未登录 Rethinking Immunological Risk: A Retrospective Cohort Study of Severe SARS-Cov-2 Infections in Individuals With Congenital Immunodeficiencies 重新思考免疫风险: 先天性免疫缺陷患者严重SARS-Cov-2感染的回顾性队列研究 Nguyen, Alan A.; Habiballah, Saddiq B.; Labere, Brenna; Day-Lewis, Megan; Elkins, Megan; Al -Musa, Amer; Chu, Anne; Jones, Jennifer; Fried, Ari J.; Mcdonald, Douglas; van Konijnenburg, David P. Hoytema; Rockowitz, Shira; Sliz, Piotr; Oettgen, Hans C.; Schneider, Lynda C.; Macginnitie, Andrew; Bartnikas, Lisa M.; Platt, Craig D.; Ohsumi, Toshiro K.; Chou, Janet 分享 收藏
Deficiency of base excision repair enzyme NEIL3 drives increased predisposition to autoimmunity Massaad, Michel J.; Zhou, Jia; Tsuchimoto, Daisuke; Chou, Janet; Jabara, Haifa; Janssen, Erin; Glauzy, Salome; Olson, Brennan G.; Morbach, Henner; Ohsumi, Toshiro K.; Schmitz, Klaus; Kyriacos, Markianos; Kane, Jennifer; Torisu, Kumiko; Nakabeppu, Yusaku; Notarangelo, Luigi D.; Chouery, Eliane; Megarbane, Andre; Kang, Peter B.; Al-Idrissi, Eman; Aldhekri, Hasan; Meffre, Eric; Mizui, Masayuki; Tsokos, George C.; Manis, John P.; Al-Herz, Waleed; Wallace, Susan S.; Geha, Raif S. 分享 收藏
Recurrent viral infections associated with a homozygous CORO1A mutation that disrupts oligomerization and cytoskeletal association 与破坏寡聚化和细胞骨架关联的纯合CORO1A突变相关的复发性病毒感染 Yee, Christina S.; Massaad, Michel J.; Bainter, Wayne; Ohsumi, Toshiro K.; Foeger, Niko; Chan, Andrew C.; Akarsu, Nurten A.; Aytekin, Caner; Ayvaz, Deniz Cagdas; Tezcan, Ilhan; Sanal, Ozden; Geha, Raif S.; Chou, Janet 分享 收藏
A Novel Microbiome Therapeutic Increases Gut Microbial Diversity and Prevents Recurrent Clostridium difficile Infection Khanna, Sahil; Pardi, Darrell S.; Kelly, Colleen R.; Kraft, Colleen S.; Dhere, Tanvi; Henn, Matthew R.; Lombardo, Mary-Jane; Vulic, Marin; Ohsumi, Toshiro; Winkler, Jonathan; Pindar, Christina; McGovern, Barbara H.; Pomerantz, Roger J.; Aunins, John G.; Cook, David N.; Hohmann, Elizabeth L. 分享 收藏
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency 编码转铁蛋白受体1的TFRC中的错义突变导致联合免疫缺陷 Jabara, Haifa H.; Boyden, Steven E.; Chou, Janet; Ramesh, Narayanaswamy; Massaad, Michel J.; Benson, Halli; Bainter, Wayne; Fraulino, David; Rahimov, Fedik; Sieff, Colin; Liu, Zhi-Jian; Alshemmari, Salem H.; Al-Ramadi, Basel K.; Al-Dhekri, Hasan; Arnaout, Rand; Abu-Shukair, Mohammad; Vatsayan, Anant; Silver, Eli; Ahuja, Sanjay; Davies, E. Graham; Sola-Visner, Martha; Ohsumi, Toshiro K.; Andrews, Nancy C.; Notarangelo, Luigi D.; Fleming, Mark D.; Al-Herz, Waleed; Kunkel, Louis M.; Geha, Raif S. 分享 收藏
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Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections Dobbs, K.; Conde, C. Dominguez; Zhang, S. -Y.; Parolini, S.; Audry, M.; Chou, J.; Haapaniemi, E.; Keles, S.; Bilic, I.; Okada, S.; Massaad, M. J.; Rounioja, S.; Alwahadneh, A. M.; Serwas, N. K.; Capuder, K.; Ciftci, E.; Felgentreff, K.; Ohsumi, T. K.; Pedergnana, V.; Boisson, B.; Haskologlu, S.; Ensari, A.; Schuster, M.; Moretta, A.; Itan, Y.; Patrizi, O.; Rozenberg, F.; Lebon, P.; Saarela, J.; Knip, M.; Petrovski, S.; Goldstein, D. B.; Parrott, R. E.; Savas, B.; Schambach, A.; Tabellini, G.; Bock, C.; Chatila, T. A.; Comeau, A. M.; Geha, R. S.; Abel, L.; Buckley, R. H.; Ikinciogullari, A.; Al-Herz, W.; Helminen, M.; Dogu, F.; Casanova, J. -L.; Boztug, K.; Notarangelo, L. D. 分享 收藏
Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like disorder caused by loss-of-function mutations in LRBA Charbonnier, Louis-Marie; Janssen, Erin; Chou, Janet; Ohsumi, Toshiro K.; Keles, Sevgi; Hsu, Joyce T.; Massaad, Michel J.; Garcia-Lloret, Maria; Hanna-Wakim, Rima; Dbaibo, Ghassan; Alangari, Abdullah A.; Alsultan, Abdulrahman; Al-Zahrani, Daifulah; Geha, Raif S.; Chatila, Talal A. 分享 收藏
Lessons in gene hunting: A RAG1 mutation presenting with agammaglobulinemia and absence of B cells Hedayat, Mona; Massaad, Michel J.; Lee, Yu Nee; Conley, Mary Ellen; Orange, Jordan S.; Ohsumi, Toshiro K.; Al-Herz, Waleed; Notarangelo, Luigi D.; Geha, Raif S.; Chou, Janet 分享 收藏
A homozygous mucosa-associated lymphoid tissue 1 (MALT1) mutation in a family with combined immunodeficiency 一个合并免疫缺陷的家庭中的纯合粘膜相关淋巴样组织1 (MALT1) 突变 Jabara, Haifa H.; Ohsumi, Toshiro; Chou, Janet; Massaad, Michel J.; Benson, Halli; Megarbane, Andre; Chouery, Eliane; Mikhael, Raymond; Gorka, Oliver; Gewies, Andreas; Portales, Pierre; Nakayama, Toshinori; Hosokawa, Hiroyuki; Revy, Patrick; Herrod, Henry; Le Deist, Francoise; Lefranc, Gerard; Ruland, Juergen; Geha, Raif S. 分享 收藏
Genome-wide Chromatin Interactions of the Nanog Locus in Pluripotency, Differentiation, and Reprogramming Apostolou, Effie; Ferrari, Francesco; Walsh, Ryan M.; Bar-Nur, Ori; Stadtfeld, Matthias; Cheloufi, Sihem; Stuart, Hannah T.; Polo, Jose M.; Ohsumi, Toshiro K.; Borowsky, Mark L.; Kharchenko, Peter V.; Park, Peter J.; Hochedlinger, Konrad 分享 收藏
Transposon activation mutagenesis as a screening tool for identifying resistance to cancer therapeutics 转座子激活诱变作为鉴定癌症治疗抗性的筛选工具 Chen, Li; Stuart, Lynda; Ohsumi, Toshiro K.; Burgess, Shawn; Varshney, Gaurav K.; Dastur, Anahita; Borowsky, Mark; Benes, Cyril; Lacy-Hulbert, Adam; Schmidt, Emmett V. 分享 收藏
Histone H3R2 Symmetric Dimethylation and Histone H3K4 Trimethylation Are Tightly Correlated in Eukaryotic Genomes Yuan, Chih-Chi; Matthews, Adam G. W.; Jin, Yi; Chen, Chang Feng; Chapman, Brad A.; Ohsumi, Toshiro K.; Glass, Karen C.; Kutateladze, Tatiana G.; Borowsky, Mark L.; Struhl, Kevin; Oettinger, Marjorie A. 分享 收藏
Genome-wide Identification of Polycomb-Associated RNAs by RIP-seq Zhao, Jing; Ohsumi, Toshiro K.; Kung, Johnny T.; Ogawa, Yuya; Grau, Daniel J.; Sarma, Kavitha; Song, Ji Joon; Kingston, Robert E.; Borowsky, Mark; Lee, Jeannie T. 分享 收藏
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Sensitive, specific polymorphism discovery in bacteria using massively parallel sequencing Nusbaum, Chad; Ohsumi, Toshiro K.; Gomez, James; Aquadro, John; Victor, Thomas C.; Warren, Robert M.; Hung, Deborah T.; Birren, Bruce W.; Lander, Eric S.; Jaffe, David B. 分享 收藏
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