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Mingmin Gu

Showing results (1-10 of 9) with videos related to

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Yi Chuan = Hereditas|May 22, 2014
[Research progress in the mouse models of Charcot-Marie-Tooth disease type 2 (CMT2)]Zhen Yu, Chunjie Luan, Mingmin Gu
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 2, 2024
[Study of the types of mutations of Thalassemia in Shanghai area]Yanying Gu, Beiying Wu, Yiyi Lu, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 8, 2015
A novel Cx50 (GJA8) p.H277Y mutation associated with autosomal dominant congenital cataract identified with targeted next-generation sequencingChong Chen, Qiao Sun, Mingmin Gu, et al.
Molecular Genetics & Genomic Medicine|September 7, 2020
Multimodal imaging and genetic characteristics of Chinese patients with USH2A-associated nonsyndromic retinitis pigmentosaChong Chen, Qiao Sun, Mingmin Gu, et al.
FEBS Letters|October 1, 2013
DHTKD1 is essential for mitochondrial biogenesis and function maintenanceWangyang Xu, Houbao Zhu, Mingmin Gu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 2, 2016
[Mutation analysis for a family affected with Charcot-Marie-Tooth disease type 4C]Zhen Yu, Jiaying Zhang, Ye Xu, et al.
Molecular and Cellular Neurosciences|June 14, 2005
Disruption of palladin results in neural tube closure defects in miceHuijun Luo, Xuesong Liu, Fang Wang, et al.
Plos One|May 3, 2011
The cytoplasmic domain of MUC1 induces hyperplasia in the mammary gland and correlates with nuclear accumulation of β-cateninYuan Li, Haiying Yi, Yixin Yao, et al.
Human Molecular Genetics|February 8, 2017
A point mutation in Fgf9 impedes joint interzone formation leading to multiple synostoses syndromeLingyun Tang, Xiaolin Wu, Hongxin Zhang, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Yi Chuan = Hereditas|May 22, 2014
[Research progress in the mouse models of Charcot-Marie-Tooth disease type 2 (CMT2)]Zhen Yu, Chunjie Luan, Mingmin Gu
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 2, 2024
[Study of the types of mutations of Thalassemia in Shanghai area]Yanying Gu, Beiying Wu, Yiyi Lu, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 8, 2015
A novel Cx50 (GJA8) p.H277Y mutation associated with autosomal dominant congenital cataract identified with targeted next-generation sequencingChong Chen, Qiao Sun, Mingmin Gu, et al.
Molecular Genetics & Genomic Medicine|September 7, 2020
Multimodal imaging and genetic characteristics of Chinese patients with USH2A-associated nonsyndromic retinitis pigmentosaChong Chen, Qiao Sun, Mingmin Gu, et al.
FEBS Letters|October 1, 2013
DHTKD1 is essential for mitochondrial biogenesis and function maintenanceWangyang Xu, Houbao Zhu, Mingmin Gu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 2, 2016
[Mutation analysis for a family affected with Charcot-Marie-Tooth disease type 4C]Zhen Yu, Jiaying Zhang, Ye Xu, et al.
Molecular and Cellular Neurosciences|June 14, 2005
Disruption of palladin results in neural tube closure defects in miceHuijun Luo, Xuesong Liu, Fang Wang, et al.
Plos One|May 3, 2011
The cytoplasmic domain of MUC1 induces hyperplasia in the mammary gland and correlates with nuclear accumulation of β-cateninYuan Li, Haiying Yi, Yixin Yao, et al.
Human Molecular Genetics|February 8, 2017
A point mutation in Fgf9 impedes joint interzone formation leading to multiple synostoses syndromeLingyun Tang, Xiaolin Wu, Hongxin Zhang, et al.
Pageof 1