论文部分内容阅读
Mapping global patterns of connectivity in the mammalian brain
【机 构】
:
Howard Hughes Medical Institute,Department of Biology,Stanford University
【出 处】
:
The 6th FAONS Congress and 11th Biennial Conference of CNS(第
【发表日期】
:
2015年3期
其他文献
C1q is the target recognition protein of the complement pathway in the innate immune response.Its C-terminal globular domain is also found in various non-complement proteins.
会议
Erasure of recent and remote hippocampus-dependent fear memory by enhancing memory forgetting throug
Erasure of fear memory is thought to be a therapeutic target for emotional disorders such as post-traumatic stress disorders.Memantine(MEM)is an N-methyl-D-aspartate glutamate receptor antagonist.
会议
Noonan syndrome(NS)is a neurodevelopmental disorder associated with congenital heart disease,short stature,facial abnormalities and cognitive deficits such as learning disabilities.
会议
Hippocampus plays an important role in the formation of memories for space and events.However,it is not fully understood how neuronal circuits are reorganized during the formation of memory for a part
会议
X-linked mental retardation(XLMR)is a heterogeneous condition affecting approximately 0.2% men,and there is currently no drug treatment.
会议
Methyl-CpG binding protein 2(MeCP2)plays critical roles in transcriptional regulation and microRNA processing.Mutations in MECP2 gene are found in 90%of patients with Rett syndrome,a severe form of de
会议
Chronic migraine is a highly disabling neurological disorder defined as a headache with frequency of ≧15 days per month for ≧3 months,in which ≧8 days are migraine attacks or responsive to migraine-sp
会议
The orexin system is involved in the regulation of pain,in addition to arousal,feeding and reward.Here,we revealed a novel analgesic mechanism mediated by orexin in the rat ventrolateral periaqueducta
Suppression of Mutant Huntingtin Allele and Improvement of Murine Motor Function and Lifespan by Sup
Huntingtons disease(HD)is an inherited genetic disorder that leads to degeneration of brain cells primarily in Striatum and Cortex and consequently results in abnormal body movements,decreased mental
遗传性运动感觉神经病变,又称做Charcot-Marie-Tooth disease(CMT),是最常见的遗传性周边神经病变,其临床症状包括渐进性肢体远程肌肉萎缩无力、脚掌形变、远程感觉丧失及肌腱反应下降。
会议