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Pengfei Liu

Showing results (1111-1120 of 1,193) with videos related to

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American Journal of Medical Genetics. Part A|April 13, 2021
Heterozygous variants in SPTBN1 cause intellectual disability and autismJill A Rosenfeld, Rui Xiao, Mir Reza Bekheirnia, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 17, 2021
Aqueous production of secondary organic aerosol from fossil-fuel emissions in winter Beijing hazeJunfeng Wang, Jianhuai Ye, Qi Zhang, et al.
Human Mutation|July 11, 2022
Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory functionSheng-Jia Lin, Barbara Vona, Hillary M Porter, et al.
Nature Genetics|October 4, 2011
Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genomeClaudia M B Carvalho, Melissa B Ramocki, Davut Pehlivan, et al.
Science (New York, N.Y.)|March 26, 2016
Homogeneously dispersed multimetal oxygen-evolving catalystsBo Zhang, Xueli Zheng, Oleksandr Voznyy, et al.
Nature Communications|February 6, 2024
Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spineSen Zhao, Hengqiang Zhao, Lina Zhao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 27, 2017
The next generation of population-based spinal muscular atrophy carrier screening: comprehensive pan-ethnic SMN1 copy-number and sequence variant analysis by massively parallel sequencingYanming Feng, Xiaoyan Ge, Linyan Meng, et al.
Journal of Human Genetics|August 18, 2018
Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD)Kun Wang, Sen Zhao, Qianqian Zhang, et al.
Genome Medicine|September 30, 2018
Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorderElizabeth A Normand, Alicia Braxton, Salma Nassef, et al.
Journal of Environmental Sciences (China)|December 29, 2025
Research progress in atmospheric haze chemistry: Formation mechanism of air pollution complex and control technologiesQingxin Ma, Peng Zhang, Tianzeng Chen, et al.
Pageof 120

Showing results (1111-1120 of 1,193) with videos related to

Sort By:
Pageof 120
American Journal of Medical Genetics. Part A|April 13, 2021
Heterozygous variants in SPTBN1 cause intellectual disability and autismJill A Rosenfeld, Rui Xiao, Mir Reza Bekheirnia, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 17, 2021
Aqueous production of secondary organic aerosol from fossil-fuel emissions in winter Beijing hazeJunfeng Wang, Jianhuai Ye, Qi Zhang, et al.
Human Mutation|July 11, 2022
Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory functionSheng-Jia Lin, Barbara Vona, Hillary M Porter, et al.
Nature Genetics|October 4, 2011
Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genomeClaudia M B Carvalho, Melissa B Ramocki, Davut Pehlivan, et al.
Science (New York, N.Y.)|March 26, 2016
Homogeneously dispersed multimetal oxygen-evolving catalystsBo Zhang, Xueli Zheng, Oleksandr Voznyy, et al.
Nature Communications|February 6, 2024
Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spineSen Zhao, Hengqiang Zhao, Lina Zhao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 27, 2017
The next generation of population-based spinal muscular atrophy carrier screening: comprehensive pan-ethnic SMN1 copy-number and sequence variant analysis by massively parallel sequencingYanming Feng, Xiaoyan Ge, Linyan Meng, et al.
Journal of Human Genetics|August 18, 2018
Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD)Kun Wang, Sen Zhao, Qianqian Zhang, et al.
Genome Medicine|September 30, 2018
Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorderElizabeth A Normand, Alicia Braxton, Salma Nassef, et al.
Journal of Environmental Sciences (China)|December 29, 2025
Research progress in atmospheric haze chemistry: Formation mechanism of air pollution complex and control technologiesQingxin Ma, Peng Zhang, Tianzeng Chen, et al.
Pageof 120