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Shanling Liu

Showing results (81-90 of 175) with videos related to

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Frontiers in Pharmacology|December 26, 2022
Natural phytochemicals prevent side effects in <i>BRCA</i>-mutated ovarian cancer and PARP inhibitor treatmentChuanlin Wang, Pengning Gao, Jiali Xu, et al.
Diagnostic Pathology|October 31, 2012
Genomic amplification of the human telomerase gene (hTERC) associated with human papillomavirus is related to the progression of uterine cervical dysplasia to invasive cancerHongqian Liu, Shanling Liu, He Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|January 25, 2022
[Preparation and evaluation of quality management samples for noninvasive prenatal screening]Cechuan Deng, Qian Zhu, Ting Bai, et al.
Evidence-Based Complementary and Alternative Medicine : Ecam|March 17, 2021
The Neuroprotective Effect of <i>Byu d Mar</i> 25 in LPS-Induced Alzheimer's Disease Mice ModelLan Liu, Yongcang Zhang, Liang Tang, et al.
International Journal of Legal Medicine|September 26, 2024
Screening a new set of microhaplotypes in exonic regions for sample identity testing and paternity testing during whole exome sequencing analysisYu Tan, Huan Tian, Yuanyuan Xiao, et al.
Molecular Neurobiology|June 3, 2025
Interactive Effect of Plasma Lipidome on Neuropsychiatric Disorders: A Bidirectional Mendelian Randomization StudyXiao Xiao, Xiaolei Luo, Yanyun Wang, et al.
Molecular Genetics & Genomic Medicine|November 6, 2023
Identification of a novel LMX1B nonsense variant associated with congenital talipes equinovarus by prenatal exome sequencing: A case reportJing Chen, Qinqin Xiang, Xiao Xiao, et al.
Patient Preference and Adherence|June 23, 2023
Correlation Analysis of the Therapy Adherence to Long-Acting Inhalers Among Patients with Stable COPDXin Tan, Shanling Liu, Li Huang, et al.
Frontiers in Genetics|September 11, 2025
Compound heterozygous missense and intronic variants in <i>B9D1</i> contribute to a recurrent Meckel syndrome pedigreeHuining Jing, Bocheng Xu, Hao Wang, et al.
BMC Medical Genomics|July 8, 2022
Carrying both COL1A2 and FBN2 gene heterozygous mutations results in a severe skeletal clinical phenotype: an affected familyJing Chen, Qinqin Xiang, Xiao Xiao, et al.
Pageof 18

Showing results (81-90 of 175) with videos related to

Sort By:
Pageof 18
Frontiers in Pharmacology|December 26, 2022
Natural phytochemicals prevent side effects in <i>BRCA</i>-mutated ovarian cancer and PARP inhibitor treatmentChuanlin Wang, Pengning Gao, Jiali Xu, et al.
Diagnostic Pathology|October 31, 2012
Genomic amplification of the human telomerase gene (hTERC) associated with human papillomavirus is related to the progression of uterine cervical dysplasia to invasive cancerHongqian Liu, Shanling Liu, He Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|January 25, 2022
[Preparation and evaluation of quality management samples for noninvasive prenatal screening]Cechuan Deng, Qian Zhu, Ting Bai, et al.
Evidence-Based Complementary and Alternative Medicine : Ecam|March 17, 2021
The Neuroprotective Effect of <i>Byu d Mar</i> 25 in LPS-Induced Alzheimer's Disease Mice ModelLan Liu, Yongcang Zhang, Liang Tang, et al.
International Journal of Legal Medicine|September 26, 2024
Screening a new set of microhaplotypes in exonic regions for sample identity testing and paternity testing during whole exome sequencing analysisYu Tan, Huan Tian, Yuanyuan Xiao, et al.
Molecular Neurobiology|June 3, 2025
Interactive Effect of Plasma Lipidome on Neuropsychiatric Disorders: A Bidirectional Mendelian Randomization StudyXiao Xiao, Xiaolei Luo, Yanyun Wang, et al.
Molecular Genetics & Genomic Medicine|November 6, 2023
Identification of a novel LMX1B nonsense variant associated with congenital talipes equinovarus by prenatal exome sequencing: A case reportJing Chen, Qinqin Xiang, Xiao Xiao, et al.
Patient Preference and Adherence|June 23, 2023
Correlation Analysis of the Therapy Adherence to Long-Acting Inhalers Among Patients with Stable COPDXin Tan, Shanling Liu, Li Huang, et al.
Frontiers in Genetics|September 11, 2025
Compound heterozygous missense and intronic variants in <i>B9D1</i> contribute to a recurrent Meckel syndrome pedigreeHuining Jing, Bocheng Xu, Hao Wang, et al.
BMC Medical Genomics|July 8, 2022
Carrying both COL1A2 and FBN2 gene heterozygous mutations results in a severe skeletal clinical phenotype: an affected familyJing Chen, Qinqin Xiang, Xiao Xiao, et al.
Pageof 18