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Duan Ma

Showing results (91-100 of 230) with videos related to

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Blood|October 4, 2003
The effect of human tissue factor pathway inhibitor-2 on the growth and metastasis of fibrosarcoma tumors in athymic miceHitendra Singh Chand, Xin Du, Duan Ma, et al.
BMC Cancer|March 19, 2013
Low expression of TFPI-2 associated with poor survival outcome in patients with breast cancerCheng Xu, Huijun Wang, Hongyu He, et al.
The Biochemical Journal|September 28, 2011
The interaction of the second Kunitz-type domain (KD2) of TFPI-2 with a novel interaction partner, prosaposin, mediates the inhibition of the invasion and migration of human fibrosarcoma cellsChundi Xu, Fenge Deng, Zuohua Mao, et al.
Acta Biochimica Et Biophysica Sinica|November 29, 2011
Virion protein 16 induces demethylation of DNA integrated within chromatin in a novel mammalian cell modelLu Yang, Huijun Wang, Xin Luo, et al.
Oxidative Medicine and Cellular Longevity|September 26, 2022
Trophoblast Exosomal UCA1 Induces Endothelial Injury through the PFN1-RhoA/ROCK Pathway in Preeclampsia: A Human-Specific Adaptive Pathogenic MechanismSuwen Wu, Yutong Cui, Huanqiang Zhao, et al.
Human Gene Therapy|August 21, 2018
Delivery of Glucosylceramidase Beta Gene Using AAV9 Vector Therapy as a Treatment Strategy in Mouse Models of Gaucher DiseaseSichen Du, Huayuan Ou, Renjie Cui, et al.
Cancer Management and Research|August 22, 2020
The Clinical Relevance and Function of Krüppel-Like Factor 16 in Breast CancerSoyeon Bang, Junhong Li, Meiqin Zhang, et al.
Journal of Translational Medicine|January 30, 2016
Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing lossJiongjiong Hu, Fei Liu, Wenjun Xia, et al.
Birth Defects Research|June 25, 2017
Hypomethylation and decreased expression of BRG1 in the myocardium of patients with congenital heart diseaseYanyan Qian, Deyong Xiao, Xiao Guo, et al.
Clinical Genetics|June 25, 2019
Novel TRRAP mutation causes autosomal dominant non-syndromic hearing lossWenjun Xia, Jiongjiong Hu, Jing Ma, et al.
Pageof 23

Showing results (91-100 of 230) with videos related to

Sort By:
Pageof 23
Blood|October 4, 2003
The effect of human tissue factor pathway inhibitor-2 on the growth and metastasis of fibrosarcoma tumors in athymic miceHitendra Singh Chand, Xin Du, Duan Ma, et al.
BMC Cancer|March 19, 2013
Low expression of TFPI-2 associated with poor survival outcome in patients with breast cancerCheng Xu, Huijun Wang, Hongyu He, et al.
The Biochemical Journal|September 28, 2011
The interaction of the second Kunitz-type domain (KD2) of TFPI-2 with a novel interaction partner, prosaposin, mediates the inhibition of the invasion and migration of human fibrosarcoma cellsChundi Xu, Fenge Deng, Zuohua Mao, et al.
Acta Biochimica Et Biophysica Sinica|November 29, 2011
Virion protein 16 induces demethylation of DNA integrated within chromatin in a novel mammalian cell modelLu Yang, Huijun Wang, Xin Luo, et al.
Oxidative Medicine and Cellular Longevity|September 26, 2022
Trophoblast Exosomal UCA1 Induces Endothelial Injury through the PFN1-RhoA/ROCK Pathway in Preeclampsia: A Human-Specific Adaptive Pathogenic MechanismSuwen Wu, Yutong Cui, Huanqiang Zhao, et al.
Human Gene Therapy|August 21, 2018
Delivery of Glucosylceramidase Beta Gene Using AAV9 Vector Therapy as a Treatment Strategy in Mouse Models of Gaucher DiseaseSichen Du, Huayuan Ou, Renjie Cui, et al.
Cancer Management and Research|August 22, 2020
The Clinical Relevance and Function of Krüppel-Like Factor 16 in Breast CancerSoyeon Bang, Junhong Li, Meiqin Zhang, et al.
Journal of Translational Medicine|January 30, 2016
Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing lossJiongjiong Hu, Fei Liu, Wenjun Xia, et al.
Birth Defects Research|June 25, 2017
Hypomethylation and decreased expression of BRG1 in the myocardium of patients with congenital heart diseaseYanyan Qian, Deyong Xiao, Xiao Guo, et al.
Clinical Genetics|June 25, 2019
Novel TRRAP mutation causes autosomal dominant non-syndromic hearing lossWenjun Xia, Jiongjiong Hu, Jing Ma, et al.
Pageof 23