dmd mouse - Axtarish в Google
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5 дней назад · Dystrophin deficiency in Dmd(mdx) mice impairs long-term, but not short-term, object recognition memory and impairs long-term spatial memory, ...
Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy.
Mdx mice show progressive cycles of skeletal muscle degeneration and regeneration that mimic human course of DMD, starting at approximately three weeks of age.
mdx mouse mdx mouse
Мышь mdx является популярной моделью для изучения мышечной дистрофии Дюшенна. Мышь mdx имеет точечную мутацию в гене DMD, изменяющую аминокислоту, кодирующую глутамин, на кодон STOP. Это заставляет мышечные клетки производить небольшой,... Википедия (Английский язык)
The mdx mouse is a popular model for studying Duchenne muscular dystrophy (DMD). The mdx mouse has a point mutation in its DMD gene, changing the amino acid ...
Mutations in this gene cause muscular dystrophy. Phenotypic variation has been observed in different backgrounds. Gene Ontology (GO)
In this section you can find previous SOPs on the mouse models in Duchenne muscular dystrophy. These have now been superseded with more recent research.
The X-linked muscular dystrophy (mdx) mouse model is used to study Duchenne muscular dystrophy. In this model, the dystrophin gene is truncated so the mouse ...
21 авг. 2020 г. · Duchenne muscular dystrophy (DMD) is an X-linked, lethal muscle degenerative disease caused by loss of dystrophin protein.
1 мая 2023 г. · These spontaneous Dmd mdx mutant mice do not express dystrophin and may be useful for studying Duchenne muscular dystrophy.
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