Detalhe da pesquisa
1.
Identification of the genetic mechanism that associates L3MBTL3 to multiple sclerosis.
Hum Mol Genet
; 31(13): 2155-2163, 2022 07 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35088080
2.
The CYP24A1 gene variant rs2762943 is associated with low serum 1,25-dihydroxyvitamin D levels in multiple sclerosis patients.
Eur J Neurol
; 30(8): 2401-2410, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37183562
3.
Targeted resequencing reveals rare variants enrichment in multiple sclerosis susceptibility genes.
Hum Mutat
; 41(7): 1308-1320, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32196808
4.
Exome sequencing study in patients with multiple sclerosis reveals variants associated with disease course.
J Neuroinflammation
; 15(1): 265, 2018 Sep 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30217166
5.
A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells.
J Clin Med
; 9(3)2020 Feb 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-32110891