Structure and activity of human TMPRSS2 protease implicated in SARS-CoV-2 activation von Fraser, Bryan J., Beldar, Serap, Seitova, Almagul, Hutchinson, Ashley, Mannar, Dhiraj, Li, Yanjun, Kwon, Daniel, Tan, Ruiyan, Wilson, Ryan P., Leopold, Karoline, Subramaniam, Sriram, Halabelian, Levon, Arrowsmith, Cheryl H., Bénard, François

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PGE1 and PGA1 bind to Nurr1 and activate its transcriptional function von Rajan, Sreekanth, Jang, Yongwoo, Kim, Chun-Hyung, Kim, Woori, Toh, Hui Ting, Jeon, Jeha, Song, Bin, Serra, Aida, Lescar, Julien, Yoo, Jun Yeob, Beldar, Serap, Ye, Hong, Kang, Congbao, Liu, Xue-Wei, Feitosa, Melissa, Kim, Yeahan, Hwang, Dabin, Goh, Geraldine, Lim, Kah-Leong, Park, Hye Min, Lee, Choong Hwan, Oh, Sungwhan F., Petsko, Gregory A., Yoon, Ho Sup, Kim, Kwang-Soo

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Sequence specificity analysis of the SETD2 protein lysine methyltransferase and discovery of a SETD2 super-substrate von Schuhmacher, Maren Kirstin, Beldar, Serap, Khella, Mina S., Bröhm, Alexander, Ludwig, Jan, Tempel, Wolfram, Weirich, Sara, Min, Jinrong, Jeltsch, Albert

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Cdyl Deficiency Brakes Neuronal Excitability and Nociception through Promoting Kcnb1 Transcription in Peripheral Sensory Neurons von Sun, Zhao‐Wei, Waybright, Jarod M., Beldar, Serap, Chen, Lu, Foley, Caroline A., Norris‐Drouin, Jacqueline L., Lyu, Tian‐Jie, Dong, Aiping, Min, Jinrong, Wang, Yu‐Pu, James, Lindsey I., Wang, Yun

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Cdyl Deficiency Brakes Neuronal Excitability and Nociception through Promoting Kcnb1 Transcription in Peripheral Sensory Neurons von Sun, Zhao‐Wei, Waybright, Jarod M., Beldar, Serap, Chen, Lu, Foley, Caroline A., Norris‐Drouin, Jacqueline L., Lyu, Tian‐Jie, Dong, Aiping, Min, Jinrong, Wang, Yu‐Pu, James, Lindsey I., Wang, Yun

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Novel immunodeficiency caused by homozygous mutation in SLC19A1 encoding the reduced folate carrier von Shiraishi, Akira, Uygun, Vedat, Sharfe, Nigel, Beldar, Serap, Sun, Mark George Ford, Dadi, Harjit, Vong, Linda, Maxson, Michelle, Karaca, Neslihan E., Mevlitoğlu, Süleyman, Grinstein, Sergio, Artan, Reha, Merico, Daniele, Roifman, Chaim M

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Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrier von Shiraishi, Akira, Uygun, Vedat, Sharfe, Nigel, Beldar, Serap, Sun, Mark G. F., Dadi, Harjit, Vong, Linda, Maxson, Michelle, Karaca, Neslihan E., Mevlitoğlu, Süleyman, Grinstein, Sergio, Artan, Reha, Merico, Daniele, Roifman, Chaim M.

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Structural Basis for the Binding Selectivity of Human CDY Chromodomains von Dong, Cheng, Liu, Yanli, Lyu, Tian-Jie, Beldar, Serap, Lamb, Kelsey N., Tempel, Wolfram, Li, Yanjun, Li, Zoey, James, Lindsey I., Qin, Su, Wang, Yun, Min, Jinrong

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A Target Class Ligandability Evaluation of WD40 Repeat-Containing Proteins von Ackloo, Suzanne, Li, Fengling, Szewczyk, Magda, Seitova, Almagul, Loppnau, Peter, Zeng, Hong, Xu, Jin, Ahmad, Shabbir, Arnautova, Yelena A, Baghaie, A. J., Beldar, Serap, Bolotokova, Albina, Centrella, Paolo A., Chau, Irene, Clark, Matthew A., Cuozzo, John W., Dehghani-Tafti, Saba, Disch, Jeremy S., Dong, Aiping, Dumas, Antoine, Feng, Jianwen A., Ghiabi, Pegah, Gibson, Elisa, Gilmer, Justin, Goldman, Brian, Green, Stuart R, Guié, Marie-Aude, Guilinger, John P., Harms, Nathan, Herasymenko, Oleksandra, Houliston, Scott, Hutchinson, Ashley, Kearnes, Steven, Keefe, Anthony D., Kimani, Serah W., Kramer, Trevor, Kutera, Maria, Kwak, Haejin A., Lento, Cristina, Li, Yanjun, Liu, Jenny, Loup, Joachim, Machado, Raquel A. C., Mulhern, Christopher J., Perveen, Sumera, Righetto, Germanna L., Riley, Patrick, Shrestha, Suman, Sigel, Eric A., Silva, Madhushika, Sintchak, Michael D., Slakman, Belinda L., Taylor, Rhys D., Thompson, James, Torng, Wen, Underkoffler, Carl, von Rechenberg, Moritz, Walsh, Ryan T., Watson, Ian, Wilson, Derek J., Wolf, Esther, Yadav, Manisha, Yazdi, Aliakbar K., Zhang, Junyi, Zhang, Ying, Santhakumar, Vijayaratnam, Edwards, Aled M., Barsyte-Lovejoy, Dalia, Schapira, Matthieu, Brown, Peter J., Halabelian, Levon, Arrowsmith, Cheryl H.

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Self-association and conformational variation of NS5A domain 1 of hepatitis C virus von Beldar, Serap, Manimekalai, Malathy Sony Subramanian, Cho, Nam-Joon, Baek, Kwanghee, Grüber, Gerhard, Yoon, Ho Sup

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Sequence specificity analysis of the SETD2 protein lysine methyltransferase and discovery of a SETD2 super-substrate (Sep, 10.1038/s42003-020-01223-6, 2020) von Schuhmacher, Maren Kirstin, Beldar, Serap, Khella, Mina S., Broehm, Alexander, Ludwig, Jan, Tempel, Wolfram, Weirich, Sara, Min, Jinrong, Jeltsch, Albert

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Author Correction: Sequence specificity analysis of the SETD2 protein lysine methyltransferase and discovery of a SETD2 super-substrate von Schuhmacher, Maren Kirstin, Beldar, Serap, Khella, Mina S., Bröhm, Alexander, Ludwig, Jan, Tempel, Wolfram, Weirich, Sara, Min, Jinrong, Jeltsch, Albert

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Proteomics of plaques and novel sources of potential biomarkers for atherosclerosis von Bleijerveld, Onno B., Zhang, Ya-Nan, Beldar, Serap, Hoefer, Imo E., Sze, Siu K., Pasterkamp, Gerard, de Kleijn, Dominique P. V.

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Expression and solubility test of SETDB1 catalytic domain constructs von Beldar, Serap, Hutchinson, Ashley, Seitova, Alma, Dong, Cheng, Lei, Ming, Li, Yanjun, Loppnau, Peter, Min, Jinrong

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WDR protein purification and druggability assessment von Halabelian, Levon, Seitova, Alma, Loppnau, Peter, Zeng, Hong, Kwak, Haejin, Li, Fengling, Ahmad, Shabbir, Beldar, Serap, Bolotokova, Albina, Chau, Irene, Dehghani-Tafti, Saba, Dong, Aiping, Ghiabi, Pegah, Ackloo, Suzanne, Green, Stuart, Herasymenko, Oleksandra, Houliston, Scott, Hutchinson, Ashley, Kimani, Serah, Kutera, Maria, Szewczyk, Magda, Li, Yanjun, Machado, Raquel, Perveen, Sumera, Righetto, Germanna, Suman, Shrestha, Silva, Madhushika, Yadav, Manisha, Yazdi, Aliakbar, Santhakumar, Vijayaratnam, Barsyte-Lovejoy, Dalia, Brown, Peter, Edwards, Aled, Schapira, Matthieu, Arrowsmith, Cheryl

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Expression test and purification of SETDB1 catalytic domain constructs' for structural studies by X-ray crystallography von Beldar, Serap, Dong, Cheng, Lei, Ming, Li, Yanjun, Loppnau, Peter, Min, Jinrong

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