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Hongen Xu

Showing results (21-30 of 63) with videos related to

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Frontiers in Genetics|December 6, 2021
Genetic and Phenotypic Variability in Chinese Patients With Branchio-Oto-Renal or Branchio-Oto SyndromeHaifeng Feng, Hongen Xu, Bei Chen, et al.
BMC Medical Genomics|April 16, 2024
Novel likely pathogenic variant in the EYA1 gene causing Branchio oto renal syndrome and the exploration of pathogenic mechanismsHui Zhang, Jian Gao, Hanjun Wang, et al.
Molecular Genetics & Genomic Medicine|April 22, 2025
SLC26A4 C.317C > A Variant: Functional Analysis and Patient-Derived Induced Pluripotent Stem Line DevelopmentYijing Li, Tao Sun, Sang Hu, et al.
Frontiers in Neurology|April 2, 2019
Multiple Distinctive Demyelinating Lesions Caused by Eosinophilic Granulomatosis With Polyangiitis: Case Report and Literature ReviewDingkang Xu, Hongen Xu, Fang Wang, et al.
BMC Medical Genomics|September 28, 2024
Validating the splicing effect of rare variants in the SLC26A4 gene using minigene assayYixin Zhao, Yan Long, Tao Shi, et al.
Cell Reports|May 28, 2026
AKT1 glutarylation regulated by GCDH and SIRT5 suppresses oncogenic signalingLongchang Bai, Ruocen Liao, Yu Zhang, et al.
Medicine|October 7, 2017
Intensity-modulated radiation therapy for patients with 1 to 3 brain metastases in recursive partitioning analysis class 3Jia Yang, Wenming Zhan, Haibo Zhang, et al.
World Journal of Surgical Oncology|December 2, 2019
Association of pre-surgery to pre-radiotherapy lymphocyte counts ratio with disease-free survival in rectal cancer patients receiving neoadjuvant concurrent chemoradiotherapyHongen Xu, Guangxian You, Minjun Zhang, et al.
Human Molecular Genetics|October 8, 2025
Atypical phenotypic characteristics, mutation analysis and treatment in a family of riboflavin transporter deficiency caused by SLC52A3 variantsPeipei Li, Ting Zhang, Hongen Xu, et al.
Biology|April 28, 2023
Molecular Mechanisms and Clinical Phenotypes of <i>GJB2</i> Missense VariantsLu Mao, Yueqiang Wang, Lei An, et al.
Pageof 7

Showing results (21-30 of 63) with videos related to

Sort By:
Pageof 7
Frontiers in Genetics|December 6, 2021
Genetic and Phenotypic Variability in Chinese Patients With Branchio-Oto-Renal or Branchio-Oto SyndromeHaifeng Feng, Hongen Xu, Bei Chen, et al.
BMC Medical Genomics|April 16, 2024
Novel likely pathogenic variant in the EYA1 gene causing Branchio oto renal syndrome and the exploration of pathogenic mechanismsHui Zhang, Jian Gao, Hanjun Wang, et al.
Molecular Genetics & Genomic Medicine|April 22, 2025
SLC26A4 C.317C > A Variant: Functional Analysis and Patient-Derived Induced Pluripotent Stem Line DevelopmentYijing Li, Tao Sun, Sang Hu, et al.
Frontiers in Neurology|April 2, 2019
Multiple Distinctive Demyelinating Lesions Caused by Eosinophilic Granulomatosis With Polyangiitis: Case Report and Literature ReviewDingkang Xu, Hongen Xu, Fang Wang, et al.
BMC Medical Genomics|September 28, 2024
Validating the splicing effect of rare variants in the SLC26A4 gene using minigene assayYixin Zhao, Yan Long, Tao Shi, et al.
Cell Reports|May 28, 2026
AKT1 glutarylation regulated by GCDH and SIRT5 suppresses oncogenic signalingLongchang Bai, Ruocen Liao, Yu Zhang, et al.
Medicine|October 7, 2017
Intensity-modulated radiation therapy for patients with 1 to 3 brain metastases in recursive partitioning analysis class 3Jia Yang, Wenming Zhan, Haibo Zhang, et al.
World Journal of Surgical Oncology|December 2, 2019
Association of pre-surgery to pre-radiotherapy lymphocyte counts ratio with disease-free survival in rectal cancer patients receiving neoadjuvant concurrent chemoradiotherapyHongen Xu, Guangxian You, Minjun Zhang, et al.
Human Molecular Genetics|October 8, 2025
Atypical phenotypic characteristics, mutation analysis and treatment in a family of riboflavin transporter deficiency caused by SLC52A3 variantsPeipei Li, Ting Zhang, Hongen Xu, et al.
Biology|April 28, 2023
Molecular Mechanisms and Clinical Phenotypes of <i>GJB2</i> Missense VariantsLu Mao, Yueqiang Wang, Lei An, et al.
Pageof 7