Down syndrome is caused by trisomy of chromosome 21. To date, a multiplicity of mouse models with Down-syndrome-related features has been developed to understand this complex human chromosomal disorder. These mouse models have been important for determining genotype-phenotype relationships and identification of dosage-sensitive genes involved in the pathophysiology of the condition, and in exploring the impact of the additional chromosome on the whole genome. Mouse models of Down syndrome have also been used to test therapeutic strategies. Here, we provide an overview of research in the last 15 years dedicated to the development and application of rodent models for Down syndrome. We also speculate on possible and probable future directions ...
Intellectual disabilities, hypotonia and cranio-facial dysmorphism are the cardinal characteristics ...
Down syndrome (DS) is a genetic complex condition which is collection of physical, mental and functi...
Down syndrome (DS) is caused by trisomy of chromosome 21 (Hsa21) and presents a complex phenotype th...
Down syndrome is caused by trisomy of chromosome 21. To date, a multiplicity of mouse models with Do...
IntroductionDown syndrome (DS), caused by human trisomy 21 (Ts21), can be considered as a prototypic...
Down syndrome, also referred to as trisomy 21, is a chromosomal abnormality in which the 21st human ...
International audienceThe genotype-phenotype relationship and the physiopathology of Down Syndrome (...
Down syndrome (DS) is mainly caused by the presence of an extra copy of human chromosome 21 (Hsa21) ...
Down syndrome (DS) is the most common genetic cause of mental disability. Based on the homology of H...
Mice trisomic for Chromosome (Chr) 16 have been used extensively as an animal model for human Down S...
Aneuploidies are common chromosomal defects that result in growth and developmental deficits and hig...
Down syndrome is the most common genetic cause of intellectual disability worldwide and affects more...
With an incidence of approximately 1 in 700 live births, Down syndrome (DS) remains the most common ...
Down syndrome (DS), trisomy for chromosome 21, is the most common genetic cause of intellectual disa...
<div><p>Down syndrome (DS), trisomy for chromosome 21, is the most common genetic cause of intellect...
Intellectual disabilities, hypotonia and cranio-facial dysmorphism are the cardinal characteristics ...
Down syndrome (DS) is a genetic complex condition which is collection of physical, mental and functi...
Down syndrome (DS) is caused by trisomy of chromosome 21 (Hsa21) and presents a complex phenotype th...
Down syndrome is caused by trisomy of chromosome 21. To date, a multiplicity of mouse models with Do...
IntroductionDown syndrome (DS), caused by human trisomy 21 (Ts21), can be considered as a prototypic...
Down syndrome, also referred to as trisomy 21, is a chromosomal abnormality in which the 21st human ...
International audienceThe genotype-phenotype relationship and the physiopathology of Down Syndrome (...
Down syndrome (DS) is mainly caused by the presence of an extra copy of human chromosome 21 (Hsa21) ...
Down syndrome (DS) is the most common genetic cause of mental disability. Based on the homology of H...
Mice trisomic for Chromosome (Chr) 16 have been used extensively as an animal model for human Down S...
Aneuploidies are common chromosomal defects that result in growth and developmental deficits and hig...
Down syndrome is the most common genetic cause of intellectual disability worldwide and affects more...
With an incidence of approximately 1 in 700 live births, Down syndrome (DS) remains the most common ...
Down syndrome (DS), trisomy for chromosome 21, is the most common genetic cause of intellectual disa...
<div><p>Down syndrome (DS), trisomy for chromosome 21, is the most common genetic cause of intellect...
Intellectual disabilities, hypotonia and cranio-facial dysmorphism are the cardinal characteristics ...
Down syndrome (DS) is a genetic complex condition which is collection of physical, mental and functi...
Down syndrome (DS) is caused by trisomy of chromosome 21 (Hsa21) and presents a complex phenotype th...