Transcriptomic and protein expression analyses of skeletal muscles isolated from Ts1cje mouse model for Down syndrome

Down Syndrome (DS) is caused by an additional copy of human chromosome 21 (HSA21). It is characterised by several clinical phenotypes such as intellectual disability, facial features, early onset dementia, weak immune system and hypotonia. Deficits in motor functions happens throughout developme...

وصف كامل

التفاصيل البيبلوغرافية
المؤلف الرئيسي: Leong, Melody Pui Yee
التنسيق: أطروحة
اللغة:الإنجليزية
منشور في: 2017
الموضوعات:
Down Syndrome
Transcriptome
الوصول للمادة أونلاين:http://psasir.upm.edu.my/id/eprint/70541/1/FPSK%28M%29%202017%2051%20-%20IR.pdf

الانترنت

http://psasir.upm.edu.my/id/eprint/70541/1/FPSK%28M%29%202017%2051%20-%20IR.pdf

مواد مشابهة