Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Chengqi Xu

Showing results (21-30 of 94) with videos related to

Pageof 10
Sort By:
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|June 14, 2017
Exomic and Epigenomic Analyses in a Pair of Monozygotic Twins Discordant for CryptorchidismPeng Lu, Pengyun Wang, Lianbing Li, et al.
Clinical Case Reports|August 28, 2018
A novel <i>FBN2</i> mutation cosegregates with congenital contractural arachnodactyly in a five-generation Chinese familyShiyuan Zhou, Fengyu Wang, Yongheng Dou, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 31, 2021
Role of epigenetic m<sup>6</sup> A RNA methylation in vascular development: mettl3 regulates vascular development through PHLPP2/mTOR-AKT signalingRamendu Parial, Hui Li, Jia Li, et al.
Experimental and Therapeutic Medicine|April 2, 2019
A family with Liddle's syndrome caused by a new c.1721 deletion mutation in the epithelial sodium channel β-subunitXia Ding, Na Jia, Cong Zhao, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 26, 2017
Identification of a molecular signaling gene-gene regulatory network between GWAS susceptibility genes ADTRP and MIA3/TANGO1 for coronary artery diseaseChunyan Luo, Fan Wang, Xiang Ren, et al.
BMC Medical Genetics|August 10, 2007
A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese familyXianqin Zhang, Lanying Chen, Jingyu Liu, et al.
Research Square|February 6, 2026
PAIRWISE: Deep Learning based Prediction of Effective Personalized Drug Combinations in CancerOlivier Elemento, Chengqi Xu, Ilkay Us, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 4, 2025
Angiogenic factor AGGF1 is a general splicing factor regulating angiogenesis and vascular development by alternative splicing of SRSF6Wenchao Lv, Jingwen Zhang, Dayin Lyu, et al.
The Journal of Biological Chemistry|May 18, 2025
LncRNA-induced lysosomal localization of NHE1 promotes increased lysosomal pH in macrophages leading to atherosclerosisPengcheng Shi, Bo Tang, Wen Xie, et al.
Pulmonary Pharmacology & Therapeutics|February 1, 2019
SUMOylation of Vps34 by SUMO1 promotes phenotypic switching of vascular smooth muscle cells by activating autophagy in pulmonary arterial hypertensionYufeng Yao, Hui Li, Xinwen Da, et al.
Pageof 10

Showing results (21-30 of 94) with videos related to

Sort By:
Pageof 10
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|June 14, 2017
Exomic and Epigenomic Analyses in a Pair of Monozygotic Twins Discordant for CryptorchidismPeng Lu, Pengyun Wang, Lianbing Li, et al.
Clinical Case Reports|August 28, 2018
A novel <i>FBN2</i> mutation cosegregates with congenital contractural arachnodactyly in a five-generation Chinese familyShiyuan Zhou, Fengyu Wang, Yongheng Dou, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 31, 2021
Role of epigenetic m<sup>6</sup> A RNA methylation in vascular development: mettl3 regulates vascular development through PHLPP2/mTOR-AKT signalingRamendu Parial, Hui Li, Jia Li, et al.
Experimental and Therapeutic Medicine|April 2, 2019
A family with Liddle's syndrome caused by a new c.1721 deletion mutation in the epithelial sodium channel β-subunitXia Ding, Na Jia, Cong Zhao, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 26, 2017
Identification of a molecular signaling gene-gene regulatory network between GWAS susceptibility genes ADTRP and MIA3/TANGO1 for coronary artery diseaseChunyan Luo, Fan Wang, Xiang Ren, et al.
BMC Medical Genetics|August 10, 2007
A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese familyXianqin Zhang, Lanying Chen, Jingyu Liu, et al.
Research Square|February 6, 2026
PAIRWISE: Deep Learning based Prediction of Effective Personalized Drug Combinations in CancerOlivier Elemento, Chengqi Xu, Ilkay Us, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 4, 2025
Angiogenic factor AGGF1 is a general splicing factor regulating angiogenesis and vascular development by alternative splicing of SRSF6Wenchao Lv, Jingwen Zhang, Dayin Lyu, et al.
The Journal of Biological Chemistry|May 18, 2025
LncRNA-induced lysosomal localization of NHE1 promotes increased lysosomal pH in macrophages leading to atherosclerosisPengcheng Shi, Bo Tang, Wen Xie, et al.
Pulmonary Pharmacology & Therapeutics|February 1, 2019
SUMOylation of Vps34 by SUMO1 promotes phenotypic switching of vascular smooth muscle cells by activating autophagy in pulmonary arterial hypertensionYufeng Yao, Hui Li, Xinwen Da, et al.
Pageof 10