Detalhe da pesquisa
1.
NLRP3 is activated in Alzheimer's disease and contributes to pathology in APP/PS1 mice.
Nature
; 493(7434): 674-8, 2013 Jan 31.
Artigo
Inglês
| MEDLINE | ID: mdl-23254930
2.
Four hypotrichosis families with mutations in the gene LSS presenting with and without neurodevelopmental phenotypes.
Am J Med Genet A
; 185(12): 3900-3904, 2021 12.
Artigo
Inglês
| MEDLINE | ID: mdl-34318586
3.
PPARγ/RXRα-induced and CD36-mediated microglial amyloid-ß phagocytosis results in cognitive improvement in amyloid precursor protein/presenilin 1 mice.
J Neurosci
; 32(48): 17321-31, 2012 Nov 28.
Artigo
Inglês
| MEDLINE | ID: mdl-23197723
4.
Mrp14 deficiency ameliorates amyloid ß burden by increasing microglial phagocytosis and modulation of amyloid precursor protein processing.
J Neurosci
; 32(49): 17824-9, 2012 Dec 05.
Artigo
Inglês
| MEDLINE | ID: mdl-23223301
5.
Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 Individuals.
JAMA Dermatol
; 158(11): 1245-1253, 2022 11 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36044230
6.
Pan-PPAR modulation effectively protects APP/PS1 mice from amyloid deposition and cognitive deficits.
Mol Neurobiol
; 51(2): 661-71, 2015 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-24838579
7.
Nitric oxide decreases the enzymatic activity of insulin degrading enzyme in APP/PS1 mice.
J Neuroimmune Pharmacol
; 7(1): 165-72, 2012 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-22227962