検索結果 - Ngo, Linh
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Bacurd2 is a novel interacting partner to Rnd2 which controls radial migration within the developing mammalian cerebral cortex 著者: Gladwyn-Ng, Ivan Enghian, Li, Shan Shan, Qu, Zhengdong, Davis, John Michael, Ngo, Linh, Haas, Matilda, Singer, Jeffrey, Heng, Julian Ik-Tsen
出版事項 2015テキスト -
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Dose Separation Does Not Overcome the Pharmacokinetic Interaction between Fosamprenavir and Lopinavir/Ritonavir 著者: Corbett, Amanda H., Patterson, Kristine B., Tien, Hsiao-Chuan, Kalvass, Leslie A., Eron, Joseph J., Ngo, Linh T., Lim, Michael L., Kashuba, Angela D. M.
出版事項 2006テキスト -
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Bacurd1/Kctd13 and Bacurd2/Tnfaip1 are interacting partners to Rnd proteins which influence the long-term positioning and dendritic maturation of cerebral cortical neurons 著者: Gladwyn-Ng, Ivan, Huang, Lieven, Ngo, Linh, Li, Shan Shan, Qu, Zhengdong, Vanyai, Hannah Kate, Cullen, Hayley Daniella, Davis, John Michael, Heng, Julian Ik-Tsen
出版事項 2016テキスト -
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Germline heterozygous mutations in Nxf1 perturb RNA metabolism and trigger thrombocytopenia and lymphopenia in mice 著者: Chappaz, Stéphane, Law, Charity W., Dowling, Mark R., Carey, Kirstyn T., Lane, Rachael M., Ngo, Linh H., Wickramasinghe, Vihandha O., Smyth, Gordon K., Ritchie, Matthew E., Kile, Benjamin T.
出版事項 2020テキスト -
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Synthesis and Selective Functionalization of Thiadiazine 1,1-Dioxides with Efficacy in a Model of Huntington’s Disease§ 著者: Terrab, Leila, Rosenker, Christopher J., Johnstone, Lisa, Ngo, Linh K., Zhang, Li, Ware, Nathaniel F., Miller, Bettina, Topacio, Andrea Z., Sannino, Sara, Brodsky, Jeffrey L., Wipf, Peter
出版事項 2020テキスト -
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Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway 著者: Edvardson, Shimon, Tian, Guoling, Cullen, Hayley, Vanyai, Hannah, Ngo, Linh, Bhat, Saiuj, Aran, Adi, Daana, Muhannad, Da’amseh, Naderah, Abu-Libdeh, Bassam, Cowan, Nicholas J., Heng, Julian Ik-Tsen, Elpeleg, Orly
出版事項 2016テキスト -
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The HSA21 gene EURL/C21ORF91 controls neurogenesis within the cerebral cortex and is implicated in the pathogenesis of Down Syndrome 著者: Li, Shan Shan, Qu, Zhengdong, Haas, Matilda, Ngo, Linh, Heo, You Jeong, Kang, Hyo Jung, Britto, Joanne Maria, Cullen, Hayley Daniella, Vanyai, Hannah Kate, Tan, Seong-Seng, Chan-Ling, Tailoi, Gunnersen, Jenny Margaret, Heng, Julian Ik-Tsen
出版事項 2016テキスト -
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De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation 著者: Haas, Matilda A., Ngo, Linh, Li, Shan Shan, Schleich, Sibylle, Qu, Zhengdong, Vanyai, Hannah K., Cullen, Hayley D., Cardona-Alberich, Aida, Gladwyn-Ng, Ivan E., Pagnamenta, Alistair T., Taylor, Jenny C., Stewart, Helen, Kini, Usha, Duncan, Kent E., Teleman, Aurelio A., Keays, David A., Heng, Julian I.-T.
出版事項 2016テキスト -
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Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities 著者: Breuss, Martin, Heng, Julian Ik-Tsen, Poirier, Karine, Tian, Guoling, Jaglin, Xavier Hubert, Qu, Zhengdong, Braun, Andreas, Gstrein, Thomas, Ngo, Linh, Haas, Matilda, Bahi-Buisson, Nadia, Moutard, Marie-Laure, Passemard, Sandrine, Verloes, Alain, Gressens, Pierre, Xie, Yunli, Robson, Kathryn J.H., Rani, Deepa Selvi, Thangaraj, Kumarasamy, Clausen, Tim, Chelly, Jamel, Cowan, Nicholas Justin, Keays, David Anthony
出版事項 2012テキスト