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Xicui Long

Showing results (1-10 of 9) with videos related to

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SAGE Open Medical Case Reports|December 2, 2024
A case report of CHARGE syndrome caused by a de novo <i>CHD7</i> gene mutationYuan Zhang, Yu Lu, Xicui Long, et al.
Cellular Signalling|June 7, 2026
CDK1 alleviates intrauterine adhesion progression by enhancing glycolysis and mitophagy in endometrial stem cellsXicui Long, Lijuan Yang, Jianghong Zhou, et al.
Acta Obstetricia Et Gynecologica Scandinavica|November 7, 2025
Global burden and between-country inequalities in Turner syndrome from 1990 to 2021Xicui Long, Yong Hu, Mingjie Wu, et al.
Case Reports in Nephrology and Dialysis|October 9, 2025
A Complement Factor B Mutation in a Chinese Family with Atypical Hemolytic Uremic Syndrome: A Case Report and Systematic ReviewWan Peng, Xicui Long, Haoran Lei, et al.
Experimental Cell Research|June 13, 2025
Estradiol inhibits endometrial injury by promoting the stability of the KLF15 protein and the recovery of mitochondrial functionJianghong Zhou, Zhenghua Xiong, Xicui Long, et al.
Frontiers in Neurology|February 23, 2026
A novel non-sense variant in <i>GSDME</i> causing exon skipping associated with DFNA5 in a large Chinese familyBingqian Yang, Mingwan Zhu, Xicui Long, et al.
BMC Cancer|October 7, 2021
Effectiveness comparisons of various therapies for FIGO stage IB2/IIA2 cervical cancer: a Bayesian network meta-analysisJing Cheng, Beibei Liu, Biao Wang, et al.
Human Genomics|May 23, 2025
CLPP Gene Variants Causing Perrault Syndrome Type 3 in Han Chinese Families: A Genotype-Phenotype StudyXicui Long, Bingqian Yang, Wei Wang, et al.
BMC Medical Genomics|August 9, 2024
Genotype-phenotype spectrum and correlation of PHARC Syndrome due to pathogenic ABHD12 variantsXicui Long, Wenyu Xiong, Xuegang Wang, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
SAGE Open Medical Case Reports|December 2, 2024
A case report of CHARGE syndrome caused by a de novo <i>CHD7</i> gene mutationYuan Zhang, Yu Lu, Xicui Long, et al.
Cellular Signalling|June 7, 2026
CDK1 alleviates intrauterine adhesion progression by enhancing glycolysis and mitophagy in endometrial stem cellsXicui Long, Lijuan Yang, Jianghong Zhou, et al.
Acta Obstetricia Et Gynecologica Scandinavica|November 7, 2025
Global burden and between-country inequalities in Turner syndrome from 1990 to 2021Xicui Long, Yong Hu, Mingjie Wu, et al.
Case Reports in Nephrology and Dialysis|October 9, 2025
A Complement Factor B Mutation in a Chinese Family with Atypical Hemolytic Uremic Syndrome: A Case Report and Systematic ReviewWan Peng, Xicui Long, Haoran Lei, et al.
Experimental Cell Research|June 13, 2025
Estradiol inhibits endometrial injury by promoting the stability of the KLF15 protein and the recovery of mitochondrial functionJianghong Zhou, Zhenghua Xiong, Xicui Long, et al.
Frontiers in Neurology|February 23, 2026
A novel non-sense variant in <i>GSDME</i> causing exon skipping associated with DFNA5 in a large Chinese familyBingqian Yang, Mingwan Zhu, Xicui Long, et al.
BMC Cancer|October 7, 2021
Effectiveness comparisons of various therapies for FIGO stage IB2/IIA2 cervical cancer: a Bayesian network meta-analysisJing Cheng, Beibei Liu, Biao Wang, et al.
Human Genomics|May 23, 2025
CLPP Gene Variants Causing Perrault Syndrome Type 3 in Han Chinese Families: A Genotype-Phenotype StudyXicui Long, Bingqian Yang, Wei Wang, et al.
BMC Medical Genomics|August 9, 2024
Genotype-phenotype spectrum and correlation of PHARC Syndrome due to pathogenic ABHD12 variantsXicui Long, Wenyu Xiong, Xuegang Wang, et al.
Pageof 1