Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5743
pubmed:dateCreated
2005-9-23
pubmed:abstractText
Aneuploidies are common chromosomal defects that result in growth and developmental deficits and high levels of lethality in humans. To gain insight into the biology of aneuploidies, we manipulated mouse embryonic stem cells and generated a trans-species aneuploid mouse line that stably transmits a freely segregating, almost complete human chromosome 21 (Hsa21). This "transchromosomic" mouse line, Tc1, is a model of trisomy 21, which manifests as Down syndrome (DS) in humans, and has phenotypic alterations in behavior, synaptic plasticity, cerebellar neuronal number, heart development, and mandible size that relate to human DS. Transchromosomic mouse lines such as Tc1 may represent useful genetic tools for dissecting other human aneuploidies.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/16179473-10196383, http://linkedlifedata.com/resource/pubmed/commentcorrection/16179473-11283700, http://linkedlifedata.com/resource/pubmed/commentcorrection/16179473-11371509, http://linkedlifedata.com/resource/pubmed/commentcorrection/16179473-15096951, http://linkedlifedata.com/resource/pubmed/commentcorrection/16179473-15183168, http://linkedlifedata.com/resource/pubmed/commentcorrection/16179473-15371516, http://linkedlifedata.com/resource/pubmed/commentcorrection/16179473-15499000, http://linkedlifedata.com/resource/pubmed/commentcorrection/16179473-15499018, http://linkedlifedata.com/resource/pubmed/commentcorrection/16179473-16179439, http://linkedlifedata.com/resource/pubmed/commentcorrection/16179473-2881207, http://linkedlifedata.com/resource/pubmed/commentcorrection/16179473-8421494, http://linkedlifedata.com/resource/pubmed/commentcorrection/16179473-9517425
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1095-9203
pubmed:author
pubmed:issnType
Electronic
pubmed:day
23
pubmed:volume
309
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2033-7
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:16179473-Aneuploidy, pubmed-meshheading:16179473-Animals, pubmed-meshheading:16179473-Behavior, Animal, pubmed-meshheading:16179473-Brain, pubmed-meshheading:16179473-Cell Count, pubmed-meshheading:16179473-Cell Line, pubmed-meshheading:16179473-Chimera, pubmed-meshheading:16179473-Chromosomes, Human, Pair 21, pubmed-meshheading:16179473-Disease Models, Animal, pubmed-meshheading:16179473-Down Syndrome, pubmed-meshheading:16179473-Embryo, Mammalian, pubmed-meshheading:16179473-Facial Bones, pubmed-meshheading:16179473-Female, pubmed-meshheading:16179473-Gene Expression, pubmed-meshheading:16179473-Genetic Engineering, pubmed-meshheading:16179473-Genetic Markers, pubmed-meshheading:16179473-Heart Defects, Congenital, pubmed-meshheading:16179473-Hippocampus, pubmed-meshheading:16179473-Humans, pubmed-meshheading:16179473-Long-Term Potentiation, pubmed-meshheading:16179473-Lymphocyte Activation, pubmed-meshheading:16179473-Male, pubmed-meshheading:16179473-Maze Learning, pubmed-meshheading:16179473-Memory, pubmed-meshheading:16179473-Mice, pubmed-meshheading:16179473-Mice, Inbred Strains, pubmed-meshheading:16179473-Mice, Transgenic, pubmed-meshheading:16179473-Neurons, pubmed-meshheading:16179473-Oligonucleotide Array Sequence Analysis, pubmed-meshheading:16179473-Phenotype, pubmed-meshheading:16179473-Skull, pubmed-meshheading:16179473-Stem Cells, pubmed-meshheading:16179473-Synaptic Transmission, pubmed-meshheading:16179473-T-Lymphocytes
pubmed:year
2005
pubmed:articleTitle
An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes.
pubmed:affiliation
Department of Neurodegenerative Disease, Institute of Neurology, Queen Square, London WC1N 3BG, UK.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't