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

Helen A L Tuppen

Showing results (1-10 of 19) with videos related to

Pageof 2
Sort By:
Methods in Molecular Biology (Clifton, N.J.)|February 22, 2023
Single Cell Analysis of Mitochondrial DNA DeletionsHelen A L Tuppen, Amy K Reeve, Amy E Vincent
Biochimica Et Biophysica Acta|September 19, 2009
Mitochondrial DNA mutations and human diseaseHelen A L Tuppen, Emma L Blakely, Douglass M Turnbull, et al.
Scientific Reports|May 20, 2015
Triplex real-time PCR--an improved method to detect a wide spectrum of mitochondrial DNA deletions in single cellsKarolina A Rygiel, John P Grady, Robert W Taylor, et al.
Plos One|December 5, 2014
Accurate measurement of mitochondrial DNA deletion level and copy number differences in human skeletal muscleJohn P Grady, Julie L Murphy, Emma L Blakely, et al.
Neuromuscular Disorders : NMD|December 16, 2014
A novel mitochondrial DNA m.7507A>G mutation is only pathogenic at high levels of heteroplasmyBeverly Jo McCann, Helen A L Tuppen, Benno Küsters, et al.
Journal of Neuromuscular Diseases|August 28, 2023
Resistance Exercise Training Rescues Mitochondrial Dysfunction in Skeletal Muscle of Patients with Myotonic Dystrophy Type 1Valeria Di Leo, Conor Lawless, Marie-Pier Roussel, et al.
European Journal of Human Genetics : EJHG|April 16, 2015
Pathogenic mitochondrial mt-tRNA(Ala) variants are uniquely associated with isolated myopathyDiana Lehmann, Kathrin Schubert, Pushpa R Joshi, et al.
Molecular Genetics and Metabolism|May 18, 2010
Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutationHelen A L Tuppen, Janev Fehmi, Birgit Czermin, et al.
Scientific Reports|January 25, 2014
Therapeutic potential of somatic cell nuclear transfer for degenerative disease caused by mitochondrial DNA mutationsGareth D Greggains, Lisa M Lister, Helen A L Tuppen, et al.
Geroscience|March 18, 2025
Effect of acipimox on skeletal muscle biochemistry, structure and function in older people with probable sarcopenia: an experimental medicine studyClaire McDonald, Craig Alderson, Matthew G Birkbeck, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Methods in Molecular Biology (Clifton, N.J.)|February 22, 2023
Single Cell Analysis of Mitochondrial DNA DeletionsHelen A L Tuppen, Amy K Reeve, Amy E Vincent
Biochimica Et Biophysica Acta|September 19, 2009
Mitochondrial DNA mutations and human diseaseHelen A L Tuppen, Emma L Blakely, Douglass M Turnbull, et al.
Scientific Reports|May 20, 2015
Triplex real-time PCR--an improved method to detect a wide spectrum of mitochondrial DNA deletions in single cellsKarolina A Rygiel, John P Grady, Robert W Taylor, et al.
Plos One|December 5, 2014
Accurate measurement of mitochondrial DNA deletion level and copy number differences in human skeletal muscleJohn P Grady, Julie L Murphy, Emma L Blakely, et al.
Neuromuscular Disorders : NMD|December 16, 2014
A novel mitochondrial DNA m.7507A>G mutation is only pathogenic at high levels of heteroplasmyBeverly Jo McCann, Helen A L Tuppen, Benno Küsters, et al.
Journal of Neuromuscular Diseases|August 28, 2023
Resistance Exercise Training Rescues Mitochondrial Dysfunction in Skeletal Muscle of Patients with Myotonic Dystrophy Type 1Valeria Di Leo, Conor Lawless, Marie-Pier Roussel, et al.
European Journal of Human Genetics : EJHG|April 16, 2015
Pathogenic mitochondrial mt-tRNA(Ala) variants are uniquely associated with isolated myopathyDiana Lehmann, Kathrin Schubert, Pushpa R Joshi, et al.
Molecular Genetics and Metabolism|May 18, 2010
Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutationHelen A L Tuppen, Janev Fehmi, Birgit Czermin, et al.
Scientific Reports|January 25, 2014
Therapeutic potential of somatic cell nuclear transfer for degenerative disease caused by mitochondrial DNA mutationsGareth D Greggains, Lisa M Lister, Helen A L Tuppen, et al.
Geroscience|March 18, 2025
Effect of acipimox on skeletal muscle biochemistry, structure and function in older people with probable sarcopenia: an experimental medicine studyClaire McDonald, Craig Alderson, Matthew G Birkbeck, et al.
Pageof 2