未登录 Noncoding variants are a rare cause of recessive developmental disorders in trans with coding variants Lord, Jenny; Oquendo, Carolina J.; Wai, Htoo A.; Holloway, John G.; Martin-Geary, Alexandra; Blakes, Alexander J. M.; Arciero, Elena; Domcke, Silvia; Childs, Anne-Marie; Low, Karen; Rankin, Julia; Baralle, Diana; Martin, Hilary C.; Whiff, Nicola 分享 收藏
Multiplex, single-cell CRISPRa screening for cell type specific regulatory elements Chardon, Florence M.; McDiarmid, Troy A.; Page, Nicholas F.; Daza, Riza M.; Martin, Beth K.; Domcke, Silvia; Regalado, Samuel G.; Lalanne, Jean-Benoit; Calderon, Diego; Li, Xiaoyi; Starita, Lea M.; Sanders, Stephan J.; Ahituv, Nadav; Shendure, Jay 分享 收藏
Multiplex profiling of developmental cis-regulatory elements with quantitative single-cell expression reporters Lalanne, Jean-Benoit; Regalado, Samuel G.; Domcke, Silvia; Calderon, Diego; Martin, Beth K.; Li, Xiaoyi; Li, Tony; Suiter, Chase C.; Lee, Choli; Trapnell, Cole; Shendure, Jay 分享 收藏
Multiplex single-cell chemical genomics reveals the kinase dependence of the response to targeted therapy McFaline-Figueroa, Jose L.; Srivatsan, Sanjay; Hill, Andrew J.; Gasperini, Molly; Jackson, Dana L.; Saunders, Lauren; Domcke, Silvia; Regalado, Samuel G.; Lazarchuck, Paul; Alvarez, Sarai; Monnat Jr, Raymond J.; Shendure, Jay; Trapnell, Cole 分享 收藏
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DNA sequence and chromatin modifiers cooperate to confer epigenetic bistability at imprinting control regions Butz, Stefan; Schmolka, Nina; Karemaker, Ino D.; Villasenor, Rodrigo; Schwarz, Isabel; Domcke, Silvia; Uijttewaal, Esther C. H.; Jude, Julian; Lienert, Florian; Krebs, Arnaud R.; de Wagenaar, Nathalie P.; Bao, Xue; Zuber, Johannes; Elling, Ulrich; Schuebeler, Dirk; Baubec, Tuncay 分享 收藏
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