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Developmental expression pattern of calmodulin gene in amphioxus Branchiostoma belcheri tsingtauense
[期刊论文] 作者：LUAN Jing,GENG Jinpei,FANG Sha,
来源：黑龙江科技学院学报 年份：2010
为探究吕家坨井田地质构造格局,根据钻孔勘探资料,采用分形理论和趋势面分析方法,研究了井田7...
[期刊论文] 作者：Wang Chong,Luan Jing,Niu Zhen-Min,Huang Qiong,Zhang Zheng-Hua,,
来源：国际皮肤性病学杂志（英文） 年份：2020
Introduction::Darier’s disease is a rare autosomal dominant skin disorder caused by mutations in ATP2A2. Recently, the high prevalence of neuropsychiatric symp...
[会议论文] 作者：Qi Luan,Jing Sun,Linchao Sun,Chunying Li,Tianwen Gao,
来源：The 10th China-Japan Joint Meeting of Dermatology(第十次中日皮肤科联合 年份：2008
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[会议论文] 作者：SHI Liang,CUI Ya-Zhou,LUAN Jing,ZHOU Xiao-Yan,HAN Jin-Xiang,
来源：第六届泛环渤海生物化学与分子生物学会2016年学术交流会 年份：2016
Human Induced pluripotent stem cells (iPSCs) have pluripotency and self-renewal in common with embryonic stem cells (ESCs),but are not associated with the e...
[会议论文] 作者：Liu Chao,Cui YaZhou,Luan Jing,Zhou XiaoYan,Han JinXiang,
来源：第八届全国医学生物化学与分子生物学、第五届全国临床应用生物化学与分子生物学、2013华东六省一市生物化学与分子生物学联合 年份：2013
Apert syndrome(AS) is an autosomal dominant syndrome,characterized by craniosynostosis, midface hypoplasia, and severe syndactyly of the hands and feet, with a prevalence of 1 in 65,000 individuals....
[会议论文] 作者：LI Cheng-Zhi,CUI Ya-Zhou,LI Hai-Ying,WANG Hua-Xin,LUAN Jing,ZHOU Xiao-Yan,HAN Jin-Xiang,
来源：第五届泛环渤海生物化学与分子生物学会学术交流会 年份：2015
Our previous experiment found that tenascin C was increased with the time-dependent mineralization and we found it was expressed in MVs.In this study,we inv...
PRELP Activates Osteoblast Mineralization in Mouse PreosteoblasticMC3T3-E1 Cells by the Wnt Signal T
[会议论文] 作者：LI Hai-Yin,CUI Ya-Zhou,LI Cheng-Zhi,WANG Hua-Xin,LUAN Jing,ZHOU Xiao-Yan,HAN Jin-Xiang,
来源：第五届泛环渤海生物化学与分子生物学会学术交流会 年份：2015
PRELP is a glycosaminoglycan and collagen binding anchor protein highly expressed in cartilage,basement membranes,and developing bone,it plays an important...
[期刊论文] 作者：Xin Wang,Yisong Wang,Dong Liu,Peigang Wang,Dongying Fan,Yuguang Guan,Tianfu Li,Guoming Luan,Jing An,,
来源：Virologica Sinica 年份：2017
Rasmussen’s encephalitis(RE) is a rare pediatric neurological disorder, the etiology of which remains unclear. It has been speculated that the immunopathogenes...
[期刊论文] 作者：Yao Zhang,Yisong Wang,Sichang Chen,Shuai Chen,Yuguang Guan,Changqing Liu,Tianfu Li,Guoming Luan,Jing,
来源：Virologica Sinica 年份：2017
Rasmussen’s encephalitis(RE) is a rare and severe progressive epileptic syndrome with unknown etiology. Infection by viruses, including human cytomegalovirus(H...
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