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Jinfu Lin

Showing results (11-20 of 17) with videos related to

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Frontiers in Neurology|December 1, 2018
HLA Polymorphism Affects Risk of <i>de novo</i> Mutation of <i>dystrophin</i> Gene and Clinical Severity of Duchenne Muscular Dystrophy in a Southern Chinese PopulationHuan Li, Lulu Xiao, Liang Wang, et al.
Disease Markers|July 19, 2018
Ratio of Creatine Kinase to Alanine Aminotransferase as a Biomarker of Acute Liver Injury in DystrophinopathyLiang Wang, Menglong Chen, Min Xu, et al.
Orphanet Journal of Rare Diseases|August 16, 2018
The clinical spectrum and genetic variability of limb-girdle muscular dystrophy in a cohort of Chinese patientsLiang Wang, Victor Wei Zhang, Shaoyuan Li, et al.
Frontiers in Neurology|August 28, 2020
Genetic Modifiers of Duchenne Muscular Dystrophy in Chinese PatientsMenglong Chen, Liang Wang, Yaqin Li, et al.
BMC Neurology|September 26, 2021
Serum creatinine as a biomarker for dystrophinopathy: a cross-sectional and longitudinal studyLiang Wang, Min Xu, Dawei Liu, et al.
Small (Weinheim an Der Bergstrasse, Germany)|August 23, 2025
In Situ Selenization Engineered Dual Schottky Heterojunctions: A Novel Architecture for High-Speed Broadband Photonic Communication Detector ArraysShaoqiu Ke, Mengyu Ge, Shengyan Zu, et al.
Genome Medicine|April 13, 2021
In vivo genome editing in mouse restores dystrophin expression in Duchenne muscular dystrophy patient muscle fibersMenglong Chen, Hui Shi, Shixue Gou, et al.
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Showing results (11-20 of 17) with videos related to

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Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Frontiers in Neurology|December 1, 2018
HLA Polymorphism Affects Risk of <i>de novo</i> Mutation of <i>dystrophin</i> Gene and Clinical Severity of Duchenne Muscular Dystrophy in a Southern Chinese PopulationHuan Li, Lulu Xiao, Liang Wang, et al.
Disease Markers|July 19, 2018
Ratio of Creatine Kinase to Alanine Aminotransferase as a Biomarker of Acute Liver Injury in DystrophinopathyLiang Wang, Menglong Chen, Min Xu, et al.
Orphanet Journal of Rare Diseases|August 16, 2018
The clinical spectrum and genetic variability of limb-girdle muscular dystrophy in a cohort of Chinese patientsLiang Wang, Victor Wei Zhang, Shaoyuan Li, et al.
Frontiers in Neurology|August 28, 2020
Genetic Modifiers of Duchenne Muscular Dystrophy in Chinese PatientsMenglong Chen, Liang Wang, Yaqin Li, et al.
BMC Neurology|September 26, 2021
Serum creatinine as a biomarker for dystrophinopathy: a cross-sectional and longitudinal studyLiang Wang, Min Xu, Dawei Liu, et al.
Small (Weinheim an Der Bergstrasse, Germany)|August 23, 2025
In Situ Selenization Engineered Dual Schottky Heterojunctions: A Novel Architecture for High-Speed Broadband Photonic Communication Detector ArraysShaoqiu Ke, Mengyu Ge, Shengyan Zu, et al.
Genome Medicine|April 13, 2021
In vivo genome editing in mouse restores dystrophin expression in Duchenne muscular dystrophy patient muscle fibersMenglong Chen, Hui Shi, Shixue Gou, et al.
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