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

Proteomic and bioinformatic profiling of neutrophils in CLL reveals functional defects that predispose to bacterial infections

CLL 中性粒细胞的蛋白质组学和生物信息学分析揭示了易发生细菌感染的功能缺陷

Nirojah Subramaniam, Jenny Bottek, Stephanie Thiebes, Kristina Zec, Matthias Kudla, Camille Soun, Elena de Dios Panal, Julia K Lill, Aaron Pfennig, Ralf Herrmann, Kirsten Bruderek, Sven Rahmann, Sven Brandau, Patricia Johansson, Hans Christian Reinhardt, Jan Dürig, Martina Seiffert, Thilo Bracht, Ba

Involvement of CXCL1/CXCR2 During Microglia Activation Following Inflammation-Sensitized Hypoxic-Ischemic Brain Injury in Neonatal Rats

CXCL1/CXCR2 参与新生大鼠炎症致敏缺氧缺血性脑损伤后小胶质细胞的激活

Meray Serdar, Karina Kempe, Ralf Herrmann, Daniel Picard, Marc Remke, Josephine Herz, Ivo Bendix, Ursula Felderhoff-Müser, Hemmen Sabir

An advanced modeling study on the impacts and atmospheric implications of multiphase dimethyl sulfide chemistry

一项关于多相二甲基硫化学反应的影响及其大气效应的高级建模研究

Hoffmann, Erik Hans; Tilgner, Andreas; Schrödner, Roland; Bräuer, Peter; Wolke, Ralf; Herrmann, Hartmut

ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies

ISPD 基因突变是先天性和肢带型肌营养不良症的常见原因

Sebahattin Cirak, Aileen Reghan Foley, Ralf Herrmann, Tobias Willer, Shu Yau, Elizabeth Stevens, Silvia Torelli, Lina Brodd, Alisa Kamynina, Petr Vondracek, Helen Roper, Cheryl Longman, Rudolf Korinthenberg, Gianni Marrosu, Peter Nürnberg; UK10K Consortium; Daniel E Michele, Vincent Plagnol, Matt Hu

DNA-methylome analysis of mouse intestinal adenoma identifies a tumour-specific signature that is partly conserved in human colon cancer

对小鼠肠道腺瘤的DNA甲基化组分析发现了一种肿瘤特异性特征,该特征在人类结肠癌中部分保守。

Grimm, Christina; Chavez, Lukas; Vilardell, Mireia; Farrall, Alexandra L; Tierling, Sascha; Böhm, Julia W; Grote, Phillip; Lienhard, Matthias; Dietrich, Jörn; Timmermann, Bernd; Walter, Jörn; Schweiger, Michal R; Lehrach, Hans; Herwig, Ralf; Herrmann, Bernhard G; Morkel, Markus

Kelch-like homologue 9 mutation is associated with an early onset autosomal dominant distal myopathy

Kelch 样同源物 9 突变与早发性常染色体显性远端肌病有关

Sebahattin Cirak, Florian von Deimling, Shrikesh Sachdev, Wesley J Errington, Ralf Herrmann, Carsten Bönnemann, Knut Brockmann, Stephan Hinderlich, Tom H Lindner, Alice Steinbrecher, Katrin Hoffmann, Gilbert G Privé, Mark Hannink, Peter Nürnberg, Thomas Voit

Intragenic deletion in the LARGE gene causes Walker-Warburg syndrome

LARGE基因内部缺失导致沃克-瓦尔堡综合征

Jeroen van Reeuwijk,Prabhjit K Grewal, Mustafa A M Salih, Daniel Beltrán-Valero de Bernabé, Jenny M McLaughlan, Caroline B Michielse, Ralf Herrmann, Jane E Hewitt, Alice Steinbrecher, Mohamed Z Seidahmed, Mohamed M Shaheed, Abdullah Abomelha, Han G Brunner, Hans van Bokhoven, Thomas Voit

Cross-species hybridisation of human and bovine orthologous genes on high density cDNA microarrays

在高密度cDNA微阵列上进行人和牛同源基因的跨物种杂交

Adjaye, James; Herwig, Ralf; Herrmann, Doris; Wruck, Wasco; Benkahla, Alia; Brink, Thore C; Nowak, Monika; Carnwath, Joseph W; Hultschig, Claus; Niemann, Heiner; Lehrach, Hans