(Q22251439)

PubMed publication ID

7 February 2023

3

Joseph D Buxbaum

Joseph D

Buxbaum

1 reference

PubMed publication ID

7 February 2023

Takeshi Sakurai

2

Takeshi

Sakurai

1 reference

PubMed publication ID

19541375

7 February 2023

language of work or name

English

0 references

publication date

July 2009

0 references

published in

Trends in Neurosciences

1 reference

The new neurobiology of autism: cortex, connectivity, and neuronal organization

volume

32

0 references

issue

7

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page(s)

402-412

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cites work

1 reference

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7 January 2021

Molecular and phenotypic characterization of ring chromosome 22

1 reference

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7 January 2021

Molecular cytogenetic analysis of a familial interstitial deletion Xp22.2-22.3 with a highly variable phenotype in female carriers.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Defining key features of the broad autism phenotype: a comparison across parents of multiple- and single-incidence autism families

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

No evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning level

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Familial aggregation of quantitative autistic traits in multiplex versus simplex autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Novel de novo SHANK3 mutation in autistic patients

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

22q13.3 deletion syndrome: a recognizable malformation syndrome associated with marked speech and language delay

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Rapamycin prevents epilepsy in a mouse model of tuberous sclerosis complex.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Deletion of alpha-neurexins does not cause a major impairment of axonal pathfinding or synapse formation.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

No effect of genetic deletion of contactin-associated protein (CASPR) on axonal orientation and synaptic plasticity.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Overlapping and differential expression of BIG-2, BIG-1, TAG-1, and F3: four members of an axon-associated cell adhesion molecule subgroup of the immunoglobulin superfamily

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

The postsynaptic density

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Autism spectrum phenotype in males and females with fragile X full mutation and premutation.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Neuroligin 1: a splice site-specific ligand for beta-neurexins

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Disruption of neurexin 1 associated with autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Structural variation of chromosomes in autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Alterations in CDH15 and KIRREL3 in patients with mild to severe intellectual disability

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Microanatomy of dendritic spines: emerging principles of synaptic pathology in psychiatric and neurological disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Neurexins induce differentiation of GABA and glutamate postsynaptic specializations via neuroligins

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

GABA and neuroligin signaling: linking synaptic activity and adhesion in inhibitory synapse development

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

L1 and NCAM adhesion molecules as signaling coreceptors in neuronal migration and process outgrowth

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

A direct role for FMRP in activity-dependent dendritic mRNA transport links filopodial-spine morphogenesis to fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Normal intelligence and social interactions in a male patient despite the deletion of NLGN4X and the VCX genes.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

A 12Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Cadherins as regulators for the emergence of neural nets from embryonic divisions

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Molecular anatomy of the postsynaptic density.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

High frequency of neurexin 1beta signal peptide structural variants in patients with autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Neurexin 1alpha structural variants associated with autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

A preformed complex of postsynaptic proteins is involved in excitatory synapse development

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Neuroligins determine synapse maturation and function

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Activity-dependent validation of excitatory versus inhibitory synapses by neuroligin-1 versus neuroligin-2

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Activity-induced protocadherin arcadlin regulates dendritic spine number by triggering N-cadherin endocytosis via TAO2beta and p38 MAP kinases

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Cdk5 promotes synaptogenesis by regulating the subcellular distribution of the MAGUK family member CASK

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Correction of fragile X syndrome in mice.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

The complexity of PDZ domain-mediated interactions at glutamatergic synapses: a case study on neuroligin

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Suppression of two major Fragile X Syndrome mouse model phenotypes by the mGluR5 antagonist MPEP.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Molecular mechanisms of dendritic spine development and remodeling

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

The mGluR theory of fragile X mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Cadherins and catenins at synapses: roles in synaptogenesis and synaptic plasticity

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Neuroligin expressed in nonneuronal cells triggers presynaptic development in contacting axons

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Dendritic Spine Pathology: Cause or Consequence of Neurological Disorders?

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

On the allelic spectrum of human disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Regulation of dendritic spine morphology and synaptic function by Shank and Homer

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Neuroligins and neurexins link synaptic function to cognitive disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Common genetic variants on 5p14.1 associate with autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Phenotypic variations on the theme of CNVs

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Common and rare variants in multifactorial susceptibility to common diseases

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Reversal of learning deficits in a Tsc2+/- mouse model of tuberous sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Determination of absolute protein numbers in single synapses by a GFP-based calibration technique.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Neurexin mediates the assembly of presynaptic terminals

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Neural recognition molecules of the immunoglobulin superfamily: signaling transducers of axon guidance and neuronal migration

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Laminar and compartmental regulation of dendritic growth in mature cortex.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Advances in autism genetics: on the threshold of a new neurobiology

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Mutation screening and association analysis of six candidate genes for autism on chromosome 7q

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Analysis of four neuroligin genes as candidates for autism.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Genetics and pathophysiology of mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

XLMR genes: update 2007.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Familial deletion within NLGN4 associated with autism and Tourette syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Association between microdeletion and microduplication at 16p11.2 and autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Postsynaptic N-methyl-D-aspartate receptor function requires alpha-neurexins

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Gamma protocadherins are required for synaptic development in the spinal cord

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Fragile X mental retardation protein deficiency leads to excessive mGluR5-dependent internalization of AMPA receptors

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Dissection of synapse induction by neuroligins: effect of a neuroligin mutation associated with autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Nectin: an adhesion molecule involved in formation of synapses

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Association of TAG-1 with Caspr2 is essential for the molecular organization of juxtaparanodal regions of myelinated fibers

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Are rare variants responsible for susceptibility to complex diseases?

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Contribution of SHANK3 mutations to autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

The allelic architecture of human disease genes: common disease-common variant... or not?

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Neural cell recognition molecule L1: relating biological complexity to human disease mutations

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Disorder-associated mutations lead to functional inactivation of neuroligins

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Recurrent 16p11.2 microdeletions in autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Disruption of the neurexin 1 gene is associated with schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Association analysis of the NrCAM gene in autism and in subsets of families with severe obsessive-compulsive or self-stimulatory behaviors.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Analysis of protocadherin alpha gene deletion variant in bipolar disorder and schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Deletions of VCX-A and NLGN4: a variable phenotype including normal intellect.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Neuroligin-3-deficient mice: model of a monogenic heritable form of autism with an olfactory deficit.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Control of excitatory and inhibitory synapse formation by neuroligins

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Reversal of neurological defects in a mouse model of Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Strong association of de novo copy number mutations with autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Identifying autism loci and genes by tracing recent shared ancestry

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

A patient with vertebral, cognitive and behavioural abnormalities and a de novo deletion of NRXN1alpha

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Disruption of contactin 4 in three subjects with autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Intranasal insulin to improve developmental delay in children with 22q13 deletion syndrome: an exploratory clinical trial.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

The postsynaptic architecture of excitatory synapses: a more quantitative view

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Cell-cell signaling during synapse formation in the CNS.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Nectin-like molecule-1/TSLL1/SynCAM3: a neural tissue-specific immunoglobulin-like cell-cell adhesion molecule localizing at non-junctional contact sites of presynaptic nerve terminals, axons and glia cell processes.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Silencing of neuroligin function by postsynaptic neurexins

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

The Arg451Cys-neuroligin-3 mutation associated with autism reveals a defect in protein processing

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Extracellular domains of alpha-neurexins participate in regulating synaptic transmission by selectively affecting N- and P/Q-type Ca2+ channels.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

N-cadherin redistribution during synaptogenesis in hippocampal neurons.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Gamma-protocadherins are targeted to subsets of synapses and intracellular organelles in neurons

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Smaller dendritic spines, weaker synaptic transmission, but enhanced spatial learning in mice lacking Shank1.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Shank expression is sufficient to induce functional dendritic spine synapses in aspiny neurons.

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Pharmacological inhibition of mTORC1 suppresses anatomical, cellular, and behavioral abnormalities in neural-specific Pten knock-out mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Neurobehavioral profile and brain imaging study of the 22q13.3 deletion syndrome in childhood

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Neural GPI-anchored cell adhesion molecules

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021

Cell adhesion molecules at the synapse

1 reference

https://api.crossref.org/works/10.1016%2FJ.TINS.2009.04.003

7 January 2021