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.
Boosting Cholesterol Efflux from Foam Cells by Sequential Administration of rHDL to Deliver MicroRNA and to Remove Cholesterol in a Triple-Cell 2D Atherosclerosis Model.
Small
; 18(13): e2105915, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35156292
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.
Pathophysiology of Atherosclerosis.
Int J Mol Sci
; 23(6)2022 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35328769
5.
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
6.
Novel Transcript Discovery Expands the Repertoire of Pathologically-Associated, Long Non-Coding RNAs in Vascular Smooth Muscle Cells.
Int J Mol Sci
; 22(3)2021 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33540814
7.
BIRC6 Is Associated with Vulnerability of Carotid Atherosclerotic Plaque.
Int J Mol Sci
; 21(24)2020 Dec 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33317170
8.
Pharmacological Targeting of the ER-Resident Chaperones GRP94 or Cyclophilin B Induces Secretion of IL-22 Binding Protein Isoform-1 (IL-22BPi1).
Int J Mol Sci
; 20(10)2019 May 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31108847
9.
Novel Insights into the Multiple Sclerosis Risk Gene ANKRD55.
J Immunol
; 196(11): 4553-65, 2016 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27183579
10.
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
11.
Cell-specific effects in different immune subsets associated with SOCS1 genotypes in multiple sclerosis.
Mult Scler
; 21(12): 1498-512, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25623250
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.
The era of GWAS is over - Yes.
Mult Scler
; 24(3): 256-257, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29251250
15.
Correction: Novel Insights into the Multiple Sclerosis Risk Gene ANKRD55.
J Immunol
; 197(10): 4177, 2016 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27815448
16.
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
17.
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
18.
Inhibition of secretion of interleukin (IL)-12/IL-23 family cytokines by 4-trifluoromethyl-celecoxib is coupled to degradation via the endoplasmic reticulum stress protein HERP.
J Biol Chem
; 285(10): 6960-9, 2010 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-20054003
19.
Pharmacogenomics and multiple sclerosis: moving toward individualized medicine.
Curr Neurol Neurosci Rep
; 11(5): 484-91, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21701907
20.
Genomic Multiple Sclerosis Risk Variants Modulate the Expression of the ANKRD55-IL6ST Gene Region in Immature Dendritic Cells.
Front Immunol
; 12: 816930, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35111166