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CDKL5 protein substitution therapy rescues neurological phenotypes of a mouse model of CDKL5 disorder

机译：CDK15蛋白替代治疗拯救了CDKL5疾病小鼠模型的神经表谱

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Stefania Trazzi; Marianna De Franceschi; Claudia Fuchs; Stefano Bastianini; Rocchina Viggiano; Leonardo Lupori; Raffaele Mazziotti; Giorgio Medici; Viviana Lo Martire; Elisa Ren; Roberto Rimondini; Giovanna Zoccoli; Renata Bartesaghi; Tommaso Pizzorusso; Elisabetta Ciani;
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1. CDKL5 protein substitution therapy rescues neurological phenotypes of a mouse model of CDKL5 disorder [J] . Trazzi Stefania, De Franceschi Marianna, Fuchs Claudia, Human Molecular Genetics . 2018,第9期

机译：CDKL5蛋白替代治疗拯救了CDKL5疾病小鼠模型的神经表谱
2. Inhibition of p21-activated kinase rescues disrupted phenotype in a mouse model of CDKL5 deficiency disorder [J] . Talamo M. C., Pellas M., Urbinati C., European neuropsychopharmacology: the journal of the European College of Neuropsychopharmacology . 2020,第1期

机译：P21活化激酶抑制在CDK15缺陷障碍的小鼠模型中损伤的表型中断
3. Pharmacotherapy with sertraline rescues brain development and behavior in a mouse model of CDKL5 deficiency disorder [J] . Neuropharmacology . 2020,第期

机译：药物治疗与塞拉尔氏素拯救了CDKL5缺陷障碍的小鼠模型中的脑部发育和行为
4. Identification of Substrates of CDKL5, a Kinase Involved in Severe Neurodevelopmental Disorders, Through siKALIP [C] . Justine V. Arrington, Juan Sebastian Paez Paez, W. Andy Tao ASMS Conference on Mass Spectrometry and Allied Topics . 2016

机译：鉴定CDK15的底物，通过Sikalip涉及严重神经发育障碍的激酶
5. Sex Chromosomes and Gonadal Hormones: Genesis and Rescue of ASD-like Phenotypes in Mouse Models [D] . Gata Garcia, Adriana Chader. 2021

机译：性染色体和性腺激素：小鼠模型中的特征和恢复ASD样表型
6. Functional and Structural Impairments in the Perirhinal Cortex of a Mouse Model of CDKL5 Deficiency Disorder Are Rescued by a TrkB Agonist [O] . Elisa Ren, Vincenzo Roncacé, Stefania Trazzi, 1974

机译：TrkB激动剂拯救了CDKL5缺乏症小鼠模型的腹膜皮质的功能和结构障碍。
7. Mapping pathological phenotypes in a mouse model of CDKL5 disorder [O] . Amendola, Elena, Zhan, Yang, Mattucci, Camilla, 2014

机译：在CDKL5疾病的小鼠模型中绘制病理表型

CDKL5 protein substitution therapy rescues neurological phenotypes of a mouse model of CDKL5 disorder

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