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
Inglês
| MEDLINE | ID: mdl-35088080
2.
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
Inglês
| MEDLINE | ID: mdl-30102396
3.
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
Inglês
| MEDLINE | ID: mdl-26152201
4.
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
Inglês
| MEDLINE | ID: mdl-26466946
5.
Genome-wide significant association with seven novel multiple sclerosis risk loci.
J Med Genet
; 52(12): 848-55, 2015 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-26475045
6.
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
Inglês
| MEDLINE | ID: mdl-25392328
7.
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
Inglês
| MEDLINE | ID: mdl-24405691
8.
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
Inglês
| MEDLINE | ID: mdl-23160276
9.
Systemic cellular migration: The forces driving the directed locomotion movement of cells.
PNAS Nexus
; 3(5): pgae171, 2024 May.
Artigo
Inglês
| MEDLINE | ID: mdl-38706727
10.
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
Inglês
| MEDLINE | ID: mdl-22194214
11.
Polymorphisms in ARNTL/BMAL1 and CLOCK Are Not Associated with Multiple Sclerosis in Spanish Population.
Biology (Basel)
; 11(10)2022 Sep 28.
Artigo
Inglês
| MEDLINE | ID: mdl-36290322
12.
Self-Organization and Information Processing: From Basic Enzymatic Activities to Complex Adaptive Cellular Behavior.
Front Genet
; 12: 644615, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-34093645
13.
Associative Conditioning Is a Robust Systemic Behavior in Unicellular Organisms: An Interspecies Comparison.
Front Microbiol
; 12: 707086, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-34349748
14.
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
Inglês
| MEDLINE | ID: mdl-32110891
15.
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
Inglês
| MEDLINE | ID: mdl-31053784
16.
The nucleus does not significantly affect the migratory trajectories of amoeba in two-dimensional environments.
Sci Rep
; 9(1): 16369, 2019 11 08.
Artigo
Inglês
| MEDLINE | ID: mdl-31704992
17.
Evidence of conditioned behavior in amoebae.
Nat Commun
; 10(1): 3690, 2019 08 15.
Artigo
Inglês
| MEDLINE | ID: mdl-31417086
18.
The high producer variant of the Fc-receptor like-3 (FCRL3) gene is involved in protection against multiple sclerosis.
J Neuroimmunol
; 195(1-2): 146-50, 2008 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-18313765
19.
Dynamic properties of calcium-activated chloride currents in Xenopus laevis oocytes.
Sci Rep
; 7: 41791, 2017 02 13.
Artigo
Inglês
| MEDLINE | ID: mdl-28198817
20.
A splice variant in the ACSL5 gene relates migraine with fatty acid activation in mitochondria.
Eur J Hum Genet
; 24(11): 1572-1577, 2016 11.
Artigo
Inglês
| MEDLINE | ID: mdl-27189022