(Q46400538)

21 December 2017

title

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

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21 December 2017

author

Bernice E. Morrow

8

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21 December 2017

Sandra Merscher

object named as

Sandra Merscher

3

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author name string

Jeffrey M Long

1

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21 December 2017

Patricia LaPorte

2

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21 December 2017

Birgit Funke

4

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21 December 2017

Bruno Saint-Jore

5

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21 December 2017

Anne Puech

6

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21 December 2017

Raju Kucherlapati

7

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21 December 2017

Arthur I Skoultchi

9

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21 December 2017

Anthony Wynshaw-Boris

10

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21 December 2017

publication date

10 August 2006

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21 December 2017

published in

Neurogenetics

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21 December 2017

volume

7

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21 December 2017

issue

4

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21 December 2017

page(s)

247-257

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21 December 2017

https://scigraph.springernature.com/pub.10.1007/s10048-006-0054-0

exact match

0 references

cites work

Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-006-0054-0

Deficits in prepulse inhibition and habituation in never-medicated, first-episode schizophrenia.

21 January 2018

1 reference

12 December 2020

A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome

1 reference

12 December 2020

Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives

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12 December 2020

Dissecting contiguous gene defects: TBX1.

1 reference

12 December 2020

Early speech and language development in children with velocardiofacial syndrome

1 reference

12 December 2020

Doublecortin is required in mice for lamination of the hippocampus but not the neocortex.

1 reference

12 December 2020

Stability of the acoustic startle reflex, prepulse inhibition, and habituation in schizophrenia.

1 reference

12 December 2020

The use of behavioral test batteries: effects of training history.

1 reference

12 December 2020

Neurobiology of Pavlovian fear conditioning.

1 reference

12 December 2020

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

1 reference

12 December 2020

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11

1 reference

12 December 2020

A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

1 reference

12 December 2020

Velo-cardio-facial syndrome: a distinctive behavioral phenotype

1 reference

12 December 2020

Follow-up of a report of a potential linkage for schizophrenia on chromosome 22q12-q13.1: Part 2

1 reference

12 December 2020

The schizophrenia phenotype in 22q11 deletion syndrome

1 reference

12 December 2020

Goosecoid-like (Gscl), a candidate gene for velocardiofacial syndrome, is not essential for normal mouse development.

1 reference

12 December 2020

Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage

1 reference

12 December 2020

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

1 reference

12 December 2020

Role of TBX1 in human del22q11.2 syndrome

1 reference

12 December 2020

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

1 reference

12 December 2020

Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

1 reference

12 December 2020

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

1 reference

12 December 2020

Developing models of DiGeorge syndrome

1 reference

12 December 2020

22q11 deletion syndrome in childhood onset schizophrenia: an update

1 reference

12 December 2020

Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.

1 reference

12 December 2020

Phenotype of adults with the 22q11 deletion syndrome: A review

1 reference

12 December 2020

Congenital heart disease in mice deficient for the DiGeorge syndrome region

1 reference

12 December 2020

Gscl, a gene within the minimal DiGeorge critical region, is expressed in primordial germ cells and the developing pons

1 reference

12 December 2020

The spectrum of the DiGeorge syndrome

1 reference

12 December 2020

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

1 reference

12 December 2020

Hippocampus and contextual fear conditioning: recent controversies and advances

1 reference

12 December 2020

Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12-q13.1: Part 1

1 reference

12 December 2020

Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region

1 reference

12 December 2020

DiGeorge syndrome: the use of model organisms to dissect complex genetics

1 reference

12 December 2020

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

1 reference

12 December 2020

The 22q11 deletion syndromes

1 reference

12 December 2020

Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse.

1 reference

12 December 2020

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population

1 reference

12 December 2020

Emotion circuits in the brain

1 reference

12 December 2020

Familial third-fourth pharyngeal pouch syndrome with apparent autosomal dominant transmission

1 reference

12 December 2020

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

1 reference

12 December 2020

Chromosomal microdeletions: dissecting del22q11 syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial DiGeorge syndrome and associated partial monosomy of chromosome 22

1 reference

12 December 2020

Targeted mutation of the murine goosecoid gene results in craniofacial defects and neonatal death

1 reference

12 December 2020

Functional analysis of Gscl in the pathogenesis of the DiGeorge and velocardiofacial syndromes.

1 reference

12 December 2020

Goosecoid is not an essential component of the mouse gastrula organizer but is required for craniofacial and rib development

1 reference

12 December 2020

Correlation between loss of middle ear bones and altered goosecoid gene expression in the branchial region following retinoic acid treatment of mouse embryos in vivo.

1 reference

12 December 2020

10.1007/S10048-006-0054-0

Identifiers

DOI

1 reference

21 December 2017

PubMed ID

16900388

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21 December 2017