Torthaí cuardaigh - Ngo, Linh
- 1 - 19 toradh as 19 á dtaispeáint
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21(st) Century Natural Product Research and Drug Development and Traditional Medicines de réir Ngo, Linh T., Okogun, Joseph I., Folk, William R.
Foilsithe / Cruthaithe 2013Téacs -
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Utilisation and safety of catheter ablation of atrial fibrillation in public and private sector hospitals de réir Ngo, Linh, Ali, Anna, Ganesan, Anand, Woodman, Richard J, Adams, Robert, Ranasinghe, Isuru
Foilsithe / Cruthaithe 2021Téacs -
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Institutional Variation in 30‐Day Complications Following Catheter Ablation of Atrial Fibrillation de réir Ngo, Linh, Ali, Anna, Ganesan, Anand, Woodman, Richard, Krumholz, Harlan M., Adams, Robert, Ranasinghe, Isuru
Foilsithe / Cruthaithe 2022Téacs -
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A diazido mannose analog as a chemoenzymatic synthon for synthesizing di-N-acetyllegionaminic acid-containing glycosides de réir Santra, Abhishek, Xiao, An, Yu, Hai, Li, Wanqing, Li, Yanhong, Ngo, Linh, McArthur, John B., Chen, Xi
Foilsithe / Cruthaithe 2018Téacs -
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Safety and Efficacy of Leadless Pacemakers: A Systematic Review and Meta‐Analysis de réir Ngo, Linh, Nour, Daniel, Denman, Russell A., Walters, Tomos E., Haqqani, Haris M., Woodman, Richard J., Ranasinghe, Isuru
Foilsithe / Cruthaithe 2021Téacs -
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Bacurd2 is a novel interacting partner to Rnd2 which controls radial migration within the developing mammalian cerebral cortex de réir Gladwyn-Ng, Ivan Enghian, Li, Shan Shan, Qu, Zhengdong, Davis, John Michael, Ngo, Linh, Haas, Matilda, Singer, Jeffrey, Heng, Julian Ik-Tsen
Foilsithe / Cruthaithe 2015Téacs -
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Incidence of New Onset Atrial Fibrillation After Cardiovascular Surgery in Vietnam: Results From A Novel Screening Strategy de réir Ngo, Linh, Duc, Thinh, Van, Ba Vu, Hoang, KienTrung, Tien Le, Dzung, Nguyen, Huu Cong, Nguyen, Thuy Tran, Freedman, Ben, Lowres, Nicole
Foilsithe / Cruthaithe 2021Téacs -
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Dose Separation Does Not Overcome the Pharmacokinetic Interaction between Fosamprenavir and Lopinavir/Ritonavir de réir 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.
Foilsithe / Cruthaithe 2006Téacs -
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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 de réir 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
Foilsithe / Cruthaithe 2016Téacs -
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Germline heterozygous mutations in Nxf1 perturb RNA metabolism and trigger thrombocytopenia and lymphopenia in mice de réir 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.
Foilsithe / Cruthaithe 2020Téacs -
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Synthesis and Selective Functionalization of Thiadiazine 1,1-Dioxides with Efficacy in a Model of Huntington’s Disease§ de réir 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
Foilsithe / Cruthaithe 2020Téacs -
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Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway de réir 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
Foilsithe / Cruthaithe 2016Téacs -
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The HSA21 gene EURL/C21ORF91 controls neurogenesis within the cerebral cortex and is implicated in the pathogenesis of Down Syndrome de réir 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
Foilsithe / Cruthaithe 2016Téacs -
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De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation de réir 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.
Foilsithe / Cruthaithe 2016Téacs -
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Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities de réir 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
Foilsithe / Cruthaithe 2012Téacs