The spinal muscular atrophy protein SMN affects Drosophila germline nuclear organization through the U body-P body pathway.
Survival motor neuron protein (SMN) is the determining factor for the human neurodegenerative disease spinal muscular atrophy (SMA). SMN is critical for small nuclear ribonucleoprotein (snRNP) assembly. Using Drosophila oogenesis as a model system, we show that mutations in smn cause abnormal nuclea...
主要な著者: | Lee, L, Davies, SE, Liu, J |
---|---|
フォーマット: | Journal article |
言語: | English |
出版事項: |
2009
|
類似資料
-
Therapeutic strategies for spinal muscular atrophy: SMN and beyond
著者:: Bowerman, M, 等
出版事項: (2017) -
Therapeutic strategies for spinal muscular atrophy: SMN and beyond
著者:: Bowerman, M, 等
出版事項: (2017) -
SMN post-translational modifications in spinal muscular atrophy
著者:: Giulietta M. Riboldi, 等
出版事項: (2023-02-01) -
Therapeutic strategies for spinal muscular atrophy: SMN and beyond
著者:: Melissa Bowerman, 等
出版事項: (2017-08-01) -
Spinal muscular atrophy in Venezuela: quantitative analysis of SMN1 and SMN2 genes
著者:: Yuri Yépez, 等
出版事項: (2020-06-01)