Genetic background modulates phenotypes of serotonin transporter Ala56 knock-in mice (Q30558687)

19 August 2017

Genetic background modulates phenotypes of serotonin transporter Ala56 knock-in mice (English)

1 reference

Jeremy Veenstra-VanderWeele

19 August 2017

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object named as

Jeremy Veenstra-Vanderweele

12

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James S. Sutcliffe

object named as

James S Sutcliffe

10

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author name string

Travis M Kerr

1

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19 August 2017

Christopher L Muller

2

1 reference

19 August 2017

Mahfuzur Miah

3

1 reference

19 August 2017

Christopher S Jetter

4

1 reference

19 August 2017

Rita Pfeiffer

5

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19 August 2017

Charisma Shah

6

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19 August 2017

Nicole Baganz

7

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19 August 2017

George M Anderson

8

1 reference

19 August 2017

Jacqueline N Crawley

9

1 reference

19 August 2017

Randy D Blakely

11

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19 August 2017

1 October 2013

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19 August 2017

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19 August 2017

4

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19 August 2017

1

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19 August 2017

35

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Behavioral and serotonergic response changes in the Dhcr7-HET mouse model of Smith-Lemli-Opitz syndrome.

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Deficits in social behavior emerge during development after pediatric traumatic brain injury in mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Autism-relevant social abnormalities and cognitive deficits in engrailed-2 knockout mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Neurobehavioral phenotyping of G(αq) knockout mice reveals impairments in motor functions and spatial working memory without changes in anxiety or behavioral despair

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Haploinsufficiency of the E3 ubiquitin ligase C-terminus of heat shock cognate 70 interacting protein (CHIP) produces specific behavioral impairments

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Autism gene variant causes hyperserotonemia, serotonin receptor hypersensitivity, social impairment and repetitive behavior

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Autism-like socio-communicative deficits and stereotypies in mice lacking heparan sulfate

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Zic2 hypomorphic mutant mice as a schizophrenia model and ZIC2 mutations identified in schizophrenia patients

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Networking in autism: leveraging genetic, biomarker and model system findings in the search for new treatments

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Automated three-chambered social approach task for mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Transgenic elimination of high-affinity antidepressant and cocaine sensitivity in the presynaptic serotonin transporter.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Modifying behavioral phenotypes in Fmr1KO mice: genetic background differences reveal autistic-like responses

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Regulation of monoamine transporters: Role of transporter phosphorylation

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Opposing alterations in anxiety and species-typical behaviours in serotonin transporter overexpressor and knockout mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Modeling rare gene variation to gain insight into the oldest biomarker in autism: construction of the serotonin transporter Gly56Ala knock-in mouse

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

A triplet repeat expansion genetic mouse model of infantile spasms syndrome, Arx(GCG)10+7, with interneuronopathy, spasms in infancy, persistent seizures, and adult cognitive and behavioral impairment

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Functional coding variation in recombinant inbred mouse lines reveals multiple serotonin transporter-associated phenotypes.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Enhanced activity of human serotonin transporter variants associated with autism

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

How the serotonin story is being rewritten by new gene-based discoveries principally related to SLC6A4, the serotonin transporter gene, which functions to influence all cellular serotonin systems.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Going with the flow: trafficking-dependent and -independent regulation of serotonin transport

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Interactions between integrin alphaIIbbeta3 and the serotonin transporter regulate serotonin transport and platelet aggregation in mice and humans

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Targeting the murine serotonin transporter: insights into human neurobiology.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Autism and the serotonin transporter: the long and short of it

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Human serotonin transporter variants display altered sensitivity to protein kinase G and p38 mitogen-activated protein kinase

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Replication of autism linkage: fine-mapping peak at 17q21.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Sex-specific genetic architecture of whole blood serotonin levels

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Evidence for sex-specific risk alleles in autism spectrum disorder

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

A new set of BXD recombinant inbred lines from advanced intercross populations in mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

A genomewide screen of 345 families for autism-susceptibility loci

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Broad and narrow heritabilities of quantitative traits in a founder population

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Modifications of the serotonergic system in mice lacking serotonin transporters: an in vivo electrophysiological study.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Evidence of linkage between the serotonin transporter and autistic disorder

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

The serotonin system in autism

20 June 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

20 June 2018

https://api.crossref.org/works/10.1186%2F2040-2392-4-35

Quantitative assessment of tactile allodynia in the rat paw

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Autism as a strongly genetic disorder: evidence from a British twin study

20 June 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

20 June 2018

https://api.crossref.org/works/10.1186%2F2040-2392-4-35

Genetic progressive hearing loss in the C57-b16 mouse. Relation of behavioral responses to chochlear anatomy

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Determination of serotonin in whole blood, platelet-rich plasma, platelet-poor plasma and plasma ultrafiltrate

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Infantile autism: a genetic study of 21 twin pairs

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

Platelet serotonin levels in pervasive developmental disorders and mental retardation: diagnostic group differences, within-group distribution, and behavioral correlates

20 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-4-35

Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-4-35

Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-4-35

Deficits in acetylcholine homeostasis, receptors and behaviors in choline transporter heterozygous mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-4-35

Ontogeny of brain and blood serotonin levels in 5-HT receptor knockout mice: potential relevance to the neurobiology of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-4-35

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/10.1186%2F2040-2392-4-35

Autism before diagnosis: crying, feeding and sleeping problems in the first two years of life

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-4-35

Temperament and its relationship to autistic symptoms in a high-risk infant sib cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-4-35

Increased expression of the 5-HT transporter confers a low-anxiety phenotype linked to decreased 5-HT transmission.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-4-35

Altered depression-related behaviors and functional changes in the dorsal raphe nucleus of serotonin transporter-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-4-35

Non-linear relationship between 5-HT transporter gene expression and frequency sensitivity of 5-HT signals

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-4-35

The MECP2 duplication syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-4-35

Genetic Progressive Hearing Loss in the C57/M6 Mouse: Relation of Behaviorial Responses to Cochlear Anatomy

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-4-35

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3851031

26 November 2018

Identifiers

DOI

10.1186/2040-2392-4-35

1 reference

Dimensions Publication ID

19 August 2017

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/2040-2392-4-35

1 reference

19 August 2017

PubMed publication ID

24083388

1 reference