Detalhe da pesquisa
1.
Rare variants in IFFO1, DTNB, NLRC3 and SLC22A10 associate with Alzheimer's disease CSF profile of neuronal injury and inflammation.
Mol Psychiatry
; 27(4): 1990-1999, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35173266
2.
Whole-exome rare-variant analysis of Alzheimer's disease and related biomarker traits.
Alzheimers Dement
; 19(6): 2317-2331, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36464806
3.
Cellular ageing, increased mortality and FTLD-TDP-associated neuropathology in progranulin knockout mice.
J Pathol
; 228(1): 67-76, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22733568
4.
TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration.
Proc Natl Acad Sci U S A
; 107(8): 3858-63, 2010 Feb 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-20133711
5.
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort.
Brain
; 134(Pt 3): 808-15, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21354975
6.
Increased caspase activation and decreased TDP-43 solubility in progranulin knockout cortical cultures.
J Neurochem
; 115(3): 735-47, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20731760
7.
Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models.
J Pathol
; 219(2): 173-81, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19557827
8.
Reduced brain volumes in mice expressing APP-Austrian mutation but not in mice expressing APP-Swedish-Austrian mutations.
Neurosci Lett
; 447(2-3): 143-7, 2008 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-18840503
9.
Overexpression of ALS-associated p.M337V human TDP-43 in mice worsens disease features compared to wild-type human TDP-43 mice.
Mol Neurobiol
; 48(1): 22-35, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23475610
10.
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study.
Lancet Neurol
; 11(1): 54-65, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22154785
11.
Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Arch Neurol
; 67(5): 606-16, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20457961