Effect of Runx2 silencing on autophagy and RANKL expression in osteoblasts
H Qin, J Cai - Archives of Oral Biology, 2018 - Elsevier
Objective This study aimed to investigate the effect of Runx2 silencing on autophagy and
RANKL expression in mouse osteoblasts, and provide an experimental basis to assess …
RANKL expression in mouse osteoblasts, and provide an experimental basis to assess …
Effect of Periostin Silencing on the Autophagy of Osteoblasts
H Qin, J Cai - Cellular reprogramming, 2019 - liebertpub.com
The objective of the present work was to investigate the effect of Periostin (POSTN) silencing
on autophagy in osteoblasts, and provide an experimental basis for studying the mechanism …
on autophagy in osteoblasts, and provide an experimental basis for studying the mechanism …
Mechanism of NF-κB signaling pathway and autophagy in the regulation of osteoblast differentiation
H Qin, HZ Xu, YQ Gong - Molecular Membrane Biology, 2016 - Taylor & Francis
Objective: The objective of the present work was to investigate a possible mechanism of NF-
κB signaling pathway and autophagy in the regulation of osteoblast differentiation, and …
κB signaling pathway and autophagy in the regulation of osteoblast differentiation, and …
HCY, CRP, Fib, WBC 水平在冠心病诊断中的临床价值.
宋玉莲， 白若岑， 刘铁峰， 柴伟… - Progress in Modern …, 2016 - search.ebscohost.com
摘要目的: 探讨血清同型半胱氨酸(HCY), C 反应蛋白, 纤维蛋白原(Fib), 白细胞(WBC)
与冠心病(CHD) 病变程度的相关性和作为检测指标的敏感性; 检测BMI 是否为CHD …
与冠心病(CHD) 病变程度的相关性和作为检测指标的敏感性; 检测BMI 是否为CHD …
构建靶向Runx2 基因成骨样细胞MC3T3-E1 慢病毒载体
秦晗， 龚永庆， 徐宏志 - 中国组织工程研究, 2018 - cjter.com
文章快速阅读: 文题释义: 颅骨锁骨发育不全(cleidocranial dysplasia, CCD):
是一种广泛累及包括锁骨, 颅骨在内的整个骨骼系统的常染色体显性遗传性疾病(MM119600) …
是一种广泛累及包括锁骨, 颅骨在内的整个骨骼系统的常染色体显性遗传性疾病(MM119600) …
超声骨刀开窗术联合正畸牵引治疗上颌唇侧埋伏阻生尖牙的疗效观察.
张明烨， 王峰， 林松杉， 黄飞… - Progress in Modern …, 2016 - search.ebscohost.com
摘要目的: 研究超声骨刀开窗术联合正畸牵引治疗上颌唇侧埋伏阻生尖牙的临床疗效. 方法:
选取2013 年7 月到2015 年4 月我院收治的上颌唇侧埋伏阻生尖牙患者110 例 …
选取2013 年7 月到2015 年4 月我院收治的上颌唇侧埋伏阻生尖牙患者110 例 …
Lentivirus-mediated Runx2 gene transfection into MC3T3-E1 cells
H Qin, Y Gong, H Xu - Chinese Journal of Tissue Engineering Research, 2018 - cjter.com
BACKGROUND: Heterozygous mutation, gene insertion and gene deletion of Runt-related
transcription factor 2 (Runx2) have been found to be important causes of cleidocranial …
transcription factor 2 (Runx2) have been found to be important causes of cleidocranial …