(Q30497935)

19 October 2017

Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice (English)

1 reference

19 October 2017

10

Antonio Baldini

1 reference

19 October 2017

Tao Yu

1

1 reference

19 October 2017

Steven J Clapcote

2

1 reference

19 October 2017

Zhongyou Li

3

1 reference

19 October 2017

Chunhong Liu

4

1 reference

19 October 2017

Annie Pao

5

1 reference

19 October 2017

Allison R Bechard

6

1 reference

19 October 2017

Sandra Carattini-Rivera

7

1 reference

19 October 2017

Sei-Ichi Matsui

8

1 reference

19 October 2017

John C Roder

9

1 reference

19 October 2017

William C Mobley

11

1 reference

19 October 2017

Allan Bradley

12

1 reference

19 October 2017

Y Eugene Yu

13

1 reference

19 October 2017

29 May 2010

1 reference

19 October 2017

10

1 reference

inferred from page(s)

published in

Mammalian Genome

1 reference

19 October 2017

21

1 reference

19 October 2017

5-6

1 reference

19 October 2017

258-267

1 reference

https://scigraph.springernature.com/pub.10.1007/s00335-010-9262-x

19 October 2017

0 references

cites work

Copy number variation in human health, disease, and evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Neurocognitive functioning of a child with partial trisomy 6 and monosomy 21

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

A recombineering based approach for high-throughput conditional knockout targeting vector construction

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Copy number variation: new insights in genome diversity

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

A deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects 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=3023176

Complex haplotypes, copy number polymorphisms and coding variation in two recently divergent mouse strains

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

The knockout mouse project

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Large-scale copy number polymorphism in the human genome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Mutagenic insertion and chromosome engineering resource (MICER).

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Survey of embryonic stem cell line source strains in the water maze reveals superior reversal learning of 129S6/SvEvTac 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=3023176

Behavioral profiles of inbred strains on novel olfactory, spatial and emotional tests for reference memory 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=3023176

Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: phenotypic consequences of gene dosage imbalance.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects 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=3023176

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge 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=3023176

Impaired hippocampal-dependent learning and functional abnormalities in the hippocampus in mice lacking serotonin(1A) receptors.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Developing genetic reagents to facilitate recovery, analysis, and maintenance of mouse mutations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Molecular characterisation of partial chromosome 21 aneuploidies by fluorescent PCR.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi 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=3023176

A system for rapid generation of coat color-tagged knockouts and defined chromosomal rearrangements 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=3023176

Hippocampus and context in classical conditioning

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Mice lacking metabotropic glutamate receptor 5 show impaired learning and reduced CA1 long-term potentiation (LTP) but normal CA3 LTP

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Monosomy 21q: two cases of del(21q) and review of the literature.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

"Compensatory" uniparental disomy of chromosome 21 in two cases

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

A case of partial monosomy 21q22.2 associated with Rieger's 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=3023176

Holoprosencephaly in an infant with a minute deletion of chromosome 21(q22.3).

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

A case of 21q-syndrome with normal SOD-1 activity

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

A new case of de novo 11q duplication in a patient with normal development and intelligence and review of the literature.

20 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00335-010-9262-X

Oxidative stress induced by intense and exhaustive exercise impairs murine cognitive function.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Modeling the monosomy for the telomeric part of human chromosome 21 reveals haploinsufficient genes modulating the inflammatory and airway responses.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Duplication of the entire 22.9 Mb human chromosome 21 syntenic region on mouse chromosome 16 causes cardiovascular and gastrointestinal abnormalities.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Effects of the rd1 mutation and host strain on hippocampal learning in mice

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studies.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

A reliable lacZ expression reporter cassette for multipurpose, knockout-first alleles.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Contextual and cued fear conditioning in C57BL/6J and DBA/2J mice: context discrimination and the effects of retention interval.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Deletion of 8p: a report of a child with normal intelligence.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

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

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Hippocampal lesions cause learning deficits in inbred mice in the Morris water maze and conditioned-fear task.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Mildly impaired water maze performance in male Fmr1 knockout mice.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Down syndrome with partial duplication and del (21) syndrome: study protocol and call for collaboration. Study I: Clinical assessment.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023176

Physical findings in 21q22 deletion suggest critical region for 21q- phenotype in q22

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20512340

12 December 2020

inferred from PubMed ID database lookup

Congenital heart disease in mice deficient for the DiGeorge syndrome region

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20512340

12 December 2020

inferred from PubMed ID database lookup

Mouse geneticists need European strategy too

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20512340

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00335-010-9262-X

1 reference

release_ksu6wk3oing3loq3hk2dkmtdvq

19 October 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ksu6wk3oing3loq3hk2dkmtdvq

24 November 2022

mapped directly with Wikidata item

1 reference

19 October 2017

1 reference