(Q34676133)

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Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndrome

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Europe PubMed Central

PubMed publication ID

3 August 2017

Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndrome (English)

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3 August 2017

Michael Andrew Quail

17

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Michael A Quail

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3 August 2017

Olivia Sheppard

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Olivia Sheppard

10

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Tomas W Fitzgerald

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Tomas Fitzgerald

16

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Frances K Wiseman

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Frances K Wiseman

2

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Kai Rothkamm

19

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Elizabeth M. C. Fisher

21

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Elizabeth M C Fisher

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3 August 2017

4

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Elena Prigmore

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3 August 2017

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Susan M Gribble

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3 August 2017

Stephen Clayton

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3 August 2017

Elizabeth Langley

5

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3 August 2017

Fengtang Yang

6

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3 August 2017

Sean Maguire

7

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3 August 2017

Beiyuan Fu

8

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3 August 2017

Diana Rajan

9

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3 August 2017

Carol Scott

11

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3 August 2017

Heidi Hauser

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3 August 2017

Philip J Stephens

13

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3 August 2017

Lucy A Stebbings

14

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3 August 2017

Bee Ling Ng

15

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3 August 2017

Ruby Banerjee

18

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3 August 2017

Victor L J Tybulewicz

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3 August 2017

Nigel P Carter

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3 August 2017

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publication date

15 April 2013

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3 August 2017

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3 August 2017

8

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3 August 2017

4

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3 August 2017

e60482

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Europe PubMed Central

PubMed publication ID

3 August 2017

copyright license

Creative Commons Attribution 4.0 International

15 April 2013

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April 2022 Public Data File from Crossref

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Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Altered regulation of tau phosphorylation in a mouse model of down syndrome aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Perturbed hematopoiesis in the Tc1 mouse model of Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Heterogeneous nuclear ribonucleoprotein E3 modestly activates splicing of tau exon 10 via its proximal downstream intron, a hotspot for frontotemporal dementia mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Upregulation of three Drosophila homologs of human chromosome 21 genes alters synaptic function: implications for Down syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Complex human chromosomal and genomic rearrangements

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Down syndrome--recent progress and future prospects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Amplification-free Illumina sequencing-library preparation facilitates improved mapping and assembly of (G+C)-biased genomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

A large genome center's improvements to the Illumina sequencing system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Species-specific transcription in mice carrying human chromosome 21

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Epidemiology of Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Construction and use of spotted large-insert clone DNA microarrays for the detection of genomic copy number changes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Flow analysis and sorting of microchromosomes (<3 Mb).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

New techniques to understand chromosome dosage: mouse models of aneuploidy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Factors affecting flow karyotype resolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Human hair keratin-associated proteins (KAPs).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Biochemical mechanisms of chromosomal translocations resulting from DNA double-strand breaks

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Initial characterization of an uromodulin-like 1 gene on human chromosome 21q22.3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

RUNX1 and GATA-1 coexpression and cooperation in megakaryocytic differentiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Radiation-induced genomic rearrangements formed by nonhomologous end-joining of DNA double-strand breaks

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Computational method to predict mitochondrially imported proteins and their targeting sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Repair of x-ray-induced DNA double-strand breaks in specific Not I restriction fragments in human fibroblasts: joining of correct and incorrect ends

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Astrocytosis and axonal proliferation in the hippocampus of S100b transgenic mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Characterization of a newly derived human sarcoma cell line (HT-1080).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626651

7 July 2018

Modeling the monosomy for the telomeric part of human chromosome 21 reveals haploinsufficient genes modulating the inflammatory and airway responses

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0060482

21 January 2018

Duplication of the entire 22.9 Mb human chromosome 21 syntenic region on mouse chromosome 16 causes cardiovascular and gastrointestinal abnormalities.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0060482

21 January 2018

Chromosome specific paints from a high resolution flow karyotype of the mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/23596509

12 December 2020

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Alopecia areata

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https://pubmed.ncbi.nlm.nih.gov/23596509

12 December 2020

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10.1371/JOURNAL.PONE.0060482

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Europe PubMed Central

PubMed publication ID

3 August 2017

2013PLoSO...860482G

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Europe PubMed Central

PubMed publication ID

3 August 2017

PubMed publication ID

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Europe PubMed Central

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3 August 2017

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