(Q35946317)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

title

Classification of human chromosome 21 gene-expression variations in Down syndrome: impact on disease phenotypes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

1 reference

1 reference

13

1 reference

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3 January 2020

author name string

Aït Yahya-Graison E

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Aubert J

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Dauphinot L

3

1 reference

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3 January 2020

Rivals I

4

1 reference

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3 January 2020

Prieur M

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Golfier G

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Rossier J

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Personnaz L

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Creau N

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Bléhaut H

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Robin S

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Delabar JM

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

language of work or name

English

0 references

publication date

19 July 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

3 January 2020

published in

1 reference

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3 January 2020

volume

81

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

page(s)

475-491

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

issue

3

1 reference

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''R"--project for statistical computing

3 January 2020

cites work

1 reference

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Trisomy for the Down syndrome 'critical region' is necessary but not sufficient for brain phenotypes of trisomic mice.

2 October 2017

1 reference

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Gene-expression variation within and among human populations

2 October 2017

1 reference

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A study of enzyme activities in a dosage series of the long arm of chromosome one in maize.

2 October 2017

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Common genetic variants account for differences in gene expression among ethnic groups

2 October 2017

1 reference

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Global variation in copy number in the human genome

2 October 2017

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An open-access long oligonucleotide microarray resource for analysis of the human and mouse transcriptomes.

2 October 2017

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Cell type-specific over-expression of chromosome 21 genes in fibroblasts and fetal hearts with trisomy 21.

2 October 2017

1 reference

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Transcriptional dysregulation in Down syndrome: predictions for altered protein complex stoichiometries and post-translational modifications, and consequences for learning/behavior genes ELK, CREB, and the estrogen and glucocorticoid receptors

2 October 2017

1 reference

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Primary and secondary transcriptional effects in the developing human Down syndrome brain and heart

2 October 2017

1 reference

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Human chromosome 21/Down syndrome gene function and pathway database

2 October 2017

1 reference

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Dosage balance in gene regulation: biological implications

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Gene expression analysis of cultured amniotic fluid cell with Down syndrome by DNA microarray

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Tissue-specific overexpression of the HSA21 gene GABPalpha: implications for DS.

2 October 2017

1 reference

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Chromosome 21 and down syndrome: from genomics to pathophysiology

2 October 2017

1 reference

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Gene expression from the aneuploid chromosome in a trisomy mouse model of down syndrome

2 October 2017

1 reference

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Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome

2 October 2017

1 reference

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A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 21q

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Study of somatic chromosomes from 9 mongoloid children

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Statistical significance for genomewide studies

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Global up-regulation of chromosome 21 gene expression in the developing down syndrome brain

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Microarray data normalization and transformation

2 October 2017

1 reference

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Nineteen additional unpredicted transcripts from human chromosome 21

2 October 2017

1 reference

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Large-scale transcriptional activity in chromosomes 21 and 22

2 October 2017

1 reference

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Developmental instability of the cerebellum and its relevance to Down syndrome.

2 October 2017

1 reference

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Assessing gene significance from cDNA microarray expression data via mixed models

2 October 2017

1 reference

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The DNA sequence of human chromosome 21

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Transcriptional map of the 2.5-Mb CBR-ERG region of chromosome 21 involved in Down syndrome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Gene identification in 1.6-Mb region of the Down syndrome region on chromosome 21

2 October 2017

1 reference

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Autosomal dosage compensation Drosophila melanogaster strains trisomic for the left arm of chromosome 2.

2 October 2017

1 reference

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Human Cu/Zn superoxide dismutase gene: molecular characterization of its two mRNA species

2 October 2017

1 reference

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Protocols to establish genotype-phenotype correlations in Down syndrome

2 October 2017

1 reference

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Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Molecular mapping of twenty-four features of Down syndrome on chromosome 21.

11 July 2018

1 reference

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Paraoxonase-1 expression is up-regulated in Down syndrome fetal liver.

11 July 2018

1 reference

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Clinical and molecular characterization of individuals with 18p deletion: a genotype-phenotype correlation.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Transcriptional disruptions in Down syndrome: a case study in the Ts1Cje mouse cerebellum during post-natal development.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Identification of a novel putative mitogen-activated kinase cascade on human chromosome 21 by computational approaches.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

The cerebellar transcriptome during postnatal development of the Ts1Cje mouse, a segmental trisomy model for Down syndrome.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Blood expression profiles for tuberous sclerosis complex 2, neurofibromatosis type 1, and Down's syndrome

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Dosage-dependent over-expression of genes in the trisomic region of Ts1Cje mouse model for Down syndrome.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Global disruption of the cerebellar transcriptome in a Down syndrome mouse model.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Gene expression profile of trisomy 21 placentas: a potential approach for designing noninvasive techniques of prenatal diagnosis.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Gene expression profile analysis in human T lymphocytes from patients with Down Syndrome

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Gene expression variation and expression quantitative trait mapping of human chromosome 21 genes

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950826

Superoxide dismutase activities of blood platelets in trisomy 21

14 November 2018

1 reference

12 December 2020

Trans-acting dosage effects on the expression of model gene systems in maize aneuploids

1 reference

12 December 2020

Natural variation in human gene expression assessed in lymphoblastoid cells

1 reference

12 December 2020

Transcriptome analysis of human autosomal trisomy

1 reference

12 December 2020

Identifiers

DOI

10.1086/520000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17701894%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

1 reference