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

A novel intronic variant in the ASAH1 gene enhances aberrant splicing, causing spinal muscular atrophy with progressive myoclonic epilepsy.

ASAH1 基因中一种新的内含子变异增强了异常剪接,导致脊髓性肌萎缩症伴进行性肌阵挛性癫痫

Bai Jinli, Li Ping, Jiao Hui, Jin Yuwei, Wang Hong, Jiang Qinglin, Song Fang, Peng Xiaoyin, Qu Yujin

Association among biomarkers, phenotypes, and motor milestones in Chinese patients with 5q spinal muscular atrophy types 1-3

中国5q脊髓性肌萎缩症1-3型患者的生物标志物、表型和运动里程碑之间的关联

Ouyang, Shijia; Peng, Xiaoyin; Huang, Wenchen; Bai, Jinli; Wang, Hong; Jin, Yuwei; Jiao, Hui; Wei, Maoti; Ge, Xiushan; Song, Fang; Qu, Yujin

Corrigendum: Association among biomarkers, phenotypes, and motor milestones in Chinese patients with 5q spinal muscular atrophy types 1-3

更正:中国5q脊髓性肌萎缩症1-3型患者的生物标志物、表型和运动里程碑之间的关联

Ouyang, Shijia; Peng, Xiaoyin; Huang, Wenchen; Bai, Jinli; Wang, Hong; Jin, Yuwei; Jiao, Hui; Wei, Maoti; Ge, Xiushan; Song, Fang; Qu, Yujin

DNMT1 is a negative regulator of osteogenesis

DNMT1是成骨作用的负调控因子

Chen Tao,Jia Liu,Ziqi Li,Pinglin Lai,Sheng Zhang,Jiankun Qu,Yujin Tang,Anling Liu,Zhipeng Zou,Xiaochun Bai,Jianwei Li

Bone mineral density and its influencing factors in Chinese children with spinal muscular atrophy types 2 and 3

中国脊髓性肌萎缩症2型和3型患儿骨矿物质密度及其影响因素

Peng, Xiaoyin; Qu, Yujin; Li, Xiaohui; Liu, Junting; Shan, Xinying; Wang, Jia; Song, Fang

Transmission characteristics of SMN from 227 spinal muscular atrophy core families in China

中国227个脊髓性肌萎缩症核心家族SMN基因的遗传特征

Cao, Yanyan; Qu, Yujin; Bai, Jinli; Cheng, Miaomiao; Jin, Yuwei; Wang, Hong; Song, Fang

X-linked ichthyosis and Crigler-Najjar syndrome I: Coexistence in a male patient with two copy number variable regions of 2q37.1 and Xp22.3

X连锁鱼鳞病和克里格勒-纳贾尔综合征I:一名男性患者同时患有这两种疾病,其2q37.1和Xp22.3两个拷贝数可变区。

Bai, Jinli; Qu, Yujin; Cao, Yanyan; Li, Yan; Zhang, Wenhui; Jin, Yuwei; Wang, Hong; Song, Fang