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A genome-scale DNA repair RNAi screen identifies SPG48 as a novel gene associated with hereditary spastic paraplegia.

机译：基因组规模的DNa修复RNai筛选将spG48鉴定为与遗传性痉挛性截瘫相关的新基因。

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Mikołaj Słabicki; Mirko Theis; Dragomir B Krastev; Sergey Samsonov; Emeline Mundwiller; Magno Junqueira; Maciej Paszkowski-Rogacz; Joan Teyra; Anne-Kristin Heninger; Ina Poser; Fabienne Prieur; Jérémy Truchetto; Christian Confavreux; Cécilia Marelli; Alexandra Durr; Jean Philippe Camdessanche; Alexis Brice; Andrej Shevchenko; M Teresa Pisabarro; Giovanni Stevanin; Frank Buchholz;
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1. A Genome-Scale DNA Repair RNAi Screen Identifies SPG48 as a Novel Gene Associated with Hereditary Spastic Paraplegia [J] . Miko?aj S?abicki, Mirko Theis, Dragomir B. Krastev, PLoS Biology . 2010,第6期

机译：基因组规模的DNA修复RNAi屏幕确定SPG48作为与遗传性痉挛性截瘫相关的新基因
2. Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia. [J] . Zhao X, Alvarado D, Rainier S, Nature Genetics . 2001,第3期

机译：新发现的GTPase基因突变导致常染色体显性遗传性痉挛性截瘫。
3. A genome-wide IR-induced RAD51 foci RNAi screen identifies CDC73 involved in chromatin remodeling for DNA repair [J] . Patrick Herr, Cecilia Lundin, Bastiaan Evers, Cell discovery. . 2015,第7期

机译：全基因组IR诱导的RAD51基因座RNAi筛选可鉴定参与染色质重塑以修复DNA的CDC73
4. Genome-scale RNA interference screen identifies key pathways and genes for improving recombinant protein production in mammalian cells [C] . Su Xiao, Yu Chi Chen, Eugene Buehler, Cell culture engineering XV . 2016

机译：基因组规模的RNA干扰筛选可识别关键途径和基因，以改善哺乳动物细胞中重组蛋白的产生
5. RNAi Screening of the Kinome Identifies PACT as a Novel Genetic Modifier of Foci Integrity in Myotonic Dystrophy type 1. [D] . O'Reilly, Sean. 2014

机译：RNAi筛查的基因组确定PACT是1型强直性营养不良中病灶完整性的新型遗传修饰因子。
6. A Genome-Scale DNA Repair RNAi Screen Identifies SPG48 as a Novel Gene Associated with Hereditary Spastic Paraplegia [O] . Mikołaj Słabicki, Mirko Theis, Dragomir B. Krastev, 2010

机译：基因组规模的DNA修复RNAi屏幕确定SPG48作为与遗传性痉挛性截瘫相关的新基因
7. A genome-scale DNA repair RNAi screen identifies SPG48 as a novel gene associated with hereditary spastic paraplegia. [O] . Słabicki, Mikołaj, Theis, Mirko, Krastev, Dragomir,, 2010

机译：基因组规模的DNA修复RNAi筛选将SPG48识别为与遗传性痉挛性截瘫相关的新基因。

A genome-scale DNA repair RNAi screen identifies SPG48 as a novel gene associated with hereditary spastic paraplegia.

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