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.
 
 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 
 
 

 
 

Garry Richard Cutting, M.D.

Garry Home|Publications|Book Chapters | Lab Members

 

 

Garry Richard Cutting, M.D.
Professor of Pediatric and Medicine
Aetna/U.S. Healthcare Professor of Medical Genetics
Director, Residency and Postdoctoral Training Program in Medical Genetics
Director, DNA Diagnostic Laboratory
The Johns Hopkins University School of Medicine
Baltimore, MD 21205
Email: gcutting@jhmi.edu
 

Garry Cutting
 

        
  Publications
 

Chu CS, Trapnell BC, Curristin S, Cutting GR, Crystal RG. Genetic basis for variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA. Nature Genetics (1993), 3:151-156.
 
Dietz HC, Francomano CA, Kendzior RJ Jr, Pyeritz, RE, Valle DV, Cutting GR.   The skipping of constitutive exons in vivo induced by nonsense mutations. (1993) Science 259:680-683.
 

Kiesewetter S, Macek M Jr., Davis C, Curristin SM, Chu C-S, Graham C, Shrimpton AE, Cashman SM, Tsui L-C, Mickle J, Amos J, Highsmith WE, Shuber A, Witt DR, Crystal RG and Cutting GR. A mutation in the cystic fibrosis transmembrane conductance regulator gene produces different phenotypes depending on chromosomal background.  Nature Genetics (1993), 5:274-278.

 

Kusama T, Wang T-L, Guggino WB, Cutting GR and Uhl GR.  GABA ρ2 receptor pharmacological profile: GABA recognition site similarities to ρ1 . Europ J Pharm-Mol Pharm (1993), 245:83-84.
 
O'Hara BR, Smith SS, Cutting GR, Uhl GR.  Population differences in dopamine D2 receptor alleles suggest caution for associational studies. Hum Hered (1993), 43:209-218.
 

Genotype-Phenotype consortium (Hamosh A, Rosenstein BJ, Nash E, Curristin SM and Cutting GR).  Correlation between genotype and phenotype in cystic fibrosis: Analysis of seven common mutations.  New Eng J Med (1993), 329: 1308-1313.
 

Carroll TP, McIntosh I, Zeitlin PL, Cutting GR, Guggino WB. Transmembrane and nucleotide-binding fold mutations alter the channels characteristics of the cystic fibrosis transmembrane conductance regulator expressed in Xenopus oocytes. Cell Physiol Biochem (1994), 4:10-18.
 
Ramsey BW, Boat TF, Accurso F, Bennett W, Boucher R, Brody A, Crystal R, Cutting GR, Davis P, Dorkin H, Fleming T, Kaplan RM, Knowles M, Konstan MW, Laube B, McElvaney G, Morgan W, Moss R, Orenstein D, Pencharz P, Rosenstein B, Schidlow D, Smith A, Spino M, Stallings V, Stecenko A, Terrin M, Weatherly M, Wilmott R, Wilson C, and Wood R.  Outcome Measures for Clinical Trials in Cystic Fibrosis. J Ped (1994), 124:177-192.
 
Wang T-L, Guggino WB, Cutting GR A novel ³ -aminobutyric acid receptor subunit (rho2) cloned from human retina forms bicuculline-insensitive homooligomeric receptors in Xenopus oocytes. J Neurosci (1994), 14:6524-6531.
 
Schwiebert EM, Flotte T, Cutting GR, Guggino WB.  CFTR and outwardly rectifying chloride channels contribute to whole cell chloride currents in normal airway epithelial cells and are defectively regulated in cystic fibrosis.  Am J Physiol (Cell) (1994), 266: 1464-1477. 
 
Smit LS, Strong TV, Wilkinson DJ, Macek Jr M, Mansoura MK, Wood DL, Cole JL, Cutting GR, Cohn JA, Dawson DC, Collins FS.  Missense mutation (G480C) in the CFTR gene associated with protein mislocalization but normal chloride channel activity.  Hum Molec Genet (1995), 4(2): 269-273.
 

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