Detalhe da pesquisa
1.
Functional consequences of postnatal interventions in a mouse model of Fragile X syndrome.
Neurobiol Dis
; 162: 105577, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34871737
2.
Astrocytic Ephrin-B1 Controls Excitatory-Inhibitory Balance in Developing Hippocampus.
J Neurosci
; 40(36): 6854-6871, 2020 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32801156
3.
Urokinase plasminogen activator mediates changes in human astrocytes modeling fragile X syndrome.
Glia
; 69(12): 2947-2962, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34427356
4.
Deletion of Fmr1 from Forebrain Excitatory Neurons Triggers Abnormal Cellular, EEG, and Behavioral Phenotypes in the Auditory Cortex of a Mouse Model of Fragile X Syndrome.
Cereb Cortex
; 30(3): 969-988, 2020 03 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-31364704
5.
Abnormal development of auditory responses in the inferior colliculus of a mouse model of Fragile X Syndrome.
J Neurophysiol
; 123(6): 2101-2121, 2020 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32319849
6.
Acute pharmacological inhibition of matrix metalloproteinase-9 activity during development restores perineuronal net formation and normalizes auditory processing in Fmr1 KO mice.
J Neurochem
; 155(5): 538-558, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32374912
7.
Multielectrode array analysis of EEG biomarkers in a mouse model of Fragile X Syndrome.
Neurobiol Dis
; 138: 104794, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32036032
8.
Beneficial effects of sound exposure on auditory cortex development in a mouse model of Fragile X Syndrome.
Neurobiol Dis
; 134: 104622, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31698054
9.
Functional Consequences of Synapse Remodeling Following Astrocyte-Specific Regulation of Ephrin-B1 in the Adult Hippocampus.
J Neurosci
; 38(25): 5710-5726, 2018 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-29793972
10.
Reduced perineuronal net expression in Fmr1 KO mice auditory cortex and amygdala is linked to impaired fear-associated memory.
Neurobiol Learn Mem
; 164: 107042, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31326533
11.
Genetic Reduction of Matrix Metalloproteinase-9 Promotes Formation of Perineuronal Nets Around Parvalbumin-Expressing Interneurons and Normalizes Auditory Cortex Responses in Developing Fmr1 Knock-Out Mice.
Cereb Cortex
; 28(11): 3951-3964, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29040407
12.
Translation-relevant EEG phenotypes in a mouse model of Fragile X Syndrome.
Neurobiol Dis
; 115: 39-48, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29605426
13.
GLT-1-Dependent Disruption of CNS Glutamate Homeostasis and Neuronal Function by the Protozoan Parasite Toxoplasma gondii.
PLoS Pathog
; 12(6): e1005643, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27281462
14.
Matrix metalloproteinase-9 deletion rescues auditory evoked potential habituation deficit in a mouse model of Fragile X Syndrome.
Neurobiol Dis
; 89: 126-35, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26850918
15.
Genetic removal of matrix metalloproteinase 9 rescues the symptoms of fragile X syndrome in a mouse model.
J Neurosci
; 34(30): 9867-79, 2014 Jul 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-25057190
16.
Cofilin under control of ß-arrestin-2 in NMDA-dependent dendritic spine plasticity, long-term depression (LTD), and learning.
Proc Natl Acad Sci U S A
; 109(7): E442-51, 2012 Feb 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-22308427
17.
Looking forward to EphB signaling in synapses.
Semin Cell Dev Biol
; 23(1): 75-82, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22040917
18.
Altered GnRH neuron and ovarian innervation characterize reproductive dysfunction linked to the Fragile X messenger ribonucleoprotein (Fmr1) gene mutation.
Front Endocrinol (Lausanne)
; 14: 1129534, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36909303
19.
An iPSC-derived astrocyte model of fragile X syndrome exhibits dysregulated cholesterol homeostasis.
Commun Biol
; 6(1): 789, 2023 07 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37516746
20.
EphA4 targeting agents protect motor neurons from cell death induced by amyotrophic lateral sclerosis -astrocytes.
iScience
; 25(9): 104877, 2022 Sep 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36034213