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The molecular basis of cognitive deficits in pervasive developmental disorders
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title
The molecular basis of cognitive deficits in pervasive developmental disorders
(English)
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PubMed
author name string
A. Bhattacharya
series ordinal
1
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E. Klann
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2
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language of work or name
English
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publication date
16 August 2012
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published in
Learning and Memory
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volume
19
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issue
9
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PubMed
page(s)
434-43
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PubMed
cites work
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28 September 2017
Experimental models of Rett syndrome based on Mecp2 dysfunction.
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28 September 2017
Normal social seeking behavior, hypoactivity and reduced exploratory range in a mouse model of Angelman syndrome
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28 September 2017
Deconstruction for reconstruction: the role of proteolysis in neural plasticity and disease
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28 September 2017
Empathizing, systemizing, and the extreme male brain theory of autism
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28 September 2017
Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult mice
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28 September 2017
Activation of multiple signaling pathways causes developmental defects in mice with a Noonan syndrome–associated Sos1 mutation
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28 September 2017
Reduced dysbindin expression mediates N-methyl-D-aspartate receptor hypofunction and impaired working memory performance
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28 September 2017
SHANK2 redemption: another synaptic protein for mental retardation and autism
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28 September 2017
Genetics of Early Onset Cognitive Impairment
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28 September 2017
Annual Research Review: Development of the cerebral cortex: implications for neurodevelopmental disorders
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28 September 2017
Altered mRNA transport, docking, and protein translation in neurons lacking fragile X mental retardation protein
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28 September 2017
Reactive oxygen species in the regulation of synaptic plasticity and memory
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28 September 2017
Neurofibromin regulates corticostriatal inhibitory networks during working memory performance
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28 September 2017
The role of G-quadruplex in RNA metabolism: involvement of FMRP and FMR2P.
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28 September 2017
Altered ultrasonic vocalizations in a tuberous sclerosis mouse model of autism
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28 September 2017
Evidence of mitochondrial dysfunction in fragile X-associated tremor/ataxia syndrome
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28 September 2017
Mice with altered serotonin 2C receptor RNA editing display characteristics of Prader-Willi syndrome
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28 September 2017
GSK3 influences social preference and anxiety-related behaviors during social interaction in a mouse model of fragile X syndrome and autism.
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28 September 2017
Serotonergic hyperinnervation and effective serotonin blockade in an FGF receptor developmental model of psychosis
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28 September 2017
Deregulation of EIF4E: a novel mechanism for autism.
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28 September 2017
Tuberous sclerosis complex activity is required to control neuronal stress responses in an mTOR-dependent manner
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28 September 2017
Hypoxanthine-guanine phosphoribosyl transferase regulates early developmental programming of dopamine neurons: implications for Lesch-Nyhan disease pathogenesis
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28 September 2017
MeCP2-mediated transcription repression in the basolateral amygdala may underlie heightened anxiety in a mouse model of Rett syndrome
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28 September 2017
Neurobehavioral abnormalities in the dysbindin-1 mutant, sandy, on a C57BL/6J genetic background
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28 September 2017
Pharmacological inhibition of mTORC1 suppresses anatomical, cellular, and behavioral abnormalities in neural-specific Pten knock-out mice
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28 September 2017
Reduced expression of the NMDA receptor-interacting protein SynGAP causes behavioral abnormalities that model symptoms of Schizophrenia
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28 September 2017
Ubiquitin, the proteasome and protein degradation in neuronal function and dysfunction
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28 September 2017
Behavior and neuropsychiatric manifestations in Angelman syndrome.
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28 September 2017
Misleading behavioural phenotype with adenylosuccinate lyase deficiency
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28 September 2017
Increased dosage of Dyrk1A alters alternative splicing factor (ASF)-regulated alternative splicing of tau in Down syndrome
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28 September 2017
Synaptic protein degradation underlies destabilization of retrieved fear memory
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28 September 2017
Cardio-facio-cutaneous and Noonan syndromes due to mutations in the RAS/MAPK signalling pathway: genotype-phenotype relationships and overlap with Costello syndrome.
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28 September 2017
Molecular epigenetics of Angelman syndrome
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28 September 2017
Transgenic mice expressing a truncated form of CREB-binding protein (CBP) exhibit deficits in hippocampal synaptic plasticity and memory storage.
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28 September 2017
What's right with my mouse model? New insights into the molecular and cellular basis of cognition from mouse models of Rubinstein-Taybi Syndrome
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28 September 2017
Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation.
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28 September 2017
Chromatin acetylation, memory, and LTP are impaired in CBP+/- mice: a model for the cognitive deficit in Rubinstein-Taybi syndrome and its amelioration.
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28 September 2017
Neurofibromin modulates adult hippocampal neurogenesis and behavioral effects of antidepressants
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31 May 2018
Restoration of normal L-type Ca2+ channel function during Timothy syndrome by ablation of an anchoring protein
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31 May 2018
CBP histone acetyltransferase activity regulates embryonic neural differentiation in the normal and Rubinstein-Taybi syndrome brain
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31 May 2018
Gene expression and mRNA editing of serotonin receptor 2C in brains of HPRT gene knock-out mice, an animal model of Lesch-Nyhan disease.
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31 May 2018
Relationship between abnormal cholesterol synthesis and retarded learning in rats
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31 May 2018
Special educational treatment of autistic children: a comparative study. II. Follow-up findings and implications for services
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31 May 2018
Minocycline treatment reverses ultrasonic vocalization production deficit in a mouse model of Fragile X Syndrome
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28 November 2018
Dysregulation of Rho GTPases in the αPix/Arhgef6 mouse model of X-linked intellectual disability is paralleled by impaired structural and synaptic plasticity and cognitive deficits
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28 November 2018
Mitochondrial dysfunction: a crucial event in okadaic acid (ICV) induced memory impairment and apoptotic cell death in rat brain
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28 November 2018
Oxidative stress in Rett syndrome: natural history, genotype, and variants.
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28 November 2018
Familial intellectual disability and autistic behavior caused by a small FMR2 gene deletion.
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28 November 2018
Brain Region-Specific Changes in Oxidative Stress and Neurotrophin Levels in Autism Spectrum Disorders (ASD)
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28 November 2018
Effects of FGF receptor peptide agonists on animal behavior under normal and pathological conditions
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28 November 2018
Disruption of hippocampus-regulated behavioural and cognitive processes by heterozygous constitutive deletion of SynGAP.
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28 November 2018
Altered neuroligin expression is involved in social deficits in a mouse model of the fragile X syndrome
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28 November 2018
A direct relationship between aggressive behavior in the resident/intruder test and cell oxidative status in adult male mice
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28 November 2018
Appetitively motivated instrumental learning in SynGAP heterozygous knockout mice
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28 November 2018
Overexpression of the cell adhesion protein neuroligin-1 induces learning deficits and impairs synaptic plasticity by altering the ratio of excitation to inhibition in the hippocampus
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28 November 2018
Neuroligin-3-deficient mice: model of a monogenic heritable form of autism with an olfactory deficit.
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28 November 2018
Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418762
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28 November 2018
Angelman syndrome due to a novel splicing mutation of the UBE3A gene.
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28 November 2018
Impaired spatial memory and altered dendritic spine morphology in angiotensin II type 2 receptor-deficient mice.
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28 November 2018
Beckwith Weidemann syndrome: a behavioral phenotype-genotype study
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28 November 2018
Reduction in memory in passive avoidance learning, exploratory behaviour and synaptic plasticity in mice with a spontaneous deletion in the ubiquitin C-terminal hydrolase L1 gene
1 reference
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28 November 2018
Loss of X-linked mental retardation gene oligophrenin1 in mice impairs spatial memory and leads to ventricular enlargement and dendritic spine immaturity
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PubMed Central
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28 November 2018
Rescue of neurological deficits in a mouse model for Angelman syndrome by reduction of alphaCaMKII inhibitory phosphorylation.
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28 November 2018
Fibroblast growth factor receptor-1 is required for long-term potentiation, memory consolidation, and neurogenesis
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PubMed Central
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28 November 2018
The near universal presence of autism spectrum disorders in children with Smith-Lemli-Opitz syndrome.
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28 November 2018
Ubiquitin C-terminal hydrolase L3 (Uchl3) is involved in working memory
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28 November 2018
Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.
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28 November 2018
Impaired long-term spatial and recognition memory and enhanced CA1 hippocampal LTP in the dystrophin-deficient Dmd(mdx) mouse.
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28 November 2018
The cognitive neuroscience of autism
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28 November 2018
Mitochondrial DNA modifies cognition in interaction with the nuclear genome and age in mice
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28 November 2018
Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice
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28 November 2018
The ubiquitin-proteasome cascade is required for mammalian long-term memory formation.
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28 November 2018
Developmental sensitivity of associative learning to cholesterol synthesis inhibitors.
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28 November 2018
Behavioral characterization of mdx3cv mice deficient in C-terminal dystrophins
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28 November 2018
Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.
1 reference
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PubMed Central
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28 November 2018
Autistic children: infancy to adulthood
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28 November 2018
Identifiers
DOI
10.1101/LM.025007.111
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PMC publication ID
3418762
1 reference
stated in
PubMed
PubMed publication ID
22904374
1 reference
stated in
PubMed
ResearchGate publication ID
230699232
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