Monitoring thioredoxin redox with a genetically encoded red fluorescent biosensor

por Fan, Yichong, Makar, Merna, Wang, Michael X., Ai, Hui-wang
Publicado 2017

Designing DNA interstrand lock for locus-specific methylation detection in a nanopore

por Kang, Insoon, Wang, Yong, Reagan, Corbin, Fu, Yumei, Wang, Michael X., Gu, Li-Qun
Publicado 2013

Occult pulmonary mucosa-associated lymphoid tissue lymphoma presenting as catastrophic antiphospholipid antibody syndrome

por REGUNATH, HARIHARAN, SHORTRIDGE, JAMES, RAZA, SHAHZAD, NISTALA, PUJA, HUFFMAN, BRANDON M., WANG, MICHAEL X., XIANG, DONG
Publicado 2013

GcsR, a TyrR-Like Enhancer-Binding Protein, Regulates Expression of the Glycine Cleavage System in Pseudomonas aeruginosa PAO1

por Sarwar, Zaara, Lundgren, Benjamin R., Grassa, Michael T., Wang, Michael X., Gribble, Megan, Moffat, Jennifer F., Nomura, Christopher T.
Publicado 2016

Erratum for Sarwar et al., GcsR, a TyrR-Like Enhancer-Binding Protein, Regulates Expression of the Glycine Cleavage System in Pseudomonas aeruginosa PAO1

por Sarwar, Zaara, Lundgren, Benjamin R., Grassa, Michael T., Wang, Michael X., Gribble, Megan, Moffat, Jennifer F., Nomura, Christopher T.
Publicado 2016

Designing highly multiplex PCR primer sets with Simulated Annealing Design using Dimer Likelihood Estimation (SADDLE)

por Xie, Nina G., Wang, Michael X., Song, Ping, Mao, Shiqi, Wang, Yifan, Yang, Yuxia, Luo, Junfeng, Ren, Shengxiang, Zhang, David Yu
Publicado 2022

Olivar: automated variant aware primer design for multiplex tiled amplicon sequencing of pathogens

por Wang, Michael X., Lou, Esther G., Sapoval, Nicolae, Kim, Eddie, Kalvapalle, Prashant, Kille, Bryce, Elworth, R. A. Leo, Liu, Yunxi, Fu, Yilei, Stadler, Lauren B., Treangen, Todd J.
Publicado 2023

A deep learning model for predicting next-generation sequencing depth from DNA sequence

por Zhang, Jinny X., Yordanov, Boyan, Gaunt, Alexander, Wang, Michael X., Dai, Peng, Chen, Yuan-Jyue, Zhang, Kerou, Fang, John Z., Dalchau, Neil, Li, Jiaming, Phillips, Andrew, Zhang, David Yu
Publicado 2021

Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability

por Teekakirikul, Polakit, Zhu, Wenjuan, Xu, Xinxiu, Young, Cullen B., Tan, Tuantuan, Smith, Amanda M., Wang, Chengdong, Peterson, Kevin A., Gabriel, George C., Ho, Sebastian, Sheng, Yi, Moreau de Bellaing, Anne, Sonnenberg, Daniel A., Lin, Jiuann-huey, Fotiou, Elisavet, Tenin, Gennadiy, Wang, Michael X., Wu, Yijen L., Feinstein, Timothy, Devine, William, Gou, Honglan, Bais, Abha S., Glennon, Benjamin J., Zahid, Maliha, Wong, Timothy C., Ahmad, Ferhaan, Rynkiewicz, Michael J., Lehman, William J., Keavney, Bernard, Alastalo, Tero-Pekka, Freckmann, Mary-Louise, Orwig, Kyle, Murray, Steve, Ware, Stephanie M., Zhao, Hui, Feingold, Brian, Lo, Cecilia W.
Publicado 2022

Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease

por Teekakirikul, Polakit, Zhu, Wenjuan, Gabriel, George C., Young, Cullen B., Williams, Kylia, Martin, Lisa J., Hill, Jennifer C., Richards, Tara, Billaud, Marie, Phillippi, Julie A., Wang, Jianbin, Wu, Yijen, Tan, Tuantuan, Devine, William, Lin, Jiuann-huey, Bais, Abha S., Klonowski, Jonathan, de Bellaing, Anne Moreau, Saini, Ankur, Wang, Michael X., Emerel, Leonid, Salamacha, Nathan, Wyman, Samuel K., Lee, Carrie, Li, Hung Sing, Miron, Anastasia, Zhang, Jingyu, Xing, Jianhua, McNamara, Dennis M., Fung, Erik, Kirshbom, Paul, Mahle, William, Kochilas, Lazaros K., He, Yihua, Garg, Vidu, White, Peter, McBride, Kim L., Benson, D. Woodrow, Gleason, Thomas G., Mital, Seema, Lo, Cecilia W.
Publicado 2021