RING1A and BMI1 bookmark active genes via ubiquitination of chromatin-associated proteins

por Arora, Mansi, Packard, Colin Z., Banerjee, Tapahsama, Parvin, Jeffrey D.
Publicado 2016

The chromatin scaffold protein SAFB1 localizes SUMO-1 to the promoters of ribosomal protein genes to facilitate transcription initiation and splicing

por Liu, Hui-wen, Banerjee, Tapahsama, Guan, Xiaoyan, Freitas, Michael A., Parvin, Jeffrey D.
Publicado 2015

DNA Repair Function Scores for 2172 Variants in the BRCA1 Amino-Terminus

por Diabate, Mariame, Islam, Muhtadi M., Nagy, Gregory, Banerjee, Tapahsama, Dhar, Shruti, Smith, Nahum, Adamovich, Aleksandra I., Starita, Lea M., Parvin, Jeffrey D.
Publicado 2023

DNA repair function scores for 2172 variants in the BRCA1 amino-terminus

por Diabate, Mariame, Islam, Muhtadi M., Nagy, Gregory, Banerjee, Tapahsama, Dhar, Shruti, Smith, Nahum, Adamovich, Aleksandra I., Starita, Lea M., Parvin, Jeffrey D.
Publicado 2023

Functional analysis of BARD1 missense variants in homology-directed repair and damage sensitivity

por Adamovich, Aleksandra I., Banerjee, Tapahsama, Wingo, Margaret, Duncan, Kathryn, Ning, Jie, Martins Rodrigues, Fernanda, Huang, Kuan-lin, Lee, Cindy, Chen, Feng, Ding, Li, Parvin, Jeffrey D.
Publicado 2019

Multiplexed assay of variant effect reveals residues of functional importance in the BRCA1 coiled-coil and serine cluster domains

por Nagy, Gregory, Diabate, Mariame, Banerjee, Tapahsama, Adamovich, Aleksandra I., Smith, Nahum, Jeon, Hyeongseon, Dhar, Shruti, Liu, Wenfang, Burgess, Katherine, Chung, Dongjun, Starita, Lea M., Parvin, Jeffrey D.
Publicado 2023

Genetic suppression reveals DNA repair-independent antagonism between BRCA1 and COBRA1 in mammary gland development

por Nair, Sreejith J., Zhang, Xiaowen, Chiang, Huai-Chin, Jahid, Md Jamiul, Wang, Yao, Garza, Paula, April, Craig, Salathia, Neeraj, Banerjee, Tapahsama, Alenazi, Fahad S., Ruan, Jianhua, Fan, Jian-Bing, Parvin, Jeffrey D., Jin, Victor X., Hu, Yanfen, Li, Rong
Publicado 2016

Patterns and functional implications of rare germline variants across 12 cancer types

por Lu, Charles, Xie, Mingchao, Wendl, Michael C., Wang, Jiayin, McLellan, Michael D., Leiserson, Mark D. M., Huang, Kuan-lin, Wyczalkowski, Matthew A., Jayasinghe, Reyka, Banerjee, Tapahsama, Ning, Jie, Tripathi, Piyush, Zhang, Qunyuan, Niu, Beifang, Ye, Kai, Schmidt, Heather K., Fulton, Robert S., McMichael, Joshua F., Batra, Prag, Kandoth, Cyriac, Bharadwaj, Maheetha, Koboldt, Daniel C., Miller, Christopher A., Kanchi, Krishna L., Eldred, James M., Larson, David E., Welch, John S., You, Ming, Ozenberger, Bradley A., Govindan, Ramaswamy, Walter, Matthew J., Ellis, Matthew J., Mardis, Elaine R., Graubert, Timothy A., Dipersio, John F., Ley, Timothy J., Wilson, Richard K., Goodfellow, Paul J., Raphael, Benjamin J., Chen, Feng, Johnson, Kimberly J., Parvin, Jeffrey D., Ding, Li
Publicado 2015