Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis (Q27301001)

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English	Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

26 June 2017

Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis (English)

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Europe PubMed Central

PubMed publication ID

26 June 2017

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26 June 2017

Margaret A. Pericak-Vance

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Margaret A Pericak-Vance

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Holly N Cukier

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Silvia De Rubeis

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Silvia De Rubeis

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Jonathan L Haines

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Jonathan L Haines

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26 June 2017

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James D Baker

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Eden R Martin

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26 June 2017

Michael L Cuccaro

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Michael L Cuccaro

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26 June 2017

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Guiqing Cai

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26 June 2017

Anthony J Griswold

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Anthony J Griswold

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26 June 2017

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Robert A Kozol

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26 June 2017

Bing Zou

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26 June 2017

Vera Mayo

4

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26 June 2017

Patrice L Whitehead

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26 June 2017

John R Gilbert

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26 June 2017

Julia E Dallman

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26 June 2017

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16 April 2015

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26 June 2017

Human Molecular Genetics

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26 June 2017

24

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26 June 2017

14

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26 June 2017

4006-4023

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26 June 2017

Disruptive CHD8 mutations define a subtype of autism early in development

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The genome of the ctenophore Mnemiopsis leidyi and its implications for cell type evolution

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21 March 2017

Function and regulation of AUTS2, a gene implicated in autism and human evolution

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21 March 2017

Pathogenic SYNGAP1 mutations impair cognitive development by disrupting maturation of dendritic spine synapses

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21 March 2017

The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome)

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21 March 2017

Consensus paper: pathological role of the cerebellum in autism

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Importance of Shank3 protein in regulating metabotropic glutamate receptor 5 (mGluR5) expression and signaling at synapses

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21 March 2017

Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3

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21 March 2017

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction

1 reference

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21 March 2017

Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication

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21 March 2017

Common circuit defect of excitatory-inhibitory balance in mouse models of autism

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21 March 2017

Functional impact of global rare copy number variation in autism spectrum disorders

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21 March 2017

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

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21 March 2017

The backbone of the post-synaptic density originated in a unicellular ancestor of choanoflagellates and metazoans

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Disrupted in schizophrenia 1 regulates neuronal progenitor proliferation via modulation of GSK3beta/beta-catenin signaling

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Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation

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21 March 2017

p53 activation by knockdown technologies

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21 March 2017

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

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21 March 2017

SynGAP regulates synaptic strength and mitogen-activated protein kinases in cultured neurons

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21 March 2017

Shank, a novel family of postsynaptic density proteins that binds to the NMDA receptor/PSD-95/GKAP complex and cortactin

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21 March 2017

Fiji: an open-source platform for biological-image analysis

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7 April 2017

Primer3 on the WWW for general users and for biologist programmers

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Minicolumnar pathology in autism

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Coupling of mGluR/Homer and PSD-95 complexes by the Shank family of postsynaptic density proteins

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21 March 2017

22q13.2q13.32 genomic regions associated with severity of speech delay, developmental delay, and physical features in Phelan-McDermid syndrome

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21 March 2017

SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patients

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21 March 2017

Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders

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21 March 2017

Direct interaction of post-synaptic density-95/Dlg/ZO-1 domain-containing synaptic molecule Shank3 with GluR1 alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptor

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21 March 2017

High-throughput sequencing of mGluR signaling pathway genes reveals enrichment of rare variants in autism

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21 March 2017

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

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Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability

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Transcriptomic analysis of autistic brain reveals convergent molecular pathology

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7 April 2017

Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting

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7 April 2017

Most genetic risk for autism resides with common variation

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28 September 2017

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Transcriptional landscape of the prenatal human brain

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Patches of disorganization in the neocortex of children with autism

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The genetic landscape of autism spectrum disorders

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28 September 2017

Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency

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28 September 2017

SHANK3 haploinsufficiency: a "common" but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders

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28 September 2017

Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus

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Autism-associated mutations in ProSAP2/Shank3 impair synaptic transmission and neurexin-neuroligin-mediated transsynaptic signaling.

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Reduced excitatory neurotransmission and mild autism-relevant phenotypes in adolescent Shank3 null mutant mice

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28 September 2017

Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways

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28 September 2017

Functional consequences of mutations in postsynaptic scaffolding proteins and relevance to psychiatric disorders.

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28 September 2017

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders

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28 September 2017

Common DISC1 polymorphisms disrupt Wnt/GSK3β signaling and brain development

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Molecular and synaptic defects in intellectual disability syndromes

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Disc1 regulates both β-catenin-mediated and noncanonical Wnt signaling during vertebrate embryogenesis

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28 September 2017

Protein interactome reveals converging molecular pathways among autism disorders

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28 September 2017

SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism.

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28 September 2017

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28 September 2017

Genetic controls balancing excitatory and inhibitory synaptogenesis in neurodevelopmental disorder models

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28 September 2017

Genetic visualization with an improved GCaMP calcium indicator reveals spatiotemporal activation of the spinal motor neurons in zebrafish

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28 September 2017

Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism

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31 May 2018

The autism susceptibility gene met regulates zebrafish cerebellar development and facial motor neuron migration

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Zinc deficiency dysregulates the synaptic ProSAP/Shank scaffold and might contribute to autism spectrum disorders

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Mutations in SYNGAP1 cause intellectual disability, autism, and a specific form of epilepsy by inducing haploinsufficiency.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

Disruption of hippocampus-regulated behavioural and cognitive processes by heterozygous constitutive deletion of SynGAP.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

Time course of the development of motor behaviors in the zebrafish embryo

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

Validation of zebrafish (Danio rerio) reference genes for quantitative real-time RT-PCR normalization.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

Sensorimotor gating in larval zebrafish.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

XNGNR1-dependent neurogenesis mediates early neural cell death.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

Molecular and behavioral changes associated with adult hippocampus-specific SynGAP1 knockout

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

Expression of three zebrafish orthologs of human FMR1-related genes and their phylogenetic relationships.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

Differential expression of two NMDA receptor interacting proteins, PSD-95 and SynGAP during mouse development.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

Transcriptional regulation of cardiac progenitor cell populations

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

The spatio-temporal expression of ProSAP/shank family members and their interaction partner LAPSER1 during Xenopus laevis development.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

DISC1 partners with GSK3beta in neurogenesis.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

Glutamic acid decarboxylase 65 and 67 kDa proteins are reduced in autistic parietal and cerebellar cortices

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

Generation of multiple classes of V0 neurons in zebrafish spinal cord: progenitor heterogeneity and temporal control of neuronal diversity.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

A phylotypic stage in vertebrate brain development: GABA cell patterns in zebrafish compared with mouse

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

A balanced translocation disruptsSYNGAP1in a patient with intellectual disability, speech impairment, and epilepsy with myoclonic absences (EMA)

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV138

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4476447

28 November 2018

Sensory activation and role of inhibitory reticulospinal neurons that stop swimming in hatchling frog tadpoles.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4476447

28 November 2018

Neural degeneration mutants in the zebrafish, Danio rerio.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4476447

28 November 2018

A novel de novo microdeletion spanning the SYNGAP1 gene on the short arm of chromosome 6 associated with mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/25882707

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hindbrain V2a neurons in the excitation of spinal locomotor circuits during zebrafish swimming

1 reference

https://pubmed.ncbi.nlm.nih.gov/25882707

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development and axonal outgrowth of identified motoneurons in the zebrafish

1 reference

https://pubmed.ncbi.nlm.nih.gov/25882707

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Optogenetic activation of excitatory premotor interneurons is sufficient to generate coordinated locomotor activity in larval zebrafish

1 reference

https://pubmed.ncbi.nlm.nih.gov/25882707

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuromuscular synaptogenesis in wild-type and mutant zebrafish

1 reference

https://pubmed.ncbi.nlm.nih.gov/25882707

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/HMG/DDV138

1 reference

Europe PubMed Central

PubMed publication ID

26 June 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 June 2017

ResearchGate publication ID

0 references

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