(Q28191044)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11377958%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

review article

1 reference

title

Chromosome 21: from sequence to applications (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11377958%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

author

Stilianos Antonarakis

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11377958%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

author name string

S E Antonarakis

series ordinal

1

0 references

language of work or name

English

0 references

publication date

1 June 2001

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11377958%20AND%20SRC:MED&resulttype=core&format=json

Current Opinion in Genetics & Development

8 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11377958%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

volume

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11377958%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

issue

3

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11377958%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

page(s)

241-246

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11377958%20AND%20SRC:MED&resulttype=core&format=json

The DNA sequence of human chromosome 21

8 November 2019

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A genetic linkage map of 17 markers on human chromosome 21

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Continuum of overlapping clones spanning the entire human chromosome 21q.

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The DNA sequence of human chromosome 22

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7 January 2021

The sequence of human chromosome 21 and implications for research into Down syndrome

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7 January 2021

A physical map of 30,000 human genes

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

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7 January 2021

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

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7 January 2021

Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis

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7 January 2021

An SNP map of the human genome generated by reduced representation shotgun sequencing

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Single nucleotide polymorphisms and the future of genetic epidemiology

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A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes

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7 January 2021

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

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7 January 2021

Exploring the new world of the genome with DNA microarrays

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7 January 2021

Serial analysis of gene expression

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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

Mass spectrometry. From genomics to proteomics

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7 January 2021

Proteomics to study genes and genomes

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7 January 2021

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

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7 January 2021

Integration of cytogenetic landmarks into the draft sequence of the human genome

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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

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

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7 January 2021

Motor dysfunction in a mouse model for Down syndrome.

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7 January 2021

Impaired short- and long-term memory in Ts65Dn mice, a model for Down syndrome.

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7 January 2021

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

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7 January 2021

Genetic dissection of region associated with behavioral abnormalities in mouse models for Down syndrome

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7 January 2021

Engineering chromosomes in mice through targeted meiotic recombination (TAMERE)

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7 January 2021

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

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7 January 2021

Partial IFN-alpha/beta and IFN-gamma receptor knockout trisomy 16 mouse fetuses show improved growth and cultured neuron viability

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7 January 2021

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

Transgenic mice with increased Cu/Zn-superoxide dismutase activity: animal model of dosage effects in 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

The genome sequence of Drosophila melanogaster

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7 January 2021

Genome sequence of the nematode C. elegans: a platform for investigating biology

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7 January 2021

Functional genomic analysis of cell division in C. elegans using RNAi of genes on chromosome III

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7 January 2021

Functional genomic analysis of C. elegans chromosome I by systematic RNA interference

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7 January 2021

Large-scale analysis of the yeast genome by transposon tagging and gene disruption

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7 January 2021

Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)

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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

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia

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7 January 2021

Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome)

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7 January 2021

Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness

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7 January 2021

Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.

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7 January 2021

A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3.

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7 January 2021

Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels

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7 January 2021

Leukaemia and transient leukaemia in Down syndrome

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7 January 2021

Risks of leukaemia and solid tumours in individuals with Down's syndrome.

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7 January 2021

Searching for genetic determinants in the new millennium

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7 January 2021

How many diseases does it take to map a gene with SNPs?

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7 January 2021

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

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7 January 2021

10.1016/S0959-437X(00)00185-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11377958%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

1 reference