Результати пошуку - Ngo, Linh
- Показ 1 - 19 результатів із 19
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Utilisation and safety of catheter ablation of atrial fibrillation in public and private sector hospitals за авторством Ngo, Linh, Ali, Anna, Ganesan, Anand, Woodman, Richard J, Adams, Robert, Ranasinghe, Isuru
Опубліковано 2021Текст -
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Institutional Variation in 30‐Day Complications Following Catheter Ablation of Atrial Fibrillation за авторством Ngo, Linh, Ali, Anna, Ganesan, Anand, Woodman, Richard, Krumholz, Harlan M., Adams, Robert, Ranasinghe, Isuru
Опубліковано 2022Текст -
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A diazido mannose analog as a chemoenzymatic synthon for synthesizing di-N-acetyllegionaminic acid-containing glycosides за авторством Santra, Abhishek, Xiao, An, Yu, Hai, Li, Wanqing, Li, Yanhong, Ngo, Linh, McArthur, John B., Chen, Xi
Опубліковано 2018Текст -
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Safety and Efficacy of Leadless Pacemakers: A Systematic Review and Meta‐Analysis за авторством Ngo, Linh, Nour, Daniel, Denman, Russell A., Walters, Tomos E., Haqqani, Haris M., Woodman, Richard J., Ranasinghe, Isuru
Опубліковано 2021Текст -
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Bacurd2 is a novel interacting partner to Rnd2 which controls radial migration within the developing mammalian cerebral cortex за авторством Gladwyn-Ng, Ivan Enghian, Li, Shan Shan, Qu, Zhengdong, Davis, John Michael, Ngo, Linh, Haas, Matilda, Singer, Jeffrey, Heng, Julian Ik-Tsen
Опубліковано 2015Текст -
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Incidence of New Onset Atrial Fibrillation After Cardiovascular Surgery in Vietnam: Results From A Novel Screening Strategy за авторством Ngo, Linh, Duc, Thinh, Van, Ba Vu, Hoang, KienTrung, Tien Le, Dzung, Nguyen, Huu Cong, Nguyen, Thuy Tran, Freedman, Ben, Lowres, Nicole
Опубліковано 2021Текст -
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Dose Separation Does Not Overcome the Pharmacokinetic Interaction between Fosamprenavir and Lopinavir/Ritonavir за авторством 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.
Опубліковано 2006Текст -
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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 за авторством 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
Опубліковано 2016Текст -
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Germline heterozygous mutations in Nxf1 perturb RNA metabolism and trigger thrombocytopenia and lymphopenia in mice за авторством 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.
Опубліковано 2020Текст -
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Synthesis and Selective Functionalization of Thiadiazine 1,1-Dioxides with Efficacy in a Model of Huntington’s Disease§ за авторством 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
Опубліковано 2020Текст -
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Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway за авторством 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
Опубліковано 2016Текст -
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The HSA21 gene EURL/C21ORF91 controls neurogenesis within the cerebral cortex and is implicated in the pathogenesis of Down Syndrome за авторством 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
Опубліковано 2016Текст -
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De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation за авторством 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.
Опубліковано 2016Текст -
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Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities за авторством 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
Опубліковано 2012Текст