Coiled bodies and gems: Janus or gemini?
作者信息
Matera A G, Frey M R
机构信息
Department of Genetics, Center for Human Genetics, Center for RNA Molecular Biology and Program in Cell Biology, Case Western Reserve University School of Medicine, Cleveland, OH 44106-4955, USA.
出版信息
Am J Hum Genet. 1998 Aug;63(2):317-21. doi: 10.1086/301992.
Abstract
摘要
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本文引用的文献
1
Of coiled bodies, gems, and salmon.关于螺旋小体、宝石和鲑鱼。
J Cell Biochem. 1998 Aug 1;70(2):181-92.
2
Heterogeneity of subcellular localization and electrophoretic mobility of survival motor neuron (SMN) protein in mammalian neural cells and tissues.哺乳动物神经细胞和组织中存活运动神经元（SMN）蛋白的亚细胞定位和电泳迁移率的异质性。
Proc Natl Acad Sci U S A. 1998 May 26;95(11):6492-7. doi: 10.1073/pnas.95.11.6492.
3
SMN oligomerization defect correlates with spinal muscular atrophy severity.SMN寡聚化缺陷与脊髓性肌萎缩症的严重程度相关。
Nat Genet. 1998 May;19(1):63-6. doi: 10.1038/ng0598-63.
4
Coiled bodies and U2 snRNA genes adjacent to coiled bodies are enriched in factors required for snRNA transcription.螺旋体以及与螺旋体相邻的U2小核RNA基因富含小核RNA转录所需的因子。
Mol Biol Cell. 1998 May;9(5):1025-36. doi: 10.1091/mbc.9.5.1025.
5
Structure and function in the nucleus.细胞核的结构与功能
Science. 1998 Apr 24;280(5363):547-53. doi: 10.1126/science.280.5363.547.
6
Human genes encoding U3 snRNA associate with coiled bodies in interphase cells and are clustered on chromosome 17p11.2 in a complex inverted repeat structure.编码U3小核仁RNA的人类基因在间期细胞中与卷曲小体相关联，并且以复杂的反向重复结构聚集在17号染色体的11.2区带上。
Nucleic Acids Res. 1997 Dec 1;25(23):4740-7. doi: 10.1093/nar/25.23.4740.
7
Spinal muscular atrophy.脊髓性肌萎缩症
Curr Opin Neurol. 1997 Oct;10(5):381-5. doi: 10.1097/00019052-199710000-00005.
8
The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis.SMN-SIP1复合物在剪接体小核核糖核蛋白（snRNP）生物合成中起关键作用。
Cell. 1997 Sep 19;90(6):1023-9. doi: 10.1016/s0092-8674(00)80368-2.
9
The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins.脊髓性肌萎缩症疾病基因产物SMN及其相关蛋白SIP1与剪接体snRNP蛋白形成复合物。
Cell. 1997 Sep 19;90(6):1013-21. doi: 10.1016/s0092-8674(00)80367-0.
10
Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos.存活运动神经元基因是人类脊髓性肌萎缩症的一个候选基因，该基因的失活会导致小鼠早期胚胎出现大量细胞死亡。
Proc Natl Acad Sci U S A. 1997 Sep 2;94(18):9920-5. doi: 10.1073/pnas.94.18.9920.
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