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Shiyu Luo

Showing results (101-110 of 107) with videos related to

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European Journal of Human Genetics : EJHG|May 15, 2025
Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndromeShiyu Luo, Valérie Gailus-Durner, Bobbi McGivern, et al.
Cell Stem Cell|May 7, 2016
Age-Related Accumulation of Somatic Mitochondrial DNA Mutations in Adult-Derived Human iPSCsEunju Kang, Xinjian Wang, Rebecca Tippner-Hedges, et al.
Plos Genetics|July 7, 2021
A homozygous stop-gain variant in ARHGAP42 is associated with childhood interstitial lung disease, systemic hypertension, and immunological findingsQifei Li, Michal Dibus, Alicia Casey, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|October 24, 2023
Stable Decoding from a Speech BCI Enables Control for an Individual with ALS without Recalibration for 3 MonthsShiyu Luo, Miguel Angrick, Christopher Coogan, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|May 19, 2021
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short statureXin Fan, Sen Zhao, Chenxi Yu, et al.
Nature|March 1, 2019
Author Correction: Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutationsEunju Kang, Jun Wu, Nuria Marti Gutierrez, et al.
Nature|December 6, 2016
Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutationsEunju Kang, Jun Wu, Nuria Marti Gutierrez, et al.
Pageof 11

Showing results (101-110 of 107) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 107 results.
European Journal of Human Genetics : EJHG|May 15, 2025
Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndromeShiyu Luo, Valérie Gailus-Durner, Bobbi McGivern, et al.
Cell Stem Cell|May 7, 2016
Age-Related Accumulation of Somatic Mitochondrial DNA Mutations in Adult-Derived Human iPSCsEunju Kang, Xinjian Wang, Rebecca Tippner-Hedges, et al.
Plos Genetics|July 7, 2021
A homozygous stop-gain variant in ARHGAP42 is associated with childhood interstitial lung disease, systemic hypertension, and immunological findingsQifei Li, Michal Dibus, Alicia Casey, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|October 24, 2023
Stable Decoding from a Speech BCI Enables Control for an Individual with ALS without Recalibration for 3 MonthsShiyu Luo, Miguel Angrick, Christopher Coogan, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|May 19, 2021
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short statureXin Fan, Sen Zhao, Chenxi Yu, et al.
Nature|March 1, 2019
Author Correction: Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutationsEunju Kang, Jun Wu, Nuria Marti Gutierrez, et al.
Nature|December 6, 2016
Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutationsEunju Kang, Jun Wu, Nuria Marti Gutierrez, et al.
Pageof 11