检索结果 - Sylvia Singh
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The COMA complex interacts with Cse4 and positions Sli15/Ipl1 at the budding yeast inner kinetochore 由 Josef Fischböck-Halwachs, Sylvia Singh, Mia Potočnjak, Götz Hagemann, Victor Solis‐Mezarino, Stephan Woike, Medini Ghodgaonkar-Steger, Florian Weissmann, Laura D. Gallego, Julie Rojas, Jessica Andréani, Alwin Köhler, Franz Herzog
出版 2019Artigo -
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SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome 由 Natalie D. Shaw, Harrison Brand, Zachary A Kupchinsky, Hemant Bengani, Lacey Plummer, Takako I. Jones, Serkan Erdin, Kathleen A. Williamson, Joe Rainger, Alexei Stortchevoi, Kaitlin E. Samocha, Benjamin Currall, Donncha S. Dunican, Ryan L. Collins, Jason R. Willer, Angela Lek, Monkol Lek, Malik Nassan, Shahrin Pereira, Tammy Kammin, Diane Lucente, Alexandra Silva, Catarina M. Seabra, Colby Chiang, Yu An, Morad Ansari, Jacqueline K. Rainger, Shelagh Joss, Jill Smith, Margaret Lippincott, Sylvia Singh, Nirav Patel, Jenny W Jing, Jennifer Law, Nalton Ferraro, Alain Verloès, Anita Rauch, Katharina Steindl, Markus Zweier, Ianina Scheer, Daisuke Sato, Nobuhiko Okamoto, Christina M. Jacobsen, Jeanie B. Tryggestad, Steven D. Chernausek, Lisa A. Schimmenti, Benjamin Brasseur, Claudia Cesaretti, José Elías García‐Ortíz, Tatiana Pineda Buitrago, Orlando Pérez Silva, Jodi D. Hoffman, W. Mühlbauer, Klaus W. Ruprecht, Bart Loeys, Masato Shino, Angela M. Kaindl, Chie Hee Cho, Cynthia C. Morton, Richard R. Meehan, Veronica van Heyningen, Eric C. Liao, Ravikumar Balasubramanian, Janet E. Hall, Stephanie B. Seminara, Daniel G. MacArthur, Steven A. Moore, Koh-ichiro Yoshiura, James F. Gusella, Joseph A. Marsh, John M. Graham, Angela E. Lin, Nicholas Katsanis, Peter L. Jones, William F. Crowley, Erica E. Davis, David Fitzpatrick, Michael E. Talkowski
出版 2017Artigo
相关主题
Biology
Gene
Genetics
Apoptosis
Aurora B kinase
Biochemistry
Calcitriol receptor
Cardiac function curve
Cardioprotection
Cell biology
Centromere
Chromosome
Chromosome segregation
DNA
Endocrinology
Epigenetics
Facioscapulohumeral muscular dystrophy
Fibrosis
Heart failure
Histone
Inflammation
Internal medicine
Kinetochore
Knockout mouse
Medicine
Microphthalmia
Missense mutation
Muscular dystrophy
Myocardial infarction
Nucleosome