Detalhe da pesquisa
1.
Electrolyte transport properties in distal small airways from cystic fibrosis pigs with implications for host defense.
Am J Physiol Lung Cell Mol Physiol
; 310(7): L670-9, 2016 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26801568
2.
Glycaemic regulation and insulin secretion are abnormal in cystic fibrosis pigs despite sparing of islet cell mass.
Clin Sci (Lond)
; 128(2): 131-42, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25142104
3.
Air trapping and airflow obstruction in newborn cystic fibrosis piglets.
Am J Respir Crit Care Med
; 188(12): 1434-41, 2013 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24168209
4.
CFTR is required for maximal transepithelial liquid transport in pig alveolar epithelia.
Am J Physiol Lung Cell Mol Physiol
; 303(2): L152-60, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22637155
5.
Drosophila are protected from Pseudomonas aeruginosa lethality by transgenic expression of paraoxonase-1.
J Clin Invest
; 118(9): 3123-31, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18704198
6.
HSP90 inhibitor geldanamycin reverts IL-13- and IL-17-induced airway goblet cell metaplasia.
J Clin Invest
; 129(2): 744-758, 2019 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30640172
7.
Postnatal airway growth in cystic fibrosis piglets.
J Appl Physiol (1985)
; 123(3): 526-533, 2017 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28620056
8.
Repurposing tromethamine as inhaled therapy to treat CF airway disease.
JCI Insight
; 1(8)2016 06 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27390778
9.
Xylitol enhances bacterial killing in the rabbit maxillary sinus.
Laryngoscope
; 114(11): 2021-4, 2004 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-15510034
10.
Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs.
J Clin Invest
; 123(6): 2685-93, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23676501
11.
Expression of human paraoxonase 1 decreases superoxide levels and alters bacterial colonization in the gut of Drosophila melanogaster.
PLoS One
; 7(8): e43777, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22952763
12.
Glucose depletion in the airway surface liquid is essential for sterility of the airways.
PLoS One
; 6(1): e16166, 2011 Jan 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-21311590
13.
The ΔF508 mutation causes CFTR misprocessing and cystic fibrosis-like disease in pigs.
Sci Transl Med
; 3(74): 74ra24, 2011 Mar 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-21411740
14.
Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth.
Sci Transl Med
; 2(29): 29ra31, 2010 Apr 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-20427821
15.
Disruption of the CFTR gene produces a model of cystic fibrosis in newborn pigs.
Science
; 321(5897): 1837-41, 2008 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-18818360
16.
Lysozyme secretion by submucosal glands protects the airway from bacterial infection.
Am J Respir Cell Mol Biol
; 32(6): 548-52, 2005 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-15746432