Resultados de procura - Ngo, Linh
- Mostrando 1 - 19 Resultados de 19
-
1
-
2
-
3
-
4
-
5
-
6
-
7
-
8
A diazido mannose analog as a chemoenzymatic synthon for synthesizing di-N-acetyllegionaminic acid-containing glycosides por Santra, Abhishek, Xiao, An, Yu, Hai, Li, Wanqing, Li, Yanhong, Ngo, Linh, McArthur, John B., Chen, Xi
Publicado 2018Text -
9
-
10
Bacurd2 is a novel interacting partner to Rnd2 which controls radial migration within the developing mammalian cerebral cortex por Gladwyn-Ng, Ivan Enghian, Li, Shan Shan, Qu, Zhengdong, Davis, John Michael, Ngo, Linh, Haas, Matilda, Singer, Jeffrey, Heng, Julian Ik-Tsen
Publicado 2015Text -
11
Incidence of New Onset Atrial Fibrillation After Cardiovascular Surgery in Vietnam: Results From A Novel Screening Strategy por Ngo, Linh, Duc, Thinh, Van, Ba Vu, Hoang, KienTrung, Tien Le, Dzung, Nguyen, Huu Cong, Nguyen, Thuy Tran, Freedman, Ben, Lowres, Nicole
Publicado 2021Text -
12
Dose Separation Does Not Overcome the Pharmacokinetic Interaction between Fosamprenavir and Lopinavir/Ritonavir por 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.
Publicado 2006Text -
13
Bacurd1/Kctd13 and Bacurd2/Tnfaip1 are interacting partners to Rnd proteins which influence the long-term positioning and dendritic maturation of cerebral cortical neurons por 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
Publicado 2016Text -
14
Germline heterozygous mutations in Nxf1 perturb RNA metabolism and trigger thrombocytopenia and lymphopenia in mice por 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.
Publicado 2020Text -
15
Synthesis and Selective Functionalization of Thiadiazine 1,1-Dioxides with Efficacy in a Model of Huntington’s Disease§ por 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
Publicado 2020Text -
16
Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway por 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
Publicado 2016Text -
17
The HSA21 gene EURL/C21ORF91 controls neurogenesis within the cerebral cortex and is implicated in the pathogenesis of Down Syndrome por 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
Publicado 2016Text -
18
De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation por 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.
Publicado 2016Text -
19
Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities por 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
Publicado 2012Text