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Showing results (341-350 of 970) with videos related to

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Journal of Cellular and Molecular Medicine|February 20, 2016
The risk of new-onset cancer associated with HFE C282Y and H63D mutations: evidence from 87,028 participantsYang-Fan Lv, Xian Chang, Rui-Xi Hua, et al.
Zhonghua Yi Xue Za Zhi|January 3, 2004
[A study of the degrees of insulin resistance and first-phase insulin secretion of beta-cells in metabolic syndrome patients with different glucose tolerance]Jie Hong, Wei-qiong Gu, Yi-fei Zhang, et al.
Zhonghua Yi Xue Za Zhi|February 16, 2012
[Clinical and genetic analysis of 11β-hydroxylase deficiency]Shou-yue Sun, Man-na Zhang, Jun Yang, et al.
Endocrine|April 22, 2009
Identification of a novel GNAS mutation for pseudohypoparathyroidism in a Chinese familyLi-Hao Sun, Bin Cui, Hong-Yan Zhao, et al.
Clinical Endocrinology|August 16, 2008
Variations in the promoter of CYP21A2 gene identified in a Chinese patient with simple virilizing form of 21-hydroxylase deficiencyHui-Jie Zhang, Jun Yang, Man-Na Zhang, et al.
Journal of Clinical Hypertension (Greenwich, Conn.)|April 5, 2013
Hormones other than aldosterone may contribute to hypertension in 3 different subtypes of primary aldosteronismFei Ye, Zheng-Yi Tang, Jing-Cheng Wu, et al.
Inorganic Chemistry|October 2, 2024
Two Thiophene-Functionalized Co-MOFs as Green Heterogeneous Catalysts for the Biginelli ReactionNana Liu, Jun Zheng, Tingting Liu, et al.
Clinical Endocrinology|January 25, 2006
Hyperglycaemia after glucose loading is a major predictor of preclinical atherosclerosis in nondiabetic subjectsYi-Fei Zhang, Jie Hong, Wei-Wei Zhan, et al.
World Journal of Surgery|February 11, 2014
Copy number variation in CCND1 gene is implicated in the pathogenesis of sporadic parathyroid carcinomaLin Zhao, Li-hao Sun, Dong-mei Liu, et al.
Zhonghua Yi Xue Za Zhi|June 14, 2005
[Hereditary spinocerebellar ataxia--a family pedigree with SCA3 gene mutation]Xiao-hua Jiang, Lei Ye, Yi Fu, et al.
Pageof 97

Showing results (341-350 of 970) with videos related to

Sort By:
Pageof 97
Journal of Cellular and Molecular Medicine|February 20, 2016
The risk of new-onset cancer associated with HFE C282Y and H63D mutations: evidence from 87,028 participantsYang-Fan Lv, Xian Chang, Rui-Xi Hua, et al.
Zhonghua Yi Xue Za Zhi|January 3, 2004
[A study of the degrees of insulin resistance and first-phase insulin secretion of beta-cells in metabolic syndrome patients with different glucose tolerance]Jie Hong, Wei-qiong Gu, Yi-fei Zhang, et al.
Zhonghua Yi Xue Za Zhi|February 16, 2012
[Clinical and genetic analysis of 11β-hydroxylase deficiency]Shou-yue Sun, Man-na Zhang, Jun Yang, et al.
Endocrine|April 22, 2009
Identification of a novel GNAS mutation for pseudohypoparathyroidism in a Chinese familyLi-Hao Sun, Bin Cui, Hong-Yan Zhao, et al.
Clinical Endocrinology|August 16, 2008
Variations in the promoter of CYP21A2 gene identified in a Chinese patient with simple virilizing form of 21-hydroxylase deficiencyHui-Jie Zhang, Jun Yang, Man-Na Zhang, et al.
Journal of Clinical Hypertension (Greenwich, Conn.)|April 5, 2013
Hormones other than aldosterone may contribute to hypertension in 3 different subtypes of primary aldosteronismFei Ye, Zheng-Yi Tang, Jing-Cheng Wu, et al.
Inorganic Chemistry|October 2, 2024
Two Thiophene-Functionalized Co-MOFs as Green Heterogeneous Catalysts for the Biginelli ReactionNana Liu, Jun Zheng, Tingting Liu, et al.
Clinical Endocrinology|January 25, 2006
Hyperglycaemia after glucose loading is a major predictor of preclinical atherosclerosis in nondiabetic subjectsYi-Fei Zhang, Jie Hong, Wei-Wei Zhan, et al.
World Journal of Surgery|February 11, 2014
Copy number variation in CCND1 gene is implicated in the pathogenesis of sporadic parathyroid carcinomaLin Zhao, Li-hao Sun, Dong-mei Liu, et al.
Zhonghua Yi Xue Za Zhi|June 14, 2005
[Hereditary spinocerebellar ataxia--a family pedigree with SCA3 gene mutation]Xiao-hua Jiang, Lei Ye, Yi Fu, et al.
Pageof 97