Detalhe da pesquisa
1.
Proximal and Distal Bronchioles Contribute to the Pathogenesis of Non-Cystic Fibrosis Bronchiectasis.
Am J Respir Crit Care Med;
209(4): 374-389, 2024 Feb 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38016030
2.
Revisiting Host-Pathogen Interactions in Cystic Fibrosis Lungs in the Era of CFTR Modulators.
Int J Mol Sci;
24(5)2023 Mar 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36902441
3.
Chronic E-Cigarette Exposure Alters Human Alveolar Macrophage Morphology and Gene Expression.
Nicotine Tob Res;
24(3): 395-399, 2022 02 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34519792
4.
IRE1α Is a Therapeutic Target for Cystic Fibrosis Airway Inflammation.
Int J Mol Sci;
22(6)2021 Mar 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33802742
5.
XBP1S Regulates MUC5B in a Promoter Variant-Dependent Pathway in Idiopathic Pulmonary Fibrosis Airway Epithelia.
Am J Respir Crit Care Med;
200(2): 220-234, 2019 07 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30973754
6.
Mucin Production and Hydration Responses to Mucopurulent Materials in Normal versus Cystic Fibrosis Airway Epithelia.
Am J Respir Crit Care Med;
197(4): 481-491, 2018 02 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29099608
7.
PLCB3 Loss of Function Reduces Pseudomonas aeruginosa-Dependent IL-8 Release in Cystic Fibrosis.
Am J Respir Cell Mol Biol;
59(4): 428-436, 2018 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29668297
8.
SPLUNC1 degradation by the cystic fibrosis mucosal environment drives airway surface liquid dehydration.
Eur Respir J;
52(4)2018 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30190268
9.
Defining Tobacco Regulatory Science Competencies.
Nicotine Tob Res;
19(2): 222-230, 2017 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27613917
10.
Role of IRE1α/XBP-1 in Cystic Fibrosis Airway Inflammation.
Int J Mol Sci;
18(1)2017 Jan 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28075361
11.
X-Box-Binding Protein 1 and Innate Immune Responses of Human Cystic Fibrosis Alveolar Macrophages.
Am J Respir Crit Care Med;
192(12): 1449-61, 2015 Dec 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26331676
12.
"Shocking" the System to Achieve Efficient Gene Targeting in Primary Human Airway Epithelia.
Am J Respir Cell Mol Biol;
62(3): 279-280, 2020 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31633992
13.
Getting neural about airway gland secretion.
Eur Respir J;
55(4)2020 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32300022
14.
Cystic Fibrosis Inflammation: Hyperinflammatory, Hypoinflammatory, or Both?
Am J Respir Cell Mol Biol;
61(3): 273-274, 2019 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30951377
15.
Cystic fibrosis airway inflammation enables elexacaftor/tezacaftor/ivacaftor-mediated rescue of N1303K CFTR mutation.
ERJ Open Res;
10(1)2024 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38226069
16.
Inflammation promotes airway epithelial ATP release via calcium-dependent vesicular pathways.
Am J Respir Cell Mol Biol;
49(5): 814-20, 2013 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23763446
17.
The cystic fibrosis airway milieu enhances rescue of F508del in a pre-clinical model.
Eur Respir J;
52(6)2018 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30287473
18.
AAV exploits subcellular stress associated with inflammation, endoplasmic reticulum expansion, and misfolded proteins in models of cystic fibrosis.
PLoS Pathog;
7(5): e1002053, 2011 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21625534
19.
A Novel Co-Culture Model Reveals Enhanced CFTR Rescue in Primary Cystic Fibrosis Airway Epithelial Cultures with Persistent Pseudomonas aeruginosa Infection.
Cells;
12(22)2023 11 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37998353
20.
Mucus-targeting therapies of defective mucus clearance for cystic fibrosis: A short review.
Curr Opin Pharmacol;
65: 102248, 2022 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35689870