Publications by authors named "Deanna M Green"

14Publications

The microbiome in pediatric cystic fibrosis patients: the role of shared environment suggests a window of intervention.

Microbiome 2014 28;2:14. Epub 2014 Apr 28.

Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, 202 Remsen Building, N. College St., Hanover, NH 03755, USA.

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July 2014

Cat and dog exposure and respiratory morbidities in cystic fibrosis.

J Pediatr 2014 Oct 12;165(4):830-5.e2. Epub 2014 Jul 12.

Eudowood Division of Pediatric Respiratory Sciences, Baltimore, MD. Electronic address:

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October 2014

Cystic fibrosis: a model for personalized genetic medicine.

Authors:
Deanna M Green

N C Med J 2013 Nov-Dec;74(6):486-7

Division of Pediatric Pulmonary and Sleep Medicine, Duke University Medical Systems, Box 102360, 350 Hanes House, 315 Trent Dr., Durham, NC 27710, USA.

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January 2014

Environmental allergies and respiratory morbidities in cystic fibrosis.

Pediatr Pulmonol 2013 Sep 9;48(9):857-64. Epub 2012 Nov 9.

Eudowood Division of Pediatric Respiratory Sciences, Johns Hopkins University, Baltimore, Maryland 21287, USA.

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September 2013

Heritability of respiratory infection with Pseudomonas aeruginosa in cystic fibrosis.

J Pediatr 2012 Aug 23;161(2):290-5.e1. Epub 2012 Feb 23.

Division of Pediatric Pulmonary and Sleep Medicine, Duke University Medical Center, Durham, NC, USA.

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August 2012

Effect of temperature on cystic fibrosis lung disease and infections: a replicated cohort study.

PLoS One 2011 18;6(11):e27784. Epub 2011 Nov 18.

Eudowood Division of Pediatric Respiratory Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.

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April 2012

Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patients.

Respir Res 2010 Oct 8;11:140. Epub 2010 Oct 8.

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

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October 2010

Location and duration of treatment of cystic fibrosis respiratory exacerbations do not affect outcomes.

Am J Respir Crit Care Med 2010 Nov 25;182(9):1137-43. Epub 2010 Jun 25.

Eudowood Division of Pediatric Respiratory Sciences, Johns Hopkins University, 200 N. Wolfe Street, David M. Rubenstein Building, 3rd Floor, Baltimore, MD 21287, USA.

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November 2010

Transient effectiveness of vitamin D2 therapy in pediatric cystic fibrosis patients.

J Cyst Fibros 2010 Mar 8;9(2):143-9. Epub 2010 Feb 8.

Eudowood Division of Pediatric Respiratory Sciences, The Johns Hopkins Medical Institutions, Baltimore, MD 21287, USA.

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March 2010

The C-terminal domain of myosin-like protein 1 (Mlp1p) is a docking site for heterogeneous nuclear ribonucleoproteins that are required for mRNA export.

Proc Natl Acad Sci U S A 2003 Feb 16;100(3):1010-5. Epub 2003 Jan 16.

Department of Biochemistry, Emory University School of Medicine, Atlanta, GA 30322, USA.

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February 2003

Domain analysis of the Saccharomyces cerevisiae heterogeneous nuclear ribonucleoprotein, Nab2p. Dissecting the requirements for Nab2p-facilitated poly(A) RNA export.

J Biol Chem 2003 Feb 19;278(9):6731-40. Epub 2002 Dec 19.

Department of Biochemistry, Graduate Program in Genetics and Molecular Biology, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

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February 2003

Nab2p is required for poly(A) RNA export in Saccharomyces cerevisiae and is regulated by arginine methylation via Hmt1p.

J Biol Chem 2002 Mar 4;277(10):7752-60. Epub 2002 Jan 4.

Department of Biochemistry, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

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March 2002