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

Zhaoxin Ma

Showing results (31-40 of 42) with videos related to

Pageof 5
Sort By:
Experimental and Therapeutic Medicine|December 14, 2018
Beneficial effects of hydrogen gas inhalation on a murine model of allergic rhinitisShengjian Fang, Xinqian Li, Xian Wei, 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.
Clinical Genetics|June 25, 2019
Novel TRRAP mutation causes autosomal dominant non-syndromic hearing lossWenjun Xia, Jiongjiong Hu, Jing Ma, et al.
International Immunopharmacology|March 19, 2022
SIRT1 alleviates IL-1β induced nucleus pulposus cells pyroptosis via mitophagy in intervertebral disc degenerationZhaoxin Ma, Pan Tang, Wei Dong, et al.
International Journal of Surgery (London, England)|January 12, 2024
The effect of perioperative sequential application of multiple doses of tranexamic acid on postoperative blood loss after PLIF: a prospective randomized controlled trialWei Dong, Yuchen Tang, Miao Lei, et al.
Molecular Medicine Reports|June 29, 2017
Peroxisome proliferator-activated receptor γ agonist suppresses mast cell maturation and induces apoptosisYu Zhang, Xinqian Li, Shengjian Fang, et al.
FEBS Letters|June 15, 2019
Mutations in TOP2B cause autosomal-dominant hereditary hearing loss via inhibition of the PI3K-Akt signalling pathwayWenjun Xia, Jiongjiong Hu, Jing Ma, et al.
Human Molecular Genetics|December 26, 2016
SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing lossZhaoxin Ma, Wenjun Xia, Fei Liu, et al.
Frontiers in Medicine|August 21, 2023
The effect of sequential perioperative intravenous tranexamic acid in reducing postoperative blood loss and hidden blood loss after posterior lumbar interbody fusion: a randomized controlled trialWei Dong, Yi Liang, Dongxu Li, et al.
Nature Communications|June 24, 2026
Breaking high-temperature dielectric energy storage limits through suppression of charge carrier transportLei Zhang, Xuan Zhao, Xi Chen, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Experimental and Therapeutic Medicine|December 14, 2018
Beneficial effects of hydrogen gas inhalation on a murine model of allergic rhinitisShengjian Fang, Xinqian Li, Xian Wei, 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.
Clinical Genetics|June 25, 2019
Novel TRRAP mutation causes autosomal dominant non-syndromic hearing lossWenjun Xia, Jiongjiong Hu, Jing Ma, et al.
International Immunopharmacology|March 19, 2022
SIRT1 alleviates IL-1β induced nucleus pulposus cells pyroptosis via mitophagy in intervertebral disc degenerationZhaoxin Ma, Pan Tang, Wei Dong, et al.
International Journal of Surgery (London, England)|January 12, 2024
The effect of perioperative sequential application of multiple doses of tranexamic acid on postoperative blood loss after PLIF: a prospective randomized controlled trialWei Dong, Yuchen Tang, Miao Lei, et al.
Molecular Medicine Reports|June 29, 2017
Peroxisome proliferator-activated receptor γ agonist suppresses mast cell maturation and induces apoptosisYu Zhang, Xinqian Li, Shengjian Fang, et al.
FEBS Letters|June 15, 2019
Mutations in TOP2B cause autosomal-dominant hereditary hearing loss via inhibition of the PI3K-Akt signalling pathwayWenjun Xia, Jiongjiong Hu, Jing Ma, et al.
Human Molecular Genetics|December 26, 2016
SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing lossZhaoxin Ma, Wenjun Xia, Fei Liu, et al.
Frontiers in Medicine|August 21, 2023
The effect of sequential perioperative intravenous tranexamic acid in reducing postoperative blood loss and hidden blood loss after posterior lumbar interbody fusion: a randomized controlled trialWei Dong, Yi Liang, Dongxu Li, et al.
Nature Communications|June 24, 2026
Breaking high-temperature dielectric energy storage limits through suppression of charge carrier transportLei Zhang, Xuan Zhao, Xi Chen, et al.
Pageof 5