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

Julia Hofhuis

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
Biomolecules|August 6, 2021
Stop Codon Context-Specific Induction of Translational ReadthroughMirco Schilff, Yelena Sargsyan, Julia Hofhuis, et al.
Plos Genetics|June 25, 2025
Defining the high-translational readthrough stop codon contextDaniela Smoljanow, Dennis Lebeda, Julia Hofhuis, et al.
Biology Direct|February 16, 2024
Tissue-specific roles of peroxisomes revealed by expression meta-analysisMatthias Plessner, Leonie Thiele, Julia Hofhuis, et al.
Methods in Molecular Biology (Clifton, N.J.)|April 15, 2017
Dual Reporter Systems for the Analysis of Translational Readthrough in MammalsJulia Hofhuis, Severin Dieterle, Rosemol George, et al.
Journal of Structural Biology|July 12, 2011
The unusual extended C-terminal helix of the peroxisomal α/β-hydrolase Lpx1 is involved in dimer contacts but dispensable for dimerizationSven Thoms, Julia Hofhuis, Christian Thöing, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 2, 2024
Systematic and quantitative analysis of stop codon readthrough in Rett syndrome nonsense mutationsDennis Lebeda, Adrian Fierenz, Lina Werfel, et al.
Open Biology|November 25, 2016
The functional readthrough extension of malate dehydrogenase reveals a modification of the genetic codeJulia Hofhuis, Fabian Schueren, Christopher Nötzel, et al.
Elife|September 24, 2014
Peroxisomal lactate dehydrogenase is generated by translational readthrough in mammalsFabian Schueren, Thomas Lingner, Rosemol George, et al.
Journal of Cell Science|January 21, 2017
Dysferlin mediates membrane tubulation and links T-tubule biogenesis to muscular dystrophyJulia Hofhuis, Kristina Bersch, Ronja Büssenschütt, et al.
Neurobiology of Disease|July 13, 2020
Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severityElinor Lazarov, Merle Hillebrand, Simone Schröder, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Biomolecules|August 6, 2021
Stop Codon Context-Specific Induction of Translational ReadthroughMirco Schilff, Yelena Sargsyan, Julia Hofhuis, et al.
Plos Genetics|June 25, 2025
Defining the high-translational readthrough stop codon contextDaniela Smoljanow, Dennis Lebeda, Julia Hofhuis, et al.
Biology Direct|February 16, 2024
Tissue-specific roles of peroxisomes revealed by expression meta-analysisMatthias Plessner, Leonie Thiele, Julia Hofhuis, et al.
Methods in Molecular Biology (Clifton, N.J.)|April 15, 2017
Dual Reporter Systems for the Analysis of Translational Readthrough in MammalsJulia Hofhuis, Severin Dieterle, Rosemol George, et al.
Journal of Structural Biology|July 12, 2011
The unusual extended C-terminal helix of the peroxisomal α/β-hydrolase Lpx1 is involved in dimer contacts but dispensable for dimerizationSven Thoms, Julia Hofhuis, Christian Thöing, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 2, 2024
Systematic and quantitative analysis of stop codon readthrough in Rett syndrome nonsense mutationsDennis Lebeda, Adrian Fierenz, Lina Werfel, et al.
Open Biology|November 25, 2016
The functional readthrough extension of malate dehydrogenase reveals a modification of the genetic codeJulia Hofhuis, Fabian Schueren, Christopher Nötzel, et al.
Elife|September 24, 2014
Peroxisomal lactate dehydrogenase is generated by translational readthrough in mammalsFabian Schueren, Thomas Lingner, Rosemol George, et al.
Journal of Cell Science|January 21, 2017
Dysferlin mediates membrane tubulation and links T-tubule biogenesis to muscular dystrophyJulia Hofhuis, Kristina Bersch, Ronja Büssenschütt, et al.
Neurobiology of Disease|July 13, 2020
Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severityElinor Lazarov, Merle Hillebrand, Simone Schröder, et al.
Pageof 2