Jornal da Síndrome de Down e Anormalidades Cromossômicas

Jornal da Síndrome de Down e Anormalidades Cromossômicas
Acesso livre

ISSN: 2472-1115

Abstrato

Mouse Models and Human Non-disjunction in Down Syndrome

Khue Vu Nguyen

Ttrisomy of human chromosome 21 (Hsa21) and Down syndrome (DS) is challenging to model in mice. Hsa21 (Orthologs) genes map to segments called Mmu16, Mmu17, and Mmu10. For DS Ts65Dn was the first viable segmental trisomy mouse model and it is a partial trisomy currently popular in preclinical evaluations of drugs for cognition in DS. Ts65Dn a limitations are as follows: (i) it is trisomic for 125 human protein-coding orthologs, but only 90 of these are Hsa21 orthologs (ii) it lacks trisomy for ~75 Hsa21 orthologs.

Isenção de responsabilidade: Este resumo foi traduzido com recurso a ferramentas de inteligência artificial e ainda não foi revisto ou verificado.
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