Isolation of an FMRP-Associated Messenger Ribonucleoprotein Particle and Identification of Nucleolin and the Fragile X-Related Proteins as Components of the Complex

The loss of FMR1 expression due to trinucleotide repeat expansion leads to fragile X syndrome, a cause of mental retardation. The encoded protein, FMRP, is a member of a gene family that also contains the fragile X-related proteins, FXR1P and FXR2P. FMRP has been shown to be a nucleocytoplasmic shut...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Ceman, Stephanie, Brown, Victoria, Warren, Stephen T.
التنسيق: Artigo
اللغة:Inglês
منشور في: American Society for Microbiology 1999
الموضوعات:
Gene Expression
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC84877/
https://ncbi.nlm.nih.gov/pubmed/10567518
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