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Shanling Liu

Showing results (91-100 of 175) with videos related to

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Diagnostic Pathology|April 18, 2015
Accumulation of invariant NKT cells with increased IFN-γ production in persistent high-risk HPV-infected high-grade cervical intraepithelial neoplasiaTing Hu, Pei Yang, Hongmei Zhu, et al.
International Journal of Clinical and Experimental Pathology|July 21, 2015
Phospho-histone H2AX is a diagnostic and prognostic marker for epithelial ovarian cancerLing Mei, Qian Hu, Jing Peng, et al.
Thoracic Cancer|April 20, 2023
GTSE1 promotes the growth of NSCLC by regulating microtubule-associated proteins through the ERK/MAPK pathwayChuanlin Wang, Meiyan Wen, Jiali Xu, et al.
Frontiers in Genetics|April 10, 2023
Case Report: The compound heterozygotes variants in <i>FLT4</i> causes autosomal recessive hereditary lymphedema in a Chinese familyQinqin Xiang, Jing Chen, Xiao Xiao, et al.
Epilepsy Research|January 24, 2021
Genetic diagnoses in pediatric patients with epilepsy and comorbid intellectual disabilityMei Yang, Bocheng Xu, Jiamin Wang, et al.
Pain Physician|July 25, 2019
The Relevance of the OPRM1 118A>G Genetic Variant for Opioid Requirement in Pain Treatment: A Meta-AnalysisXueying Zhang, Yongxin Liang, Nannan Zhang, et al.
Molecular Genetics & Genomic Medicine|August 1, 2022
A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosisQianying Zhao, Qinqin Xiang, Yu Tan, et al.
Medicine|February 2, 2024
Preimplantation genetic testing for X-linked chronic granulomatous disease induced by a CYBB gene variant: A case reportXinlian Chen, Cuiting Peng, Han Chen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 27, 2023
[Clinical manifestations and genetic analysis of 4 patients with variants of FBN1 gene]Xin Liu, Mei Yang, Hanbing Xie, et al.
Prenatal Diagnosis|August 29, 2019
Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in fetuses with ultrasound anomalies in the urinary systemTing Hu, Zhu Zhang, Jiamin Wang, et al.
Pageof 18

Showing results (91-100 of 175) with videos related to

Sort By:
Pageof 18
Diagnostic Pathology|April 18, 2015
Accumulation of invariant NKT cells with increased IFN-γ production in persistent high-risk HPV-infected high-grade cervical intraepithelial neoplasiaTing Hu, Pei Yang, Hongmei Zhu, et al.
International Journal of Clinical and Experimental Pathology|July 21, 2015
Phospho-histone H2AX is a diagnostic and prognostic marker for epithelial ovarian cancerLing Mei, Qian Hu, Jing Peng, et al.
Thoracic Cancer|April 20, 2023
GTSE1 promotes the growth of NSCLC by regulating microtubule-associated proteins through the ERK/MAPK pathwayChuanlin Wang, Meiyan Wen, Jiali Xu, et al.
Frontiers in Genetics|April 10, 2023
Case Report: The compound heterozygotes variants in <i>FLT4</i> causes autosomal recessive hereditary lymphedema in a Chinese familyQinqin Xiang, Jing Chen, Xiao Xiao, et al.
Epilepsy Research|January 24, 2021
Genetic diagnoses in pediatric patients with epilepsy and comorbid intellectual disabilityMei Yang, Bocheng Xu, Jiamin Wang, et al.
Pain Physician|July 25, 2019
The Relevance of the OPRM1 118A>G Genetic Variant for Opioid Requirement in Pain Treatment: A Meta-AnalysisXueying Zhang, Yongxin Liang, Nannan Zhang, et al.
Molecular Genetics & Genomic Medicine|August 1, 2022
A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosisQianying Zhao, Qinqin Xiang, Yu Tan, et al.
Medicine|February 2, 2024
Preimplantation genetic testing for X-linked chronic granulomatous disease induced by a CYBB gene variant: A case reportXinlian Chen, Cuiting Peng, Han Chen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 27, 2023
[Clinical manifestations and genetic analysis of 4 patients with variants of FBN1 gene]Xin Liu, Mei Yang, Hanbing Xie, et al.
Prenatal Diagnosis|August 29, 2019
Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in fetuses with ultrasound anomalies in the urinary systemTing Hu, Zhu Zhang, Jiamin Wang, et al.
Pageof 18