(Q36662954)

English

The telomeric part of the human chromosome 21 from Cstb to Prmt2 is not necessary for the locomotor and short-term memory deficits observed in the Tc1 mouse model of Down syndrome

scientific article published on 31 October 2010

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

The telomeric part of the human chromosome 21 from Cstb to Prmt2 is not necessary for the locomotor and short-term memory deficits observed in the Tc1 mouse model of Down syndrome (English)

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

1 reference

based on heuristic

inferred from title

object named as

Arnaud Duchon

1

0 references

object named as

Yann Herault

7

0 references

Elizabeth M. C. Fisher

6

object named as

Elizabeth M C Fisher

1 reference

Europe PubMed Central

15 August 2017

PMC publication ID

author name string

Stéphanie Pothion

2

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Véronique Brault

3

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Andrew J Sharp

4

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Victor L J Tybulewicz

5

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Europe PubMed Central

PMC publication ID

15 August 2017

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publication date

31 October 2010

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Behavioural Brain Research

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Europe PubMed Central

PMC publication ID

15 August 2017

217

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

2

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

271-281

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Behavioral and genetic investigations of low exploratory behavior in Il18r1(-/-) mice: we can't always blame it on the targeted gene

1 reference

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Down's syndrome-like cardiac developmental defects in embryos of the transchromosomic Tc1 mouse

1 reference

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Tumour angiogenesis is reduced in the Tc1 mouse model of Down's syndrome

1 reference

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

1 reference

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A mouse model of Down syndrome trisomic for all human chromosome 21 syntenic regions

1 reference

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Clinical, cytogenetic, and molecular characterization of a girl with some clinical features of Down syndrome resulting from a pure partial trisomy 21q22.11-qter due to a de novo intrachromosomal duplication

1 reference

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Communication breaks-Down: from neurodevelopment defects to cognitive disabilities in Down syndrome

1 reference

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Trends in Down's syndrome live births and antenatal diagnoses in England and Wales from 1989 to 2008: analysis of data from the National Down Syndrome Cytogenetic Register

1 reference

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A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome

1 reference

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1 reference

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1 reference

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Aneuploidy: from a physiological mechanism of variance to Down syndrome

1 reference

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1 reference

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30 September 2017

Impairments in motor coordination without major changes in cerebellar plasticity in the Tc1 mouse model of Down syndrome

1 reference

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Genetics. It's the sequence, stupid!

1 reference

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Cautionary insights on knockout mouse studies: the gene or not the gene?

1 reference

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Inducing segmental aneuploid mosaicism in the mouse through targeted asymmetric sister chromatid event of recombination

1 reference

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Preservation of long-term memory and synaptic plasticity despite short-term impairments in the Tc1 mouse model of Down syndrome

1 reference

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A mutation in mouse Disc1 that models a schizophrenia risk allele leads to specific alterations in neuronal architecture and cognition

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Social approach and repetitive behavior in eleven inbred mouse strains

1 reference

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Deletion polymorphism of Disc1 is common to all 129 mouse substrains: implications for gene-targeting studies of brain function

1 reference

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30 September 2017

Motor development and neuropsychological patterns in persons with Down syndrome

1 reference

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30 September 2017

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

1 reference

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30 September 2017

An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes

1 reference

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30 September 2017

A chromosome 21 critical region does not cause specific Down syndrome phenotypes.

1 reference

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Flanking gene and genetic background problems in genetically manipulated mice

1 reference

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Verbal short-term memory in Down's syndrome: an articulatory loop deficit?

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App gene dosage modulates endosomal abnormalities of Alzheimer's disease in a segmental trisomy 16 mouse model of down syndrome

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No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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Verbal and visuospatial working memory deficits in children with Down syndrome.

1 reference

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Prehension in young children with Down syndrome.

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Working memory and Down syndrome

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/21047530

12 December 2020

based on heuristic

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based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.BBR.2010.10.023

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

ResearchGate publication ID

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