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Showing results (461-470 of 530) with videos related to

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Molecular Psychiatry|July 31, 2003
Family-based association study of DTNBP1 in 6p22.3 and schizophreniaJ X Tang, J Zhou, J B Fan, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|August 12, 2016
[Clinical and genetic analysis of an infant with isolated 17, 20-lyase deficiency]D Y Zhou, W J Qiu, M S Xu, et al.
BMC Medical Genetics|March 19, 2009
Functional and genetic analysis in type 2 diabetes of liver X receptor alleles--a cohort studyIngrid Dahlman, Maria Nilsson, Harvest F Gu, et al.
Springerplus|April 27, 2017
Evaluation of common variants in <i>MG53</i> and the risk of type 2 diabetes and insulin resistance in Han ChineseSong Yang, Hailong Zhao, Kuangfeng Xu, et al.
Cell Death & Disease|August 30, 2018
JAZF1 ameliorates age and diet-associated hepatic steatosis through SREBP-1c -dependent mechanismQin Wei, Baoyong Zhou, Gangyi Yang, et al.
Human Molecular Genetics|May 2, 2008
Evidence that the gene encoding insulin degrading enzyme influences human lifespanMun-Gwan Hong, Chandra Reynolds, Margaret Gatz, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|December 7, 2018
High Circulating Alarin Levels Are Associated with Presence of Metabolic SyndromeXia Fang, Tingran Zhang, Mengliu Yang, et al.
Molecular Psychiatry|August 4, 2004
No association between polymorphisms of methylenetetrahydrofolate reductase gene and schizophrenia in both Chinese and Scottish populationsL Yu, T Li, Z Robertson, et al.
Molecular Psychiatry|January 13, 2006
Family-based association study of Epsin 4 and SchizophreniaR Q Tang, X Z Zhao, Y Y Shi, et al.
Brain & Development|July 28, 2024
Clinical, biochemical and genetic characteristics and long-term follow-up of five patients with malonyl-CoA decarboxylase deficiencyJ M Zhang, L L Hao, W J Qiu, et al.
Pageof 53

Showing results (461-470 of 530) with videos related to

Sort By:
Pageof 53
Molecular Psychiatry|July 31, 2003
Family-based association study of DTNBP1 in 6p22.3 and schizophreniaJ X Tang, J Zhou, J B Fan, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|August 12, 2016
[Clinical and genetic analysis of an infant with isolated 17, 20-lyase deficiency]D Y Zhou, W J Qiu, M S Xu, et al.
BMC Medical Genetics|March 19, 2009
Functional and genetic analysis in type 2 diabetes of liver X receptor alleles--a cohort studyIngrid Dahlman, Maria Nilsson, Harvest F Gu, et al.
Springerplus|April 27, 2017
Evaluation of common variants in <i>MG53</i> and the risk of type 2 diabetes and insulin resistance in Han ChineseSong Yang, Hailong Zhao, Kuangfeng Xu, et al.
Cell Death & Disease|August 30, 2018
JAZF1 ameliorates age and diet-associated hepatic steatosis through SREBP-1c -dependent mechanismQin Wei, Baoyong Zhou, Gangyi Yang, et al.
Human Molecular Genetics|May 2, 2008
Evidence that the gene encoding insulin degrading enzyme influences human lifespanMun-Gwan Hong, Chandra Reynolds, Margaret Gatz, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|December 7, 2018
High Circulating Alarin Levels Are Associated with Presence of Metabolic SyndromeXia Fang, Tingran Zhang, Mengliu Yang, et al.
Molecular Psychiatry|August 4, 2004
No association between polymorphisms of methylenetetrahydrofolate reductase gene and schizophrenia in both Chinese and Scottish populationsL Yu, T Li, Z Robertson, et al.
Molecular Psychiatry|January 13, 2006
Family-based association study of Epsin 4 and SchizophreniaR Q Tang, X Z Zhao, Y Y Shi, et al.
Brain & Development|July 28, 2024
Clinical, biochemical and genetic characteristics and long-term follow-up of five patients with malonyl-CoA decarboxylase deficiencyJ M Zhang, L L Hao, W J Qiu, et al.
Pageof 53