Detalles de la búsqueda
1.
Identification of single nucleotide variants in SLC26A9 gene in patients with cystic fibrosis (p.Phe508del homozygous) and its association to Orkambi® (Lumacaftor and Ivacaftor) response in vitro.
Gene
; 871: 147428, 2023 Jun 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-37068695
2.
Novel, rare and common pathogenic variants in the CFTR gene screened by high-throughput sequencing technology and predicted by in silico tools.
Sci Rep
; 9(1): 6234, 2019 04 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-30996306
3.
Extent of rescue of F508del-CFTR function by VX-809 and VX-770 in human nasal epithelial cells correlates with SNP rs7512462 in SLC26A9 gene in F508del/F508del Cystic Fibrosis patients.
Biochim Biophys Acta Mol Basis Dis
; 1865(6): 1323-1331, 2019 06 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30716472
4.
Association of clinical severity of cystic fibrosis with variants in the SLC gene family (SLC6A14, SLC26A9, SLC11A1 and SLC9A3).
Gene
; 629: 117-126, 2017 Sep 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-28756021
Resultados
1 -
4
de 4
1
Próxima >
>>