Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice (Q30481665)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

title

Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

1 reference

GOA release 2020-03-11

1 reference

1

1 reference

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22 January 2020

Kathryn M Harper

2

1 reference

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22 January 2020

author name string

Takeshi Hiramoto

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Takehito Sawamura

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

MoonSook Lee

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Gina Kang

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Kenji Tanigaki

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Mahalah Buell

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Mark A Geyer

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

William S Trimble

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Soh Agatsuma

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Noboru Hiroi

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

publication date

24 February 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

published in

Human Molecular Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

volume

18

1 reference

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22 January 2020

issue

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

page(s)

1652-1660

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT.

22 January 2020

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20 June 2018

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20 June 2018

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20 June 2018

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1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features.

20 June 2018

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Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome

20 June 2018

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20 June 2018

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Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome

20 June 2018

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Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

20 June 2018

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Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: Neuropsychological and behavioral implications

20 June 2018

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A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice

20 June 2018

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Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome

20 June 2018

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Microduplication and triplication of 22q11.2: a highly variable syndrome

20 June 2018

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Adolescents and young adults with 22q11 deletion syndrome: psychopathology in an at-risk group.

20 June 2018

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Associations between prepulse inhibition and executive visual attention in children with the 22q11 deletion syndrome

20 June 2018

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Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome

20 June 2018

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A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome

20 June 2018

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Dopamine-dependent neurodegeneration in rats induced by viral vector-mediated overexpression of the parkin target protein, CDCrel-1

20 June 2018

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Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients

20 June 2018

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Mouse genetic models for prepulse inhibition: an early review

20 June 2018

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Knockout mice: simple solutions to the problems of genetic background and flanking genes

20 June 2018

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Abnormalities of SNARE mechanism proteins in anterior frontal cortex in severe mental illness

20 June 2018

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The septin CDCrel-1 is dispensable for normal development and neurotransmitter release

20 June 2018

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20 June 2018

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Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

20 June 2018

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Differential localization of septins in the mouse brain

20 June 2018

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A common molecular basis for rearrangement disorders on chromosome 22q11

20 June 2018

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The septin CDCrel-1 binds syntaxin and inhibits exocytosis

20 June 2018

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Localization of a novel septin protein, hCDCrel-1, in neurons of human brain

20 June 2018

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Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior

20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.

20 June 2018

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Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects.

21 January 2018

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Autistic disorder and 22q11.2 duplication.

21 January 2018

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An investigation of the neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS).

21 January 2018

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Risk factors for the emergence of psychotic disorders in adolescents with 22q11.2 deletion syndrome.

21 January 2018

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Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion).

21 January 2018

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Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome

21 January 2018

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Abnormalities of presynaptic protein CDCrel-1 in striatum of rats reared in social isolation: relevance to neural connectivity in schizophrenia.

21 January 2018

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Pleiotropic impact of constitutive fosB inactivation on nicotine-induced behavioral alterations and stress-related traits in mice.

21 January 2018

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QTL analysis of multiple behavioral measures of anxiety in mice

21 January 2018

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COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome

21 January 2018

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Monoamine oxidase A knockout mice exhibit impaired nicotine preference but normal responses to novel stimuli.

21 January 2018

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Innate versus learned odour processing in the mouse olfactory bulb

21 January 2018

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Microduplication 22q11.2 in a child with autism spectrum disorder: clinical and genetic study.

21 January 2018

1 reference

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22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes.

26 November 2018

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Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion.

26 November 2018

1 reference

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Comparing phenotypes in patients with idiopathic autism to patients with velocardiofacial syndrome (22q11 DS) with and without autism

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19240081

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The intrafamilial variability of the 22q11.2 microduplication encompasses a spectrum from minor cognitive deficits to severe congenital anomalies

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19240081

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Duplication of the 22q11.2 region associated with congenital cardiac disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19240081

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDP086

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19240081%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

1 reference