with the endocytic compartment in non-neuronal cells.

A. Czernik, C. Marino, F. Gorelick, 1994, European journal of cell biology.

Cysteine String Protein Interacts with and Modulates the Maturation of the Cystic Fibrosis Transmembrane Conductance Regulator*

Hui Zhang, R. Frizzell, C. Marino, 2002, The Journal of Biological Chemistry.

The ΔF508 mutation shortens the biochemical half-life of plasma membrane CFTR in polarized epithelial cells

G. Heda, C. Marino, M. Tanwani, 2001 .

The Delta F508 mutation shortens the biochemical half-life of plasma membrane CFTR in polarized epithelial cells.

G. Heda, C. Marino, M. Tanwani, 2001, American journal of physiology. Cell physiology.

Subcellular distribution of CFTR in rat intestine supports a physiologic role for CFTR regulation by vesicle traffic

E. V. van Donselaar, H. Geuze, P. Peters, 2000, Histochemistry and Cell Biology.

The D F508 mutation shortens the biochemical half-life of plasma membrane CFTR in polarized epithelial cells

G. Heda, C. Marino, M. Tanwani, 2000 .

Vasoactive intestinal peptide, forskolin, and genistein increase apical CFTR trafficking in the rectal gland of the spiny dogfish, Squalus acanthias. Acute regulation of CFTR trafficking in an intact epithelium.

J. Forrest, R. Lehrich, P. Webster, 1998, The Journal of clinical investigation.

Immuno and functional characterization of CFTR in submandibular and pancreatic acinar and duct cells.

M. G. Lee, S. Muallem, S. Freedman, 1997, The American journal of physiology.

Subcellular localization of CFTR to endosomes in a ductal epithelium.

A. Nairn, P. Webster, C. Marino, 1994, The American journal of physiology.

Surface expression of the cystic fibrosis transmembrane conductance regulator mutant DeltaF508 is markedly upregulated by combination treatment with sodium butyrate and low temperature.

G. Heda, C. Marino, 2000, Biochemical and biophysical research communications.

A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo.

P. French, B. Scholte, C. Marino, 1996, The Journal of clinical investigation.

Expansion of Pdx1-expressing pancreatic epithelium and islet neogenesis in transgenic mice overexpressing transforming growth factor alpha.

M. Washington, S. Leach, R. Coffey, 1999, Gastroenterology.

Scientific advances in cystic fibrosis.

C. Marino, F. Gorelick, 1992, Gastroenterology.

Localization of the cystic fibrosis transmembrane conductance regulator in pancreas.

J. Cohn, C. Marino, F. Gorelick, 1991, The Journal of clinical investigation.

Albendazole-induced pseudomembranous colitis.

F. Altice, C. Marino, V. Shah, 1996, The American journal of gastroenterology.

Characterization of cAMP‐dependent protein kinase activation by CCK in rat pancreas

S. Leach, L. Miller, C. Marino, 1993, FEBS letters.

Neurologic complications of pancreas and small bowel transplantation.

M. Jacewicz, C. Marino, 2014, Handbook of clinical neurology.

Expression and distribution of the Na+-[Formula: see text] cotransporter in human pancreas.

W. Boron, C. Marino, B. Schmitt, 1999, American journal of physiology. Gastrointestinal and liver physiology.

Expression and distribution of the Na+-[Formula: see text] cotransporter in human pancreas.

W. Boron, C. Marino, B. Schmitt, 1999, American journal of physiology. Gastrointestinal and liver physiology.

Endoscopic removal of a toothpick from the transverse colon.

C. Marino, R. Patil, K. Monkemuller, 1996, The American journal of gastroenterology.

Dynamic Association of Proteasomal Machinery with the Centrosome

Min Goo Lee, S. Muallem, P. Thomas, 1999, The Journal of cell biology.

Biochemical methods to assess CFTR expression and membrane localization.

G. Lukács, M. Amaral, C. Farinha, 2004, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Malignant ascites: new concepts in pathophysiology, diagnosis, and management.

C. Marino, N. Aslam, 2001, Archives of internal medicine.

New Concepts in Pathophysiology, Diagnosis, and Management

C. Marino, N. Aslam, 2016 .

cAMP-dependent exocytosis and vesicle traffic regulate CFTR and fluid transport in rat jejunum in vivo.

C. Marino, N. Ameen, P. Salas, 2003, American journal of physiology. Cell physiology.

PANCREATIC AND SALIVARY GLANDS

C. Marino, F. Gorelick, 2009 .

Characterization of the cystic fibrosis transmembrane conductance regulator in a colonocyte cell line.

A. Nairn, J. Cohn, C. Marino, 1992, Proceedings of the National Academy of Sciences of the United States of America.

A unique subset of rat and human intestinal villus cells express the cystic fibrosis transmembrane conductance regulator.

M. Kashgarian, C. Marino, T. Ardito, 1995, Gastroenterology.

expedited article Expression and distribution of the Na 1 -HCO 3 cotransporter in human pancreas

W. Boron, C. Marino, B. Schmitt, 1999 .

Immunolocalization of CFTR in intact tissue and cultured cells.

C. Marino, 2002, Methods in molecular medicine.