(Q52185557)

26 April 2018

review article

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title

Down syndrome and mouse models. (English)

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26 April 2018

ORCID Public Data File 2021

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1 reference

author name string

Kola I

series ordinal

1

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26 April 2018

Hertzog PJ

series ordinal

2

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26 April 2018

publication date

1 June 1998

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26 April 2018

Current Opinion in Genetics & Development

published in

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26 April 2018

volume

8

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26 April 2018

issue

3

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26 April 2018

page(s)

316-321

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26 April 2018

Simple minded mice from 'in vivo' libraries

cites work

1 reference

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7 January 2021

Animal models in the study of the biological function of genes on human chromosome 21 and their role in the pathophysiology of Down syndrome

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7 January 2021

Mouse trisomy 16: an animal model of human trisomy 21 (Down syndrome)

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7 January 2021

Developmental abnormalities and age-related neurodegeneration in a mouse model of Down syndrome

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7 January 2021

Down's syndrome-like skeletal abnormalities in Ets2 transgenic mice

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7 January 2021

A behavioral assessment of Ts65Dn mice: a putative Down syndrome model.

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7 January 2021

A mouse model for Down syndrome exhibits learning and behaviour deficits.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980088-9

7 January 2021

Ts1Cje, a partial trisomy 16 mouse model for Down syndrome, exhibits learning and behavioral abnormalities

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980088-9

7 January 2021

Astrocytosis and axonal proliferation in the hippocampus of S100b transgenic mice

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980088-9

7 January 2021

Functional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndrome

1 reference

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7 January 2021

Alterations of central noradrenergic transmission in Ts65Dn mouse, a model for Down syndrome

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7 January 2021

Cholinergic, serotonergic and catecholaminergic neurons are not affected in Ts65Dn mice.

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7 January 2021

Cell damage by excess CuZnSOD and Down's syndrome

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7 January 2021

Constitutive overexpression of Cu/Zn superoxide dismutase exacerbates kainic acid-induced apoptosis of transgenic-Cu/Zn superoxide dismutase neurons

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7 January 2021

Thymic abnormalities and enhanced apoptosis of thymocytes and bone marrow cells in transgenic mice overexpressing Cu/Zn-superoxide dismutase: implications for Down syndrome

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7 January 2021

Overexpression of liver-type phosphofructokinase (PFKL) in transgenic-PFKL mice: implication for gene dosage in trisomy 21

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7 January 2021

Oxidative stress mediates impairment of muscle function in transgenic mice with elevated level of wild-type Cu/Zn superoxide dismutase

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7 January 2021

Reversible impairment of long-term potentiation in transgenic Cu/Zn-SOD mice.

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7 January 2021

Positional cloning of the APECED gene

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7 January 2021

An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains

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7 January 2021

10.1016/S0959-437X(98)80088-9

Identifiers

DOI

1 reference

26 April 2018

1 reference

26 April 2018