Detalhe da pesquisa
1.
Loss of anion transport without increased sodium absorption characterizes newborn porcine cystic fibrosis airway epithelia.
Cell
; 143(6): 911-23, 2010 Dec 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-21145458
2.
Cystic Fibrosis Transmembrane Conductance Regulator in Sarcoplasmic Reticulum of Airway Smooth Muscle. Implications for Airway Contractility.
Am J Respir Crit Care Med
; 193(4): 417-26, 2016 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26488271
3.
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
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.
Pulmonary neuroendocrine cells sense succinate to stimulate myoepithelial cell contraction.
Dev Cell
; 57(18): 2221-2236.e5, 2022 09 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-36108628
6.
Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children.
Am J Respir Crit Care Med
; 182(10): 1251-61, 2010 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20622026
7.
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
8.
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
9.
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