Launspach JL - Search Results

1

Absence of amiloride-sensitive sodium absorption in the airway of an infant with pseudohypoaldosteronism.

Prince LS, Launspach JL, Geller DS, Lifton RP, Pratt JH, Zabner J, Welsh MJ. Prince LS, et al. Among authors: launspach jl. J Pediatr. 1999 Dec;135(6):786-9. doi: 10.1016/s0022-3476(99)70105-8. J Pediatr. 1999. PMID: 10586189 Free article.

2

The osmolyte xylitol reduces the salt concentration of airway surface liquid and may enhance bacterial killing.

Zabner J, Seiler MP, Launspach JL, Karp PH, Kearney WR, Look DC, Smith JJ, Welsh MJ. Zabner J, et al. Among authors: launspach jl. Proc Natl Acad Sci U S A. 2000 Oct 10;97(21):11614-9. doi: 10.1073/pnas.97.21.11614. Proc Natl Acad Sci U S A. 2000. PMID: 11027360 Free PMC article.

3

Comparison of DNA-lipid complexes and DNA alone for gene transfer to cystic fibrosis airway epithelia in vivo.

Zabner J, Cheng SH, Meeker D, Launspach J, Balfour R, Perricone MA, Morris JE, Marshall J, Fasbender A, Smith AE, Welsh MJ. Zabner J, et al. J Clin Invest. 1997 Sep 15;100(6):1529-37. doi: 10.1172/JCI119676. J Clin Invest. 1997. PMID: 9294121 Free PMC article. Clinical Trial.

4

Increasing epithelial junction permeability enhances gene transfer to airway epithelia In vivo.

Wang G, Zabner J, Deering C, Launspach J, Shao J, Bodner M, Jolly DJ, Davidson BL, McCray PB Jr. Wang G, et al. Am J Respir Cell Mol Biol. 2000 Feb;22(2):129-38. doi: 10.1165/ajrcmb.22.2.3938. Am J Respir Cell Mol Biol. 2000. PMID: 10657931

5

Sequential magnetic resonance imaging analysis of the maxillary sinuses: implications for a model of gene therapy in cystic fibrosis.

Graham SM, Launspach JL, Welsh MJ, Zabner J. Graham SM, et al. Among authors: launspach jl. J Laryngol Otol. 1999 Apr;113(4):329-35. doi: 10.1017/s0022215100143907. J Laryngol Otol. 1999. PMID: 10474667

6

Repeat administration of an adenovirus vector encoding cystic fibrosis transmembrane conductance regulator to the nasal epithelium of patients with cystic fibrosis.

Zabner J, Ramsey BW, Meeker DP, Aitken ML, Balfour RP, Gibson RL, Launspach J, Moscicki RA, Richards SM, Standaert TA, et al. Zabner J, et al. J Clin Invest. 1996 Mar 15;97(6):1504-11. doi: 10.1172/JCI118573. J Clin Invest. 1996. PMID: 8617884 Free PMC article. Clinical Trial.

7

Ivacaftor-induced sweat chloride reductions correlate with increases in airway surface liquid pH in cystic fibrosis.

Abou Alaiwa MH, Launspach JL, Grogan B, Carter S, Zabner J, Stoltz DA, Singh PK, McKone EF, Welsh MJ. Abou Alaiwa MH, et al. Among authors: launspach jl. JCI Insight. 2018 Aug 9;3(15):e121468. doi: 10.1172/jci.insight.121468. eCollection 2018 Aug 9. JCI Insight. 2018. PMID: 30089726 Free PMC article.

8

Ivacaftor-Induced Proteomic Changes Suggest Monocyte Defects May Contribute to the Pathogenesis of Cystic Fibrosis.

Hisert KB, Schoenfelt KQ, Cooke G, Grogan B, Launspach JL, Gallagher CG, Donnelly SC, Welsh MJ, Singh PK, McKone EF, Becker L. Hisert KB, et al. Among authors: launspach jl. Am J Respir Cell Mol Biol. 2016 Apr;54(4):594-7. doi: 10.1165/rcmb.2015-0322LE. Am J Respir Cell Mol Biol. 2016. PMID: 27035067 Free PMC article. No abstract available.

9

Meal-induced secretion of gastrointestinal regulatory peptides is not affected by sleep.

Soffer EE, Adrian TE, Launspach J, Zimmerman B. Soffer EE, et al. Neurogastroenterol Motil. 1997 Mar;9(1):7-12. doi: 10.1046/j.1365-2982.1997.d01-1.x. Neurogastroenterol Motil. 1997. PMID: 9058386

10

Sonographic evidence of abnormal tracheal cartilage ring structure in cystic fibrosis.

Diwakar A, Adam RJ, Michalski AS, Tamegnon MM, Fischer AJ, Launspach JL, Horan RA, Kao SC, Chaloner K, Meyerholz DK, Stoltz DA. Diwakar A, et al. Among authors: launspach jl. Laryngoscope. 2015 Oct;125(10):2398-404. doi: 10.1002/lary.25255. Epub 2015 Mar 30. Laryngoscope. 2015. PMID: 25827636 Free PMC article.

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