Sökresultat - Meijian Guan
- Visas 1 - 7 av 7 resultat
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The TLR9 Ligand, CpG‐ODN, Induces Protection against Cerebral Ischemia/Reperfusion Injury via Activation of PI3K/Akt Signaling av Chen Lu, Tuanzhu Ha, Xiaohui Wang, Li Liu, Xia Zhang, Erinmarie Olson Kimbrough, Zhanxin Sha, Meijian Guan, John B. Schweitzer, John H. Kalbfleisch, David L. Williams, Chuanfu Li
Publicerad 2014Artigo -
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Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with nondiabetic nephropathy than strong APOL1–s... av Carl D. Langefeld, Mary E. Comeau, Maggie C. Y. Ng, Meijian Guan, Latchezar Dimitrov, Poorva Mudgal, Mitzie Spainhour, Bruce A. Julian, Jeffrey C. Edberg, Jennifer A. Croker, Jasmin Divers, Andrew A. Hicks, Donald W. Bowden, Gary Kok Yew Chan, Lijun Ma, Colin N. A. Palmer, Robert P. Kimberly, Barry I. Freedman
Publicerad 2018Revisão -
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Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans av Meijian Guan, Jacob M. Keaton, Latchezar Dimitrov, Andrew A. Hicks, Jianzhao Xu, Colin N. A. Palmer, Lijun Ma, Swapan K. Das, Yii‐Der Ida Chen, Josef Coresh, Myriam Fornage, Nora Franceschini, Holly Kramer, Carl D. Langefeld, Josyf C. Mychaleckyj, Rulan S. Parekh, Wendy S. Post, Laura J. Rasmussen‐Torvik, Stephen S. Rich, Jerome I. Rotter, John R. Sedor, Denyse Thornley‐Brown, Adrienne Tin, James G. Wilson, Barry I. Freedman, Donald W. Bowden, Maggie Ng
Publicerad 2019Artigo -
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Assessing reproducibility of inherited variants detected with short-read whole genome sequencing av Bohu Pan, Luyao Ren, Vitor Onuchic, Meijian Guan, Rebecca Kusko, Steve Bruinsma, Len Trigg, Andreas Scherer, Baitang Ning, Chaoyang Zhang, Christine Glidewell-Kenney, Chunlin Xiao, Eric Donaldson, Fritz J. Sedlazeck, Gary P. Schroth, Gökhan Yavaş, Haiying Grunenwald, Haodong Chen, Heather Meinholz, Joe Meehan, Jing Wang, Jingcheng Yang, Jonathan Foox, Jun Shang, Kelci Miclaus, Lianhua Dong, Leming Shi, Marghoob Mohiyuddin, Mehdi Pirooznia, Ping Gong, Rooz Golshani, Russ Wolfinger, Samir Lababidi, Sayed Mohammad Ebrahim Sahraeian, Stephen T. Sherry, Tao Han, Tao Chen, Tieliu Shi, Wanwan Hou, Weigong Ge, Wen Zou, Wenjing Guo, Wenjun Bao, Wenzhong Xiao, Xiaohui Fan, Yoichi Gondo, Ying Yu, Yongmei Zhao, Zhenqiang Su, Zhichao Liu, Weida Tong, Wenming Xiao, Justin M. Zook, Yuanting Zheng, Huixiao Hong
Publicerad 2022Artigo -
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A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequency av Wendell Jones, Binsheng Gong, Natalia Novoradovskaya, Dan Li, Rebecca Kusko, Todd Richmond, Donald J. Johann, Halil Bişğin, Sayed Mohammad Ebrahim Sahraeian, Pierre R. Bushel, Mehdi Pirooznia, Katherine Wilkins, Marco Chierici, Wenjun Bao, Lee S Basehore, Anne Bergstrom Lucas, Daniel L. Burgess, Daniel Butler, Simon Cawley, Chia-Jung Chang, Guangchun Chen, Tao Chen, Yun-Ching Chen, Daniel J. Craig, Ángela del Pozo, Jonathan Foox, Margherita Francescatto, Yutao Fu, Cesare Furlanello, Kristina Giorda, Kira P. Grist, Meijian Guan, Yingyi Hao, Scott Happe, Gunjan Hariani, Nathan Haseley, Jeff S. Jasper, Giuseppe Jurman, David P. Kreil, Paweł P. Łabaj, Kevin Lai, Jianying Li, Quan‐Zhen Li, Yulong Li, Zhiguang Li, Zhichao Liu, Mario Solís, Kelci Miclaus, Raymond D. Miller, Vinay Kumar Mittal, Marghoob Mohiyuddin, Carlos Pabón-Peña, Barbara L. Parsons, Fujun Qiu, Andreas Scherer, Tieliu Shi, Suzy Stiegelmeyer, Chen Suo, Nikola Tom, Dong Wang, Zhining Wen, Leihong Wu, Wenzhong Xiao, Chang Xu, Ying Yu, Jiyang Zhang, Yifan Zhang, Zhihong Zhang, Yuanting Zheng, Christopher E. Mason, James C. Willey, Weida Tong, Leming Shi, Joshua Xu
Publicerad 2021Artigo -
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Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing av Wenming Xiao, Luyao Ren, Zhong Chen, Li Tai Fang, Yongmei Zhao, Justin Lack, Meijian Guan, Bin Zhu, Erich Jaeger, Liz Kerrigan, Thomas Blomquist, Tiffany Hung, Marc Sultan, Kenneth B. Idler, Charles Lu, Andreas Scherer, Rebecca Kusko, Malcolm Moos, Chunlin Xiao, Stephen T. Sherry, Ogan D. Abaan, Wanqiu Chen, Xin Chen, Jessica Nordlund, Ulrika Liljedahl, Roberta Maestro, Maurizio Polano, Jir̆ı́ Drábek, Petr Vojta, Sulev Kõks, Ene Reimann, Bindu Swapna Madala, Tim R. Mercer, Chris Miller, Howard J. Jacob, Tiffany Truong, Ali Moshrefi, Aparna Natarajan, Ana Granat, Gary P. Schroth, Rasika Kalamegham, Eric Peters, Virginie Petitjean, Ashley Walton, Tsai-Wei Shen, Keyur Talsania, Cristobal Juan Vera, Kurt J. Langenbach, Maryellen de Mars, Jennifer Hipp, James C. Willey, Jing Wang, Jyoti Shetty, Yuliya Kriga, Arati Raziuddin, Bao Tran, Yuanting Zheng, Ying Yu, Margaret C. Cam, Parthav Jailwala, Cu Nguyen, Daoud Meerzaman, Qingrong Chen, Chunhua Yan, Ben Ernest, Urvashi Mehra, Roderick V. Jensen, Wendell Jones, Jian‐Liang Li, Brian N. Papas, Mehdi Pirooznia, Yunching Chen, Fayaz Seifuddin, Zhipan Li, Xue‐Lu Liu, Wolfgang Resch, Jingya Wang, Leihong Wu, Gökhan Yavaş, Corey J. Miles, Baitang Ning, Weida Tong, Christopher E. Mason, Eric Donaldson, Samir Lababidi, Louis M. Staudt, Živana Težak, Huixiao Hong, Charles Wang, Leming Shi
Publicerad 2021Artigo
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Relaterade ämnen
Biology
Gene
Genetics
Computational biology
Genotype
Internal medicine
Mathematics
Medicine
Single-nucleotide polymorphism
Statistics
Chemistry
DNA sequencing
Diabetes mellitus
Disease
Endocrinology
Genetic association
Genome
Genome-wide association study
Kidney disease
Nephropathy
Reproducibility
Whole genome sequencing
Allele
Allele frequency
Artificial intelligence
Artificial neural network
Biochemistry
Bioinformatics
Cancer genome sequencing
Cell biology