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

SOD2 is a regulator of proteasomal degradation promoting an adaptive cellular starvation response.

SOD2 是蛋白酶体降解的调节因子,可促进细胞适应性饥饿反应

Ibrahim Nurul Khalida, Schreek Sabine, Cinar Buesra, Stasche Anna Sophie, Lee Su Hyun, Zeug Andre, Dolgner Tim, Niessen Julia, Ponimaskin Evgeni, Shcherbata Halyna, Fehlhaber Beate, Bourquin Jean-Pierre, Bornhauser Beat, Stanulla Martin, Pich Andreas, Gutierrez Alejandro, Hinze Laura

Chemotherapy-related hyperbilirubinemia in pediatric acute lymphoblastic leukemia: a genome-wide association study from the AIEOP-BFM ALL study group

儿童急性淋巴细胞白血病化疗相关性高胆红素血症:来自 AIEOP-BFM ALL 研究组的全基因组关联研究

Junk, Stefanie V; Schaeffeler, Elke; Zimmermann, Martin; Möricke, Anja; Beier, Rita; Schütte, Peter; Fedders, Birthe; Alten, Julia; Hinze, Laura; Klein, Norman; Kulozik, Andreas; Muckenthaler, Martina U; Koehler, Rolf; Borkhardt, Arndt; Vijayakrishnan, Jayaram; Ellinghaus, David; Forster, Michael; Franke, Andre; Wintering, Astrid; Kratz, Christian P; Schrappe, Martin; Schwab, Matthias; Houlston, Richard S; Cario, Gunnar; Stanulla, Martin

Detection of Cancer Mutations by Urine Liquid Biopsy as a Potential Tool in the Clinical Management of Bladder Cancer Patients

尿液活检检测癌症突变作为膀胱癌患者临床管理的潜在工具

Ibrahim, Nurul Khalida; Eraky, Ahmed; Eggers, Jan; Steiert, Tim Alexander; Sebens, Susanne; Jünemann, Klaus-Peter; Hendricks, Alexander; Bang, Corinna; Stanulla, Martin; Franke, Andre; Hamann, Claudius; Röcken, Christoph; Arnold, Norbert; Hinze, Laura; Forster, Michael

Acquired von Willebrand syndrome (AVWS) type 2, characterized by decreased high molecular weight multimers, is common in children with severe pulmonary hypertension (PH)

获得性血管性血友病(AVWS)2 型,其特征是高分子量多聚体减少,常见于患有严重肺动脉高压(PH)的儿童。

Wieland, Ivonne; Diekmann, Franziska; Carlens, Julia; Hinze, Laura; Lambeck, Katharina; Jack, Thomas; Hansmann, Georg

Hepatic sinusoidal obstruction syndrome and short-term application of 6-thioguanine in pediatric acute lymphoblastic leukemia

肝窦阻塞综合征及6-硫鸟嘌呤短期应用治疗儿童急性淋巴细胞白血病

Stanulla, Martin; Schaeffeler, Elke; Möricke, Anja; Buchmann, Swantje; Zimmermann, Martin; Igel, Svitlana; Schmiegelow, Kjeld; Flotho, Christian; Hartmann, Hans; Illsinger, Sabine; Sauerbrey, Axel; Junk, Stefanie V; Schütte, Peter; Hinze, Laura; Lauten, Melchior; Modlich, Simon; Kolb, Reinhard; Rossig, Claudia; Schwabe, Georg; Gnekow, Astrid K; Fleischhack, Gudrun; Schlegel, Paul Gerhard; Schünemann, Holger J; Kratz, Christian P; Cario, Gunnar; Schrappe, Martin; Schwab, Matthias

Impact of NUDT15 genetics on severe thiopurine-related hematotoxicity in patients with European ancestry

NUDT15基因对欧洲血统患者严重硫嘌呤相关血液毒性的影响

Schaeffeler, Elke; Jaeger, Simon U; Klumpp, Verena; Yang, Jun J; Igel, Svitlana; Hinze, Laura; Stanulla, Martin; Schwab, Matthias