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

Howard Gamper

Showing results (41-50 of 48) with videos related to

Pageof 5
Sort By:
You have reached the last page of results.This site can display upto 48 results.
Nucleic Acids Research|December 14, 2016
A genetically encoded fluorescent tRNA is active in live-cell protein synthesisIsao Masuda, Takao Igarashi, Reiko Sakaguchi, et al.
Biorxiv : the Preprint Server for Biology|December 18, 2023
Post-Transcriptional Methylation of Mitochondrial-tRNA Differentially Contributes to Mitochondrial PathologySunita Maharjan, Howard Gamper, Yuka Yamaki, et al.
Biorxiv : the Preprint Server for Biology|April 8, 2024
Probing enzyme-dependent pseudouridylation using direct RNA sequencing to assess neuronal epitranscriptome plasticityOleksandra Fanari, Sepideh Tavakoli, Yuchen Qiu, et al.
Cell Systems|March 21, 2025
Probing enzyme-dependent pseudouridylation using direct RNA sequencing to assess epitranscriptome plasticity in a neuronal cell lineOleksandra Fanari, Sepideh Tavakoli, Yuchen Qiu, et al.
Nature Communications|October 18, 2024
Post-transcriptional methylation of mitochondrial-tRNA differentially contributes to mitochondrial pathologySunita Maharjan, Howard Gamper, Yuka Yamaki, et al.
Nature Communications|January 26, 2025
Genome-wide profiling of tRNA modifications by Induro-tRNAseq reveals coordinated changesYuko Nakano, Howard Gamper, Henri McGuigan, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2026
Molecular mechanism of IF1- and IF2-driven translation initiation in bacteriaGabriel Soares Guerra, Hassan Zafar, Xueliang Ge, et al.
American Journal of Human Genetics|March 31, 2015
Loss-of-function alanyl-tRNA synthetase mutations cause an autosomal-recessive early-onset epileptic encephalopathy with persistent myelination defectCas Simons, Laurie B Griffin, Guy Helman, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Nucleic Acids Research|December 14, 2016
A genetically encoded fluorescent tRNA is active in live-cell protein synthesisIsao Masuda, Takao Igarashi, Reiko Sakaguchi, et al.
Biorxiv : the Preprint Server for Biology|December 18, 2023
Post-Transcriptional Methylation of Mitochondrial-tRNA Differentially Contributes to Mitochondrial PathologySunita Maharjan, Howard Gamper, Yuka Yamaki, et al.
Biorxiv : the Preprint Server for Biology|April 8, 2024
Probing enzyme-dependent pseudouridylation using direct RNA sequencing to assess neuronal epitranscriptome plasticityOleksandra Fanari, Sepideh Tavakoli, Yuchen Qiu, et al.
Cell Systems|March 21, 2025
Probing enzyme-dependent pseudouridylation using direct RNA sequencing to assess epitranscriptome plasticity in a neuronal cell lineOleksandra Fanari, Sepideh Tavakoli, Yuchen Qiu, et al.
Nature Communications|October 18, 2024
Post-transcriptional methylation of mitochondrial-tRNA differentially contributes to mitochondrial pathologySunita Maharjan, Howard Gamper, Yuka Yamaki, et al.
Nature Communications|January 26, 2025
Genome-wide profiling of tRNA modifications by Induro-tRNAseq reveals coordinated changesYuko Nakano, Howard Gamper, Henri McGuigan, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2026
Molecular mechanism of IF1- and IF2-driven translation initiation in bacteriaGabriel Soares Guerra, Hassan Zafar, Xueliang Ge, et al.
American Journal of Human Genetics|March 31, 2015
Loss-of-function alanyl-tRNA synthetase mutations cause an autosomal-recessive early-onset epileptic encephalopathy with persistent myelination defectCas Simons, Laurie B Griffin, Guy Helman, et al.
Pageof 5