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Xiangjun Huang

Showing results (21-30 of 27) with videos related to

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Current Genomics|August 2, 2018
An <i>OTOF</i> Frameshift Variant Associated with Auditory Neuropathy Spectrum DisorderHong Xia, Xiangjun Huang, Hongbo Xu, et al.
Plos One|August 27, 2015
Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing LossHong Xia, Xiangjun Huang, Yi Guo, et al.
Biosensors & Bioelectronics|April 29, 2022
In-situ preparation of lactate-sensing membrane for the noninvasive and wearable analysis of sweatDanfeng Jiang, Changshun Xu, Qingwen Zhang, et al.
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.
Journal of Cellular Biochemistry|January 19, 2019
A novel splice-site mutation in the ATP2C1 gene of a Chinese family with Hailey-Hailey diseaseHeng Xiao, Xiangjun Huang, Hongbo Xu, 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.
Biosensors & Bioelectronics|October 13, 2022
A miniaturized electrochemical device based on the nitrogen, carbon-codoped bimetal for real-time monitoring of acetaminophen and dopamine in urineDanfeng Jiang, Xiangjun Huang, Qingwen Zhang, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Current Genomics|August 2, 2018
An <i>OTOF</i> Frameshift Variant Associated with Auditory Neuropathy Spectrum DisorderHong Xia, Xiangjun Huang, Hongbo Xu, et al.
Plos One|August 27, 2015
Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing LossHong Xia, Xiangjun Huang, Yi Guo, et al.
Biosensors & Bioelectronics|April 29, 2022
In-situ preparation of lactate-sensing membrane for the noninvasive and wearable analysis of sweatDanfeng Jiang, Changshun Xu, Qingwen Zhang, et al.
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.
Journal of Cellular Biochemistry|January 19, 2019
A novel splice-site mutation in the ATP2C1 gene of a Chinese family with Hailey-Hailey diseaseHeng Xiao, Xiangjun Huang, Hongbo Xu, 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.
Biosensors & Bioelectronics|October 13, 2022
A miniaturized electrochemical device based on the nitrogen, carbon-codoped bimetal for real-time monitoring of acetaminophen and dopamine in urineDanfeng Jiang, Xiangjun Huang, Qingwen Zhang, et al.
Pageof 3