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8篇 您的检索式：作者名="Simon Shaw"

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		题名	作者	年代	出处	被引量
	1	Endovascular Treatment of Visceral Aneurysms Associated with Pancreatitis and a Suggested Classification with Therapeutic Implications显示文摘	Anthony A. Nicholson Jai Patel Simon McPherson David R. Shaw David Kessel	2006	Journal of Vascular and Interventional Radiology2006，，8：	1
	2	Pathogen evolution and disease emergence in carnivores显示文摘	McCarthy Alex J Shaw Marie-Anne Goodman Simon J	2007	Proceedings of The Royal Society B2007，，1629：	1
	3	Comparison of microfluidic digital PCR and conventional quantitative PCR for measuring copy number variation显示文摘	Alexandra S. Whale Jim F. Huggett Simon Cowen Valerie Speirs Jacqui Shaw Stephen Ellison Carole A. Foy Daniel J. Scott	2012	Nucleic Acids Research2012，，11：	1
	4	Chess Playing Programs and the Pruning显示文摘	Newell A Shaw J Simon H		0，，：	1
	5	Presence and severity of non-alcoholic fatty liver disease in a large prospective primary care cohort显示文摘	Matthew J. Armstrong Diarmaid D. Houlihan Louise Bentham Jean C. Shaw Robert Cramb Simon Olliff Paramjit S. Gill James M. Neuberger Richard J. Lilford Philip N. Newsome	2011	Journal of Hepatology2011，，1：	1
	6	A study on the rate of degradation of the bioabsorbable polymer polyglycolic acid ( PGA ) 显示文摘	SIMON Shawe FRASER Buchanan DAVID Farrar	2006	Material Science2006，41，15：	1
	7	Is Foxglove Effective in Heart Failure?显示文摘	Parminder S Chaggar Steven M Shaw Simon G Williams	2015	Cardiovasc Ther2015，，4：	1
	8	Designing sgRNAs for CRISPR-BEST base editing applications with CRISPyweb 2.0显示文摘CRISPR/Cas9 systems are an established tool in genome engineering.As double strand breaks caused by the standard Cas9-based knock-out techniques can be problematic in some organisms,new systems were developed that can efficiently create knock-outs without causing double strand breaks to elegantly sidestep these issues.The recently published CRISPR-BEST base editor system for actinobacteria is built around a C to T or A to G base exchange.These base editing systems however require additional constraints to be considered for designing the sgRNAs.Here,we present an updated version of the interactive CRISPy-web single guide RNA design tool http://gffzz2b22c00a04674870s5npbwxp5pn506upq.ffgz.tsg.suse.edu.cn/that was built to support“classical”CRISPR and now also CRISPRBEST workflows.	Kai Blin Simon Shaw Yaojun Tong Tilmann Weber	2020	Synthetic and Systems Biotechnology2020，5，2：	0

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