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

The transcriptomic signature of DEPDC5 KO induced mTOR hyperactivation in human neurons and its response to rapamycin treatment

DEPDC5 KO 诱导的人类神经元 mTOR 过度激活的转录组特征及其对雷帕霉素治疗的反应

Jones, Mattson S O; Lindlar, Silvia; Ludwig, Johannes; Waltes, Regina; Kumar, Afsheen; V Brauchitsch, Sophie; Rossi, Andrea; Ullrich, Evelyn; Momma, Stefan; Freitag, Christine M; Hefendehl, Jasmin K; Klein, Karl Martin; Rosenow, Felix; Haslinger, Denise; Chiocchetti, Andreas G

The phenotypic and genotypic spectrum of epilepsy and intellectual disability in adults: Implications for genetic testing

成人癫痫和智力障碍的表型和基因型谱:对基因检测的启示

von Brauchitsch, Sophie; Haslinger, Denise; Lindlar, Silvia; Thiele, Holger; Bernsen, Natalie; Zahnert, Felix; Reif, Philipp S; Balcik, Yunus; Au, Ping Yee Billie; Josephson, Colin B; Altmüller, Janine; Strzelczyk, Adam; Knake, Susanne; Rosenow, Felix; Chiocchetti, Andreas; Klein, Karl Martin

Spectroscopic and in vitro Investigations of Fe2+ /α-Ketoglutarate-Dependent Enzymes Involved in Nucleic Acid Repair and Modification

参与核酸修复和修饰的 Fe2+ /α-酮戊二酸依赖性酶的光谱和体外研究

David Schmidl, Niko S W Lindlar Né Jonasson, Annika Menke, Sabine Schneider, Lena J Daumann

Drug-Resistant Juvenile Myoclonic Epilepsy: Misdiagnosis of Progressive Myoclonus Epilepsy

耐药性青少年肌阵挛性癫痫:误诊为进行性肌阵挛性癫痫

Martin, Sarah; Strzelczyk, Adam; Lindlar, Silvia; Krause, Kristina; Reif, Philipp S; Menzler, Katja; Chiocchetti, Andreas G; Rosenow, Felix; Knake, Susanne; Klein, Karl Martin

Loss of the Chr16p11.2 ASD candidate gene QPRT leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model

Chr16p11.2 ASD 候选基因 QPRT 的缺失导致 SH-SY5Y 神经元细胞模型中神经元分化异常

Denise Haslinger, Regina Waltes, Afsheen Yousaf, Silvia Lindlar, Ines Schneider, Chai K Lim, Meng-Miao Tsai, Boyan K Garvalov, Amparo Acker-Palmer, Nicolas Krezdorn, Björn Rotter, Till Acker, Gilles J Guillemin, Simone Fulda, Christine M Freitag, Andreas G Chiocchetti

Transcriptomic signatures of neuronal differentiation and their association with risk genes for autism spectrum and related neuropsychiatric disorders

神经元分化的转录组特征及其与自闭症谱系和相关神经精神疾病风险基因的关联

A G Chiocchetti, D Haslinger, J L Stein, L de la Torre-Ubieta, E Cocchi, T Rothämel, S Lindlar, R Waltes, S Fulda, D H Geschwind, C M Freitag