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.
Tigecycline Opposes Bortezomib Effect on Myeloma Cells Decreasing Mitochondrial Reactive Oxygen Species Production.
Int J Mol Sci
; 25(9)2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38732105
3.
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
4.
Unraveling the Influence of HHEX Risk Polymorphism rs7923837 on Multiple Sclerosis Pathogenesis.
Int J Mol Sci
; 23(14)2022 Jul 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35887298
5.
Impact of Multiple Sclerosis Risk Polymorphism rs7665090 on MANBA Activity, Lysosomal Endocytosis, and Lymphocyte Activation.
Int J Mol Sci
; 23(15)2022 Jul 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-35897697
6.
NLRP3 inflammasome as prognostic factor and therapeutic target in primary progressive multiple sclerosis patients.
Brain
; 143(5): 1414-1430, 2020 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32282893
7.
Expression patterns common and unique to ulcerative colitis and celiac disease.
Ann Hum Genet
; 83(2): 86-94, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30402962
8.
Influence of HLA on clinical and analytical features of pediatric celiac disease.
BMC Gastroenterol
; 19(1): 91, 2019 Jun 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-31196071
9.
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
10.
HLA-DQ distribution and risk assessment of celiac disease in a Spanish center.
Rev Esp Enferm Dig
; 110(7): 421-426, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29699404
11.
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
12.
NLRP3 inflammasome is associated with the response to IFN-ß in patients with multiple sclerosis.
Brain
; 138(Pt 3): 644-52, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25586466
13.
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
14.
HLA alleles as biomarkers of high-titre neutralising antibodies to interferon-ß therapy in multiple sclerosis.
J Med Genet
; 51(6): 395-400, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24748646
15.
Response to Infliximab in Crohn's Disease: Genetic Analysis Supporting Expression Profile.
Mediators Inflamm
; 2015: 318207, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26339133
16.
High-density SNP mapping of the HLA region identifies multiple independent susceptibility loci associated with selective IgA deficiency.
PLoS Genet
; 8(1): e1002476, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22291608
17.
Genetic variation in the lymphotoxin-α (LTA)/tumour necrosis factor-α (TNFα) locus as a risk factor for idiopathic achalasia.
Gut
; 63(9): 1401-9, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24259423
18.
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
19.
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
20.
Alternative splicing and proteolytic rupture contribute to the generation of soluble IL-6 receptors (sIL-6R) in rheumatoid arthritis.
Cytokine
; 61(3): 720-3, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23375120