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Fragile X protein family member FXR1P is regulated by microRNAs

FXR1P is one of two autosomal paralogs of the fragile X mental retardation protein FMRP. The absence of FMRP causes fragile X syndrome, the leading cause of hereditary mental retardation. FXR1P plays an important role in normal muscle development and has been implicated in facioscapulohumeral muscul...

詳細記述

保存先:
書誌詳細
主要な著者: Cheever, Anne, Blackwell, Ernest, Ceman, Stephanie
フォーマット: Artigo
言語:Inglês
出版事項: Cold Spring Harbor Laboratory Press 2010
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2905753/
https://ncbi.nlm.nih.gov/pubmed/20519410
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1261/rna.2022210
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