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Bing Wen

Showing results (81-90 of 436) with videos related to

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Acta Cardiologica|July 31, 2008
Distribution and effect of apo A-IV genotype on plasma lipid and apolipoprotein levels in a Chinese populationHuai Bai, Rui Liu, Yu Liu, et al.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae|June 18, 2005
[Clinical analysis of proteinuria and glomerular lesions in Henoch-Schönlein purpura nephritis of adults]Dong-yan Liu, Yu-bing Wen, Hang Li, et al.
Zhonghua Yi Xue Za Zhi|January 19, 2013
[IgG4-related systemic diseases: a report of eight cases]Ke Zheng, Xue-Mei Li, Jian-Fang Cai, et al.
Acta Cytologica|November 9, 2010
Malignant fibrous histiocytoma like pleomorphic leiomyosarcoma with laryngeal cancer as a second primary neoplasm: a case reportQing-Lian Wen, Mao-Bin Meng, Bing-Wen Zou, et al.
Neuropsychiatric Disease and Treatment|March 14, 2019
Clinical feature and outcome of late-onset cobalamin C disease patients with neuropsychiatric presentations: a Chinese case seriesSheng-Jun Wang, Chuan-Zhu Yan, Bing Wen, et al.
Sichuan Da Xue Xue Bao. Yi Xue Ban = Journal of Sichuan University. Medical Science Edition|December 22, 2007
[Inhibitory effect of isorhamnetin and hesperidin on the oxidation of high-density lipoproteins (HDL) induced by Cu2+]Rui Liu, Fang Meng, Huai Bai, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 13, 2006
[Analysis of cholesterol ester transfer protein gene Taq IB and -629 C/A polymorphisms in patients with endogenous hypertriglyceridemia in Chinese population]Yin Wu, Huai Bai, Rui Liu, et al.
Neurobiology of Disease|May 10, 2011
Splice isoform-specific suppression of the Cav2.1 variant underlying spinocerebellar ataxia type 6Wei-Ling Tsou, Bing-Wen Soong, Henry L Paulson, et al.
Acta Neurologica Taiwanica|June 4, 2015
[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)]Yun-Chung Chen, Cheng-Tsung Hsiao, Bing-Wen Soong, et al.
Brain : a Journal of Neurology|May 24, 2003
A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23Ming-Yi Chung, Yi-Chun Lu, Nai-Chia Cheng, et al.
Pageof 44

Showing results (81-90 of 436) with videos related to

Sort By:
Pageof 44
Acta Cardiologica|July 31, 2008
Distribution and effect of apo A-IV genotype on plasma lipid and apolipoprotein levels in a Chinese populationHuai Bai, Rui Liu, Yu Liu, et al.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae|June 18, 2005
[Clinical analysis of proteinuria and glomerular lesions in Henoch-Schönlein purpura nephritis of adults]Dong-yan Liu, Yu-bing Wen, Hang Li, et al.
Zhonghua Yi Xue Za Zhi|January 19, 2013
[IgG4-related systemic diseases: a report of eight cases]Ke Zheng, Xue-Mei Li, Jian-Fang Cai, et al.
Acta Cytologica|November 9, 2010
Malignant fibrous histiocytoma like pleomorphic leiomyosarcoma with laryngeal cancer as a second primary neoplasm: a case reportQing-Lian Wen, Mao-Bin Meng, Bing-Wen Zou, et al.
Neuropsychiatric Disease and Treatment|March 14, 2019
Clinical feature and outcome of late-onset cobalamin C disease patients with neuropsychiatric presentations: a Chinese case seriesSheng-Jun Wang, Chuan-Zhu Yan, Bing Wen, et al.
Sichuan Da Xue Xue Bao. Yi Xue Ban = Journal of Sichuan University. Medical Science Edition|December 22, 2007
[Inhibitory effect of isorhamnetin and hesperidin on the oxidation of high-density lipoproteins (HDL) induced by Cu2+]Rui Liu, Fang Meng, Huai Bai, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 13, 2006
[Analysis of cholesterol ester transfer protein gene Taq IB and -629 C/A polymorphisms in patients with endogenous hypertriglyceridemia in Chinese population]Yin Wu, Huai Bai, Rui Liu, et al.
Neurobiology of Disease|May 10, 2011
Splice isoform-specific suppression of the Cav2.1 variant underlying spinocerebellar ataxia type 6Wei-Ling Tsou, Bing-Wen Soong, Henry L Paulson, et al.
Acta Neurologica Taiwanica|June 4, 2015
[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)]Yun-Chung Chen, Cheng-Tsung Hsiao, Bing-Wen Soong, et al.
Brain : a Journal of Neurology|May 24, 2003
A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23Ming-Yi Chung, Yi-Chun Lu, Nai-Chia Cheng, et al.
Pageof 44