Detalhe da pesquisa
1.
Roles for neuronal and glial autophagy in synaptic pruning during development.
Neurobiol Dis
; 122: 49-63, 2019 02.
Artigo
Inglês
| MEDLINE | ID: mdl-29709573
2.
Fragility and robustness of self-sustained oscillations in an epidemiological model on small-world networks.
Chaos
; 29(2): 023119, 2019 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-30823719
3.
Mitochondrial abnormalities in temporal lobe of autistic brain.
Neurobiol Dis
; 54: 349-61, 2013 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-23333625
4.
Lingo-1 expression is increased in essential tremor cerebellum and is present in the basket cell pinceau.
Acta Neuropathol
; 125(6): 879-89, 2013 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-23543187
5.
Synaptic hyperexcitability of cytomegalic pyramidal neurons contributes to epileptogenesis in tuberous sclerosis complex.
Cell Rep
; 40(3): 111085, 2022 07 19.
Artigo
Inglês
| MEDLINE | ID: mdl-35858542
6.
Mutant glucocerebrosidase impairs α-synuclein degradation by blockade of chaperone-mediated autophagy.
Sci Adv
; 8(6): eabm6393, 2022 02 11.
Artigo
Inglês
| MEDLINE | ID: mdl-35138901
7.
Huntington disease oligodendrocyte maturation deficits revealed by single-nucleus RNAseq are rescued by thiamine-biotin supplementation.
Nat Commun
; 13(1): 7791, 2022 12 21.
Artigo
Inglês
| MEDLINE | ID: mdl-36543778
8.
Oligomers of mutant glial fibrillary acidic protein (GFAP) Inhibit the proteasome system in alexander disease astrocytes, and the small heat shock protein alphaB-crystallin reverses the inhibition.
J Biol Chem
; 285(14): 10527-37, 2010 Apr 02.
Artigo
Inglês
| MEDLINE | ID: mdl-20110364
9.
Autophagy induced by Alexander disease-mutant GFAP accumulation is regulated by p38/MAPK and mTOR signaling pathways.
Hum Mol Genet
; 17(11): 1540-55, 2008 Jun 01.
Artigo
Inglês
| MEDLINE | ID: mdl-18276609
10.
Widespread Alterations in Translation Elongation in the Brain of Juvenile Fmr1 Knockout Mice.
Cell Rep
; 26(12): 3313-3322.e5, 2019 03 19.
Artigo
Inglês
| MEDLINE | ID: mdl-30893603
11.
Mitochondrial dysfunction and mitophagy defect triggered by heterozygous GBA mutations.
Autophagy
; 15(1): 113-130, 2019 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30160596
12.
An affinity/avidity model of peripheral T cell regulation.
J Clin Invest
; 115(2): 302-12, 2005 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-15668735
13.
Ultraflexible Transparent Film Heater Made of Ag Nanowire/PVA Composite for Rapid-Response Thermotherapy Pads.
ACS Appl Mater Interfaces
; 9(7): 6644-6651, 2017 Feb 22.
Artigo
Inglês
| MEDLINE | ID: mdl-28150931
14.
[Genome-wide search for linkage to attention deficit hyperactivity disorder (ADHD) on the X chromosome].
Yi Chuan
; 28(1): 26-30, 2006 Jan.
Artigo
Chinês
| MEDLINE | ID: mdl-16469712
15.
Ligation-free ribosome profiling of cell type-specific translation in the brain.
Genome Biol
; 17(1): 149, 2016 07 05.
Artigo
Inglês
| MEDLINE | ID: mdl-27380875
16.
Decreased Coenzyme Q10 Levels in Multiple System Atrophy Cerebellum.
J Neuropathol Exp Neurol
; 75(7): 663-72, 2016 07.
Artigo
Inglês
| MEDLINE | ID: mdl-27235405
17.
Genetic studies of A2M and BACE1 genes in Chinese Han Alzheimer's disease patients.
Neuroreport
; 16(9): 1023-6, 2005 Jun 21.
Artigo
Inglês
| MEDLINE | ID: mdl-15931081
18.
No association between attention-deficit hyperactivity disorder and catechol-O-methyltransferase gene in Chinese.
Yi Chuan Xue Bao
; 32(8): 784-8, 2005 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-16231731
19.
Genetic study of apolipoprotein E gene, alpha-1 antichymotrypsin gene in sporadic Parkinson disease.
Am J Med Genet
; 114(4): 446-9, 2002 May 08.
Artigo
Inglês
| MEDLINE | ID: mdl-11992569
20.
Alpha-2 macroglobulin I1000 V polymorphism in Chinese sporadic Alzheimer's disease and Parkinson's disease.
Neurosci Lett
; 328(2): 195-7, 2002 Aug 09.
Artigo
Inglês
| MEDLINE | ID: mdl-12133586