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Chuan Liu

Showing results (741-750 of 1,812) with videos related to

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American Journal of Human Biology : the Official Journal of the Human Biology Council|September 5, 2001
Morphological growth of Han boys and girls born and raised near sea level and at high altitude in western ChinaCharles A. Weitz, Ralph M. Garruto, Chen-Ting Chin, et al.
The Journal of International Medical Research|September 26, 2019
Dissecting basilar artery aneurysm manifesting as sudden sensorineural hearing loss: a case report and literature reviewYi-Zhi Zhang, Qiu-Hui Chen, Zhan-Chuan Liu, et al.
Molecular Genetics and Genomics : MGG|February 12, 2014
Association between the CYP1A2-164 A/C polymorphism and colorectal cancer susceptibility: a meta-analysisJianbing Hu, Chuan Liu, Qinghua Yin, et al.
Journal of Biotechnology|August 16, 2024
Development of Stephania tetrandra S. MOORE hairy root culture process for tetrandrine productionHsuan-Chieh Liu, Hsiao-Sung Chan, Parushi Nargotra, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|October 31, 2015
Association between the CYP1A2 rs762551 Polymorphism and Bladder Cancer Susceptibility: a Meta-Analysis Based on Case-Control StudiesYong Zeng, Hua-Yong Jiang, Li Wei, et al.
The Annals of Thoracic Surgery|February 26, 2016
Prognosis of Patients With Pathologic T0 N+ Esophageal Squamous Cell Carcinoma After Chemoradiotherapy and Surgical Resection: Results From a Nationwide StudyYin-Kai Chao, Hui-Shan Chen, Bing-Yen Wang, et al.
Mbio|July 21, 2022
VEGF-Mediated Augmentation of Autophagic and Lysosomal Activity in Endothelial Cells Defends against Intracellular Streptococcus pyogenesShiou-Ling Lu, Hiroko Omori, Yi Zhou, et al.
International Journal of Ophthalmology|September 21, 2020
Preliminary report on screening IGSF3 gene mutation in families with congenital absence of lacrimal puncta and canaliculiFei Wang, Hai Tao, Cui Han, et al.
Cardiology in the Young|November 22, 2019
A novel <i>MYBPC3</i> c.2737+1 (IVS26) G>T mutation responsible for high-risk hypertrophic cardiomyopathyWuyang Tong, Wei Liu, Hong Guo, et al.
Frontiers in Immunology|October 3, 2022
Research hotspot and trend analysis in the diagnosis of inflammatory bowel disease: A machine learning bibliometric analysis from 2012 to 2021Chuan Liu, Rong Yu, Jixiang Zhang, et al.
Pageof 182

Showing results (741-750 of 1,812) with videos related to

Sort By:
Pageof 182
American Journal of Human Biology : the Official Journal of the Human Biology Council|September 5, 2001
Morphological growth of Han boys and girls born and raised near sea level and at high altitude in western ChinaCharles A. Weitz, Ralph M. Garruto, Chen-Ting Chin, et al.
The Journal of International Medical Research|September 26, 2019
Dissecting basilar artery aneurysm manifesting as sudden sensorineural hearing loss: a case report and literature reviewYi-Zhi Zhang, Qiu-Hui Chen, Zhan-Chuan Liu, et al.
Molecular Genetics and Genomics : MGG|February 12, 2014
Association between the CYP1A2-164 A/C polymorphism and colorectal cancer susceptibility: a meta-analysisJianbing Hu, Chuan Liu, Qinghua Yin, et al.
Journal of Biotechnology|August 16, 2024
Development of Stephania tetrandra S. MOORE hairy root culture process for tetrandrine productionHsuan-Chieh Liu, Hsiao-Sung Chan, Parushi Nargotra, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|October 31, 2015
Association between the CYP1A2 rs762551 Polymorphism and Bladder Cancer Susceptibility: a Meta-Analysis Based on Case-Control StudiesYong Zeng, Hua-Yong Jiang, Li Wei, et al.
The Annals of Thoracic Surgery|February 26, 2016
Prognosis of Patients With Pathologic T0 N+ Esophageal Squamous Cell Carcinoma After Chemoradiotherapy and Surgical Resection: Results From a Nationwide StudyYin-Kai Chao, Hui-Shan Chen, Bing-Yen Wang, et al.
Mbio|July 21, 2022
VEGF-Mediated Augmentation of Autophagic and Lysosomal Activity in Endothelial Cells Defends against Intracellular Streptococcus pyogenesShiou-Ling Lu, Hiroko Omori, Yi Zhou, et al.
International Journal of Ophthalmology|September 21, 2020
Preliminary report on screening IGSF3 gene mutation in families with congenital absence of lacrimal puncta and canaliculiFei Wang, Hai Tao, Cui Han, et al.
Cardiology in the Young|November 22, 2019
A novel <i>MYBPC3</i> c.2737+1 (IVS26) G>T mutation responsible for high-risk hypertrophic cardiomyopathyWuyang Tong, Wei Liu, Hong Guo, et al.
Frontiers in Immunology|October 3, 2022
Research hotspot and trend analysis in the diagnosis of inflammatory bowel disease: A machine learning bibliometric analysis from 2012 to 2021Chuan Liu, Rong Yu, Jixiang Zhang, et al.
Pageof 182