Detalhe da pesquisa
1.
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum.
Physiol Rev
; 103(1): 433-513, 2023 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35951482
2.
Early endocannabinoid-mediated depolarization-induced suppression of excitation delays the appearance of the epileptic phenotype in synapsin II knockout mice.
Cell Mol Life Sci
; 81(1): 37, 2024 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38214769
3.
The intramembrane COOH-terminal domain of PRRT2 regulates voltage-dependent Na+ channels.
J Biol Chem
; 299(5): 104632, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36958475
4.
Biomolecular Corona of Gold Nanoparticles: The Urgent Need for Strong Roots to Grow Strong Branches.
Small
; 20(15): e2306474, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38085683
5.
Low glycemic index diet restrains epileptogenesis in a gender-specific fashion.
Cell Mol Life Sci
; 80(12): 356, 2023 Nov 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37947886
6.
Catalytic Bioswitch of Platinum Nanozymes: Mechanistic Insights of Reactive Oxygen Species Scavenging in the Neurovascular Unit.
Nano Lett
; 23(10): 4660-4668, 2023 05 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37155280
7.
Interactions of Graphene Oxide and Few-Layer Graphene with the Blood-Brain Barrier.
Nano Lett
; 23(7): 2981-2990, 2023 04 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36917703
8.
Alterations in KIDINS220/ARMS Expression Impact Sensory Processing and Social Behavior in Adult Mice.
Int J Mol Sci
; 25(4)2024 Feb 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38397009
9.
Neuron-restrictive silencer factor/repressor element 1-silencing transcription factor (NRSF/REST) controls spatial K+ buffering in primary cortical astrocytes.
J Neurochem
; 165(5): 701-721, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36636908
10.
Missense mutations in the membrane domain of PRRT2 affect its interaction with Nav1.2 voltage-gated sodium channels.
Neurobiol Dis
; 183: 106177, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37271286
11.
A developmental stage- and Kidins220-dependent switch in astrocyte responsiveness to brain-derived neurotrophic factor.
J Cell Sci
; 134(16)2021 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34279618
12.
Dual Thermal- and Oxidation-Responsive Polymers Synthesized by a Sequential ROP-to-RAFT Procedure Inherently Temper Neuroinflammation.
Biomacromolecules
; 24(10): 4478-4493, 2023 10 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36757736
13.
Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis.
Brain
; 145(8): 2687-2703, 2022 08 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35675510
14.
The light-dependent pseudo-capacitive charging of conjugated polymer nanoparticles coupled with the depolarization of the neuronal membrane.
Phys Chem Chem Phys
; 26(1): 47-56, 2023 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38054374
15.
Ca2+ binding to synapsin I regulates resting Ca2+ and recovery from synaptic depression in nerve terminals.
Cell Mol Life Sci
; 79(12): 600, 2022 Nov 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36409372
16.
Synaptic genes and neurodevelopmental disorders: From molecular mechanisms to developmental strategies of behavioral testing.
Neurobiol Dis
; 173: 105856, 2022 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36070836
17.
Presynaptic L-Type Ca2+ Channels Increase Glutamate Release Probability and Excitatory Strength in the Hippocampus during Chronic Neuroinflammation.
J Neurosci
; 40(36): 6825-6841, 2020 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32747440
18.
Increased responsiveness at the cerebellar input stage in the PRRT2 knockout model of paroxysmal kinesigenic dyskinesia.
Neurobiol Dis
; 152: 105275, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33515674
19.
The epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neurons.
Hum Mol Genet
; 28(4): 584-597, 2019 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30335140
20.
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations.
J Clin Immunol
; 41(4): 756-768, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33464451