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

Xiaoliu Shi

Showing results (21-30 of 49) with videos related to

Pageof 5
Sort By:
Journal of Clinical Laboratory Analysis|June 13, 2020
Identification of a nonsense mutation in TNNI3K associated with cardiac conduction diseaseJiang Liu, Da Liu, Muzheng Li, et al.
Toxins|April 30, 2016
The Spider Venom Peptide Lycosin-II Has Potent Antimicrobial Activity against Clinically Isolated BacteriaYongjun Wang, Ling Wang, Huali Yang, et al.
Molecular Genetics & Genomic Medicine|December 6, 2020
A novel SLC37A4 missense mutation in GSD-Ib without hepatomegaly causes enhanced leukocytes endoplasmic reticulum stress and apoptosisQianyun Xu, Haiyan Tang, Liping Duan, et al.
Nature Metabolism|January 2, 2025
Cellular Feimin enhances exercise performance by suppressing muscle thermogenesisYing Peng, Liangjie Jia, Xiao Hu, et al.
Environmental Science & Technology|October 4, 2024
The Role of Human Adiponectin Receptor 1 in 2-Ethylhexyl Diphenyl Phosphate Induced Lipid Metabolic DisruptionJiafan Feng, Xiaochun Ma, Ying Liu, et al.
Journal of Hazardous Materials|September 6, 2024
Perinatal exposure to PBEB aggravates liver injury via macrophage-derived TWEAK in male adult offspring mice under western dietWanyue Wang, Xiaoliu Shi, Jiafan Feng, et al.
Brain and Behavior|December 4, 2018
A novel EMD mutation in a Chinese family with initial diagnosis of conduction cardiomyopathyJunfeng Zhou, Hui Li, Xiangping Li, et al.
Plos One|May 12, 2009
Functional analysis of a dominant negative mutation of interferon regulatory factor 5Long Yang, Tiejun Zhao, Xiaoliu Shi, et al.
Medical Molecular Morphology|April 19, 2019
A novel splicing mutation of PTCH1 in a Chinese family with nevoid basal cell carcinoma syndromeJunfeng Zhou, Guiying Zhang, Meng Shi, et al.
Pain|March 6, 2020
Alcohol-aggravated episodic pain in humans with SCN11A mutation and ALDH2 polymorphismLuyao Yang, Lulu Li, Haiyan Tang, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
Journal of Clinical Laboratory Analysis|June 13, 2020
Identification of a nonsense mutation in TNNI3K associated with cardiac conduction diseaseJiang Liu, Da Liu, Muzheng Li, et al.
Toxins|April 30, 2016
The Spider Venom Peptide Lycosin-II Has Potent Antimicrobial Activity against Clinically Isolated BacteriaYongjun Wang, Ling Wang, Huali Yang, et al.
Molecular Genetics & Genomic Medicine|December 6, 2020
A novel SLC37A4 missense mutation in GSD-Ib without hepatomegaly causes enhanced leukocytes endoplasmic reticulum stress and apoptosisQianyun Xu, Haiyan Tang, Liping Duan, et al.
Nature Metabolism|January 2, 2025
Cellular Feimin enhances exercise performance by suppressing muscle thermogenesisYing Peng, Liangjie Jia, Xiao Hu, et al.
Environmental Science & Technology|October 4, 2024
The Role of Human Adiponectin Receptor 1 in 2-Ethylhexyl Diphenyl Phosphate Induced Lipid Metabolic DisruptionJiafan Feng, Xiaochun Ma, Ying Liu, et al.
Journal of Hazardous Materials|September 6, 2024
Perinatal exposure to PBEB aggravates liver injury via macrophage-derived TWEAK in male adult offspring mice under western dietWanyue Wang, Xiaoliu Shi, Jiafan Feng, et al.
Brain and Behavior|December 4, 2018
A novel EMD mutation in a Chinese family with initial diagnosis of conduction cardiomyopathyJunfeng Zhou, Hui Li, Xiangping Li, et al.
Plos One|May 12, 2009
Functional analysis of a dominant negative mutation of interferon regulatory factor 5Long Yang, Tiejun Zhao, Xiaoliu Shi, et al.
Medical Molecular Morphology|April 19, 2019
A novel splicing mutation of PTCH1 in a Chinese family with nevoid basal cell carcinoma syndromeJunfeng Zhou, Guiying Zhang, Meng Shi, et al.
Pain|March 6, 2020
Alcohol-aggravated episodic pain in humans with SCN11A mutation and ALDH2 polymorphismLuyao Yang, Lulu Li, Haiyan Tang, et al.
Pageof 5