Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Che-Sheng Ho

Showing results (61-70 of 71) with videos related to

Pageof 8
Sort By:
Cells|January 20, 2019
Oxidative Insults and Mitochondrial DNA Mutation Promote Enhanced Autophagy and Mitophagy Compromising Cell Viability in Pluripotent Cell Model of Mitochondrial DiseaseDar-Shong Lin, Yu-Wen Huang, Che-Sheng Ho, et al.
Medicine|October 30, 2015
Outcome of Preterm Infants With Postnatal Cytomegalovirus Infection via Breast Milk: A Two-Year Prospective Follow-Up StudyWai-Tim Jim, Nan-Chang Chiu, Che-Sheng Ho, et al.
Oncotarget|November 2, 2017
Inflexibility of AMPK-mediated metabolic reprogramming in mitochondrial diseaseDar-Shong Lin, Shu-Huei Kao, Che-Sheng Ho, et al.
Gene|June 28, 2015
Mitigation of cerebellar neuropathy in globoid cell leukodystrophy mice by AAV-mediated gene therapyDar-Shong Lin, Chung-Der Hsiao, Allan Yueh-Luen Lee, et al.
American Journal of Medical Genetics. Part A|March 11, 2006
Clinical characteristics and survival of trisomy 18 in a medical center in Taipei, 1988-2004Hsiang-Yu Lin, Shuan-Pei Lin, Yen-Jiun Chen, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 30, 2007
Clinical characteristics and survival of trisomy 13 in a medical center in Taiwan, 1985-2004Hsiang-Yu Lin, Shuan-Pei Lin, Yen-Jiun Chen, et al.
American Journal of Medical Genetics. Part A|November 5, 2011
Compound heterozygous mutations in PYCR1 further expand the phenotypic spectrum of De Barsy syndromeDar-Shong Lin, Jui-Hsing Chang, Hsuan-Liang Liu, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 30, 2007
Prader-Willi syndrome in TaiwanHsiang-Yu Lin, Shuan-Pei Lin, Jui-Lung Yen, et al.
Diagnostics (Basel, Switzerland)|April 13, 2023
Application of Drug Testing Platforms in Circulating Tumor Cells and Validation of a Patient-Derived Xenograft Mouse Model in Patient with Primary Intracranial Ependymomas with Extraneural MetastasesMuh-Lii Liang, Ting-Chi Yeh, Man-Hsu Huang, et al.
Scientific Reports|October 13, 2021
Clinical spectrum and the comorbidities of Dravet syndrome in Taiwan and the possible molecular mechanismsChia-Hsuan Huang, Pi-Lien Hung, Pi-Chuan Fan, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
Cells|January 20, 2019
Oxidative Insults and Mitochondrial DNA Mutation Promote Enhanced Autophagy and Mitophagy Compromising Cell Viability in Pluripotent Cell Model of Mitochondrial DiseaseDar-Shong Lin, Yu-Wen Huang, Che-Sheng Ho, et al.
Medicine|October 30, 2015
Outcome of Preterm Infants With Postnatal Cytomegalovirus Infection via Breast Milk: A Two-Year Prospective Follow-Up StudyWai-Tim Jim, Nan-Chang Chiu, Che-Sheng Ho, et al.
Oncotarget|November 2, 2017
Inflexibility of AMPK-mediated metabolic reprogramming in mitochondrial diseaseDar-Shong Lin, Shu-Huei Kao, Che-Sheng Ho, et al.
Gene|June 28, 2015
Mitigation of cerebellar neuropathy in globoid cell leukodystrophy mice by AAV-mediated gene therapyDar-Shong Lin, Chung-Der Hsiao, Allan Yueh-Luen Lee, et al.
American Journal of Medical Genetics. Part A|March 11, 2006
Clinical characteristics and survival of trisomy 18 in a medical center in Taipei, 1988-2004Hsiang-Yu Lin, Shuan-Pei Lin, Yen-Jiun Chen, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 30, 2007
Clinical characteristics and survival of trisomy 13 in a medical center in Taiwan, 1985-2004Hsiang-Yu Lin, Shuan-Pei Lin, Yen-Jiun Chen, et al.
American Journal of Medical Genetics. Part A|November 5, 2011
Compound heterozygous mutations in PYCR1 further expand the phenotypic spectrum of De Barsy syndromeDar-Shong Lin, Jui-Hsing Chang, Hsuan-Liang Liu, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 30, 2007
Prader-Willi syndrome in TaiwanHsiang-Yu Lin, Shuan-Pei Lin, Jui-Lung Yen, et al.
Diagnostics (Basel, Switzerland)|April 13, 2023
Application of Drug Testing Platforms in Circulating Tumor Cells and Validation of a Patient-Derived Xenograft Mouse Model in Patient with Primary Intracranial Ependymomas with Extraneural MetastasesMuh-Lii Liang, Ting-Chi Yeh, Man-Hsu Huang, et al.
Scientific Reports|October 13, 2021
Clinical spectrum and the comorbidities of Dravet syndrome in Taiwan and the possible molecular mechanismsChia-Hsuan Huang, Pi-Lien Hung, Pi-Chuan Fan, et al.
Pageof 8