Abstract Chronic otitis media (OM) is common in Down syndrome (DS), but underlying aetiology is unclear. We analysed the entire available mouse resource of partial trisomy models of DS looking for histological evidence of chronic middle-ear inflammation. We found a highly penetrant OM in the Dp(16)1Yey mouse, which carries a complete trisomy of MMU16. No OM was found in the Dp(17)1Yey mouse or the Dp(10)1Yey mouse, suggesting disease loci are located only on MMU16. The Ts1Cje, Ts1RhR, Ts2Yah, and Ts65Dn trisomies and the transc-homosomic Tc1 mouse did not develop OM. On the basis of these findings, we propose a two-locus model for chronic middle-ear inflammation in DS, based upon epistasis of the regions of HSA21 not in trisomy in the Tc1 m...
poster abstractDown syndrome (DS) is caused by a nondisjunction event called Trisomy 21 and is known...
International audienceWe hypothesize that the trisomy 21 (Down syndrome) is the additive and interac...
Down syndrome is the most common genetic cause of intellectual disability worldwide and affects more...
Chronic otitis media (OM) is an archetypal complex disease, which is particularly prevalent in child...
Down syndrome is one of the most common congenital disorders leading to a wide range of health probl...
Down syndrome is one of the most common congenital disorders leading to a wide range of health probl...
Surveying the Down syndrome mouse model resource identifies critical regions responsible for chronic...
Intellectual disabilities, hypotonia and cranio-facial dysmorphism are the cardinal characteristics ...
Background Down's syndrome (DS), or trisomy 21, is a complex developmental disorder that exhibits ma...
Trisomy 21 occurs in approximately 1 out of 750 live births and causes brachycephaly, a small oral c...
Down syndrome (DS) is the result of trisomy of human chromosome 21 (Hsa 21) and occurs in approximat...
Down syndrome, also referred to as trisomy 21, is a chromosomal abnormality in which the 21st human ...
Down syndrome (DS) is a genetic pathology due to the triplication of human chromosome 21. In additio...
Otitis media (OM) is a common cause of childhood hearing loss. The large medical costs involved in t...
Otitis media (OM) is a common cause of childhood hearing loss. The large medical costs involved in t...
poster abstractDown syndrome (DS) is caused by a nondisjunction event called Trisomy 21 and is known...
International audienceWe hypothesize that the trisomy 21 (Down syndrome) is the additive and interac...
Down syndrome is the most common genetic cause of intellectual disability worldwide and affects more...
Chronic otitis media (OM) is an archetypal complex disease, which is particularly prevalent in child...
Down syndrome is one of the most common congenital disorders leading to a wide range of health probl...
Down syndrome is one of the most common congenital disorders leading to a wide range of health probl...
Surveying the Down syndrome mouse model resource identifies critical regions responsible for chronic...
Intellectual disabilities, hypotonia and cranio-facial dysmorphism are the cardinal characteristics ...
Background Down's syndrome (DS), or trisomy 21, is a complex developmental disorder that exhibits ma...
Trisomy 21 occurs in approximately 1 out of 750 live births and causes brachycephaly, a small oral c...
Down syndrome (DS) is the result of trisomy of human chromosome 21 (Hsa 21) and occurs in approximat...
Down syndrome, also referred to as trisomy 21, is a chromosomal abnormality in which the 21st human ...
Down syndrome (DS) is a genetic pathology due to the triplication of human chromosome 21. In additio...
Otitis media (OM) is a common cause of childhood hearing loss. The large medical costs involved in t...
Otitis media (OM) is a common cause of childhood hearing loss. The large medical costs involved in t...
poster abstractDown syndrome (DS) is caused by a nondisjunction event called Trisomy 21 and is known...
International audienceWe hypothesize that the trisomy 21 (Down syndrome) is the additive and interac...
Down syndrome is the most common genetic cause of intellectual disability worldwide and affects more...