Detalhe da pesquisa
1.
A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2.
Hum Mutat
; 41(1): 169-181, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31464095
2.
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.
Brain
; 140(6): 1561-1578, 2017 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28459997
3.
SARS-CoV-2-mediated dysregulation of metabolism and autophagy uncovers host-targeting antivirals.
Nat Commun
; 12(1): 3818, 2021 06 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34155207
4.
Toll-like receptor 2 gene polymorphisms Arg677Trp and Arg753Gln in chronic obstructive pulmonary disease.
Lung
; 187(3): 173-8, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19381722
5.
MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEÉ4 Noncarriers: Results from the Dementia Genetics Spanish Consortium.
J Alzheimers Dis
; 49(2): 343-52, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26444794
6.
Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes.
Neurobiol Aging
; 35(11): 2657.e13-2657.e19, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25042114