Detalhe da pesquisa
1.
High Epstein-Barr virus capsid antigen IgG level associates with the carriership of CD8+ T cell somatic mutations in the STAT3 SH2 domain.
Clin Immunol
; 255: 109733, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37572949
2.
Cultured lymphocytes' mitochondrial genome integrity is not altered by cladribine.
Clin Exp Immunol
; 214(3): 304-313, 2023 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37860849
3.
Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patients.
BMC Cardiovasc Disord
; 21(1): 126, 2021 03 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33673806
4.
A novel class of somatic mutations in blood detected preferentially in CD8+ cells.
Clin Immunol
; 175: 75-81, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27932211
5.
[The pathogenesis of amyotrophic lateral sclerosis and frontal lobe dementia is unraveling: pathology of the nucleus and glutamate sensitivity]. / Amyotrofisen lateraaliskleroosin ja otsalohkodementian patogeneesi avautuu: Tumapatologia ja glutamaattiherkkyys.
Duodecim
; 132(5): 423-31, 2016.
Artigo
em Fi
| MEDLINE | ID: mdl-27089615
6.
Use of IgE and IgG4 epitope binding to predict the outcome of oral immunotherapy in cow's milk allergy.
Pediatr Allergy Immunol
; 25(3): 227-35, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24393339
7.
High prevalence of low-allele-fraction somatic mutations in STAT3 in peripheral blood CD8+ cells in multiple sclerosis patients and controls.
PLoS One
; 17(11): e0278245, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36441748
8.
CD8+ cell somatic mutations in multiple sclerosis patients and controls-Enrichment of mutations in STAT3 and other genes implicated in hematological malignancies.
PLoS One
; 16(12): e0261002, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34874980
9.
Oligogenic basis of sporadic ALS: The example of SOD1 p.Ala90Val mutation.
Neurol Genet
; 5(3): e335, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-31086828
10.
Common origin of the gelsolin gene variant in 62 Finnish AGel amyloidosis families.
Eur J Hum Genet
; 26(1): 117-123, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29167514
11.
Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+).
Neurol Genet
; 4(1): e211, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-29379882
12.
Phosphorylation of Parkin at serine 65 is essential for its activation in vivo.
Open Biol
; 8(11)2018 11 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30404819
13.
Exome and regulatory element sequencing of neuromyelitis optica patients.
J Neuroimmunol
; 289: 139-42, 2015 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26616883
14.
Genome-wide association study of neocortical Lewy-related pathology.
Ann Clin Transl Neurol
; 2(9): 920-31, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26401513
15.
Anima: modular workflow system for comprehensive image data analysis.
Front Bioeng Biotechnol
; 2: 25, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25126541
16.
C9ORF72 expansion does not affect the phenotype in Nasu-Hakola disease with the DAP12 mutation.
Neurobiol Aging
; 35(7): 1780.e13-7, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24612676