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

Muscle phenotype of AGAT- and GAMT-deficient mice after simvastatin exposure

辛伐他汀暴露后 AGAT 和 GAMT 缺乏小鼠的肌肉表型

Ali Sasani, Sönke Hornig, Ricarda Grzybowski, Kathrin Cordts, Erik Hanff, Dimitris Tsikas, Rainer Böger, Christian Gerloff, Dirk Isbrandt, Axel Neu, Edzard Schwedhelm, Chi-Un Choe

de novo MEPCE nonsense variant associated with a neurodevelopmental disorder causes disintegration of 7SK snRNP and enhanced RNA polymerase II activation

与神经发育障碍相关的MEPCE新发无义突变导致7SK snRNP解体和RNA聚合酶II活性增强。

Pauline E Schneeberger ,Tatjana Bierhals ,Axel Neu ,Maja Hempel ,Kerstin Kutsche

Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits

新型 GFM2 变异与早发性线粒体疾病的神经系统表现以及 OXPHOS 亚基表达受损有关

Ruth I C Glasgow, Kyle Thompson, Inês A Barbosa, Langping He, Charlotte L Alston, Charu Deshpande, Michael A Simpson, Andrew A M Morris, Axel Neu, Ulrike Löbel, Julie Hall, Holger Prokisch, Tobias B Haack, Maja Hempel, Robert McFarland, Robert W Taylor

Transcriptomic and metabolic analyses reveal salvage pathways in creatine-deficient AGAT(-/-) mice

转录组学和代谢分析揭示肌酸缺乏的 AGAT(-/-) 小鼠的挽救途径

Malte Stockebrand, Ali Sasani Nejad, Axel Neu, Kusum K Kharbanda, Kathrin Sauter, Stefan Schillemeit, Dirk Isbrandt, Chi-Un Choe