日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Sulfur-containing class of broad-spectrum antivirals improves influenza virus vaccine development

含硫广谱抗病毒药物可促进流感病毒疫苗的研发

Buchholz, David W; Pacheco, Armando; Pal, Sreetama; Monreal, I Abrrey; Xu, Shi; Imbiakha, Brian; Sahler, Julie; Jager, Mason; Lai, Alex Liqi; Contreras, Erik M; Ezzatpour, Shahrzad; Cook, Brandan; Ralalage, Elshan; Liu, Qian; Yeo, Yao Yu; Ma, Andrew; Byun, Haewon; Shah, Obaed; Zamora, J Lizbeth Reyes; Shil, Niraj K; Jones-Burrage, Sara; Pritchard, Suzanne M; Yang, Chuntao; Zhao, Yu; Mohamed, Zeinab J; Xu, Cheyan; Jung, Michael J; Van de Walle, Gerlinde R; Mukhopadhyay, Suchetana; Shimamura, Masako; Goodman, Alan G; Hardy, Michele; Bose, Santanu; Nicola, Anthony V; Freed, Jack H; August, Avery; Daniel, Susan; Chlanda, Petr; Jones, Jace W; Xian, Ming; Aguilar, Hector C

Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatonia

DENND2B基因变异与神经发育障碍、精神病和紧张症的易感性相关。

Murthy, Harsha; Hoang, Ny; Stark, Jamie C; Cui, Sunny; Pannia, Emanuela; Tsoi, Chung Ting; Harris, Simon; Ceolin, C'airah; Verhaeghe, Lauren; Scholten, Sydney; Baribeau, Danielle; Summers, Jane; Costain, Gregory; Selvanayagam, Thanuja; Howe, Jennifer L; Lewis, M E Suzanne; Brunet, Theresa; Rieger, Susanne; Rosenfeld, Jill A; Craigen, William J; Burrage, Lindsay C; Christie, Michelle R; Baldwin, Deborah; Wentzensen, Ingrid M; Keren, Boris; Cogne, Benjamin; Isidor, Bertrand; Afenjar, Alexandra; Elshafie, Reem M; Bastaki, Laila; Alkanderi, Sumaya; Myers, Kenneth A; Demarest, Scott; Angione, Katie; Abbott, Megan; Campeau, Philippe M; Dowling, James J; Mendoza-Londono, Roberto; Scherer, Stephen W; Deshwar, Ashish R; Vorstman, Jacob

Setd1a Loss-of-function Disrupts Epigenetic Regulation of Ribosomal Genes via Altered DNA Methylation

Setd1a功能缺失通过改变DNA甲基化破坏核糖体基因的表观遗传调控

Clifton, Nicholas E; Policicchio, Stefania; Walker, Emma M; Castanho, Isabel; Bosworth, Matthew L; Saravanaraj, Kirtikesav S; Burrage, Joe; Hall, Jeremy; Dempster, Emma L; Hannon, Eilis; Isles, Anthony R; Mill, Jonathan

Fock state probability changes in open quantum systems

开放量子系统中的Fock态概率变化

Burrage, Clare; Käding, Christian

Two commonly reported incidental variants in OTC are associated with late-onset disease

OTC基因中两种常见的偶然变异与晚发性疾病相关。

Lang, Steven H; Lo, Russell S; Cromie, Gareth A; Dudley, Aimée M; Mew, Nicholas Ah; Simpson, Kara; Sutton, Vernon Reid; Darilek, Sandra; Ali, Saima; Snyder, Matthew T; Lee, Brendan; Marom, Ronit; Nagamani, Sandesh C S; Burrage, Lindsay C

Nitrite supplementation alleviates cerebrovascular dysfunction in chronically stressed mice, but cognitive decline remains

亚硝酸盐补充剂可缓解慢性应激小鼠的脑血管功能障碍,但认知能力下降仍然存在。

Burrage, Emily; Coblentz, Tyler; Prabhu, Saina S; Eminhizer, Nicole M; Childers, Ryan; Bryner, Randall W; Lewis, Sara E; Maxwell, Brooke A; DeVallance, Evan R; Kelley, Eric E; Chantler, Paul D

Integrative exome sequencing and machine learning identify MICB and interferon pathway genes as contributors to SSc risk

整合外显子组测序和机器学习技术发现,MICB 和干扰素通路基因是系统性硬化症风险的促成因素。

Ketkar, Shamika; Dai, Hongzheng; Burrage, Lindsay; Murdock, David; Dawson, Brian; Acosta-Herrera, Marialbert; Kerick, Martin; Martin, Javier; Wilhelm, Kevin; Asmussen, Jennifer Kay; Lichtarge, Olivier; Center, Regeneron Genetics; Assassi, Shervin; Mayes, Maureen D; Lee, Brendan H

Harnessing 12-lead ECG and MRI data to personalise repolarisation profiles in cardiac digital twin models for enhanced virtual drug testing

利用12导联心电图和磁共振成像数据,在心脏数字孪生模型中个性化定制复极化曲线,以增强虚拟药物测试效果

Camps, Julia; Wang, Zhinuo Jenny; Doste, Ruben; Berg, Lucas Arantes; Holmes, Maxx; Lawson, Brodie; Tomek, Jakub; Burrage, Kevin; Bueno-Orovio, Alfonso; Rodriguez, Blanca

Amyotrophic lateral sclerosis and frontotemporal dementia mutation reduces endothelial TDP-43 and causes blood-brain barrier defects

肌萎缩侧索硬化症和额颞叶痴呆的基因突变会降低内皮细胞TDP-43的水平,并导致血脑屏障缺陷。

Ashok Cheemala,Amy L Kimble,Emily N Burrage,Stephen B Helming,Jordan D Tyburski,Nathan K Leclair,Omar M Omar,Aamir R Zuberi,Melissa Murphy,Evan R Jellison,Bo Reese,Xiangyou Hu,Cathleen M Lutz,Riqiang Yan,Patrick A Murphy

Amyotrophic lateral sclerosis and frontotemporal dementia mutation reduces endothelial TDP-43 and causes blood-brain barrier defects

肌萎缩侧索硬化症和额颞叶痴呆的基因突变会降低内皮细胞TDP-43的水平,并导致血脑屏障缺陷。

Ashok Cheemala ,Amy L Kimble ,Emily N Burrage ,Stephen B Helming ,Jordan D Tyburski ,Nathan K Leclair ,Omar M Omar ,Aamir R Zuberi ,Melissa Murphy ,Evan R Jellison ,Bo Reese ,Xiangyou Hu ,Cathleen M Lutz ,Riqiang Yan ,Patrick A Murphy