Mice trisomic for Chromosome (Chr) 16 have been used extensively as an animal model for human Down Syndrome (Trisomy 21). This system has drawbacks, however: trisomy for all of Chr 16 is incompatible with postnatal survival and produces trisomy for many more genes than those conserved in human Chr 21. We report here the development and preliminary characterization of mice that are trisomic for only the segment of mouse Chr 16 that is conserved in human Chr 21. While these segmentally trisomic mice, Ts(17(16)) 65Dn, do not appear to have all the features characteristic of Down Syndrome, they represent a mouse model that survives to adulthood and may be useful to study features of Down Syndrome that develop later in life, such as sus...
Human trisomy 21, which results in Down syndrome (DS), is one of the most complicated congenital gen...
Human trisomy 21, which results in Down syndrome (DS), is one of the most complicated congenital gen...
Intellectual disabilities, hypotonia and cranio-facial dysmorphism are the cardinal characteristics ...
International audienceWe hypothesize that the trisomy 21 (Down syndrome) is the additive and interac...
Fluorescent in situ hybridization (FISH) -- using mouse chromosome paints, probes for the mouse majo...
Down syndrome is caused by trisomy of chromosome 21. To date, a multiplicity of mouse models with Do...
Down syndrome is caused by trisomy of chromosome 21. To date, a multiplicity of mouse models with Do...
Down syndrome, also referred to as trisomy 21, is a chromosomal abnormality in which the 21st human ...
Trisomy 21 or Down syndrome (DS) is the most frequent genetic cause of mental retardation, affecting...
Down syndrome results from triplication of human chromosome 21. The distal end of mouse chromosome 1...
Aneuploidies are common chromosomal defects that result in growth and developmental deficits and hig...
IntroductionDown syndrome (DS), caused by human trisomy 21 (Ts21), can be considered as a prototypic...
With an incidence of approximately 1 in 700 live births, Down syndrome (DS) remains the most common ...
Ts65Dn is a mouse model of Down syndrome: a syndrome that results from chromosome (Chr) 21 trisomy a...
Down syndrome (DS) is mainly caused by the presence of an extra copy of human chromosome 21 (Hsa21) ...
Human trisomy 21, which results in Down syndrome (DS), is one of the most complicated congenital gen...
Human trisomy 21, which results in Down syndrome (DS), is one of the most complicated congenital gen...
Intellectual disabilities, hypotonia and cranio-facial dysmorphism are the cardinal characteristics ...
International audienceWe hypothesize that the trisomy 21 (Down syndrome) is the additive and interac...
Fluorescent in situ hybridization (FISH) -- using mouse chromosome paints, probes for the mouse majo...
Down syndrome is caused by trisomy of chromosome 21. To date, a multiplicity of mouse models with Do...
Down syndrome is caused by trisomy of chromosome 21. To date, a multiplicity of mouse models with Do...
Down syndrome, also referred to as trisomy 21, is a chromosomal abnormality in which the 21st human ...
Trisomy 21 or Down syndrome (DS) is the most frequent genetic cause of mental retardation, affecting...
Down syndrome results from triplication of human chromosome 21. The distal end of mouse chromosome 1...
Aneuploidies are common chromosomal defects that result in growth and developmental deficits and hig...
IntroductionDown syndrome (DS), caused by human trisomy 21 (Ts21), can be considered as a prototypic...
With an incidence of approximately 1 in 700 live births, Down syndrome (DS) remains the most common ...
Ts65Dn is a mouse model of Down syndrome: a syndrome that results from chromosome (Chr) 21 trisomy a...
Down syndrome (DS) is mainly caused by the presence of an extra copy of human chromosome 21 (Hsa21) ...
Human trisomy 21, which results in Down syndrome (DS), is one of the most complicated congenital gen...
Human trisomy 21, which results in Down syndrome (DS), is one of the most complicated congenital gen...
Intellectual disabilities, hypotonia and cranio-facial dysmorphism are the cardinal characteristics ...