Project supported by the National Natural Science Foundation of China (Grant No. 39625007) and the China Medical Board. USA (Grant No. 95-617).
To study the time- and tissue-specificity of alternative splicing of the FMRl gene, we analyzed the alternative splicing pattern of the FMRl gene in human tissues from adult and fetus using RT-PCR coupled with capilla...
Project supported by the National Natural Science Foundation of China (Grant No. 39625007) and the Trans-Centary Training Program Foundation of the State Education Commission.
Fragile X syndrome can be caused by lack of expression of the FMRl gene, which encodes an RNA binding protein. Extensive alternative splicing of the FMRl gene has been observed in human and mice. Five regions of the F...