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5篇 您的检索式：作者名="Keyur R. Patel"

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		题名	作者	年代	出处	被引量
	1	Clinical Validation of a Next-Generation Sequencing Screen for Mutational Hotspots in 46 Cancer-Related Genes显示文摘	Rajesh R. Singh Keyur P. Patel Mark J. Routbort Neelima Reddy Bedia Barkoh Brian Handal Rashmi Kanagal-Shamanna Wesley O. Greaves L. Jeffrey Medeiros Kenneth Aldape Rajyalakshmi Luthra	2013	The Journal of Molecular Diagnostics2013，，：	1
	2	Using Capsule Endoscopy to Identify GI Tract Lesions in Cirrhotic Patients With Portal Hypertension and Chronic Anemia显示文摘	Karen R. Canlas Brian M. Dobozi Sauyu Lin Alastair D. Smith Don C. Rockey Andrew J. Muir Naurang M. Agrawal Martin H. Poleski Keyur Patel John G. McHutchison	2008	Journal of Clinical Gastroenterology2008，，7：	1
	3	Steatosis Is an Independent Predictor of Relapse Following Rapid Virologic Response in Patients With HCV Genotype 3显示文摘	Samir R. Shah Keyur Patel Patrick Marcellin Graham R. Foster Michael Manns Shyam Kottilil Letha Healey Erik Pulkstenis G. Mani Subramanian John G. McHutchison Mark S. Sulkowski Stefan Zeuzem David R. Nelson	2011	Clinical Gastroenterology and Hepatology2011，，8：	1
	4	TET2 mutations, myelodysplastic features, and a distinct immunoprofile characterize blastic plasmacytoid dendritic cell neoplasm in the bone marrow显示文摘	Khaled Alayed Keyur P. Patel Sergej Konoplev Rajesh R. Singh Mark J. Routbort Neelima Reddy Naveen Pemmaraju Liping Zhang Abdulaziz Al Shaikh Tariq N. Aladily Nitin Jain Rajyalakshmi Luthra L. Jeffrey Medeiros Joseph D. Khoury	2013	Hematol2013，，12：	1
	5	Simultaneous analysis of allopurinol and oxypurinol using a validated liquid chromatography–tandem mass spectrometry method in human plasma显示文摘The present study describes a simple, reliable and reproducible liquid chromatography–tandem mass spectrometry method(LC–MS/MS) for the simultaneous determination of allopurinol and its active metabolite,oxypurinol in human plasma for a pharmacokinetic/bioequivalence study. After protein precipitation(PPT) of100 μL plasma sample with 1.0% formic acid in acetonitrile, the recovery of the analytes and allopurinol-d2 as an internal standard ranged from 85.36% to 91.20%. The analytes were separated on Hypersil Gold(150 mm×4.6 mm, 5 μm) column using 0.1% formic acid-acetonitrile(98:2, v/v) as the mobile phase.Quantification was done using electrospray ionization in the positive mode. The calibration concentration range was established from 60.0 to 6000 ng/m L for allopurinol and 80.0–8000 ng/m L for oxypurinol. Matrix effect in human plasma, expressed as IS-normalized matrix factors ranged from 1.003 to 1.030 for both the analytes. The developed method was found suitable for a clinical study with 300 mg allopurinol tablet formulation in healthy subjects.	Dhiraj M. Rathod Keyur R. Patel Hiren N. Mistri Arvind G. Jangid Pranav S. Shrivastav Mallika Sanyal	2017	Journal of Pharmaceutical Analysis2017，7，1：	0

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