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Hongen Xu

Showing results (1-10 of 63) with videos related to

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Human Molecular Genetics|January 7, 2016
Genomic determinants of somatic copy number alterations across human cancersYanping Zhang, Hongen Xu, Dmitrij Frishman
Journal of Applied Genetics|August 31, 2019
Differentially methylated region in bovine MIMT1 detected by small-scale whole-genome methylation sequencingKarolina Rutkowska, Hongen Xu, Krzysztof Flisikowski
Database : the Journal of Biological Databases and Curation|April 25, 2018
FishTEDB: a collective database of transposable elements identified in the complete genomes of fishFeng Shao, Jianrong Wang, Hongen Xu, et al.
Frontiers in Pediatrics|December 2, 2022
Case report: Clinical and genetic analysis of a family with nonsyndromic auditory neuropathyLan Jiang, Hongen Xu, Danhua Liu, et al.
BMC Medical Genomics|October 31, 2023
Phenotypic variability in two female siblings with oocyte maturation arrest due to a TUBB8 variantQian Dou, HongEn Xu, LiYing Ma, et al.
Molecular Medicine Reports|August 22, 2019
Identification of key genes in osteosarcoma by meta‑analysis of gene expression microarrayJunkui Sun, Hongen Xu, Muge Qi, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 29, 2023
[Analysis of phenotype and pathogenic variants in a Chinese pedigree affected with Multiple synostoses syndrome type 1]Wenyuan Zhang, Lu Mao, Jinhui Zhang, et al.
American Journal of Medical Genetics. Part A|January 4, 2025
A Missense Variant in the IKZF2 Gene Identified in a Genetically Undiagnosed Family With Hearing LossTeng Zhang, Qiang Li, Hanjun Wang, et al.
Stem Cell Research|December 5, 2021
Establishment of an induced pluripotent stem cell line (ZZUPMCi001-A) derived from peripheral blood mononuclear cells in a patient with type 1 Waardenburg syndromeXiaoxuan Wang, Sen Zhang, Sang Hu, et al.
Heliyon|October 24, 2024
The role of m5C RNA modification in cancer development and therapyLi Yu, Hongen Xu, Hanchu Xiong, et al.
Pageof 7

Showing results (1-10 of 63) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|January 7, 2016
Genomic determinants of somatic copy number alterations across human cancersYanping Zhang, Hongen Xu, Dmitrij Frishman
Journal of Applied Genetics|August 31, 2019
Differentially methylated region in bovine MIMT1 detected by small-scale whole-genome methylation sequencingKarolina Rutkowska, Hongen Xu, Krzysztof Flisikowski
Database : the Journal of Biological Databases and Curation|April 25, 2018
FishTEDB: a collective database of transposable elements identified in the complete genomes of fishFeng Shao, Jianrong Wang, Hongen Xu, et al.
Frontiers in Pediatrics|December 2, 2022
Case report: Clinical and genetic analysis of a family with nonsyndromic auditory neuropathyLan Jiang, Hongen Xu, Danhua Liu, et al.
BMC Medical Genomics|October 31, 2023
Phenotypic variability in two female siblings with oocyte maturation arrest due to a TUBB8 variantQian Dou, HongEn Xu, LiYing Ma, et al.
Molecular Medicine Reports|August 22, 2019
Identification of key genes in osteosarcoma by meta‑analysis of gene expression microarrayJunkui Sun, Hongen Xu, Muge Qi, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 29, 2023
[Analysis of phenotype and pathogenic variants in a Chinese pedigree affected with Multiple synostoses syndrome type 1]Wenyuan Zhang, Lu Mao, Jinhui Zhang, et al.
American Journal of Medical Genetics. Part A|January 4, 2025
A Missense Variant in the IKZF2 Gene Identified in a Genetically Undiagnosed Family With Hearing LossTeng Zhang, Qiang Li, Hanjun Wang, et al.
Stem Cell Research|December 5, 2021
Establishment of an induced pluripotent stem cell line (ZZUPMCi001-A) derived from peripheral blood mononuclear cells in a patient with type 1 Waardenburg syndromeXiaoxuan Wang, Sen Zhang, Sang Hu, et al.
Heliyon|October 24, 2024
The role of m5C RNA modification in cancer development and therapyLi Yu, Hongen Xu, Hanchu Xiong, et al.
Pageof 7