Differential gene expression studies to explore the molecular pathophysiology of Down syndrome (Q57161912)

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2 December 2019

review article

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title

Differential gene expression studies to explore the molecular pathophysiology of Down syndrome (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11690624%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

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Stilianos Antonarakis

1

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2 December 2019

Roman Chrast

3

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2 December 2019

Hamish S. Scott

4

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2 December 2019

author name string

R Lyle

2

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2 December 2019

publication date

1 October 2001

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2 December 2019

published in

Brain Research Reviews

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volume

36

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2 December 2019

issue

2-3

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2 December 2019

page(s)

265-274

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Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse.

2 December 2019

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Characterization of transgenic mice with an increased content of chromosomal protein HMG-14 in their chromatin

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Mice trisomic for a bacterial artificial chromosome with the single-minded 2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome

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7 January 2021

The mouse brain transcriptome by SAGE: differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals

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7 January 2021

Mouse trisomy 16 as an animal model of human trisomy 21 (Down syndrome): Production of viable trisomy 16 ↔ diploid mouse chimeras

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7 January 2021

Down syndrome, Alzheimer's disease and the trisomy 16 mouse

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

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7 January 2021

Transgenic mice with increased Cu/Zn-superoxide dismutase activity: animal model of dosage effects in 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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The sequence of human chromosome 21 and implications for research into Down syndrome

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7 January 2021

Loss of cholinergic phenotype in basal forebrain coincides with cognitive decline in a mouse model of Down's syndrome

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7 January 2021

Human minibrain homologue (MNBH/DYRK1): characterization, alternative splicing, differential tissue expression, and overexpression in Down syndrome

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7 January 2021

The DNA sequence of human chromosome 21

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Engineering chromosomes in mice through targeted meiotic recombination (TAMERE)

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

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7 January 2021

Hippocampal volume and neuronal number in Ts65Dn mice: a murine model of Down syndrome.

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7 January 2021

Structure of chromosomal duplicons and their role in mediating human genomic disorders

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7 January 2021

Synaptic deficit in the temporal cortex of partial trisomy 16 (Ts65Dn) mice.

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Introduction and expression of the 400 kilobase amyloid precursor protein gene in transgenic mice [corrected]

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7 January 2021

Patterns of Meiotic Recombination on the Long Arm of Human Chromosome 21

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Amygdala and hippocampal volumes in children with Down syndrome: a high-resolution MRI study

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Selective neuroanatomic abnormalities in Down's syndrome and their cognitive correlates: evidence from MRI morphometry.

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7 January 2021

Too much of a good thing: mechanisms of gene action in Down syndrome.

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7 January 2021

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

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7 January 2021

Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice.

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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

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7 January 2021

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

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7 January 2021

Serial analysis of gene expression

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7 January 2021

Engineering mouse chromosomes with Cre-loxP: range, efficiency, and somatic applications

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Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11690624%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

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