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Items: 25


Implementation of cystic fibrosis clinical pathways improved physician adherence to care guidelines.

Singh SB, Shelton AU, Greenberg B, Starner TD.

Pediatr Pulmonol. 2017 Feb;52(2):175-181. doi: 10.1002/ppul.23635. Epub 2016 Oct 31.


Development of an in vitro colonization model to investigate Staphylococcus aureus interactions with airway epithelia.

Kiedrowski MR, Paharik AE, Ackermann LW, Shelton AU, Singh SB, Starner TD, Horswill AR.

Cell Microbiol. 2016 May;18(5):720-32. doi: 10.1111/cmi.12543. Epub 2016 Jan 12.


Highly differentiated human airway epithelial cells: a model to study host cell-parasite interactions in pertussis.

Guevara C, Zhang C, Gaddy JA, Iqbal J, Guerra J, Greenberg DP, Decker MD, Carbonetti N, Starner TD, McCray PB Jr, Mooi FR, Gómez-Duarte OG.

Infect Dis (Lond). 2016;48(3):177-88. doi: 10.3109/23744235.2015.1100323. Epub 2015 Oct 22.


Multiple-Breath Washout as a Lung Function Test in Cystic Fibrosis. A Cystic Fibrosis Foundation Workshop Report.

Subbarao P, Milla C, Aurora P, Davies JC, Davis SD, Hall GL, Heltshe S, Latzin P, Lindblad A, Pittman JE, Robinson PD, Rosenfeld M, Singer F, Starner TD, Ratjen F, Morgan W.

Ann Am Thorac Soc. 2015 Jun;12(6):932-9. doi: 10.1513/AnnalsATS.201501-021FR.


Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D-CFTR mutation and preserved spirometry: a randomised controlled trial.

Davies J, Sheridan H, Bell N, Cunningham S, Davis SD, Elborn JS, Milla CE, Starner TD, Weiner DJ, Lee PS, Ratjen F.

Lancet Respir Med. 2013 Oct;1(8):630-638. doi: 10.1016/S2213-2600(13)70182-6. Epub 2013 Sep 10.


Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.

Abou Alaiwa MH, Beer AM, Pezzulo AA, Launspach JL, Horan RA, Stoltz DA, Starner TD, Welsh MJ, Zabner J.

J Cyst Fibros. 2014 Jul;13(4):373-7. doi: 10.1016/j.jcf.2013.12.006. Epub 2014 Jan 11.


Growth of preschool age children receiving daily inhaled corticosteroids.

Singh SB, Weinberger MM, Zimmerman MB, Starner TD.

Allergy Asthma Proc. 2013 Nov-Dec;34(6):511-8. doi: 10.2500/aap.2013.34.3700.


Tracheomalacia is associated with lower FEV1 and Pseudomonas acquisition in children with CF.

Fischer AJ, Singh SB, Adam RJ, Stoltz DA, Baranano CF, Kao S, Weinberger MM, McCray PB Jr, Starner TD.

Pediatr Pulmonol. 2014 Oct;49(10):960-70. doi: 10.1002/ppul.22922. Epub 2013 Oct 25.


Multicenter intestinal current measurements in rectal biopsies from CF and non-CF subjects to monitor CFTR function.

Clancy JP, Szczesniak RD, Ashlock MA, Ernst SE, Fan L, Hornick DB, Karp PH, Khan U, Lymp J, Ostmann AJ, Rezayat A, Starner TD, Sugandha SP, Sun H, Quinney N, Donaldson SH, Rowe SM, Gabriel SE.

PLoS One. 2013 Sep 10;8(9):e73905. doi: 10.1371/journal.pone.0073905. eCollection 2013.


The air-liquid interface and use of primary cell cultures are important to recapitulate the transcriptional profile of in vivo airway epithelia.

Pezzulo AA, Starner TD, Scheetz TE, Traver GL, Tilley AE, Harvey BG, Crystal RG, McCray PB Jr, Zabner J.

Am J Physiol Lung Cell Mol Physiol. 2011 Jan;300(1):L25-31. doi: 10.1152/ajplung.00256.2010. Epub 2010 Oct 22.


Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth.

Stoltz DA, Meyerholz DK, Pezzulo AA, Ramachandran S, Rogan MP, Davis GJ, Hanfland RA, Wohlford-Lenane C, Dohrn CL, Bartlett JA, Nelson GA 4th, Chang EH, Taft PJ, Ludwig PS, Estin M, Hornick EE, Launspach JL, Samuel M, Rokhlina T, Karp PH, Ostedgaard LS, Uc A, Starner TD, Horswill AR, Brogden KA, Prather RS, Richter SS, Shilyansky J, McCray PB Jr, Zabner J, Welsh MJ.

Sci Transl Med. 2010 Apr 28;2(29):29ra31. doi: 10.1126/scitranslmed.3000928.


Pseudomonas aeruginosa rugose small-colony variants have adaptations that likely promote persistence in the cystic fibrosis lung.

Starkey M, Hickman JH, Ma L, Zhang N, De Long S, Hinz A, Palacios S, Manoil C, Kirisits MJ, Starner TD, Wozniak DJ, Harwood CS, Parsek MR.

J Bacteriol. 2009 Jun;191(11):3492-503. doi: 10.1128/JB.00119-09. Epub 2009 Mar 27.


Disruption of the CFTR gene produces a model of cystic fibrosis in newborn pigs.

Rogers CS, Stoltz DA, Meyerholz DK, Ostedgaard LS, Rokhlina T, Taft PJ, Rogan MP, Pezzulo AA, Karp PH, Itani OA, Kabel AC, Wohlford-Lenane CL, Davis GJ, Hanfland RA, Smith TL, Samuel M, Wax D, Murphy CN, Rieke A, Whitworth K, Uc A, Starner TD, Brogden KA, Shilyansky J, McCray PB Jr, Zabner J, Prather RS, Welsh MJ.

Science. 2008 Sep 26;321(5897):1837-41. doi: 10.1126/science.1163600.


Subinhibitory concentrations of azithromycin decrease nontypeable Haemophilus influenzae biofilm formation and Diminish established biofilms.

Starner TD, Shrout JD, Parsek MR, Appelbaum PC, Kim G.

Antimicrob Agents Chemother. 2008 Jan;52(1):137-45. Epub 2007 Oct 22.


Modulation of airway inflammation by Haemophilus influenzae isolates associated with chronic obstructive pulmonary disease exacerbation.

Look DC, Chin CL, Manzel LJ, Lehman EE, Humlicek AL, Shi L, Starner TD, Denning GM, Murphy TF, Sethi S.

Proc Am Thorac Soc. 2006 Aug;3(6):482-3. No abstract available.


Haemophilus influenzae forms biofilms on airway epithelia: implications in cystic fibrosis.

Starner TD, Zhang N, Kim G, Apicella MA, McCray PB Jr.

Am J Respir Crit Care Med. 2006 Jul 15;174(2):213-20. Epub 2006 May 4.


Pathogenesis of early lung disease in cystic fibrosis: a window of opportunity to eradicate bacteria.

Starner TD, McCray PB Jr; American College of Physicians; American Physiological Society.

Ann Intern Med. 2005 Dec 6;143(11):816-22. Review. No abstract available.


TGF-alpha regulates TLR expression and function on epidermal keratinocytes.

Miller LS, Sørensen OE, Liu PT, Jalian HR, Eshtiaghpour D, Behmanesh BE, Chung W, Starner TD, Kim J, Sieling PA, Ganz T, Modlin RL.

J Immunol. 2005 May 15;174(10):6137-43.


Haemophilus influenzae from patients with chronic obstructive pulmonary disease exacerbation induce more inflammation than colonizers.

Chin CL, Manzel LJ, Lehman EE, Humlicek AL, Shi L, Starner TD, Denning GM, Murphy TF, Sethi S, Look DC.

Am J Respir Crit Care Med. 2005 Jul 1;172(1):85-91. Epub 2005 Apr 1.


Lysozyme secretion by submucosal glands protects the airway from bacterial infection.

Dajani R, Zhang Y, Taft PJ, Travis SM, Starner TD, Olsen A, Zabner J, Welsh MJ, Engelhardt JF.

Am J Respir Cell Mol Biol. 2005 Jun;32(6):548-52. Epub 2005 Mar 3.


Expression and activity of beta-defensins and LL-37 in the developing human lung.

Starner TD, Agerberth B, Gudmundsson GH, McCray PB Jr.

J Immunol. 2005 Feb 1;174(3):1608-15.


CCL20 is an inducible product of human airway epithelia with innate immune properties.

Starner TD, Barker CK, Jia HP, Kang Y, McCray PB Jr.

Am J Respir Cell Mol Biol. 2003 Nov;29(5):627-33. Epub 2003 May 14.


The solution structures of the human beta-defensins lead to a better understanding of the potent bactericidal activity of HBD3 against Staphylococcus aureus.

Schibli DJ, Hunter HN, Aseyev V, Starner TD, Wiencek JM, McCray PB Jr, Tack BF, Vogel HJ.

J Biol Chem. 2002 Mar 8;277(10):8279-89. Epub 2001 Dec 11.


Cathelicidin peptides inhibit multiply antibiotic-resistant pathogens from patients with cystic fibrosis.

Saiman L, Tabibi S, Starner TD, San Gabriel P, Winokur PL, Jia HP, McCray PB Jr, Tack BF.

Antimicrob Agents Chemother. 2001 Oct;45(10):2838-44.

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