Biochemistry of Autoinflammatory Diseases: Catalyzing Monogenic Disease

od Beck, David B., Aksentijevich, Ivona
Izdano u Front Immunol (2019)

Deubiquitylases in developmental ubiquitin signaling and congenital diseases

od Basar, Mohammed A., Beck, David B., Werner, Achim
Izdano u Cell Death Differ (2020)

PR-Set7 and H4K20me1: at the crossroads of genome integrity, cell cycle, chromosome condensation, and transcription

od Beck, David B., Oda, Hisanobu, Shen, Steven S., Reinberg, Danny
Izdano 2012

Extending the phenotypic spectrum of Sengers syndrome: Congenital lactic acidosis with synthetic liver dysfunction

od Beck, David B., Cusmano-Ozog, Kristina, Andescavage, Nickie, Leon, Eyby
Izdano u Transl Sci Rare Dis (2018)

The Role of Host Genetic Factors in Coronavirus Susceptibility: Review of Animal and Systematic Review of Human Literature

od LoPresti, Marissa, Beck, David B, Duggal, Priya, Cummings, Derek A.T., Solomon, Benjamin D
Izdano u medRxiv (2020)

The Role of Host Genetic Factors in Coronavirus Susceptibility: Review of Animal and Systematic Review of Human Literature

od LoPresti, Marissa, Beck, David B., Duggal, Priya, Cummings, Derek A.T., Solomon, Benjamin D.
Izdano u Am J Hum Genet (2020)

The role of PR-Set7 in replication licensing depends on Suv4-20h

od Beck, David B., Burton, Adam, Oda, Hisanobu, Ziegler-Birling, Céline, Torres-Padilla, Maria-Elena, Reinberg, Danny
Izdano 2012

Regulation of the Histone H4 Monomethylase PR-Set7 by CRL4(Cdt2) Mediated PCNA Dependent Degradation during DNA Damage

od Oda, Hisanobu, Hübner, Michael R., Beck, David B., Vermeulen, Michiel, Hurwitz, Jerard, Spector, David L., Reinberg, Danny
Izdano 2010

Vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome—clinical presentation of a newly described somatic, autoinflammatory syndrome

od Alhomida, Faris, Beck, David B., George, Tracy I., Shaffer, Andrew, Lebiedz-Odrobina, Dorota, Kovacsovics, Tibor, Madigan, Lauren M.
Izdano u JAAD Case Rep (2021)

The C-Terminal Domain of RNA Polymerase II Is Modified by Site-Specific Methylation

od Sims, Robert J., Rojas, Luis Alejandro, Beck, David B., Bonasio, Roberto, Schüller, Roland, Drury, William J., Eick, Dirk, Reinberg, Danny
Izdano 2011

The use of leukocytes’ secretome to individually target biological therapy in autoimmune arthritis: a case report

od Poubelle, Patrice E., Pagé, Nathalie, Longchamps, Marie-Pier, Sampaio Moura, Natalia, Beck, David B., Aksentijevich, Ivona, Tessier, Philippe A., Pelletier, Martin
Izdano u Clin Transl Med (2019)

In Vivo Proximity Labeling for the Detection of Protein–Protein and Protein–RNA Interactions

od Beck, David B., Narendra, Varun, Drury, William J., Casey, Ryan, Jansen, Pascal W. T. C., Yuan, Zuo-Fei, Garcia, Benjamin A., Vermeulen, Michiel, Bonasio, Roberto
Izdano u J Proteome Res (2014)

Second Case of HOIP Deficiency Expands Clinical Features and Defines Inflammatory Transcriptome Regulated by LUBAC

od Oda, Hirotsugu, Beck, David B., Kuehn, Hye Sun, Sampaio Moura, Natalia, Hoffmann, Patrycja, Ibarra, Maria, Stoddard, Jennifer, Tsai, Wanxia Li, Gutierrez-Cruz, Gustavo, Gadina, Massimo, Rosenzweig, Sergio D., Kastner, Daniel L., Notarangelo, Luigi D., Aksentijevich, Ivona
Izdano u Front Immunol (2019)

Human iPSC-Derived Neuronal Cells From CTBP1-Mutated Patients Reveal Altered Expression of Neurodevelopmental Gene Networks

od Vijayalingam, S., Ezekiel, Uthayashanker R., Xu, Fenglian, Subramanian, T., Geerling, Elizabeth, Hoelscher, Brittany, San, KayKay, Ganapathy, Aravinda, Pemberton, Kyle, Tycksen, Eric, Pinto, Amelia K., Brien, James D., Beck, David B., Chung, Wendy K., Gurnett, Christina A., Chinnadurai, G.
Izdano u Front Neurosci (2020)

The tumor suppressor SirT2 regulates cell cycle progression and genome stability by modulating the mitotic deposition of H4K20 methylation

od Serrano, Lourdes, Martínez-Redondo, Paloma, Marazuela-Duque, Anna, Vazquez, Berta N., Dooley, Scott J., Voigt, Philipp, Beck, David B., Kane-Goldsmith, Noriko, Tong, Qiang, Rabanal, Rosa M., Fondevila, Dolors, Muñoz, Purificación, Krüger, Marcus, Tischfield, Jay A., Vaquero, Alejandro
Izdano 2013

A pathogenic CtBP1 missense mutation causes altered cofactor binding and transcriptional activity

od Beck, David B., Subramanian, T., Vijayalingam, S., Ezekiel, Uthayashankar R., Donkervoort, Sandra, Yang, Michele L., Dubbs, Holly A., Ortiz-Gonzalez, Xilma R., Lakhani, Shenela, Segal, Devorah, Au, Margaret, Graham, John M., Verma, Sumit, Waggoner, Darrel, Shinawi, Marwan, Bönnemann, Carsten G., Chung, Wendy K., Chinnadurai, G.
Izdano u Neurogenetics (2019)

Deficiency of Adenosine Deaminase 2 (DADA2): hidden variants, reduced penetrance, and unusual inheritance

od Schnappauf, Oskar, Zhou, Qing, Moura, Natalia Sampaio, Ombrello, Amanda K., Michael, Drew G., Deuitch, Natalie, Barron, Karyl, Stone, Deborah L., Hoffmann, Patrycja, Hershfield, Michael, Applegate, Carolyn, Bjornsson, Hans T., Beck, David B., Witmer, P. Dane, Sobreira, Nara, Wohler, Elizabeth, Chiorini, John A., Dalgard, Clifton L., Kastner, Daniel L., Aksentijevich, Ivona
Izdano u J Clin Immunol (2020)

Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation

od Beck, David B., Basar, Mohammed A., Asmar, Anthony J., Thompson, Joyce J., Oda, Hirotsugu, Uehara, Daniela T., Saida, Ken, Pajusalu, Sander, Talvik, Inga, D’Souza, Precilla, Bodurtha, Joann, Mu, Weiyi, Barañano, Kristin W., Miyake, Noriko, Wang, Raymond, Kempers, Marlies, Tamada, Tomoko, Nishimura, Yutaka, Okada, Satoshi, Kosho, Tomoki, Dale, Ryan, Mitra, Apratim, Macnamara, Ellen, Matsumoto, Naomichi, Inazawa, Johji, Walkiewicz, Magdalena, Õunap, Katrin, Tifft, Cynthia J., Aksentijevich, Ivona, Kastner, Daniel L., Rocha, Pedro P., Werner, Achim
Izdano u Sci Adv (2021)

Bi-allelic Mutations in Phe-tRNA Synthetase Associated with a Multi-system Pulmonary Disease Support Non-translational Function

od Xu, Zhiwen, Lo, Wing-Sze, Beck, David B., Schuch, Luise A., Oláhová, Monika, Kopajtich, Robert, Chong, Yeeting E., Alston, Charlotte L., Seidl, Elias, Zhai, Liting, Lau, Ching-Fun, Timchak, Donna, LeDuc, Charles A., Borczuk, Alain C., Teich, Andrew F., Juusola, Jane, Sofeso, Christina, Müller, Christoph, Pierre, Germaine, Hilliard, Tom, Turnpenny, Peter D., Wagner, Matias, Kappler, Matthias, Brasch, Frank, Bouffard, John Paul, Nangle, Leslie A., Yang, Xiang-Lei, Zhang, Mingjie, Taylor, Robert W., Prokisch, Holger, Griese, Matthias, Chung, Wendy K., Schimmel, Paul
Izdano u Am J Hum Genet (2018)

Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency

od Beck, David B., Petracovici, Ana, He, Chongsheng, Moore, Hannah W., Louie, Raymond J., Ansar, Muhammad, Douzgou, Sofia, Sithambaram, Sivagamy, Cottrell, Trudie, Santos-Cortez, Regie Lyn P., Prijoles, Eloise J., Bend, Renee, Keren, Boris, Mignot, Cyril, Nougues, Marie-Christine, Õunap, Katrin, Reimand, Tiia, Pajusalu, Sander, Zahid, Muhammad, Saqib, Muhammad Arif Nadeem, Buratti, Julien, Seaby, Eleanor G., McWalter, Kirsty, Telegrafi, Aida, Baldridge, Dustin, Shinawi, Marwan, Leal, Suzanne M., Schaefer, G. Bradley, Stevenson, Roger E., Banka, Siddharth, Bonasio, Roberto, Fahrner, Jill A.
Izdano u Am J Hum Genet (2020)