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.
No evidence for association between rs10191329 severity locus and longitudinal disease severity in 1813 relapse-onset multiple sclerosis patients from the MSBase registry.
Mult Scler
; : 13524585241240406, 2024 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38511853
3.
Not all roads lead to the immune system: the genetic basis of multiple sclerosis severity.
Brain
; 146(6): 2316-2331, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36448302
4.
Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease.
PLoS Genet
; 15(6): e1008180, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31170158
5.
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
6.
SP140 regulates the expression of immune-related genes associated with multiple sclerosis and other autoimmune diseases by NF-κB inhibition.
Hum Mol Genet
; 27(23): 4012-4023, 2018 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30102396
7.
A functional variant that affects exon-skipping and protein expression of SP140 as genetic mechanism predisposing to multiple sclerosis.
Hum Mol Genet
; 24(19): 5619-27, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26152201
8.
The multiple sclerosis-associated regulatory variant rs10877013 affects expression of CYP27B1 and VDR under inflammatory or vitamin D stimuli.
Mult Scler
; 22(8): 999-1006, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26466946
9.
Genome-wide significant association with seven novel multiple sclerosis risk loci.
J Med Genet
; 52(12): 848-55, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26475045
10.
A new risk variant for multiple sclerosis at the immunoglobulin heavy chain locus associates with intrathecal IgG, IgM index and oligoclonal bands.
Mult Scler
; 21(9): 1104-11, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25392328
11.
HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRV.
Retrovirology
; 11: 2, 2014 Jan 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-24405691
12.
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis.
Brain
; 136(Pt 6): 1778-82, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23739915
13.
Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis.
J Med Genet
; 50(1): 25-33, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23160276
14.
Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects.
J Med Genet
; 49(9): 558-62, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22972946
15.
Role of the small GTPase Rab27a during herpes simplex virus infection of oligodendrocytic cells.
BMC Microbiol
; 12: 265, 2012 Nov 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-23164453
16.
Replication study of 10 genes showing evidence for association with multiple sclerosis: validation of TMEM39A, IL12B and CBLB [correction of CLBL] genes.
Mult Scler
; 18(7): 959-65, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22194214
17.
Characterization of the MAL2-positive compartment in oligodendrocytes.
Exp Cell Res
; 315(19): 3453-65, 2009 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19683524
18.
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
19.
Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk.
J Med Genet
; 50(3): 140-3, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23315543
20.
Splice-site variant in ACSL5: a marker promoting opposing effect on cell viability and protein expression.
Eur J Hum Genet
; 27(12): 1836-1844, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31053784