(Q38291113)

1 September 2017

title

Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model (English)

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1 September 2017

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Wen-Sung Lai

4

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Paul Pavlidis

object named as

Paul Pavlidis

8

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Joseph A Gogos

11

object named as

Joseph A Gogos

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1 September 2017

Kimberly L Stark

1

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1 September 2017

Bin Xu

2

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1 September 2017

Anindya Bagchi

3

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1 September 2017

Hui Liu

5

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1 September 2017

Ruby Hsu

6

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1 September 2017

Xiang Wan

7

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1 September 2017

Alea A Mills

9

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1 September 2017

Maria Karayiorgou

10

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1 September 2017

language of work or name

English

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publication date

11 May 2008

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1 September 2017

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1 September 2017

volume

40

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1 September 2017

issue

6

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1 September 2017

page(s)

751-760

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

1 September 2017

cites work

1 reference

Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.

21 January 2018

1 reference

Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion

21 January 2018

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Genetic, developmental, and physical factors associated with attention deficit hyperactivity disorder in patients with velocardiofacial syndrome.

21 January 2018

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Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome

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Structural variation of chromosomes in autism spectrum disorder

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Approaching a consensus cognitive battery for clinical trials in schizophrenia: the NIMH-MATRICS conference to select cognitive domains and test criteria

21 January 2018

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Neuropsychological characteristics of children with the 22q11 Deletion Syndrome: a descriptive analysis

21 January 2018

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Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

21 January 2018

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

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Genetic variation in the 22q11 locus and susceptibility to schizophrenia

21 January 2018

1 reference

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

21 January 2018

1 reference

Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia

21 January 2018

1 reference

Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice

21 January 2018

1 reference

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome

21 January 2018

1 reference

Strong evidence that GNB1L is associated with schizophrenia

21 January 2018

1 reference

Neural circuit regulation of prepulse inhibition of startle in the rat: current knowledge and future challenges

21 January 2018

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The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

1 reference

A system for rapid generation of coat color-tagged knockouts and defined chromosomal rearrangements in mice

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

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Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning

21 January 2018

1 reference

Disc1 is mutated in the 129S6/SvEv strain and modulates working memory in mice

21 January 2018

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Theta rhythms coordinate hippocampal-prefrontal interactions in a spatial memory task

21 January 2018

1 reference

Transient and selective overexpression of dopamine D2 receptors in the striatum causes persistent abnormalities in prefrontal cortex functioning.

21 January 2018

1 reference

Altered expression of hippocampal dentate granule neuron genes in a mouse model of human 22q11 deletion syndrome

21 January 2018

1 reference

Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome

21 January 2018

1 reference

Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia.

21 January 2018

1 reference

A large imprinted microRNA gene cluster at the mouse Dlk1-Gtl2 domain

21 January 2018

1 reference

MicroRNA biogenesis: drosha can't cut it without a partner

21 January 2018

1 reference

Identification of new central nervous system specific mouse microRNAs

21 January 2018

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The neuronal microRNA system

21 January 2018

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Prediction of mammalian microRNA targets

21 January 2018

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Combinatorial microRNA target predictions

21 January 2018

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Inbred strain differences in prepulse inhibition of the mouse startle response

21 January 2018

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A brain-specific microRNA regulates dendritic spine development

21 January 2018

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Imaging neuronal subsets in transgenic mice expressing multiple spectral variants of GFP

21 January 2018

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Structural basis of long-term potentiation in single dendritic spines

21 January 2018

1 reference

Modeling madness in mice: one piece at a time

21 January 2018

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DGCR8 is essential for microRNA biogenesis and silencing of embryonic stem cell self-renewal

21 January 2018

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Dysregulation of cardiogenesis, cardiac conduction, and cell cycle in mice lacking miRNA-1-2

21 January 2018

1 reference

siRNAs can function as miRNAs

21 January 2018

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Synaptic protein synthesis associated with memory is regulated by the RISC pathway in Drosophila

21 January 2018

1 reference

21 January 2018

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Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG.138

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1 September 2017

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