Detalhe da pesquisa
1.
Distinct roles for SOX2 and SOX21 in differentiation, distribution and maturation of pulmonary neuroendocrine cells.
Cell Mol Life Sci
; 80(3): 79, 2023 Mar 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36867267
2.
Point mutation I634A in the glucocorticoid receptor causes embryonic lethality by reduced ligand binding.
J Biol Chem
; 298(2): 101574, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35007536
3.
Disease modeling following organoid-based expansion of airway epithelial cells.
Am J Physiol Lung Cell Mol Physiol
; 321(4): L775-L786, 2021 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34378410
4.
Real-Life Safety and Effectiveness of Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis.
Am J Respir Crit Care Med
; 201(2): 188-197, 2020 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31601120
5.
Tezacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del.
N Engl J Med
; 377(21): 2013-2023, 2017 11 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-29099344
6.
Inhibition of retinoic acid signaling induces aberrant pericyte coverage and differentiation resulting in vascular defects in congenital diaphragmatic hernia.
Am J Physiol Lung Cell Mol Physiol
; 317(3): L317-L331, 2019 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31268349
7.
Treatment of rat congenital diaphragmatic hernia with sildenafil and NS-304, selexipag's active compound, at the pseudoglandular stage improves lung vasculature.
Am J Physiol Lung Cell Mol Physiol
; 315(2): L276-L285, 2018 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29745254
8.
Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR.
N Engl J Med
; 373(3): 220-31, 2015 07 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-25981758
9.
Generation of a biotinylatable Sox2 mouse model to identify Sox2 complexes in vivo.
Transgenic Res
; 27(1): 75-85, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29383478
10.
Nutritional Status in the First 2 Years of Life in Cystic Fibrosis Diagnosed by Newborn Screening.
J Pediatr Gastroenterol Nutr
; 67(1): 123-130, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29543697
11.
Reclassifying inconclusive diagnosis for cystic fibrosis with new generation sweat test.
Eur Respir J
; 60(2)2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35777769
12.
Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome and Cystic Fibrosis Screen Positive, Inconclusive Diagnosis.
J Pediatr
; 181S: S45-S51.e1, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28129812
13.
Diagnosis of Cystic Fibrosis in Screened Populations.
J Pediatr
; 181S: S33-S44.e2, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28129810
14.
Nutritional Status Improved in Cystic Fibrosis Patients with the G551D Mutation After Treatment with Ivacaftor.
Dig Dis Sci
; 61(1): 198-207, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26250833
15.
Unique Tracheal Fluid MicroRNA Signature Predicts Response to FETO in Patients With Congenital Diaphragmatic Hernia.
Ann Surg
; 262(6): 1130-40, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25563880
16.
Comprehensive CFTR gene analysis of the French cystic fibrosis screened newborn cohort: implications for diagnosis, genetic counseling, and mutation-specific therapy.
Genet Med
; 17(2): 108-16, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25122143
17.
Sox2 regulates the emergence of lung basal cells by directly activating the transcription of Trp63.
Am J Respir Cell Mol Biol
; 51(2): 311-22, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24669837
18.
CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders.
J Med Genet
; 50(4): 220-7, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23378603
19.
Efficacy and safety of ivacaftor in patients aged 6 to 11 years with cystic fibrosis with a G551D mutation.
Am J Respir Crit Care Med
; 187(11): 1219-25, 2013 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23590265
20.
ESPEN-ESPGHAN-ECFS guideline on nutrition care for cystic fibrosis.
Clin Nutr
; 43(2): 413-445, 2024 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38169175