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Tian-Fu Li

Showing results (21-30 of 27) with videos related to

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BMC Ophthalmology|September 9, 2014
A novel P20R mutation in the alpha-B crystallin gene causes autosomal dominant congenital posterior polar cataracts in a Chinese familyXin-Yi Xia, Qiu-Yue Wu, Li-Mei An, et al.
Molecular Cytogenetics|March 4, 2014
A parthenogenetic maternal and double paternal contribution to an ovotesticular disorder of sex developmentXin-Yi Xia, Wei-Ping Wang, Tian-Fu Li, et al.
Plos One|June 21, 2014
A novel p. Gly630Ser mutation of COL2A1 in a Chinese family with presentations of Legg-Calvé-Perthes disease or avascular necrosis of the femoral headNa Li, Jian Yu, Xiang Cao, et al.
Journal of Child Neurology|October 8, 2015
Analysis of Altered Micro RNA Expression Profiles in Focal Cortical Dysplasia IIBLin Li, Chang-Qing Liu, Tian-Fu Li, et al.
Molecular Medicine Reports|March 12, 2015
A patient with unusual features and a 69.5 Mb duplication from a de novo extra der (9): a case reportYu-Chun Zhou, Cui Zhang, Jin-Sheng Zhai, et al.
Journal of Neuroinflammation|March 26, 2022
Rasmussen's encephalitis is characterized by relatively lower production of IFN-β and activated cytotoxic T cell upon herpes viruses infectionYi-Song Wang, Dong Liu, Xin Wang, et al.
ASN Neuro|November 16, 2022
Translocation of High Mobility Group Box 1 From the Nucleus to the Cytoplasm in Depressed Patients With EpilepsyXiao-Li Li, Shu Wang, Chong-Yang Tang, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
BMC Ophthalmology|September 9, 2014
A novel P20R mutation in the alpha-B crystallin gene causes autosomal dominant congenital posterior polar cataracts in a Chinese familyXin-Yi Xia, Qiu-Yue Wu, Li-Mei An, et al.
Molecular Cytogenetics|March 4, 2014
A parthenogenetic maternal and double paternal contribution to an ovotesticular disorder of sex developmentXin-Yi Xia, Wei-Ping Wang, Tian-Fu Li, et al.
Plos One|June 21, 2014
A novel p. Gly630Ser mutation of COL2A1 in a Chinese family with presentations of Legg-Calvé-Perthes disease or avascular necrosis of the femoral headNa Li, Jian Yu, Xiang Cao, et al.
Journal of Child Neurology|October 8, 2015
Analysis of Altered Micro RNA Expression Profiles in Focal Cortical Dysplasia IIBLin Li, Chang-Qing Liu, Tian-Fu Li, et al.
Molecular Medicine Reports|March 12, 2015
A patient with unusual features and a 69.5 Mb duplication from a de novo extra der (9): a case reportYu-Chun Zhou, Cui Zhang, Jin-Sheng Zhai, et al.
Journal of Neuroinflammation|March 26, 2022
Rasmussen's encephalitis is characterized by relatively lower production of IFN-β and activated cytotoxic T cell upon herpes viruses infectionYi-Song Wang, Dong Liu, Xin Wang, et al.
ASN Neuro|November 16, 2022
Translocation of High Mobility Group Box 1 From the Nucleus to the Cytoplasm in Depressed Patients With EpilepsyXiao-Li Li, Shu Wang, Chong-Yang Tang, et al.
Pageof 3