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Junhui Yi

Showing results (11-20 of 18) with videos related to

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Molecular Medicine Reports|January 24, 2017
Identification of a missense mutation in the tyrosinase gene in a Chinese family with oculocutaneous albinism type 1Qian Lu, Lamei Yuan, Hongbo Xu, et al.
The Science of the Total Environment|December 17, 2019
Fabrication and characterization of ZnTiO<sub>3</sub>/Zn<sub>2</sub>Ti<sub>3</sub>O<sub>8</sub>/ZnO ternary photocatalyst for synergetic removal of aqueous organic pollutants and Cr(<sub>VI</sub>) ionsFanyun Chen, Changlin Yu, Longfu Wei, et al.
Molecular Medicine Reports|July 22, 2017
A homozygous MYO7A mutation associated to Usher syndrome and unilateral auditory neuropathy spectrum disorderHong Xia, Pengzhi Hu, Lamei Yuan, et al.
Optometry and Vision Science : Official Publication of the American Academy of Optometry|January 31, 2015
Identification of a novel GJA3 mutation in congenital nuclear cataractLamei Yuan, Yi Guo, Junhui Yi, et al.
Bioscience Reports|February 14, 2018
Identification of a Novel Mutation in the ABCA4 Gene in a Chinese Family with Retinitis Pigmentosa Using Exome SequencingXiangjun Huang, Lamei Yuan, Hongbo Xu, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|May 3, 2018
Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar KeratodermaHeng Xiao, Yi Guo, Junhui Yi, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|February 12, 2014
Heterogeneous phenotype in a family with the FERM domain-containing 7 gene R335X mutationYi Guo, Zhi Song, Hongbo Xu, et al.
Indian Journal of Biochemistry & Biophysics|April 30, 2014
Identification of a GJA3 mutation in a Chinese family with congenital nuclear cataract using exome sequencingYi Guo, Lamei Yuan, Junhui Yi, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Molecular Medicine Reports|January 24, 2017
Identification of a missense mutation in the tyrosinase gene in a Chinese family with oculocutaneous albinism type 1Qian Lu, Lamei Yuan, Hongbo Xu, et al.
The Science of the Total Environment|December 17, 2019
Fabrication and characterization of ZnTiO<sub>3</sub>/Zn<sub>2</sub>Ti<sub>3</sub>O<sub>8</sub>/ZnO ternary photocatalyst for synergetic removal of aqueous organic pollutants and Cr(<sub>VI</sub>) ionsFanyun Chen, Changlin Yu, Longfu Wei, et al.
Molecular Medicine Reports|July 22, 2017
A homozygous MYO7A mutation associated to Usher syndrome and unilateral auditory neuropathy spectrum disorderHong Xia, Pengzhi Hu, Lamei Yuan, et al.
Optometry and Vision Science : Official Publication of the American Academy of Optometry|January 31, 2015
Identification of a novel GJA3 mutation in congenital nuclear cataractLamei Yuan, Yi Guo, Junhui Yi, et al.
Bioscience Reports|February 14, 2018
Identification of a Novel Mutation in the ABCA4 Gene in a Chinese Family with Retinitis Pigmentosa Using Exome SequencingXiangjun Huang, Lamei Yuan, Hongbo Xu, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|May 3, 2018
Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar KeratodermaHeng Xiao, Yi Guo, Junhui Yi, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|February 12, 2014
Heterogeneous phenotype in a family with the FERM domain-containing 7 gene R335X mutationYi Guo, Zhi Song, Hongbo Xu, et al.
Indian Journal of Biochemistry & Biophysics|April 30, 2014
Identification of a GJA3 mutation in a Chinese family with congenital nuclear cataract using exome sequencingYi Guo, Lamei Yuan, Junhui Yi, et al.
Pageof 2