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Wenzhen Fu

Showing results (21-30 of 33) with videos related to

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International Journal of Molecular Medicine|March 8, 2018
Novel mutations of the SERPINF1 and FKBP10 genes in Chinese families with autosomal recessive osteogenesis imperfectaHao Zhang, Yang Xu, Hua Yue, et al.
Molecular Medicine Reports|December 31, 2016
[Corrigendum] Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfectaHao Zhang, Hua Yue, Chun Wang, et al.
Molecular Medicine Reports|October 26, 2016
Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfectaHao Zhang, Hua Yue, Chun Wang, et al.
Mlife|July 1, 2024
Cinnamaldehyde targets SarA to enhance β-lactam antibiotic activity against methicillin-resistant <i>Staphylococcus aureus</i>Jianguo Li, Tingyin Lu, Yuefei Chu, et al.
Evidence-Based Complementary and Alternative Medicine : Ecam|April 4, 2022
Association between NF-<i>κ</i>B Signal Pathway-Related Gene Polymorphisms and Response to Alendronate Treatment in Postmenopausal Chinese Women with Low Bone Mineral DensityXiaoyi Shen, Sasa Tan, Xianzhen Feng, et al.
The Journal of Clinical Endocrinology and Metabolism|January 16, 2014
Associations of serum sclerostin and polymorphisms in the SOST gene with bone mineral density and markers of bone metabolism in postmenopausal Chinese womenJinwei He, Hao Zhang, Chun Wang, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|April 16, 2024
Clinical features, treatment, and follow-up of OPPG and high-bone-mass disorders: LRP5 is a key regulator of bone massNa Ren, Shanshan Lv, Xiang Li, et al.
Menopause (New York, N.Y.)|June 7, 2012
Association of ALOX12 and ALOX15 gene polymorphisms with age at menarche and natural menopause in Chinese womenWenjin Xiao, Yaohua Ke, Jinwei He, et al.
Frontiers in Cell and Developmental Biology|September 24, 2021
Genetics Evaluation of Targeted Exome Sequencing in 223 Chinese Probands With Genetic Skeletal DysplasiasShanshan Lv, Jiao Zhao, Lei Xi, et al.
American Journal of Human Genetics|December 27, 2011
Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathyZhenlin Zhang, Weibo Xia, Jinwei He, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
International Journal of Molecular Medicine|March 8, 2018
Novel mutations of the SERPINF1 and FKBP10 genes in Chinese families with autosomal recessive osteogenesis imperfectaHao Zhang, Yang Xu, Hua Yue, et al.
Molecular Medicine Reports|December 31, 2016
[Corrigendum] Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfectaHao Zhang, Hua Yue, Chun Wang, et al.
Molecular Medicine Reports|October 26, 2016
Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfectaHao Zhang, Hua Yue, Chun Wang, et al.
Mlife|July 1, 2024
Cinnamaldehyde targets SarA to enhance β-lactam antibiotic activity against methicillin-resistant <i>Staphylococcus aureus</i>Jianguo Li, Tingyin Lu, Yuefei Chu, et al.
Evidence-Based Complementary and Alternative Medicine : Ecam|April 4, 2022
Association between NF-<i>κ</i>B Signal Pathway-Related Gene Polymorphisms and Response to Alendronate Treatment in Postmenopausal Chinese Women with Low Bone Mineral DensityXiaoyi Shen, Sasa Tan, Xianzhen Feng, et al.
The Journal of Clinical Endocrinology and Metabolism|January 16, 2014
Associations of serum sclerostin and polymorphisms in the SOST gene with bone mineral density and markers of bone metabolism in postmenopausal Chinese womenJinwei He, Hao Zhang, Chun Wang, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|April 16, 2024
Clinical features, treatment, and follow-up of OPPG and high-bone-mass disorders: LRP5 is a key regulator of bone massNa Ren, Shanshan Lv, Xiang Li, et al.
Menopause (New York, N.Y.)|June 7, 2012
Association of ALOX12 and ALOX15 gene polymorphisms with age at menarche and natural menopause in Chinese womenWenjin Xiao, Yaohua Ke, Jinwei He, et al.
Frontiers in Cell and Developmental Biology|September 24, 2021
Genetics Evaluation of Targeted Exome Sequencing in 223 Chinese Probands With Genetic Skeletal DysplasiasShanshan Lv, Jiao Zhao, Lei Xi, et al.
American Journal of Human Genetics|December 27, 2011
Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathyZhenlin Zhang, Weibo Xia, Jinwei He, et al.
Pageof 4