Selective cleavage of AChR cRNAs harbouring mutations underlying the slow channel myasthenic syndrome by hammerhead ribozymes

Amr Abdelgany John Ealing Matthew Wood and David Beeson*

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Selective cleavage of AChR cRNAs harbouring mutations underlying the slow channel myasthenic syndrome by hammerhead ribozymes

机译：锤头状核酶对具有慢通道肌无力综合症基础突变的AChR cRNA的选择性切割

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《Journal of RNA i and Gene Silencing》 |2005年第2005期|共页
作者
Amr Abdelgany John Ealing Matthew Wood and David Beeson*;
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中图分类遗传学;
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入库时间 2022-08-18 17:10:22

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1. A new mouse model for the slow-channel congenital myasthenic syndrome induced by the AChR εL221F mutation [J] . ChevessierF., PeterC., MersdorfU., Neurobiology of disease . 2012,第3期

机译：AChRεL221F突变诱发慢通道先天性肌无力综合征的新小鼠模型
2. Mutations in congenital myasthenic syndromes reveal an varepsilon subunit C-terminal cysteine, C470, crucial for maturation and surface expression of adult AChR. [J] . Ealing J, Brownlow S, Oosterhuis H, Human Molecular Genetics . 2002,第24期

机译：先天性肌无力综合症的突变显示了缬草酸亚基C末端半胱氨酸C470，对成人AChR的成熟和表面表达至关重要。
3. A kinetic and thermodynamic analysis of cleavage site mutations in the hammerhead ribozyme. [J] . Baidya N, Uhlenbeck OC Biochemistry . 1997,第5期

机译：锤头核酶裂解位点突变的动力学和热力学分析。
4. Identification of DPAGT1 as a new gene in which mutations cause a congenital myasthenic syndrome [C] . Katsiaryna Belaya, Sarah Finlayson, Judith Cossins, International Conference on Myasthenia Gravis and Related Disorders . 2012

机译：鉴定DPAGT1作为突变引起先天性染发素综合征的新基因
5. Functional analysis of hERG potassium channels and mutations underlying the Long QT Syndrome. [D] . Saenen, Johan B. 2007

机译：hERG钾通道和长QT综合征基础突变的功能分析。
6. Selective cleavage of AChR cRNAs harbouring mutations underlying the slow channel myasthenic syndrome by hammerhead ribozymes [O] . Amr Abdelgany, John Ealing, Matthew Wood, 2005

机译：锤头状核酶对具有慢通道肌无力综合症基础突变的AChR cRNA的选择性切割
7. New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome [O] . A. Engel 1996

机译：乙酰胆碱受体亚基基因的新突变揭示了慢速通道先天性敏感综合征中的异质性

Selective cleavage of AChR cRNAs harbouring mutations underlying the slow channel myasthenic syndrome by hammerhead ribozymes

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