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

Characterization of transcriptional profiles associated with stress-induced neuronal activation in Arc-GFP mice

对Arc-GFP小鼠应激诱导神经元激活相关的转录谱进行表征

Butto, Tamer; Chongtham, Monika Chanu; Mungikar, Kanak; Hartwich, Dewi; Linke, Matthias; Ruffini, Nicolas; Radyushkin, Konstantin; Schweiger, Susann; Winter, Jennifer; Gerber, Susanne

A case of an Angelman-syndrome caused by an intragenic duplication of UBE3A uncovered by adaptive nanopore sequencing

通过自适应纳米孔测序发现一例由UBE3A基因内重复引起的Angelman综合征病例

Holthöfer, Laura; Diederich, Stefan; Haug, Verena; Lehmann, Lioba; Hewel, Charlotte; Paul, Norbert W; Schweiger, Susann; Gerber, Susanne; Linke, Matthias

SARS-CoV-2 surveillance in a hospital and control of an outbreak on a geriatric ward using whole genome sequencing

利用全基因组测序技术对医院内的SARS-CoV-2进行监测,并控制老年病房的疫情暴发。

Schmidt, Hanno; Lemmermann, Niels; Linke, Matthias; Bikár, Sven-Ernö; Runkel, Stefan; Schweiger-Seemann, Susann; Gerber, Susanne; Michel, André; Hankeln, Thomas; Veith, Marina; Kohnen, Wolfgang; Plachter, Bodo

Hypermethylation of RAD9A intron 2 in childhood cancer patients, leukemia and tumor cell lines suggest a role for oncogenic transformation

儿童癌症患者、白血病和肿瘤细胞系中 RAD9A 内含子 2 的过度甲基化提示其在致癌转化中发挥作用

Galetzka, Danuta; Böck, Julia; Wagner, Lukas; Dittrich, Marcus; Sinizyn, Olesja; Ludwig, Marco; Rossmann, Heidi; Spix, Claudia; Radsak, Markus; Scholz-Kreisel, Peter; Mirsch, Johanna; Linke, Matthias; Brenner, Walburgis; Marron, Manuela; Poplawski, Alicia; Haaf, Thomas; Schmidberger, Heinz; Prawitt, Dirk

Early life adversity targets the transcriptional signature of hippocampal NG2+ glia and affects voltage gated sodium (Na(v)) channels properties

早期生活逆境会影响海马NG2+胶质细胞的转录特征,并影响电压门控钠(Na(v))通道的特性。

Treccani, Giulia; Yigit, Hatice; Lingner, Thomas; Schleuβner, Vanessa; Mey, Franziska; van der Kooij, Michael A; Wennström, Malin; Herzog, David P; Linke, Matthias; Fricke, Markus; Schmeisser, Michael J; Wegener, Gregers; Mittmann, Thomas; Trotter, Jacqueline; Müller, Marianne B

Dppa3 expression is critical for generation of fully reprogrammed iPS cells and maintenance of Dlk1-Dio3 imprinting

Dppa3表达对于生成完全重编程的iPS细胞和维持Dlk1-Dio3印记至关重要。

Xu, Xingbo; Smorag, Lukasz; Nakamura, Toshinobu; Kimura, Tohru; Dressel, Ralf; Fitzner, Antje; Tan, Xiaoying; Linke, Matthias; Zechner, Ulrich; Engel, Wolfgang; Pantakani, D V Krishna

Myofibrillar instability exacerbated by acute exercise in filaminopathy

肌原纤维病中的急性运动加剧了肌原纤维的不稳定性

Frédéric Chevessier, Julia Schuld, Zacharias Orfanos, Anne-C Plank, Lucie Wolf, Alexandra Maerkens, Andreas Unger, Ursula Schlötzer-Schrehardt, Rudolf A Kley, Stephan Von Hörsten, Katrin Marcus, Wolfgang A Linke, Matthias Vorgerd, Peter F M van der Ven, Dieter O Fürst, Rolf Schröder

Growth hormone replacement therapy regulates microRNA-29a and targets involved in insulin resistance

生长激素替代疗法调节 microRNA-29a 和与胰岛素抵抗有关的靶点

Artur Galimov, Angelika Hartung, Roman Trepp, Alexander Mader, Martin Flück, Axel Linke, Matthias Blüher, Emanuel Christ, Jan Krützfeldt

Sirtuin-6-dependent genetic and epigenetic alterations are associated with poor clinical outcome in hepatocellular carcinoma patients

Sirtuin-6依赖的遗传和表观遗传改变与肝细胞癌患者的不良临床预后相关。

Marquardt, Jens U; Fischer, Kerstin; Baus, Katharina; Kashyap, Anubha; Ma, Shengyun; Krupp, Markus; Linke, Matthias; Teufel, Andreas; Zechner, Ulrich; Strand, Dennis; Thorgeirsson, Snorri S; Galle, Peter R; Strand, Susanne

Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences.

在小鼠模型和患有普拉德-威利综合征的人类中,印记 Ndn/NDN 等位基因沉默的随机丧失会产生功能性后果

Rieusset Anne, Schaller Fabienne, Unmehopa Unga, Matarazzo Valery, Watrin Françoise, Linke Matthias, Georges Beatrice, Bischof Jocelyn, Dijkstra Femke, Bloemsma Monique, Corby Severine, Michel François J, Wevrick Rachel, Zechner Ulrich, Swaab Dick, Dudley Keith, Bezin Laurent, Muscatelli Françoise