Detalhe da pesquisa
1.
Adult-born neurons maintain hippocampal cholinergic inputs and support working memory during aging.
Mol Psychiatry
; 2023 Jul 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37479778
2.
Ablation of proliferating neural stem cells during early life is sufficient to reduce adult hippocampal neurogenesis.
Hippocampus
; 28(8): 586-601, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29742815
3.
Transgenic rescue of phenotypic deficits in a mouse model of alternating hemiplegia of childhood.
Neurogenetics
; 17(1): 57-63, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26463346
4.
Deficits in social behavioral tests in a mouse model of alternating hemiplegia of childhood.
J Neurogenet
; 30(1): 42-9, 2016 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27276195
5.
Mania-like behavior induced by genetic dysfunction of the neuron-specific Na+,K+-ATPase α3 sodium pump.
Proc Natl Acad Sci U S A
; 108(44): 18144-9, 2011 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22025725
6.
Adult-born neurons maintain hippocampal cholinergic inputs and support working memory during aging.
Res Sq
; 2023 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-36778445
7.
Mutation I810N in the alpha3 isoform of Na+,K+-ATPase causes impairments in the sodium pump and hyperexcitability in the CNS.
Proc Natl Acad Sci U S A
; 106(33): 14085-90, 2009 Aug 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-19666602
8.
Circadian Disruptions in the Myshkin Mouse Model of Mania Are Independent of Deficits in Suprachiasmatic Molecular Clock Function.
Biol Psychiatry
; 84(11): 827-837, 2018 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28689605
9.
Characterization of cognitive deficits in mice with an alternating hemiplegia-linked mutation.
Behav Neurosci
; 129(6): 822-31, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26501181
10.
Adolescent but not adult-born neurons are critical for susceptibility to chronic social defeat.
Front Behav Neurosci
; 8: 289, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25221485
11.
Alternating hemiplegia of childhood-related neural and behavioural phenotypes in Na+,K+-ATPase α3 missense mutant mice.
PLoS One
; 8(3): e60141, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23527305