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Sha Tang

Showing results (161-170 of 448) with videos related to

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Phytomedicine : International Journal of Phytotherapy and Phytopharmacology|March 29, 2022
Capsaicin ameliorates renal fibrosis by inhibiting TGF-β1-Smad2/3 signalingZhenyu Liu, Weili Wang, Xueqin Li, et al.
Journal of Family Medicine and Primary Care|July 19, 2024
Effect of different endometrial preparation methods on pregnancy outcome of FET in women with a normal menstrual cycleHui-Juan Guan, Huai-Yun Tang, Hui Li, et al.
Toxicology Letters|January 3, 2017
4-Nonylphenol induces autophagy and attenuates mTOR-p70S6K/4EBP1 signaling by modulating AMPK activation in Sertoli cellsPeng Duan, Chunhui Hu, Chao Quan, et al.
Brain Research|June 16, 2010
R492X mutation in PTEN-induced putative kinase 1 induced cellular mitochondrial dysfunction and oxidative stressXiang-Li Yuan, Ji-Feng Guo, Zhen-Hua Shi, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 11, 2008
[The clinical characteristics of a pedigree with incompletely penetrated autosomal dominant hereditary spastic paraplegia and its exclusion analysis of genetic loci]Guo-hua Zhao, Zhi-jun Ren, Xiao-min Liu, et al.
The International Journal of Neuroscience|July 26, 2005
Association analysis of serotonin transporter promoter gene polymorphism with ADHD and related symptomatologyAi-Ling Zhao, Lin-Yan Su, Yu-Hu Zhang, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|October 26, 2006
[Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China]Xing-wang Song, Bei-sha Tang, Hong Jiang, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 25, 2012
Characterization of a recurrent 3.8kb deletion involving exons 17a and 17b within the CFTR geneSha Tang, Siby P Moonnumakal, Blair Stevens, et al.
BMC Medical Genetics|November 7, 2015
Germline activating MTOR mutation arising through gonadal mosaicism in two brothers with megalencephaly and neurodevelopmental abnormalitiesCameron Mroske, Kristen Rasmussen, Deepali N Shinde, et al.
Parkinson'S Disease|October 1, 2015
Effect of GBA Mutations on Phenotype of Parkinson's Disease: A Study on Chinese Population and a Meta-AnalysisYuan Zhang, Qi-Ying Sun, Yu-Wen Zhao, et al.
Pageof 45

Showing results (161-170 of 448) with videos related to

Sort By:
Pageof 45
Phytomedicine : International Journal of Phytotherapy and Phytopharmacology|March 29, 2022
Capsaicin ameliorates renal fibrosis by inhibiting TGF-β1-Smad2/3 signalingZhenyu Liu, Weili Wang, Xueqin Li, et al.
Journal of Family Medicine and Primary Care|July 19, 2024
Effect of different endometrial preparation methods on pregnancy outcome of FET in women with a normal menstrual cycleHui-Juan Guan, Huai-Yun Tang, Hui Li, et al.
Toxicology Letters|January 3, 2017
4-Nonylphenol induces autophagy and attenuates mTOR-p70S6K/4EBP1 signaling by modulating AMPK activation in Sertoli cellsPeng Duan, Chunhui Hu, Chao Quan, et al.
Brain Research|June 16, 2010
R492X mutation in PTEN-induced putative kinase 1 induced cellular mitochondrial dysfunction and oxidative stressXiang-Li Yuan, Ji-Feng Guo, Zhen-Hua Shi, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 11, 2008
[The clinical characteristics of a pedigree with incompletely penetrated autosomal dominant hereditary spastic paraplegia and its exclusion analysis of genetic loci]Guo-hua Zhao, Zhi-jun Ren, Xiao-min Liu, et al.
The International Journal of Neuroscience|July 26, 2005
Association analysis of serotonin transporter promoter gene polymorphism with ADHD and related symptomatologyAi-Ling Zhao, Lin-Yan Su, Yu-Hu Zhang, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|October 26, 2006
[Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China]Xing-wang Song, Bei-sha Tang, Hong Jiang, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 25, 2012
Characterization of a recurrent 3.8kb deletion involving exons 17a and 17b within the CFTR geneSha Tang, Siby P Moonnumakal, Blair Stevens, et al.
BMC Medical Genetics|November 7, 2015
Germline activating MTOR mutation arising through gonadal mosaicism in two brothers with megalencephaly and neurodevelopmental abnormalitiesCameron Mroske, Kristen Rasmussen, Deepali N Shinde, et al.
Parkinson'S Disease|October 1, 2015
Effect of GBA Mutations on Phenotype of Parkinson's Disease: A Study on Chinese Population and a Meta-AnalysisYuan Zhang, Qi-Ying Sun, Yu-Wen Zhao, et al.
Pageof 45