机译:缺乏ProSAP1 / Shank2的小鼠的自闭症样行为和多动
Institute for Anatomy and Cell Biology, Ulm University, 89081 Ulm, GermanyHuman Genetics and Cognitive Functions, Institut Pasteur, 75724 Paris CEDEX 15, France CNRS, URA 2182 'Genes, Synapses and Cognition', Institut Pasteur, 75724 Paris CEDEX 15, France University Paris Diderot, Sorbonne Paris Cite, Human Genetics and Cognitive Functions, 75013 Paris, France;
Neuroscience Research Center, Cluster of Excellence NeuroCure, Charite, 10117 Berlin, Germany;
Institute for Anatomy and Cell Biology, Ulm University, 89081 Ulm, Germany;
Neuroscience Research Center, Cluster of Excellence NeuroCure, Charite, 10117 Berlin, Germany;
Institute for Anatomy and Cell Biology, Ulm University, 89081 Ulm, Germany;
Institute for Anatomy and Cell Biology, Ulm University, 89081 Ulm, Germany;
Institute for Anatomy and Cell Biology, Ulm University, 89081 Ulm, Germany;
Institute for Anatomy and Cell Biology, Ulm University, 89081 Ulm, Germany Klinikumrechtsder lsar, Technische Universitaet Muenchen,Neurosurgery Department, Ismaninger Str. 22,81675 Munich, Germany;
PG Neuroplasticity, Leibniz Institute for Neurobiology, 39118 Magdeburg, Germany;
Laboratory of Biological Psychology, Department of Psychology, Catholic University of Leuven, 3000 Leuven, Belgium;
Institute of Experimental Pathology (ZMBE), University of Muenster, 48149 Muenster, Germany Interdisciplinary Center for Clinical Research (IZKF), University of Muenster, 48149 Muenster, Germany;
Max Planck Institute for Brain Research, Department of Synaptic Plasticity, 60528 Frankfurt, Germany;
Department of Neurochemistry, Leibniz Institute for Neurobiology, 39118 Magdeburg, Germany;
Neurogenetics Special Laboratory, Leibniz Institute for Neurobiology, 39118 Magdeburg, Germany;
Human Genetics and Cognitive Functions, Institut Pasteur, 75724 Paris CEDEX 15, France CNRS, URA 2182 'Genes, Synapses and Cognition', Institut Pasteur, 75724 Paris CEDEX 15, France University Paris Diderot, Sorbonne Paris Cite, Human Genetics and Cognitive Functions, 75013 Paris, France;
University Paris 06, CNRS.UMR 7102,75005 Paris, France;
Human Genetics and Cognitive Functions, Institut Pasteur, 75724 Paris CEDEX 15, France CNRS, URA 2182 'Genes, Synapses and Cognition', Institut Pasteur, 75724 Paris CEDEX 15, France University Paris Diderot, Sorbonne Paris Cite, Human Genetics and Cognitive Functions, 75013 Paris, France;
Human Genetics and Cognitive Functions, Institut Pasteur, 75724 Paris CEDEX 15, France CNRS, URA 2182 'Genes, Synapses and Cognition', Institut Pasteur, 75724 Paris CEDEX 15, France University Paris Diderot, Sorbonne Paris Cite, Human Genetics and Cognitive Functions, 75013 Paris, France;
Human Genetics and Cognitive Functions, Institut Pasteur, 75724 Paris CEDEX 15, France CNRS, URA 2182 'Genes, Synapses and Cognition', Institut Pasteur, 75724 Paris CEDEX 15, France University Paris Diderot, Sorbonne Paris Cite, Human Genetics and Cognitive Functions, 75013 Paris, France;
Institute for Anatomy and Cell Biology, Ulm University, 89081 Ulm, Germany;
Neuroscience Research Center, Cluster of Excellence NeuroCure, Charite, 10117 Berlin, Germany;
Neuroscience Research Center, Cluster of Excellence NeuroCure, Charite, 10117 Berlin, Germany;
PG Neuroplasticity, Leibniz Institute for Neurobiology, 39118 Magdeburg, Germany;
Human Genetics and Cognitive Functions, Institut Pasteur, 75724 Paris CEDEX 15, France CNRS, URA 2182 'Genes, Synapses and Cognition', Institut Pasteur, 75724 Paris CEDEX 15, France University Paris Diderot, Sorbonne Paris Cite, Human Genetics and Cognitive Functions, 75013 Paris, France;
Department of Neurochemistry, Leibniz Institute for Neurobiology, 39118 Magdeburg, Germany;
Institute for Anatomy and Cell Biology, Ulm University, 89081 Ulm, Germany;
机译:N-甲基-D-天冬氨酸受体功能的早期校正改善了成人Shank2( - / - )小鼠中的自闭症状社会行为
机译:缺乏功能性速激肽-1(NK1)受体的小鼠的行为和神经化学异常:注意缺陷多动障碍模型
机译:缺乏白细胞共同抗原相关(LAR)蛋白酪氨酸磷酸酶结构域的小鼠在两次试验水迷宫中显示出空间学习障碍,并在多项行为测试中表现出过度活跃。
机译:缺乏过氧化合物酶体增殖物激活受体-α(PPAR-α)正常MiCeand中脂肪生成和胆固基因表达的功能效率
机译:缺乏Stat3-beta(全身性炎症的整体抑制因子)的小鼠的动脉粥样硬化加速。
机译:小白蛋白神经元中的Shank2缺失导致小鼠中度活动过度增强的自我修饰和癫痫发作易感性
机译:SAPAP4缺陷小鼠中的认知障碍和自闭症行为