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

A Massively Parallel CRISPR-Based Screening Platform for Modifiers of Neuronal Activity.

基于 CRISPR 的大规模并行筛选平台,用于筛选神经元活动调节剂

Boggess Steven C, Gandhi Vaidehi, Tsai Ming-Chi, Marzette Emily, Teyssier Noam, Yu-Ying Chou Joanna, Hu Xiaoyu, Cramer Amber, Yadanar Lin, Shroff Kunal, Jeong Claire G, Eidenschenk Celine, Hanson Jesse E, Tian Ruilin, Kampmann Martin

Optimization of a Novel DEL Hit That Binds in the Cbl-b SH2 Domain and Blocks Substrate Binding

优化一种新型DEL先导化合物,该化合物能与Cbl-b SH2结构域结合并阻断底物结合

Liang, Jun; Lambrecht, Michael J; Arenzana, Teresita L; Aubert-Nicol, Samuel; Bao, Linda; Broccatelli, Fabio; Cai, Jianping; Eidenschenk, Celine; Everett, Christine; Garner, Thomas; Gruber, Felix; Haghshenas, Pouyan; Huestis, Malcolm P; Hsu, Peter L; Kou, Ponien; Jakalian, Araz; Larouche-Gauthier, Robin; Leclerc, Jean-Philippe; Leung, Dennis H; Martin, Aaron; Murray, Jeremy; Prangley, Madeleine; Rutz, Sascha; Kakiuchi-Kiyota, Satoko; Satz, Alexander Lee; Skelton, Nicholas J; Steffek, Micah; Stoffler, Daniel; Sudhamsu, Jawahar; Tan, Sophia; Wang, Jian; Wang, Shouliang; Wang, Qiuyue; Wendorff, Timothy J; Wichert, Moreno; Yadav, Arun; Yu, Christine; Wang, Xiaojing

Ru(II)-diimine complexes and cytochrome P450 working hand-in-hand

Ru(II)-二亚胺配合物与细胞色素P450协同作用

Eidenschenk, Celine; Cheruzel, Lionel

ENU-induced phenovariance in mice: inferences from 587 mutations

ENU诱导的小鼠表型变异:来自587个突变的推断

Arnold, Carrie N; Barnes, Michael J; Berger, Michael; Blasius, Amanda L; Brandl, Katharina; Croker, Ben; Crozat, Karine; Du, Xin; Eidenschenk, Celine; Georgel, Philippe; Hoebe, Kasper; Huang, Hua; Jiang, Zhengfan; Krebs, Philippe; La Vine, Diantha; Li, Xiaohong; Lyon, Stephen; Moresco, Eva Marie Y; Murray, Anne R; Popkin, Daniel L; Rutschmann, Sophie; Siggs, Owen M; Smart, Nora G; Sun, Lei; Tabeta, Koichi; Webster, Victoria; Tomisato, Wataru; Won, Sungyong; Xia, Yu; Xiao, Nengming; Beutler, Bruce

A mutation of Ikbkg causes immune deficiency without impairing degradation of IkappaB alpha.

Ikbkg 的突变会导致免疫缺陷,但不会损害 IkappaB α 的降解

Siggs Owen M, Berger Michael, Krebs Philippe, Arnold Carrie N, Eidenschenk Celine, Huber Christoph, Pirie Elaine, Smart Nora G, Khovananth Kevin, Xia Yu, McInerney Gerald, Karlsson Hedestam Gunilla B, Nemazee David, Beutler Bruce

Commitment to the regulatory T cell lineage requires CARMA1 in the thymus but not in the periphery.

向调节性 T 细胞谱系分化需要胸腺中的 CARMA1,但不需要外周组织中的 CARMA1

Barnes Michael J, Krebs Philippe, Harris Nathaniel, Eidenschenk Celine, Gonzalez-Quintial Rosana, Arnold Carrie N, Crozat Karine, Sovath Sosathya, Moresco Eva Marie, Theofilopoulos Argyrios N, Beutler Bruce, Hoebe Kasper

The Tpl2 mutation Sluggish impairs type I IFN production and increases susceptibility to group B streptococcal disease

Tpl2 突变 Sluggish 会损害 I 型干扰素的产生,并增加对 B 族链球菌疾病的易感性。

Xiao, Nengming; Eidenschenk, Celine; Krebs, Philippe; Brandl, Katharina; Blasius, Amanda L; Xia, Yu; Khovananth, Kevin; Smart, Nora G; Beutler, Bruce

Inflammation and autoimmunity caused by a SHP1 mutation depend on IL-1, MyD88, and a microbial trigger

由SHP1基因突变引起的炎症和自身免疫依赖于IL-1、MyD88和微生物触发因子。

Croker, Ben A; Lawson, Brian R; Rutschmann, Sophie; Berger, Michael; Eidenschenk, Celine; Blasius, Amanda L; Moresco, Eva Marie Y; Sovath, Sosathya; Cengia, Louise; Shultz, Leonard D; Theofilopoulos, Argyrios N; Pettersson, Sven; Beutler, Bruce Alan