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

Ou Wang

Showing results (241-250 of 425) with videos related to

Pageof 43
Sort By:
Endocrine|January 15, 2022
High incidence of hypertension-mediated organ damage in a series of Chinese patients with 17α-hydroxylase deficiencyZhiyuan Zhao, Lin Lu, Ou Wang, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 23, 2010
Two unrelated Chinese patients with hyperinsulinism /hyperammonemia (HI/HA) syndrome due to mutations in glutamate dehydrogenase geneChengming Diao, Shi Chen, Xinhua Xiao, et al.
Cell Cycle (Georgetown, Tex.)|May 15, 2012
Cellular and molecular evidence for malignancy-inhibitory functions of p15RSXiaocui Zhang, Qiuju Cao, Xiaodan Liu, et al.
Calcified Tissue International|March 21, 2009
A recurrent mutation c.617G>A in the ACVR1 gene causes fibrodysplasia ossificans progressiva in two Chinese patientsYue Sun, Weibo Xia, Yan Jiang, et al.
The Journal of Clinical Endocrinology and Metabolism|January 12, 2024
Genetic Analysis, Phenotypic Spectrum and Functional Study of Rare Osteogenesis Imperfecta Caused by CRTAP VariantsBingna Zhou, Peng Gao, Jing Hu, et al.
Wei Sheng Yan Jiu = Journal of Hygiene Research|December 20, 2023
[Analysis of diet structure of Kashin-beck disease area in Chamdo-Lhorong of Tibet in 2021]Tong Jiang, Zhu Pu, Ou Wang, et al.
Molecular Genetics & Genomic Medicine|November 9, 2020
A novel mutation in PLS3 causes extremely rare X-linked osteogenesis imperfectaJing Hu, Lu-Jiao Li, Wen-Bin Zheng, et al.
Frontiers in Endocrinology|July 22, 2022
Bone Microarchitecture in Obese Postmenopausal Chinese Women: The Chinese Vertebral Osteoporosis Study (ChiVOS)Wenting Qi, Yan Jiang, Wei Liu, et al.
Molecular and Cellular Endocrinology|October 11, 2014
Aromatase deficiency in a Chinese adult man caused by novel compound heterozygous CYP19A1 mutations: effects of estrogen replacement therapy on the bone, lipid, liver and glucose metabolismZhike Chen, Ou Wang, Min Nie, et al.
Acta Pharmacologica Sinica|August 18, 2015
Physical performance and life quality in postmenopausal women supplemented with vitamin D: a two-year prospective studyLi-hong Gao, Wen-jun Zhu, Yu-juan Liu, et al.
Pageof 43

Showing results (241-250 of 425) with videos related to

Sort By:
Pageof 43
Endocrine|January 15, 2022
High incidence of hypertension-mediated organ damage in a series of Chinese patients with 17α-hydroxylase deficiencyZhiyuan Zhao, Lin Lu, Ou Wang, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 23, 2010
Two unrelated Chinese patients with hyperinsulinism /hyperammonemia (HI/HA) syndrome due to mutations in glutamate dehydrogenase geneChengming Diao, Shi Chen, Xinhua Xiao, et al.
Cell Cycle (Georgetown, Tex.)|May 15, 2012
Cellular and molecular evidence for malignancy-inhibitory functions of p15RSXiaocui Zhang, Qiuju Cao, Xiaodan Liu, et al.
Calcified Tissue International|March 21, 2009
A recurrent mutation c.617G>A in the ACVR1 gene causes fibrodysplasia ossificans progressiva in two Chinese patientsYue Sun, Weibo Xia, Yan Jiang, et al.
The Journal of Clinical Endocrinology and Metabolism|January 12, 2024
Genetic Analysis, Phenotypic Spectrum and Functional Study of Rare Osteogenesis Imperfecta Caused by CRTAP VariantsBingna Zhou, Peng Gao, Jing Hu, et al.
Wei Sheng Yan Jiu = Journal of Hygiene Research|December 20, 2023
[Analysis of diet structure of Kashin-beck disease area in Chamdo-Lhorong of Tibet in 2021]Tong Jiang, Zhu Pu, Ou Wang, et al.
Molecular Genetics & Genomic Medicine|November 9, 2020
A novel mutation in PLS3 causes extremely rare X-linked osteogenesis imperfectaJing Hu, Lu-Jiao Li, Wen-Bin Zheng, et al.
Frontiers in Endocrinology|July 22, 2022
Bone Microarchitecture in Obese Postmenopausal Chinese Women: The Chinese Vertebral Osteoporosis Study (ChiVOS)Wenting Qi, Yan Jiang, Wei Liu, et al.
Molecular and Cellular Endocrinology|October 11, 2014
Aromatase deficiency in a Chinese adult man caused by novel compound heterozygous CYP19A1 mutations: effects of estrogen replacement therapy on the bone, lipid, liver and glucose metabolismZhike Chen, Ou Wang, Min Nie, et al.
Acta Pharmacologica Sinica|August 18, 2015
Physical performance and life quality in postmenopausal women supplemented with vitamin D: a two-year prospective studyLi-hong Gao, Wen-jun Zhu, Yu-juan Liu, et al.
Pageof 43