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Xiangjun Huang

Showing results (11-20 of 27) with videos related to

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Burns : Journal of the International Society for Burn Injuries|November 10, 2024
Formononetin alleviates thermal injury-induced skin fibroblast apoptosis and promotes cell proliferation and migrationMeiyue Yang, Zhibo Yang, Xiangjun Huang, et al.
Molecular Genetics & Genomic Medicine|July 25, 2019
Identification of a novel EVC variant in a Han-Chinese family with Ellis-van Creveld syndromeXiangjun Huang, Yi Guo, Hongbo Xu, et al.
Neuroscience Letters|May 15, 2016
A homozygous parkin p.G284R mutation in a Chinese family with autosomal recessive juvenile parkinsonismHan Chen, Xiangjun Huang, Lamei Yuan, et al.
Plos One|June 2, 2015
Identification of a Novel Mutation in the COL2A1 Gene in a Chinese Family with Spondyloepiphyseal Dysplasia CongenitaXiangjun Huang, Xiong Deng, Hongbo Xu, et al.
European Journal of Nuclear Medicine and Molecular Imaging|February 11, 2022
Optimal PET-based radiomic signature construction based on the cross-combination method for predicting the survival of patients with diffuse large B-cell lymphomaChong Jiang, Ang Li, Yue Teng, et al.
Plos One|December 12, 2024
Correction: DNAH11 compound heterozygous variants cause heterotaxy and congenital heart diseaseHong Xia, Xiangjun Huang, Sheng Deng, et al.
Plos One|June 16, 2021
DNAH11 compound heterozygous variants cause heterotaxy and congenital heart diseaseHong Xia, Xiangjun Huang, Sheng Deng, et al.
European Radiology|March 17, 2022
Radiomics signature from [<sup>18</sup>F]FDG PET images for prognosis predication of primary gastrointestinal diffuse large B cell lymphomaChong Jiang, Xiangjun Huang, Ang Li, et al.
Genetics and Molecular Biology|March 1, 2019
GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorderHong Xia, Xiangjun Huang, Hongbo Xu, et al.
Frontiers in Genetics|June 13, 2022
Identification of <i>DNAH17</i> Variants in Han-Chinese Patients With Left-Right Asymmetry DisordersXuehui Yu, Lamei Yuan, Sheng Deng, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Burns : Journal of the International Society for Burn Injuries|November 10, 2024
Formononetin alleviates thermal injury-induced skin fibroblast apoptosis and promotes cell proliferation and migrationMeiyue Yang, Zhibo Yang, Xiangjun Huang, et al.
Molecular Genetics & Genomic Medicine|July 25, 2019
Identification of a novel EVC variant in a Han-Chinese family with Ellis-van Creveld syndromeXiangjun Huang, Yi Guo, Hongbo Xu, et al.
Neuroscience Letters|May 15, 2016
A homozygous parkin p.G284R mutation in a Chinese family with autosomal recessive juvenile parkinsonismHan Chen, Xiangjun Huang, Lamei Yuan, et al.
Plos One|June 2, 2015
Identification of a Novel Mutation in the COL2A1 Gene in a Chinese Family with Spondyloepiphyseal Dysplasia CongenitaXiangjun Huang, Xiong Deng, Hongbo Xu, et al.
European Journal of Nuclear Medicine and Molecular Imaging|February 11, 2022
Optimal PET-based radiomic signature construction based on the cross-combination method for predicting the survival of patients with diffuse large B-cell lymphomaChong Jiang, Ang Li, Yue Teng, et al.
Plos One|December 12, 2024
Correction: DNAH11 compound heterozygous variants cause heterotaxy and congenital heart diseaseHong Xia, Xiangjun Huang, Sheng Deng, et al.
Plos One|June 16, 2021
DNAH11 compound heterozygous variants cause heterotaxy and congenital heart diseaseHong Xia, Xiangjun Huang, Sheng Deng, et al.
European Radiology|March 17, 2022
Radiomics signature from [<sup>18</sup>F]FDG PET images for prognosis predication of primary gastrointestinal diffuse large B cell lymphomaChong Jiang, Xiangjun Huang, Ang Li, et al.
Genetics and Molecular Biology|March 1, 2019
GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorderHong Xia, Xiangjun Huang, Hongbo Xu, et al.
Frontiers in Genetics|June 13, 2022
Identification of <i>DNAH17</i> Variants in Han-Chinese Patients With Left-Right Asymmetry DisordersXuehui Yu, Lamei Yuan, Sheng Deng, et al.
Pageof 3