Audiogenic seizure susceptibility is reduced in fragile X knockout mice after introduction of FMR1 transgenes.
about
Emerging pharmacotherapies for neurodevelopmental disordersFragile X syndrome and targeted treatment trials.Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by the small-molecule PAK inhibitor FRAX486.Sensory processing in autism spectrum disorders and Fragile X syndrome-From the clinic to animal models.Matrix metalloproteinase-9 deletion rescues auditory evoked potential habituation deficit in a mouse model of Fragile X SyndromeAuditory processing in fragile x syndrome.Resilience to audiogenic seizures is associated with p-ERK1/2 dephosphorylation in the subiculum of Fmr1 knockout mice.mGlu5 positive allosteric modulation normalizes synaptic plasticity defects and motor phenotypes in a mouse model of Rett syndromeDysregulation of group-I metabotropic glutamate (mGlu) receptor mediated signalling in disorders associated with Intellectual Disability and AutismPharmacogenetic inhibition of eIF4E-dependent Mmp9 mRNA translation reverses fragile X syndrome-like phenotypes.Glutamate receptor dysfunction and drug targets across models of autism spectrum disordersPathological plasticity in fragile X syndrome.CGG-repeat length and neuropathological and molecular correlates in a mouse model for fragile X-associated tremor/ataxia syndrome.Fragile X mental retardation protein replacement restores hippocampal synaptic function in a mouse model of fragile X syndrome.Dysfunctional mTORC1 Signaling: A Convergent Mechanism between Syndromic and Nonsyndromic Forms of Autism Spectrum Disorder?The role of GABAergic system in neurodevelopmental disorders: a focus on autism and epilepsy.Genetic and Pharmacological Reversibility of Phenotypes in Mouse Models of Autism Spectrum Disorder.Human pluripotent stem cells in modeling human disorders: the case of fragile X syndrome.Establishment of Reporter Lines for Detecting Fragile X Mental Retardation (FMR1) Gene Reactivation in Human Neural Cells.Altered surface mGluR5 dynamics provoke synaptic NMDAR dysfunction and cognitive defects in Fmr1 knockout mice.Developmental Emergence of Phenotypes in the Auditory Brainstem Nuclei of Fmr1 Knockout Mice.Fragile X syndrome: From protein function to therapy.Sensory Processing Phenotypes in Fragile X Syndrome
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P2860
Audiogenic seizure susceptibility is reduced in fragile X knockout mice after introduction of FMR1 transgenes.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh-hant
name
Audiogenic seizure susceptibil ...... troduction of FMR1 transgenes.
@en
Audiogenic seizure susceptibil ...... troduction of FMR1 transgenes.
@nl
type
label
Audiogenic seizure susceptibil ...... troduction of FMR1 transgenes.
@en
Audiogenic seizure susceptibil ...... troduction of FMR1 transgenes.
@nl
prefLabel
Audiogenic seizure susceptibil ...... troduction of FMR1 transgenes.
@en
Audiogenic seizure susceptibil ...... troduction of FMR1 transgenes.
@nl
P2093
P50
P1476
Audiogenic seizure susceptibil ...... troduction of FMR1 transgenes.
@en
P2093
Ben A Oostra
Carmela M Bonaccorso
Cathy E Bakker
David L Nelson
Giuseppe Calabrese
Judith R Brouwer
Simona D'Antoni
P304
P356
10.1016/J.EXPNEUROL.2006.08.007
P407
P577
2006-09-27T00:00:00Z