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

CRISPR-GPT for agentic automation of gene-editing experiments

CRISPR-GPT用于基因编辑实验的自动化

Qu, Yuanhao; Huang, Kaixuan; Yin, Ming; Zhan, Kanghong; Liu, Dyllan; Yin, Di; Cousins, Henry C; Johnson, William A; Wang, Xiaotong; Shah, Mihir; Altman, Russ B; Zhou, Denny; Wang, Mengdi; Cong, Le

Beta cell-targeted PD-1 agonist inhibits cell-mediated autoimmunity in pancreas tissue slices

靶向β细胞的PD-1激动剂抑制胰腺组织切片中的细胞介导的自身免疫

Becker, Matthew W; Brown, Matthew E; Wiseman, Katherine; Chiodetti, Ana Laura; Huber, Mollie K; Cuaycal, Alexandra E; Sintara, Pumin; Ferreira, Sandra M; Smurlick, Dylan; Barra, Jessie M; Ladd, Andrew M; Drotar, Denise M; Atkinson, Mark A; Weber, Peter; Al-Mossawi, Hussein; Russ, Holger A; Mahon, Tara M; Brusko, Todd M; Bossi, Giovanna; Phelps, Edward A

Loss of function variants in the primate-specific gene ZNF808 cause neonatal, transient and adult-onset diabetes

灵长类特异性基因 ZNF808 的功能缺失变异会导致新生儿糖尿病、暂时性糖尿病和成人发病型糖尿病。

Russ-Silsby, James; Colclough, Kevin; Johnson, Matthew B; Wakeling, Matthew N; Owens, Nick D L; Amaratunga, Shenali A; Flanagan, Sarah E; Patel, Kashyap A; Hattersley, Andrew T; De Franco, Elisa

TDP-43 directly inhibits mRNA accumulation in neurites through modulation of mRNA stability.

TDP-43 通过调节 mRNA 稳定性直接抑制神经突中 mRNA 的积累。

Moffatt Charlie, Arora Ankita, Vaeth Katherine F, Guzman Bryan B, Bhardwaj Gurprit, Hoelscher Audrey, Gifford Levi B, Russ Holger A, Dominguez Daniel, Taliaferro J Matthew

Bi-allelic variants in the non-protein-coding minor spliceosome components RNU6ATAC and RNU4ATAC cause syndromic monogenic autoimmune diabetes

非蛋白质编码的次要剪接体组分 RNU6ATAC 和 RNU4ATAC 的双等位基因变异会导致综合征型单基因自身免疫性糖尿病

Johnson, Matthew B; Russ-Silsby, James; Blair, Paul A; Govier, Molly; Bonfield, Georgia; Domingo-Vila, Clara; Wakeling, Matthew N; Oram, Richard A; Flanagan, Sarah E; Tree, Timothy I M; Patel, Kashyap A; Hattersley, Andrew T; De Franco, Elisa

Biallelic Pathogenic Variants in IL2RA Cause Neonatal-Onset Monogenic Autoimmune Diabetes

IL2RA基因的双等位致病变异导致新生儿期发病的单基因自身免疫性糖尿病

Bonfield, Georgia; Russ-Silsby, James; Ramchand, Suraj; Luckett, Amber M; Wakeling, Matthew N; Kulkarni, Abhishek; Nagesh, V Sri; Deeb, Asma; Ravikumar, K G; Nguyen, Phuong T K; Hattersley, Andrew T; Oram, Richard A; Flanagan, Sarah E; De Franco, Elisa; Johnson, Matthew B

Deciphering the Transcriptomic Signatures of Aging Across Organs in Mice

解读小鼠各器官衰老转录组特征

Morsy, Sarah; Scifo, Enzo; Xie, Kan; Schaaf, Kristina; Russ, Jenny; Paulusch, Stefan; De Domenico, Elena; Salomoni, Paolo; Bano, Daniele; Ehninger, Dan

Comparative effectiveness and persistence of ixekizumab and other b/tsDMARDs in patients with PsA from a real-world setting: 12-month results from the PRO-SPIRIT study

来自真实世界的研究:伊克珠单抗与其他生物/靶向合成DMARDs在银屑病关节炎患者中的疗效和持久性比较:PRO-SPIRIT研究的12个月结果

Marzo-Ortega, Helena; Sewerin, Philipp; Selmi, Carlo; Russ, Hagen; Ng, Khai Jing; Ngantcha, Marcus; Gerwien, Jens Gammeltoft; Kennedy, Dominika; Gallego-Flores, Adela; de la Torre, Inmaculada; Gladman, Dafna D; Coates, Laura C

Identification of an episignature for the MEF2C-associated syndrome

鉴定MEF2C相关综合征的表观遗传特征

Silva, Ananília; Haghshenas, Sadegheh; van der Laan, Liselot; Levy, Michael A; Relator, Raissa; McConkey, Haley; Kerkhof, Jennifer; Skinner, Steve A; Faivre, Laurence; Lespinasse, James; Vitobello, Antonio; Valenzuela, Irene; Scheffer, Ingrid E; Russ-Hall, Sophie J; Myers, Kenneth A; Tedder, Matthew L; Sadikovic, Bekim; Cooley Coleman, Jessica A

Personalized virtual reality in hemodialysis patients: a multicenter pilot study

个性化虚拟现实技术在血液透析患者中的应用:一项多中心试点研究

Russ, Philipp; Wenzel, Leo T; Bedenbender, Simon; Maeske, Michèle; Einloft, Jonas; Meyer, Hendrik L; Ganser, Andre; Bange, Gert; Hirsch, Martin C; Neubauer, Andreas; Benoehr, Peter; Grgic, Ivica