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Shaobin Lin

Showing results (71-80 of 92) with videos related to

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Analytica Chimica Acta|November 3, 2024
Sensitive and quick electrochemiluminescence biosensor for the detection of reactive oxygen species in seminal plasma based on the valence regulation of gold nanoclustersLingjun Cheng, Yuanyuan Yang, Shaobin Lin, et al.
Journal of Medical Genetics|June 2, 2019
Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF)Wensheng Liu, Yanwei Sha, Yang Li, et al.
Transfusion|March 16, 2017
Noninvasive fetal genotyping of paternally inherited alleles using targeted massively parallel sequencing in parentage testing casesDonggui Yang, Hao Liang, Yu Gao, et al.
Annals of Human Genetics|December 17, 2019
DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagellaYanwei Sha, Xiaoli Wei, Lu Ding, et al.
International Journal of Legal Medicine|April 22, 2017
An SNP panel for the analysis of paternally inherited alleles in maternal plasma using ion Torrent PGMDonggui Yang, Hao Liang, Shaobin Lin, et al.
Environment International|January 1, 2024
Overall and individual associations between per- and polyfluoroalkyl substances and liver function indices and the metabolic mechanismYiran Chen, Yan Wu, Jiayun Lv, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 3, 2019
Exome sequencing identifies compound heterozygous KCTD7 mutations in a girl with progressivemyoclonus epilepsyLibin Mei, Yanru Huang, Jing Chen, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 23, 2011
Paraplegia and paraparesis from intrathecal methotrexate and cytarabine contaminated with trace amounts of vincristine in China during 2007Guang Zeng, Huilai Ma, Xiangbo Wang, et al.
Systems Biology in Reproductive Medicine|September 11, 2019
<i>CCDC9</i> is identified as a novel candidate gene of severe asthenozoospermiaYanwei Sha, Yankai Xu, Xiaoli Wei, et al.
Annals of Human Genetics|February 17, 2017
Comprehensive Genome Profiling of Single Sperm Cells by Multiple Annealing and Looping-Based Amplification Cycles and Next-Generation Sequencing from Carriers of Robertsonian TranslocationYanwei Sha, Yankun Sha, Zhiyong Ji, et al.
Pageof 10

Showing results (71-80 of 92) with videos related to

Sort By:
Pageof 10
Analytica Chimica Acta|November 3, 2024
Sensitive and quick electrochemiluminescence biosensor for the detection of reactive oxygen species in seminal plasma based on the valence regulation of gold nanoclustersLingjun Cheng, Yuanyuan Yang, Shaobin Lin, et al.
Journal of Medical Genetics|June 2, 2019
Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF)Wensheng Liu, Yanwei Sha, Yang Li, et al.
Transfusion|March 16, 2017
Noninvasive fetal genotyping of paternally inherited alleles using targeted massively parallel sequencing in parentage testing casesDonggui Yang, Hao Liang, Yu Gao, et al.
Annals of Human Genetics|December 17, 2019
DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagellaYanwei Sha, Xiaoli Wei, Lu Ding, et al.
International Journal of Legal Medicine|April 22, 2017
An SNP panel for the analysis of paternally inherited alleles in maternal plasma using ion Torrent PGMDonggui Yang, Hao Liang, Shaobin Lin, et al.
Environment International|January 1, 2024
Overall and individual associations between per- and polyfluoroalkyl substances and liver function indices and the metabolic mechanismYiran Chen, Yan Wu, Jiayun Lv, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 3, 2019
Exome sequencing identifies compound heterozygous KCTD7 mutations in a girl with progressivemyoclonus epilepsyLibin Mei, Yanru Huang, Jing Chen, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 23, 2011
Paraplegia and paraparesis from intrathecal methotrexate and cytarabine contaminated with trace amounts of vincristine in China during 2007Guang Zeng, Huilai Ma, Xiangbo Wang, et al.
Systems Biology in Reproductive Medicine|September 11, 2019
<i>CCDC9</i> is identified as a novel candidate gene of severe asthenozoospermiaYanwei Sha, Yankai Xu, Xiaoli Wei, et al.
Annals of Human Genetics|February 17, 2017
Comprehensive Genome Profiling of Single Sperm Cells by Multiple Annealing and Looping-Based Amplification Cycles and Next-Generation Sequencing from Carriers of Robertsonian TranslocationYanwei Sha, Yankun Sha, Zhiyong Ji, et al.
Pageof 10