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Richard Boucher

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Citations 516
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Recent Articles
11.
Blouquit S, Regnier A, Dannhoffer L, Fermanian C, Naline E, Boucher R, et al.
Am J Respir Crit Care Med . 2006 Apr; 174(3):299-305. PMID: 16645176
Rationale: Small airways constitute a major site of pathology in cystic fibrosis (CF) and provide most of the surface area of the conducting airways of the lung. Little is known,...
12.
Geary C, Akinbi H, Korfhagen T, Fabre J, Boucher R, Rice W
Am J Physiol Lung Cell Mol Physiol . 2005 Jul; 289(5):L890-5. PMID: 16024720
Purinergic receptors are expressed throughout the respiratory system in diverse cell types. The efficiency of mucus clearance in the airways, the cascade leading to tissue injury, and inflammation are modulated...
13.
Gray T, Coakley R, Hirsh A, Thornton D, Kirkham S, Koo J, et al.
Am J Physiol Lung Cell Mol Physiol . 2003 Oct; 286(2):L320-30. PMID: 14527933
Mucociliary transport in the airways significantly depends on the liquid and mucin components of the airway surface liquid (ASL). The regulation of ASL water and mucin content during pathological conditions...
14.
Collier D, Anderson L, McKnight S, Noah T, Knowles M, Boucher R, et al.
FEMS Microbiol Lett . 2002 Oct; 215(1):41-6. PMID: 12393198
Pseudomonas aeruginosa is an opportunistic pathogen that is a major cause of mortality in cystic fibrosis (CF) patients. This bacterium has numerous genes controlled by cell to cell signaling, which...
15.
Schwab U, Leigh M, Ribeiro C, Yankaskas J, Burns K, Gilligan P, et al.
Infect Immun . 2002 Jul; 70(8):4547-55. PMID: 12117967
Burkholderia cepacia has emerged as a serious respiratory pathogen in cystic fibrosis (CF) patients. The clinical course of B. cepacia infections is variable, but approximately 20% of patients eventually succumb...