Professional Memberships
National Societies:
American Association for the Advancement of Science
American Thoracic Society (Associate) Chair, Pediatric Assembly (5/2007-5/2009)
American College of Chest Physicians (Fellow)
American Physiological Society
Local Societies:
Maryland Lung Association
National Scientific Committees:
Question Writing Committee, General Pediatrics, American Board of Pediatrics (2013-present)
Member, Lung Cellular and Molecular Immunology study section (2008-2012)
Gilead Sciences Research Scholars Program review committee (2011)
Member, CRRC, NCRR, GCRC study section (2003-2007)
Chair-Elect, Subboard of Pediatric Pulmonology, American Board of Pediatrics
Chair, Pediatric Program Subcommittee of the American Thoracic Society
Subboard of Pediatric Pulmonology, American Board of Pediatrics (1999 - 2005)
National Institutes of Health Medical Biochemistry Study Section (1996- 2000)
National Institutes of Health, Special Emphasis Panels, Program Project Reviews (1994-96)
International Scientific Committees:
American Thoracic Society Pediatric Planning Committee (2010-present)
American Thoracic Society Pediatric Program Committee Chair Elect (2007)
American Thoracic Society Program Review Committee (2004-05)
Canadian Cystic Fibrosis Foundation Scientific Review Committee (2000-2003)
American Thoracic Society Program Planning Committee (2002)
Local Scientific Committees:
Maryland Lung Association, Executive Committee (1998-2000)
Maryland Lung Association, awards and grant committee (1991-95)
Publications
Henry KR, Lee S, Walker D, Zeitlin PL. Direct interactions between ENaC gamma subunit and ClCN2 in cystic fibrosis epithelial cells. Physiol Rep. 2015 Jan 27;3(1). pii: e12264. doi: 10.14814/phy2.12264. Print 2015 Jan 1.
Mayer-Hamblett N, Rosenfeld M, Treggiari MM, Konstan MW, Retsch-Bogart G, Morgan W, Wagener J, Gibson RL, Khan U, Emerson J, Thompson V, Elkin EP, Ramsey BW; EPIC; ESCF Investigators (Zeitlin PL). Standard care versus protocol based therapy for new onset Pseudomonas aeruginosa in cystic fibrosis. Pediatr Pulmonol. 2013 Oct;48(10):943-53.
Kerem E, Konstan MW, De Boeck K, Accurso FJ, Sermet-Gaudelus I, Wilschanski M, Elborn JS, Melotti P, Bronsveld I, Fajac I, Malfroot A, Rosenbluth DB, Walker PA, McColley SA, Knoop C, Quattrucci S, Rietschel E, Zeitlin PL, Barth J, Elfring GL, Welch EM, Branstrom A, Spiegel RJ, Peltz SW, Ajayi T, Rowe SM; for the Cystic Fibrosis Ataluren Study Group. Ataluren for the treatment of nonsense-mutation cystic fibrosis: a randomised, double-blind, placebo-controlled phase 3 trial. Lancet Respir Med. 2014 May 15. pii: S2213-2600(14)70100-6. In press.
Lee S, Henderson MJ, Schiffhauer E, Despanie J, Henry K, Kang PW, Walker D, McClure ML, Wilson L, Sorscher EJ, Zeitlin PL. Interference with ubiquitination in CFTR modifies stability of core glycosylated and cell surface pools. Mol Cell Biol. 2014 Apr 28. [Epub ahead of print] PMCID: PMC4097669.
Schiffhauer, E, Vij N, Kovbasnjuk, O, Kang PW, Walker D, Lee S, Zeitlin, PL. Dual activation of CFTR and CLCN2 by lubiprostone in murine nasal epithelial. Am J Physiol Lung Cell Mol Physiol 2013 Mar 1;304(5):L324-31.