外显子组测序在人类疾病中的应用
饶书权， 杜廷福， 许琪 - 遗传, 2014 - chinagene.cn
… Exome sequencing supports a de novo mutational paradigm for schizophrenia. Nat Genet,
2011, … Strong association of de novo copy number mutations with sporadic schizophrenia. Nat …
2011, … Strong association of de novo copy number mutations with sporadic schizophrenia. Nat …
医学研究生" 高通量测序技术" 应用能力的培养.
郭俊， 李小燕， 蔡伦， 王绿娅… - Progress in Modern …, 2016 - search.ebscohost.com
… Next generation sequencing technology and its applicationin … encephalopathies identifies
de novo mutations in CHD2 and … Exome sequencing identifies MLL2 mutations as a cause of …
de novo mutations in CHD2 and … Exome sequencing identifies MLL2 mutations as a cause of …
天然膳食化合物作为抗阿尔茨海默病药物的遗传和表观遗传靶标
WO Castillo-Ordoñez, N Cajas-Salazar… - 中国神经再生研究 …, 2024 - sjzsyj.com.cn
… paradigms. In its broadest meaning, epigenetics is an additional layer of information and
processes that sits atop the genome … genome sequencing studies have revealed that mutations …
processes that sits atop the genome … genome sequencing studies have revealed that mutations …
前脑兴奋性神经元特异性Brpf1 缺失可减弱兴奋性突触传递并损害空间和恐惧记
B Zhao, H Zhang, Y Liu, G Zu, Y Zhang, J Hu… - 中国神经再生研究 …, 2024 - sjzsyj.com.cn
… Brpf1, KAT6A, and KAT6B mutations were identified as the … impairment in patients with
BRPF1 mutation. Key Words: … Arboleda-Tham syndrome by whole genome sequencing in …
BRPF1 mutation. Key Words: … Arboleda-Tham syndrome by whole genome sequencing in …
肠道微生物群与神经退行性疾病相关性分析: 一项基于宏基因组学的综述
X Liu, Y Liu, J Liu, H Zhang, C Shan, Y Guo… - 中国神经再生研究 …, 2024 - sjzsyj.com.cn
… next-generation sequencing (Simner et al., 2018; Gu et al., 2019; Wensel et al., 2022). Compared
with metagenomic next-generation sequencing… support of high-throughput sequencing …
with metagenomic next-generation sequencing… support of high-throughput sequencing …