Identification of a MIP mutation that activates a cryptic acceptor splice site in the 3′ untranslated region

Chongfei JinJin JiangWei WangKe Yao

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Identification of a MIP mutation that activates a cryptic acceptor splice site in the 3′ untranslated region

机译：识别激活3'非翻译区中隐性受体剪接位点的MIP突变

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《Molecular vision》 |2010年第2010期|共页
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Chongfei JinJin JiangWei WangKe Yao;
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中图分类生物化学;
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1. Identification of a MIP mutation that activates a cryptic acceptor splice site in the 3′ untranslated region [J] . Jiang Jin, Jin Chongfei, Wang Wei, Molecular vision . 2010,第2010期

机译：识别激活3'非翻译区中隐性受体剪接位点的MIP突变
2. Complete androgen insensitivity syndrome caused by c.1769-1G??C mutation and activation of a cryptic splice acceptor site in the androgen receptor gene [J] . Song Wang, Peng Xia, Nicholas A. Cacalano, Steroids: An International Journal . 2018,第期

机译：由C.1769-1G引起的完全雄激素不敏感综合征？＆αc突变和激活雄激素受体基因中的隐秘接头受体位点
3. Novel cryptic splice acceptor site activating mutation in the LAMB3 gene with founder effect causes serial Herlitz-type junctional epidermolysis bullosa [J] . Mayer B., Sillo P., Mazan M., The Journal of investigative dermatology. . 2014,第Suppla2期

机译：具有创建者作用的LAMB3基因中的新型隐性剪接受体位点激活突变导致系列Herlitz型连接性表皮松解大疱
4. Predicting Human Acceptor Splice Site Regions using Text Distance Methods [C] . Cristian G. Zimbru, Nicoleta Andreescu, Adela Chirita-Emandi, E-Health and Bioengineering Conference . 2020

机译：使用文本距离方法预测人类受体剪接部位区域
5. Diverse mechanisms of human genetic disease: Splice order determination in the COL1A2 gene. Effects that influence splice site mutations in osteogenesis imperfecta and a translocation disrupting SNRPN gene causes Prader-Willi syndrome. [D] . Kuslich, Christine D. 1999

机译：人类遗传疾病的多种机制：COL1A2基因的剪接顺序确定。影响成骨不全症中剪接位点突变和易位破坏SNRPN基因的效应会导致Prader-Willi综合征。
6. Identification of a MIP mutation that activates a cryptic acceptor splice site in the 3′ untranslated region [O] . Chongfei Jin, Jin Jiang, Wei Wang, 2010

机译：鉴定激活3非翻译区中隐性受体剪接位点的MIP突变
7. Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bβ-chain gene causing activation of cryptic splice sites [O] . Silvia Spena, Stefano Duga, Rosanna Asselta, 2002

机译：先天性阿博因素血症：首先鉴定纤维蛋白原Bβ链基因的剪接突变，导致隐秘剪接位点的激活

Identification of a MIP mutation that activates a cryptic acceptor splice site in the 3′ untranslated region

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