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

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

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

http://www.wikidata.org/entity/Q34676133

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Quantitative genetics of CTCF binding reveal local sequence effects and different modes of X-chromosome association Dissecting Alzheimer disease in Down syndrome using mouse models Down Syndrome Cognitive Phenotypes Modeled in Mice Trisomic for All HSA 21 Homologues Dosage of the Abcg1-U2af1 region modifies locomotor and cognitive deficits observed in the Tc1 mouse model of Down syndrome Obesity, starch digestion and amylase: association between copy number variants at human salivary (AMY1) and pancreatic (AMY2) amylase genes.Genome resilience and prevalence of segmental duplications following fast neutron irradiation of soybean.Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences.Successful transmission and transcriptional deployment of a human chromosome via mouse male meiosis Alterations to dendritic spine morphology, but not dendrite patterning, of cortical projection neurons in Tc1 and Ts1Rhr mouse models of Down syndrome Expansion of the HSFY gene family in pig lineages : HSFY expansion in suids Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells.The pig X and Y Chromosomes: structure, sequence, and evolution Tc1 mouse model of trisomy-21 dissociates properties of short- and long-term recognition memory.Genomic Alteration in Head and Neck Squamous Cell Carcinoma (HNSCC) Cell Lines Inferred from Karyotyping, Molecular Cytogenetics, and Array Comparative Genomic Hybridization.Involvement of Potassium and Cation Channels in Hippocampal Abnormalities of Embryonic Ts65Dn and Tc1 Trisomic Mice Fully-Automated μMRI Morphometric Phenotyping of the Tc1 Mouse Model of Down Syndrome.Successful Generation of Human Induced Pluripotent Stem Cell Lines from Blood Samples Held at Room Temperature for up to 48 hr.Genetic dissection of Down syndrome-associated congenital heart defects using a new mouse mapping panel.Protection of CpG islands from DNA methylation is DNA-encoded and evolutionarily conserved.Cognitive Impairment, Neuroimaging, and Alzheimer Neuropathology in Mouse Models of Down Syndrome.Evidence for evolutionary divergence of activity-dependent gene expression in developing neurons Changing Paradigms in Down Syndrome: The First International Conference of the Trisomy 21 Research Society.The impact of trisomy 21 on foetal haematopoiesis.Haematopoietic development and leukaemia in Down syndrome.Stem and progenitor cell dysfunction in human trisomies.Mouse models of Down syndrome: gene content and consequences.Mouse-based genetic modeling and analysis of Down syndrome.Revealing hidden complexities of genomic rearrangements generated with Cas9.Rodent models in Down syndrome research: impact and future opportunities.In vivo and ex vivo analyses of amyloid toxicity in the Tc1 mouse model of Down syndrome.Triplications of human chromosome 21 orthologous regions in mice result in expansion of megakaryocyte-erythroid progenitors and reduction of granulocyte-macrophage progenitors.Alcohol and endogenous aldehydes damage chromosomes and mutate stem cells.Recurrent Rearrangements of Human Amylase Genes Create Multiple Independent CNV Series.Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration.The Malaria-Protective Human Glycophorin Structural Variant DUP4 Shows Somatic Mosaicism and Association with Hemoglobin Levels

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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.

http://www.wikidata.org/entity/Q34676133

description

2013 nî lūn-bûn

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2013 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2013 թվականի ապրիլին հրատարակված գիտական հոդված

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2013年の論文

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Massively parallel sequencing ...... he Tc1 model of Down syndrome.

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Massively parallel sequencing ...... he Tc1 model of Down syndrome.

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Massively parallel sequencing ...... he Tc1 model of Down syndrome.

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Massively parallel sequencing ...... he Tc1 model of Down syndrome.

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Massively parallel sequencing ...... he Tc1 model of Down syndrome.

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Massively parallel sequencing ...... he Tc1 model of Down syndrome.

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Massively parallel sequencing ...... he Tc1 model of Down syndrome.

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Bee Ling Ng

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Beiyuan Fu

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Diana Rajan

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Elena Prigmore

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Fengtang Yang

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Heidi Hauser

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Lucy A Stebbings

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Nigel P Carter

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P2860

Species-specific transcription in mice carrying human chromosome 21

Astrocytosis and axonal proliferation in the hippocampus of S100b transgenic mice.

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

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

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

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

Computational method to predict mitochondrially imported proteins and their targeting sequences

RUNX1 and GATA-1 coexpression and cooperation in megakaryocytic differentiation.

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

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

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Elizabeth M. C. Fisher

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