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Shangzhi Huang

Showing results (1-10 of 74) with videos related to

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Journal of Biochemistry and Molecular Biology|December 21, 2004
Identification of the DNA binding element of the human ZNF333 proteinZhe Jing, Yaping Liu, Min Dong, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 4, 2015
[A novel indel NF1 mutation identified in a patient with neurofibromatosis type 1]Tieshan Zhu, Shangzhi Huang, Jian Wu, et al.
Biochemical and Biophysical Research Communications|December 12, 2018
Histone deacetylases HDA6 and HDA9 coordinately regulate valve cell elongation through affecting auxin signaling in ArabidopsisLiangbing Yuan, Xue Chen, Huhui Chen, et al.
Molecular Vision|October 7, 2011
Identification of a novel FBN1 gene mutation in a Chinese family with Marfan syndromeBo Meng, Hongyi Li, Tao Yang, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|September 8, 2012
CYP17A1 mutations identified in 17 Chinese patients with 17α-hydroxylase/17,20-lyase deficiencyFengxia Yao, Shangzhi Huang, Xiaodi Kang, et al.
Ophthalmic Research|March 27, 2009
Autosomal-dominant cerulean cataract in a chinese family associated with gene conversion mutation in beta-B2-crystallinLi Wang, Hui Lin, Jingzhi Gu, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|April 16, 2011
Dihydrofolate reductase transcript level is not suitable for methotrexate-resistance prediction in choriocarcinoma cell lineBing Han, Yang Xiang, Yun Wang, et al.
Genes & Nutrition|September 21, 2015
Multiple effects of curcumin on promoting expression of the exon 7-containing SMN2 transcriptDairong Feng, Yi Cheng, Yan Meng, et al.
Molecular Vision|January 21, 2012
A novel splicing mutation of the FRMD7 gene in a Chinese family with X-linked congenital nystagmusYing Hu, Jing Shen, Shuihua Zhang, et al.
BMC Genomics|May 28, 2011
Analysis of common bean expressed sequence tags identifies sulfur metabolic pathways active in seed and sulfur-rich proteins highly expressed in the absence of phaseolin and major lectinsFuqiang Yin, Agnieszka Pajak, Ralph Chapman, et al.
Pageof 8

Showing results (1-10 of 74) with videos related to

Sort By:
Pageof 8
Journal of Biochemistry and Molecular Biology|December 21, 2004
Identification of the DNA binding element of the human ZNF333 proteinZhe Jing, Yaping Liu, Min Dong, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 4, 2015
[A novel indel NF1 mutation identified in a patient with neurofibromatosis type 1]Tieshan Zhu, Shangzhi Huang, Jian Wu, et al.
Biochemical and Biophysical Research Communications|December 12, 2018
Histone deacetylases HDA6 and HDA9 coordinately regulate valve cell elongation through affecting auxin signaling in ArabidopsisLiangbing Yuan, Xue Chen, Huhui Chen, et al.
Molecular Vision|October 7, 2011
Identification of a novel FBN1 gene mutation in a Chinese family with Marfan syndromeBo Meng, Hongyi Li, Tao Yang, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|September 8, 2012
CYP17A1 mutations identified in 17 Chinese patients with 17α-hydroxylase/17,20-lyase deficiencyFengxia Yao, Shangzhi Huang, Xiaodi Kang, et al.
Ophthalmic Research|March 27, 2009
Autosomal-dominant cerulean cataract in a chinese family associated with gene conversion mutation in beta-B2-crystallinLi Wang, Hui Lin, Jingzhi Gu, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|April 16, 2011
Dihydrofolate reductase transcript level is not suitable for methotrexate-resistance prediction in choriocarcinoma cell lineBing Han, Yang Xiang, Yun Wang, et al.
Genes & Nutrition|September 21, 2015
Multiple effects of curcumin on promoting expression of the exon 7-containing SMN2 transcriptDairong Feng, Yi Cheng, Yan Meng, et al.
Molecular Vision|January 21, 2012
A novel splicing mutation of the FRMD7 gene in a Chinese family with X-linked congenital nystagmusYing Hu, Jing Shen, Shuihua Zhang, et al.
BMC Genomics|May 28, 2011
Analysis of common bean expressed sequence tags identifies sulfur metabolic pathways active in seed and sulfur-rich proteins highly expressed in the absence of phaseolin and major lectinsFuqiang Yin, Agnieszka Pajak, Ralph Chapman, et al.
Pageof 8