Related references
Note: Only part of the references are listed.Down syndrome
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AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY (2011)
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Specific targeting of the GABA-A receptor α5 subtype by a selective inverse agonist restores cognitive deficits in Down syndrome mice
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Comprehensive behavioral phenotyping of Ts65Dn mouse model of Down Syndrome: Activation of pradrenergic receptor by xamoterol as a potential cognitive enhancer
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Down's syndrome-like cardiac developmental defects in embryos of the transchromosomic Tc1 mouse
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Enlarged Brain Ventricles and Impaired Neurogenesis in the Ts1Cje and Ts2Cje Mouse Models of Down Syndrome
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A mouse model of Down syndrome trisomic for all human chromosome 21 syntenic regions
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Increased male reproductive success in Ts65Dn Down syndrome mice
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Gabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: A potential model of autism spectrum disorder
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Characterization of the cardiac phenotype in neonatal Ts65Dn mice
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Genomic instability within centromeres of interspecific marsupial hybrids
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APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy
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Understanding the basis for Down syndrome phenotypes
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An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes
A O'Doherty et al.
SCIENCE (2005)
Hippocampal long-term potentiation suppressed by increased inhibition in the Ts65Dn mouse, a genetic model of Down syndrome
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Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes
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Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions
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Hippocampal cytotoxic lesion effects on species-typical behaviours in mice
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Mice containing a human chromosome 21 model behavioral impairment and cardiac anomalies of Down's syndrome
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J Inoue et al.
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The DNA sequence of human chromosome 21
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Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse
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Stability of transferred human chromosome fragments in cultured cells and in mice
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