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

Global and regional ocean mass budget closure since 2003

自2003年以来,全球和区域海洋质量收支平衡已实现

Ludwigsen, Carsten Bjerre; Andersen, Ole Baltazar; Marzeion, Ben; Malles, Jan-Hendrik; Müller Schmied, Hannes; Döll, Petra; Watson, Christopher; King, Matt A

IsoSearch: An Untargeted and Unbiased Metabolite and Lipid Isotopomer Tracing Strategy from HR-LC-MS/MS Datasets

IsoSearch:一种基于 HR-LC-MS/MS 数据集的无靶向、无偏代谢物和脂质同位素追踪策略

He Huang, Min Yuan, Phillip Seitzer, Susan Ludwigsen, John M Asara

Concerted regulation of ISWI by an autoinhibitory domain and the H4 N-terminal tail

自抑制结构域和 H4 N 端尾对 ISWI 的协同调控

Johanna Ludwigsen, Sabrina Pfennig, Ashish K Singh, Christina Schindler, Nadine Harrer, Ignasi Forné, Martin Zacharias, Felix Mueller-Planitz

Nucleosome spacing generated by ISWI and CHD1 remodelers is constant regardless of nucleosome density

无论核小体密度如何,ISWI 和 CHD1 重塑物产生的核小体间距都是恒定的

Corinna Lieleg, Philip Ketterer, Johannes Nuebler, Johanna Ludwigsen, Ulrich Gerland, Hendrik Dietz, Felix Mueller-Planitz, Philipp Korber

EU Life revives funding debate

欧盟生命科学项目重新引发资金辩论

Ludwigsen, Johanna; Klinker, Henrike; Mueller-Planitz, Felix; Hunter, Philip

Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy

对扩张型心肌病患者中发现的TNNT2突变进行临床和功能表征

Hershberger, Ray E; Pinto, Jose Renato; Parks, Sharie B; Kushner, Jessica D; Li, Duanxiang; Ludwigsen, Susan; Cowan, Jason; Morales, Ana; Parvatiyar, Michelle S; Potter, James D

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

对 324 例无亲缘关系的特发性或家族性扩张型心肌病患者进行 Lamin A/C 基因突变分析

Parks, Sharie B; Kushner, Jessica D; Nauman, Deirdre; Burgess, Donna; Ludwigsen, Susan; Peterson, Amanda; Li, Duanxiang; Jakobs, Petra; Litt, Michael; Porter, Charles B; Rahko, Peter S; Hershberger, Ray E

Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy

在313例家族性或特发性扩张型心肌病患者中,鉴定出MYH7、TNNT2、SCN5A、CSRP3、LBD3和TCAP基因的编码序列突变。

Hershberger, Ray E; Parks, Sharie B; Kushner, Jessica D; Li, Duanxiang; Ludwigsen, Susan; Jakobs, Petra; Nauman, Deirdre; Burgess, Donna; Partain, Julie; Litt, Michael

Anaemia of rheumatoid arthritis: serum erythropoietin concentrations and red cell distribution width in relation to iron status

类风湿性关节炎贫血:血清促红细胞生成素浓度和红细胞分布宽度与铁状态的关系

Nielsen, O J; Andersen, L S; Ludwigsen, E; Bouchelouche, P; Hansen, T M; Birgens, H; Hansen, N E