檢索結果 - Cai, Xuyu
- Showing 1 - 15 results of 15
-
1
-
2
-
3
-
4
-
5
-
6
-
7
Targeted and genome-wide sequencing reveal single nucleotide variations impacting specificity of Cas9 in human stem cells 由 Yang, Luhan, Grishin, Dennis, Wang, Gang, Aach, John, Zhang, Cheng-Zhong, Chari, Raj, Homsy, Jason, Cai, Xuyu, Zhao, Yue, Fan, Jian-Bing, Seidman, Christine, Seidman, Jonathan, Pu, William, Church, George
出版 2014Text -
8
Enrichment of short mutant cell-free DNA fragments enhanced detection of pancreatic cancer() 由 Liu, Xiaoyu, Liu, Lingxiao, Ji, Yuan, Li, Changyu, Wei, Tao, Yang, Xuerong, Zhang, Yuefang, Cai, Xuyu, Gao, Yangbin, Xu, Weihong, Rao, Shengxiang, Jin, Dayong, Lou, Wenhui, Qiu, Zilong, Wang, Xiaolin
出版 2019Text -
9
Single-Neuron Sequencing Analysis of L1 Retrotransposition and Somatic Mutation in the Human Brain 由 Evrony, Gilad D., Cai, Xuyu, Lee, Eunjung, Hills, L. Benjamin, Elhosary, P. Christina, Lehmann, Hillel S., Parker, J.J., Atabay, Kutay D., Gilmore, Edward C., Poduri, Annapurna, Park, Peter J., Walsh, Christopher A.
出版 2012Text -
10
A novel cell‐free DNA methylation‐based model improves the early detection of colorectal cancer 由 Wu, Xianrui, Zhang, Yunfeng, Hu, Tuo, He, Xiaowen, Zou, Yifeng, Deng, Qiling, Ke, Jia, Lian, Lei, He, Xiaosheng, Zhao, Dezhi, Cai, Xuyu, Chen, Zhiwei, Wu, Xiaojian, Fan, Jian‐Bing, Gao, Feng, Lan, Ping
出版 2021Text -
11
Non-invasive diagnosis of early-stage lung cancer using high-throughput targeted DNA methylation sequencing of circulating tumor DNA (ctDNA) 由 Liang, Wenhua, Zhao, Yue, Huang, Weizhe, Gao, Yangbin, Xu, Weihong, Tao, Jinsheng, Yang, Meng, Li, Lequn, Ping, Wei, Shen, Hui, Fu, Xiangning, Chen, Zhiwei, Laird, Peter W., Cai, Xuyu, Fan, Jian-Bing, He, Jianxing
出版 2019Text -
12
Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly 由 Alkuraya, Fowzan S., Cai, Xuyu, Emery, Carina, Mochida, Ganeshwaran H., Al-Dosari, Mohammed S., Felie, Jillian M., Hill, R. Sean, Barry, Brenda J., Partlow, Jennifer N., Gascon, Generoso G., Kentab, Amal, Jan, Mohammad, Shaheen, Ranad, Feng, Yuanyi, Walsh, Christopher A.
出版 2011Text -
13
Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly 由 Alkuraya, Fowzan S., Cai, Xuyu, Emery, Carina, Mochida, Ganeshwaran H., Al-Dosari, Mohammed S., Felie, Jillian M., Hill, R. Sean, Barry, Brenda J., Partlow, Jennifer N., Gascon, Generoso G., Kentab, Amal, Jan, Mohammad, Shaheen, Ranad, Feng, Yuanyi, Walsh, Christopher A.
出版 2011Text -
14
Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations 由 Poduri, Annapurna, Evrony, Gilad D., Cai, Xuyu, Elhosary, Princess Christina, Beroukhim, Rameen, Lehtinen, Maria K., Hills, L. Benjamin, Heinzen, Erin L., Hill, Anthony, Hill, R. Sean, Barry, Brenda J., Bourgeois, Blaise F.D., Riviello, James J., Barkovich, A. James, Black, Peter M., Ligon, Keith L., Walsh, Christopher A.
出版 2012Text -
15
Development and validation of an ultra-deep next-generation sequencing assay for testing of plasma cell-free DNA from patients with advanced cancer 由 Janku, Filip, Zhang, Shile, Waters, Jill, Liu, Li, Huang, Helen J., Subbiah, Vivek, Hong, David S., Karp, Daniel D., Fu, Siqing, Cai, Xuyu, Ramzanali, Nishma M., Madwani, Kiran, Cabrilo, Goran, Andrews, Debra D., Zhao, Yue, Javle, Milind, Kopetz, E. Scott, Luthra, Rajyalakshmi, Kim, Hyunsung J., Gnerre, Sante, Satya, Ravi Vijaya, Chuang, Han-Yu, Kruglyak, Kristina M., Toung, Jonathan, Zhao, Chen, Shen, Richard, Heymach, John V., Meric-Bernstam, Funda, Mills, Gordon B., Fan, Jian-Bing, Salathia, Neeraj S.
出版 2017Text