GENE THERAPY VECTOR

CLINICAL CENTER GENOTYPING CENTER
Information regarding Cystic Fibrosis, the types of research being performed to finds its cure.  Learn more about gene therapy, and treatments for Cystic Fibrosis as well as volunteering opportunities.
The Center has many research laboratories dedicated to finding a cure for Cystic Fibrosis.  Meet the different lab directors, their lab members and the laboratories particular focus.
A complete list of publications from the Centers lab directors that are related to Cystic Fibrosis.
Apply for open positions at the Cystic Fibrosis Research Development Center.
Visit other websites of organizations and associations affiliated with Cystic Fibrosis.
Letter from the Director addressing the Centers continued plan for the future.
 
 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 
 

 

 

Pamela L. Zeitlin, M.D., Ph.D.

Pam Home | Publications | Book Chapters | Lab Members

   

Pamela L. Zeitlin, M.D., Ph.D.
Professor of Pediatrics
The Johns Hopkins University School of Medicine
Baltimore, MD 21205
Email: pzeitlin@jhmi.edu

 

Pamela Zeitlin
 

       
  Publications (peer reviewed)
 

Zeitlin PL, Segovia E, McNamara J.  Critical evaluation of the hematoxylin-basic fuchsin picric acid stain as an indication of early muscle ischemia.  Hawaii Med. J. 33:65-69, 1974.

 
Hubbard AD, Wall P, Zeitlin PL, Hong S.  Studies of the galactose-specific recognition  system of mammalian liver, 39th Ann. Proc. Electron Microscopy Soc. Amer. (Bailey, G.W., ed), pp. 524-527, 1981.
 
Zeitlin PL, Hubbard A.  Cell surface distribution and intracellular fate of asialoglycoproteins: A morphological and biochemical study of isolated rat hepatocytes and monolayer cultures.  J. Cell Biol. 92:634-647, 1982. 
 

Zeitlin PL, Loughlin G, Guggino W.  Ion transport in cultured fetal and adult rabbit tracheal epithelia.  Am. J. Physiol. 254:C691-C698, 1988.

 
Zeitlin PL, Wagner M, Markakis D, Loughlin GM and Guggino WB.  Steroid hormones: Modulators of Na+ absorption and C1-secretion in cultured tracheal epithelia.  Proc. Natl. Acad. Sci, USA 86:2502-2505, 1989.Zeitlin PL, Wagner M, Markakis D, Loughlin GM and Guggino WB.  Steroid hormones: Modulators of Na+ absorption and C1-secretion in cultured tracheal epithelia.  Proc. Natl. Acad. Sci, USA 86:2502-2505, 1989.
 

Hwang T, Lu L, Zeitlin PL, Gruenert DC, Huganir R, and Guggino WB.  C1-channels in CF: Lack of activation by Protein Kinase C and cAMP-Dependent Protein Kinase.  Science 244:1351-1353, 1989.

 
Lu L, Zeitlin PL, Guggino WB and Craig R.  Gene transfer by lipofection in rabbit and human secretory epithelial cells.  Pfluegers Arch 415:198-203, 1989.
 
Zeitlin PL, Lu L, Hwang TC, Rhim J, Cutting G, Stetten G, Kieffer KA, Craig R, and Guggino WB.  A cystic fibrosis bronchial epithelial cell line:  Immortalization by adeno-12-SV40 infection.  Am. J. Resp. Cell Mol. Biol 4:313-319, 1991.
 
Trapnell BC, Zeitlin PL, Chu CS, Yoshimura K, Nakamura H, Guggino WB, Bargon J, Banks Y, Dalemans W, Pavirani A, Lecocq JP, and Crystal RG.  Down-regulation of cystic fibrosis gene mRNA transcript levels and induction of the cystic fibrosis chloride secretory phenotype in epithelial cells by phorbol ester.  J. Biol. Chem 266:10219-10323, 1991.
 
Crawford I, Maloney PC, Zeitlin PL, Guggino WB, Hyde SC, Turley H, Gatter KC, Harris A, and Higgins CF.  Immunocytochemical localization of the cystic fibrosis gene product CFTR.  Proc. Natl. Acad. Sci. USA. 88:9262-9266, 1991.
 
Hamosh A, Trapnell BC, Zeitlin PL, Rafizadeh CM, Rosenstein BJ, Crystal RG, and Cutting GR.  Severe deficiency of CFTR mRNA carrying nonsense mutations R553X and W136X in respiratory epithelial cells of patients with Cystic Fibrosis.  J. Clin. Invest. 88:1800-1885, 1991.
 

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