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

First-in-class MKK4 inhibitors enhance liver regeneration and prevent liver failure.

首创的 MKK4 抑制剂可增强肝脏再生并预防肝衰竭

Zwirner Stefan, Abu Rmilah Anan A, Klotz Sabrina, Pfaffenroth Bent, Kloevekorn Philip, Moschopoulou Athina A, Schuette Svenja, Haag Mathias, Selig Roland, Li Kewei, Zhou Wei, Nelson Erek, Poso Antti, Chen Harvey, Amiot Bruce, Jia Yao, Minshew Anna, Michalak Gregory, Cui Wei, Rist Elke, Longerich Thomas, Jung Birgit, Felgendreff Philipp, Trompak Omelyan, Premsrirut Prem K, Gries Katharina, Muerdter Thomas E, Heinkele Georg, Wuestefeld Torsten, Shapiro David, Weissbach Markus, Koenigsrainer Alfred, Sipos Bence, Ab Eiso, Zacarias Magdalena Ortiz, Theisgen Stephan, Gruenheit Nicole, Biskup Saskia, Schwab Matthias, Albrecht Wolfgang, Laufer Stefan, Nyberg Scott, Zender Lars

Dynamics of Ligand Binding to a Rigid Glycosidase*

配体与刚性糖苷酶结合的动力学*

Ben Bdira, Fredj; Waudby, Christopher A; Volkov, Alexander N; Schröder, Sybrin P; Ab, Eiso; Codée, Jeroen D C; Overkleeft, Hermen S; Aerts, Johannes M F G; van Ingen, Hugo; Ubbink, Marcellus

Correction to: (1)H, (13)C, (15)N backbone and IVL methyl group resonance assignment of the fungal β-glucosidase from Trichoderma reesei

更正:里氏木霉真菌β-葡萄糖苷酶的(1)H、(13)C、(15)N骨架和IVL甲基共振归属

Makraki, Eleni; Carneiro, Marta G; Heyam, Alex; Ab, Eiso; Siegal, Gregg; Hubbard, Roderick E

Application of fragment-based drug discovery to membrane proteins: identification of ligands of the integral membrane enzyme DsbB

将基于片段的药物发现方法应用于膜蛋白:鉴定整合膜酶DsbB的配体

Früh, Virginie; Zhou, Yunpeng; Chen, Dan; Loch, Caroline; Ab, Eiso; Grinkova, Yelena N; Verheij, Herman; Sligar, Stephen G; Bushweller, John H; Siegal, Gregg

The high-resolution NMR structure of the R21A Spc-SH3:P41 complex: understanding the determinants of binding affinity by comparison with Abl-SH3

R21A Spc-SH3:P41复合物的高分辨率核磁共振结构:通过与Abl-SH3的比较了解结合亲和力的决定因素

Casares, Salvador; Ab, Eiso; Eshuis, Henk; Lopez-Mayorga, Obdulio; van Nuland, Nico A J; Conejero-Lara, Francisco

DWNN, a novel ubiquitin-like domain, implicates RBBP6 in mRNA processing and ubiquitin-like pathways

DWNN是一种新型的类泛素结构域,表明RBBP6参与mRNA加工和类泛素通路。

Pugh, David J R; Ab, Eiso; Faro, Andrew; Lutya, Portia T; Hoffmann, Eberhard; Rees, D Jasper G