Advances in behavioral genetics: mouse models of autism (Q36937876)

17 August 2017

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title

Advances in behavioral genetics: mouse models of autism (English)

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17 August 2017

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Moy SS

1

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PubMed ID

17848915

17 August 2017

Nadler JJ

series ordinal

2

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PubMed ID

17848915

17 August 2017

language of work or name

English

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publication date

11 September 2007

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17 August 2017

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17 August 2017

13

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17 August 2017

4-26

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17 August 2017

1

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https://scigraph.springernature.com/pub.10.1038/sj.mp.4002082

17 August 2017

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cites work

Genetics of austim: complex aetiology for a heterogeneous disorder

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Epidemiological trends in rates of autism.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The Epidemiology of Autism Spectrum Disorders *

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Autism and environmental genomics

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Heritable and nonheritable risk factors for autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Searching for ways out of the autism maze: genetic, epigenetic and environmental clues

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

A genomic screen of autism: evidence for a multilocus etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The search for autism disease genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Animal models of restricted repetitive behavior in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

A question of balance: a proposal for new mouse models of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Linking etiologies in humans and animal models: studies of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Mouse behavioral tasks relevant to autism: phenotypes of 10 inbred strains

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Sociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behavior in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Automated apparatus for quantitation of social approach behaviors in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Social approach-avoidance behavior of inbred mouse strains towards DBA/2 mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

A mouse model system for genetic analysis of sociability: C57BL/6J versus BALB/cJ inbred mouse strains

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Assessing autism-like behavior in mice: variations in social interactions among inbred strains

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Varieties of repetitive behavior in autism: comparisons to mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Annotation: Repetitive Behaviour in Autism: A Review of Psychological Research

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Repetitive and stereotyped behaviours in pervasive developmental disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Early features of autism: Repetitive behaviours in young children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Repetitive Behavior Profiles in Asperger Syndrome and High-Functioning Autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Genetic heterogeneity between the three components of the autism spectrum: a twin study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The genetic relationship between individual differences in social and nonsocial behaviours characteristic of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Transgenic and knock-out mouse pups: the growing need for behavioral analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Animal models of mental retardation: from gene to cognitive function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Behavioral phenotyping of mouse models of neurodevelopmental disorders: relevant social behavior patterns across the life span.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

En2 knockout mice display neurobehavioral and neurochemical alterations relevant to autism spectrum disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

A new neurobehavioral model of autism in mice: pre- and postnatal exposure to sodium valproate.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

An altered neonatal behavioral phenotype in Mecp2 mutant mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Deficit in attachment behavior in mice lacking the mu-opioid receptor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Neurobehavioural disorders in the infant reeler mouse model: interaction of genetic vulnerability and consequences of maternal separation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Expanded characterization of the social interaction abnormalities in mice lacking Dvl1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Pervasive social deficits, but normal parturition, in oxytocin receptor-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Juvenile 5HT(1B) receptor knockout mice exhibit reduced pharmacological sensitivity to 5HT(1A) receptor activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Maternal effects in infant and adult phenotypes of 5HT1A and 5HT1B receptor knockout mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Anxiety, motor activation, and maternal-infant interactions in 5HT1B knockout mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Developmental abnormalities and age-related neurodegeneration in a mouse model of Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Infant vocalization, adult aggression, and fear behavior of an oxytocin null mutant mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

A review of the methods of studies on infant ultrasound production and maternal retrieval in small rodents

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

An analysis of autism in fifty males with the fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Fragile X mice develop sensory hyperreactivity to auditory stimuli

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

A phenotypic and molecular characterization of the fmr1-tm1Cgr fragile X mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Transgenic mouse model for the fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Altered anxiety-related and social behaviors in the Fmr1 knockout mouse model of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Social behavior deficits in the Fmr1 mutant mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Behavioral and neuroanatomical characterization of the Fmr1 knockout mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

(Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical features

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Enriched environment promotes behavioral and morphological recovery in a mouse model for the fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Inhibition of p21-activated kinase rescues symptoms of fragile X syndrome in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Fragile X mouse: strain effects of knockout phenotype and evidence suggesting deficient amygdala function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Spatial learning, contextual fear conditioning and conditioned emotional response in Fmr1 knockout mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Alterations in the auditory startle response in Fmr1 targeted mutant mouse models of fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Fmr1 knockout mouse has a distinctive strain-specific learning impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Sensorimotor gating abnormalities in young males with fragile X syndrome and Fmr1-knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Sensorimotor gating deficits in adults with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Brain anatomy and sensorimotor gating in Asperger's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Learning and memory in the FMR1 knockout mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Psychiatric endophenotypes and the development of valid animal models.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Rett syndrome: of girls and mice--lessons for regression in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

MeCP2 dysfunction in Rett syndrome and related disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Evidence for abnormal early development in a mouse model of Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Postnatal loss of methyl-CpG binding protein 2 in the forebrain is sufficient to mediate behavioral aspects of Rett syndrome in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Enhanced anxiety and stress-induced corticosterone release are associated with increased Crh expression in a mouse model of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Autism and 15q11-q13 disorders: behavioral, genetic, and pathophysiological issues

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Neurological aspects of the Angelman syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Rescue of neurological deficits in a mouse model for Angelman syndrome by reduction of alphaCaMKII inhibitory phosphorylation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Repetitive and ritualistic behaviour in children with Prader-Willi syndrome and children with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader-Willi syndrome mouse models

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

A mouse model for Prader-Willi syndrome imprinting-centre mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Disruption of the mouse necdin gene results in early post-natal lethality

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Differences between mentally retarded and normally intelligent autistic children

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Plasma oxytocin levels in autistic children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Superior disembedding performance of high-functioning individuals with autism spectrum disorders and their parents: the need for subtle measures

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Dendritic spine abnormalities in the occipital cortex of C57BL/6 Fmr1 knockout mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Dynamic translational and proteasomal regulation of fragile X mental retardation protein controls mGluR-dependent long-term depression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Altered synaptic plasticity in a mouse model of fragile X mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Metabotropic receptor-dependent long-term depression persists in the absence of protein synthesis in the mouse model of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Reduced cortical synaptic plasticity and GluR1 expression associated with fragile X mental retardation protein deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Absence of metabotropic glutamate receptor-mediated plasticity in the neocortex of fragile X mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

mRNPs, polysomes or granules: FMRP in neuronal protein synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Transcription, translation and fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Local protein synthesis and spine morphogenesis: Fragile X syndrome and beyond.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Therapeutic implications of the mGluR theory of fragile X mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The mGluR theory of fragile X mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Synaptogenesis: a balancing act between excitation and inhibition

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Suppressed GABAergic inhibition as a common factor in suspected etiologies of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Model of autism: increased ratio of excitation/inhibition in key neural systems

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Decreased expression of the GABAA receptor in fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Expression profiling suggests underexpression of the GABA(A) receptor subunit delta in the fragile X knockout mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Decreased GABA(A) receptor expression in the seizure-prone fragile X mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Major defects in neocortical GABAergic inhibitory circuits in mice lacking the fragile X mental retardation protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Necdin promotes GABAergic neuron differentiation in cooperation with Dlx homeodomain proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Calcium/calmodulin-dependent kinase II and long-term potentiation enhance synaptic transmission by the same mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Calcium/calmodulin-dependent protein kinase II regulates hippocampal synaptic transmission.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

An essential role for postsynaptic calmodulin and protein kinase activity in long-term potentiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Deficient hippocampal long-term potentiation in alpha-calcium-calmodulin kinase II mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

alphaCaMKII Is essential for cerebellar LTD and motor learning.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Reversal of synaptic memory by Ca2+/calmodulin-dependent protein kinase II inhibitor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Dysregulated metabotropic glutamate receptor-dependent translation of AMPA receptor and postsynaptic density-95 mRNAs at synapses in a mouse model of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Fragile X syndrome and autism at the intersection of genetic and neural networks

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The genetics of autistic disorders and its clinical relevance: a review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Toward a developmental neurobiology of autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Neuroligins and neurexins: linking cell adhesion, synapse formation and cognitive function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The neuroligin and neurexin families: from structure to function at the synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Neuroligins determine synapse maturation and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Neurexophilin 3 is highly localized in cortical and cerebellar regions and is functionally important for sensorimotor gating and motor coordination

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Association of Reelin gene polymorphisms with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Analysis of the RELN gene as a genetic risk factor for autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Reelin gene alleles and susceptibility to autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Lack of evidence for an association between WNT2 and RELN polymorphisms and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Analysis of reelin as a candidate gene for autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Reelin glycoprotein in autism and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Reelin signaling is impaired in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Reelin glycoprotein: structure, biology and roles in health and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Behavioral phenotype of the reeler mutant mouse: effects of RELN gene dosage and social isolation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Neuroanatomical phenotypes in the reeler mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Altered cortico-striatal synaptic plasticity and related behavioural impairments in reeler mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Neurobehavioral evaluation of Reln-rl-orl mutant mice and correlations with cytochrome oxidase activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Reelin signaling facilitates maturation of CA1 glutamatergic synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Functional dissection of Reelin signaling by site-directed disruption of Disabled-1 adaptor binding to apolipoprotein E receptor 2: distinct roles in development and synaptic plasticity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Reelin and ApoE receptors cooperate to enhance hippocampal synaptic plasticity and learning

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Executive functions in the heterozygous reeler mouse model of schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The phenotypic characteristics of heterozygous reeler mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Olfactory discrimination learning deficit in heterozygous reeler mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Cognitive disruption and altered hippocampus synaptic function in Reelin haploinsufficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Assessment of cognitive function in the heterozygous reeler mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The heterozygous reeler mouse: behavioural phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Down-regulation of dendritic spine and glutamic acid decarboxylase 67 expressions in the reelin haploinsufficient heterozygous reeler mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Oxytocin receptors in brain cortical regions are reduced in haploinsufficient (+/-) reeler mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Sex differences in oxytocin and vasopressin: implications for autism spectrum disorders?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Central serotonin2C receptor: from physiology to pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Neuronal 5-HT metabotropic receptors: fine-tuning of their structure, signaling, and roles in synaptic modulation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Magnetic resonance imaging and head circumference study of brain size in autism: birth through age 2 years.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Modeling early cortical serotonergic deficits in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Serotonin1A receptor acts during development to establish normal anxiety-like behaviour in the adult

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The developmental role of serotonin: news from mouse molecular genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Neuronal localization of 5-HT1A receptor mRNA and protein in rat embryonic brain stem cultures.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

5-HT1a receptors mediate the neurotrophic effect of serotonin on developing dentate granule cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Aggressive behavior and altered amounts of brain serotonin and norepinephrine in mice lacking MAOA

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Lack of barrels in the somatosensory cortex of monoamine oxidase A-deficient mice: role of a serotonin excess during the critical period.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Reduced programmed cell death in brains of serotonin transporter knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Altered neocortical cell density and layer thickness in serotonin transporter knockout mice: a quantitation study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Hypolocomotion, anxiety and serotonin syndrome-like behavior contribute to the complex phenotype of serotonin transporter knockout mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Insertion mutation at the C-terminus of the serotonin transporter disrupts brain serotonin function and emotion-related behaviors in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Abnormal anxiety-related behavior in serotonin transporter null mutant mice: the influence of genetic background

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Neurotrophin signal transduction in the nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Transient receptor potential channels as novel effectors of brain-derived neurotrophic factor signaling: potential implications for Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Serotonin transporter function, but not expression, is dependent on brain-derived neurotrophic factor (BDNF): in vivo studies in BDNF-deficient mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Examination of behavioral deficits triggered by targeting Bdnf in fetal or postnatal brains of mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Regulation of serotonin-1A receptor function in inducible brain-derived neurotrophic factor knockout mice after administration of corticosterone.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Severe deficits in 5-HT2A -mediated neurotransmission in BDNF conditional mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Brain-derived neurotrophic factor-deficient mice develop aggressiveness and hyperphagia in conjunction with brain serotonergic abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Dysregulation of brain-derived neurotrophic factor expression and neurosecretory function in Mecp2 null mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Brain-derived neurotrophic factor conditional knockouts show gender differences in depression-related behaviors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Essential role of brain-derived neurotrophic factor in adult hippocampal function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Analysis of pyramidal neuron morphology in an inducible knockout of brain-derived neurotrophic factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Relationship of brain-derived neurotrophic factor and its receptor TrkB to altered inhibitory prefrontal circuitry in schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Experimental gene interaction studies with SERT mutant mice as models for human polygenic and epistatic traits and disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Loss of brain-derived neurotrophic factor gene allele exacerbates brain monoamine deficiencies and increases stress abnormalities of serotonin transporter knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Gender-dependent modulation of brain monoamines and anxiety-like behaviors in mice with genetic serotonin transporter and BDNF deficiencies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Autism in tuberous sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Pten regulates neuronal arborization and social interaction in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Pten is essential for embryonic development and tumour suppression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Beyond PTEN mutations: the PI3K pathway as an integrator of multiple inputs during tumorigenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Role for Akt3/protein kinase Bgamma in attainment of normal brain size

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Essential role of protein kinase B gamma (PKB gamma/Akt3) in postnatal brain development but not in glucose homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Regulation of neuronal morphology and function by the tumor suppressors Tsc1 and Tsc2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Neocortical hyperexcitability in a human case of tuberous sclerosis complex and mice lacking neuronal expression of TSC1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

A mouse model of tuberous sclerosis: neuronal loss of Tsc1 causes dysplastic and ectopic neurons, reduced myelination, seizure activity, and limited survival

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Glutamatergic regulation of the p70S6 kinase in primary mouse neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Disruption of PTEN coupling with 5-HT2C receptors suppresses behavioral responses induced by drugs of abuse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

An Akt/beta-arrestin 2/PP2A signaling complex mediates dopaminergic neurotransmission and behavior

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Brain-derived neurotrophic factor induces mammalian target of rapamycin-dependent local activation of translation machinery and protein synthesis in neuronal dendrites

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Regulation of Akt and glycogen synthase kinase-3 beta phosphorylation by sodium valproate and lithium

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

A clinical study of 57 children with fetal anticonvulsant syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Characteristics of fetal anticonvulsant syndrome associated autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Fetal valproate syndrome and autism: additional evidence of an association

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Attentional skills during the first 6 months of age in autism spectrum disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Selected neurotrophins, neuropeptides, and cytokines: developmental trajectory and concentrations in neonatal blood of children with autism or Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

21 January 2018

The teratology of autism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Perinatal complications as predictors of infantile autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Timing of prenatal stressors and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Value of a clinical morphology examination in autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Autism associated with conditions characterized by developmental errors in early embryogenesis: a mini review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Subtypes of autism by cluster analysis based on structural MRI data.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Long term health and neurodevelopment in children exposed to antiepileptic drugs before birth

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Autism and Möbius sequence: an exploratory study of children in northeastern Brazil

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Autistic disorder and viral infections

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Alterations in behavior in adult offspring mice following maternal inflammation during pregnancy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Immune activation during pregnancy in mice leads to dopaminergic hyperfunction and cognitive impairment in the offspring: a neurodevelopmental animal model of schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Prenatal viral infection in mouse causes differential expression of genes in brains of mouse progeny: a potential animal model for schizophrenia and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The time of prenatal immune challenge determines the specificity of inflammation-mediated brain and behavioral pathology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Altered expression of pro-inflammatory and developmental genes in the fetal brain in a mouse model of maternal infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Prenatal exposure of rats to valproic acid reproduces the cerebellar anomalies associated with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Maternal administration of thalidomide or valproic acid causes abnormal serotonergic neurons in the offspring: implication for pathogenesis of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Behavioral alterations in rats prenatally exposed to valproic acid: animal model of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Induction of the homeotic gene Hoxa1 through valproic acid's teratogenic mechanism of action.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Developmental defects of the ear, cranial nerves and hindbrain resulting from targeted disruption of the mouse homeobox gene Hox-1.6

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Neuronal defects in the hindbrain of Hoxa1, Hoxb1 and Hoxb2 mutants reflect regulatory interactions among these Hox genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Embryological origin for autism: developmental anomalies of the cranial nerve motor nuclei

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Converging evidence for brain stem injury in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Discovery of allelic variants of HOXA1 and HOXB1: genetic susceptibility to autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

No association between allelic variants of HOXA1/HOXB1 and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Differences in gene expression between wild type and Hoxa1 knockout embryonic stem cells after retinoic acid treatment or leukemia inhibitory factor (LIF) removal

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Teratogenic effects mediated by inhibition of histone deacetylases: evidence from quantitative structure activity relationships of 20 valproic acid derivatives

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Mode of action: inhibition of histone deacetylase, altering WNT-dependent gene expression, and regulation of beta-catenin--developmental effects of valproic acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Evidence supporting WNT2 as an autism susceptibility gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Aberrant beta-catenin signaling in tuberous sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Hamartin and tuberin modulate gene transcription via beta-catenin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Wnt signaling through Dishevelled, Rac and JNK regulates dendritic development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Signaling across the synapse: a role for Wnt and Dishevelled in presynaptic assembly and neurotransmitter release

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Environmental mercury release, special education rates, and autism disorder: an ecological study of Texas

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Sonic hedgehog regulates Gli activator and repressor functions with spatial and temporal precision in the mid/hindbrain region

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The level of sonic hedgehog signaling regulates the complexity of cerebellar foliation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Negative regulation of Hedgehog signaling by the cholesterogenic enzyme 7-dehydrocholesterol reductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

A defective response to Hedgehog signaling in disorders of cholesterol biosynthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Specific congenital heart defects in RSH/Smith-Lemli-Opitz syndrome: postulated involvement of the sonic hedgehog pathway in syndromes with postaxial polydactyly or heterotaxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The near universal presence of autism spectrum disorders in children with Smith-Lemli-Opitz syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Behavior phenotype in the RSH/Smith-Lemli-Opitz syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Mutations in the Delta7-sterol reductase gene in patients with the Smith-Lemli-Opitz syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Loss of apolipoprotein E exacerbates the neonatal lethality of the Smith-Lemli-Opitz syndrome mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7-Dehydrocholesterol-dependent proteolysis of HMG-CoA reductase suppresses sterol biosynthesis in a mouse model of Smith-Lemli-Opitz/RSH syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Biochemical, phenotypic and neurophysiological characterization of a genetic mouse model of RSH/Smith--Lemli--Opitz syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Partial rescue of neonatal lethality of Dhcr7 null mice by a nestin promoter-driven DHCR7 transgene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Abnormal serotonergic development in a mouse model for the Smith-Lemli-Opitz syndrome: implications for autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Development and characterization of a hypomorphic Smith-Lemli-Opitz syndrome mouse model and efficacy of simvastatin therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Abnormalities of cholesterol metabolism in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Engrailed genes control developmental fate of serotonergic and noradrenergic neurons in mid- and hindbrain in a gene dose-dependent manner

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Slow progressive degeneration of nigral dopaminergic neurons in postnatal Engrailed mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Engrailed genes are cell-autonomously required to prevent apoptosis in mesencephalic dopaminergic neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Midbrain dopaminergic neurons: control of their cell fate by the engrailed transcription factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The mouse Engrailed genes: a window into autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Subtle Cerebellar Phenotype in Mice Homozygous for a Targeted Deletion of the En-2 Homeobox

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

A forkhead-domain gene is mutated in a severe speech and language disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

A genetic variant that disrupts MET transcription is associated with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Gene expression profiling of lymphoblastoid cell lines from monozygotic twins discordant in severity of autism reveals differential regulation of neurologically relevant genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

An epigenetic mouse model for molecular and behavioral neuropathologies related to schizophrenia vulnerability

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Valproate corrects the schizophrenia-like epigenetic behavioral modifications induced by methionine in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Histone hyperacetylation induces demethylation of reelin and 67-kDa glutamic acid decarboxylase promoters

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Reelin and glutamic acid decarboxylase67 promoter remodeling in an epigenetic methionine-induced mouse model of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

DNA methyltransferase inhibitors coordinately induce expression of the human reelin and glutamic acid decarboxylase 67 genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Reelin down-regulation in mice and psychosis endophenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Epigenetic regulation in psychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Systematic mapping of genetic interactions in Caenorhabditis elegans identifies common modifiers of diverse signaling pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Atrophin 2 recruits histone deacetylase and is required for the function of multiple signaling centers during mouse embryogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Disruption of Trrap causes early embryonic lethality and defects in cell cycle progression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The lack of chromosomal protein Hmg1 does not disrupt cell growth but causes lethal hypoglycaemia in newborn mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Molecular mechanisms of canalization: Hsp90 and beyond

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Hsp90 and environmental impacts on epigenetic states: a model for the trans-generational effects of diethylstibesterol on uterine development and cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The stress or heat shock (HS) response: insights from transgenic mouse models

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

How commonly are known medical conditions associated with autism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Presynaptic FMR1 genotype influences the degree of synaptic connectivity in a mosaic mouse model of fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Birth order effects on autism symptom domains.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Corticosterone response to acute stress in a mouse model of Fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

RNA cargoes associating with FMRP reveal deficits in cellular functioning in Fmr1 null mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Are serotonin transporter knockout mice 'depressed'?: hypoactivity but no anhedonia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The behavioral salience of tones as indicated by prepulse inhibition of the startle response: relationship to hearing loss and central neural plasticity in C57BL/6J mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Pups call, mothers rush: does maternal responsiveness affect the amount of ultrasonic vocalizations in mouse pups?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Epigenetic sources of behavioral differences in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Maternal care effects on the hippocampal transcriptome and anxiety-mediated behaviors in the offspring that are reversible in adulthood

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Maternal care, hippocampal synaptogenesis and cognitive development in rats.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Reversal of maternal programming of stress responses in adult offspring through methyl supplementation: altering epigenetic marking later in life.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Ube3a expression is not altered in Mecp2 mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Reversal of neurological defects in a mouse model of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Large-scale gene expression differences across brain regions and inbred strains correlate with a behavioral phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Complex trait analysis of gene expression uncovers polygenic and pleiotropic networks that modulate nervous system function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Identifying loci for behavioral traits using genome‐tagged mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Mapping of quantitative trait loci with knockout/congenic strains

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

The Prader-Willi phenotype of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

Early Environmental Regulation of Hippocampal Glucocorticoid Receptor Gene Expression: Characterization of Intracellular Mediators and Potential Genomic Target Sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

2-year-old boy who has been diagnosed with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Mouse models for autism: report from a meeting.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Mouse models of autism spectrum disorders: the challenge for behavioral genetics

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Annotation: Repetitive behaviour in autism: a review of psychological research

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Spatial Reversal as a Measure of Executive Functioning in Children With Autism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Derangements of hippocampal calcium/calmodulin-dependent protein kinase II in a mouse model for Angelman mental retardation syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Signaling cascade regulating long-term potentiation of GABA(A) receptor responsiveness in cerebellar Purkinje neurons.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Refinement of thalamocortical arbors and emergence of barrel domains in the primary somatosensory cortex: a study of normal and monoamine oxidase a knock-out mice

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Barrel pattern formation requires serotonin uptake by thalamocortical afferents, and not vesicular monoamine release.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Receptor tyrosine kinase B-mediated excitatory synaptogenesis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Conditional deletion of brain-derived neurotrophic factor in the postnatal brain leads to obesity and hyperactivity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Essential versus complex autism: definition of fundamental prognostic subtypes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Autism in thalidomide embryopathy: a population study.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Maternal influenza infection causes marked behavioral and pharmacological changes in the offspring.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Discovery of allelic variants ofHOXA1 andHOXB1: Genetic susceptibility to autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Autism spectrum disorders in relation to distribution of hazardous air pollutants in the san francisco bay area

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Sonic hedgehog protein promotes bone marrow-derived endothelial progenitor cell proliferation, migration and VEGF production via PI 3-kinase/Akt signaling pathways

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Impaired motor learning performance in cerebellar En-2 mutant mice.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Pattern deformities and cell loss in Engrailed-2 mutant mice suggest two separate patterning events during cerebellar development.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Combined signaling through ERK, PI3K/AKT, and RAC1/p38 is required for met-triggered cortical neuron migration

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Genetic disruption of cortical interneuron development causes region- and GABA cell type-specific deficits, epilepsy, and behavioral dysfunction.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Mouse brain organization revealed through direct genome-scale TF expression analysis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Chaperoning of glucocorticoid receptors

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002082

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4002082

1 reference

17 August 2017

1 reference

PubMed ID

17848915