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

Hubert J M Smeets

Showing results (11-20 of 80) with videos related to

Pageof 8
Sort By:
Mitochondrion|January 25, 2019
A zebrafish model to study small-fiber neuropathy reveals a potential role for GDAP1Ivo Eijkenboom, Jo M Vanoevelen, Janneke G J Hoeijmakers, et al.
Biochemical and Biophysical Research Communications|October 5, 2010
Functional annotation of heart enriched mitochondrial genes GBAS and CHCHD10 through guilt by associationRuben S R M Martherus, Willem Sluiter, Erika D J Timmer, et al.
Human Mutation|April 17, 2009
Identifying sequence variants in the human mitochondrial genome using high-resolution melt (HRM) profilingSteven F Dobrowolski, Alexandra T M Hendrickx, Bianca J C van den Bosch, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 12, 2017
A comprehensive strategy for exome-based preconception carrier screeningSuzanne C E H Sallevelt, Bart de Koning, Radek Szklarczyk, et al.
International Journal of Molecular Sciences|February 13, 2026
Fusion Between Control Mesoangioblasts and mtDNA-Mutant Myotubes Preserves Myotube Morphology and Mitochondrial Network OrganizationSomaieh Ahmadian, Patrick J Lindsey, Monique Ummelen, et al.
Brain Communications|February 21, 2022
Neurodegenerative and functional signatures of the cerebellar cortex in m.3243A > G patientsRoy A M Haast, Irenaeus F M De Coo, Dimo Ivanov, et al.
Frontiers in Cell and Developmental Biology|June 30, 2020
<i>Tfam</i> Knockdown Results in Reduction of mtDNA Copy Number, OXPHOS Deficiency and Abnormalities in Zebrafish EmbryosAuke B C Otten, Rick Kamps, Patrick Lindsey, et al.
Annals of the New York Academy of Sciences|August 28, 2015
Preventing the transmission of mitochondrial DNA disorders using prenatal or preimplantation genetic diagnosisHubert J M Smeets, Suzanne C E H Sallevelt, Jos C F M Dreesen, et al.
Alcoholism, Clinical and Experimental Research|January 9, 2007
A functional polymorphism of the mu-opioid receptor gene (OPRM1) influences cue-induced craving for alcohol in male heavy drinkersEsther van den Wildenberg, Reinout W Wiers, Joelle Dessers, et al.
European Journal of Human Genetics : EJHG|July 23, 2015
Pathogenic CWF19L1 variants as a novel cause of autosomal recessive cerebellar ataxia and atrophyMinh Nguyen, Iris Boesten, Debby M E I Hellebrekers, et al.
Pageof 8

Showing results (11-20 of 80) with videos related to

Sort By:
Pageof 8
Mitochondrion|January 25, 2019
A zebrafish model to study small-fiber neuropathy reveals a potential role for GDAP1Ivo Eijkenboom, Jo M Vanoevelen, Janneke G J Hoeijmakers, et al.
Biochemical and Biophysical Research Communications|October 5, 2010
Functional annotation of heart enriched mitochondrial genes GBAS and CHCHD10 through guilt by associationRuben S R M Martherus, Willem Sluiter, Erika D J Timmer, et al.
Human Mutation|April 17, 2009
Identifying sequence variants in the human mitochondrial genome using high-resolution melt (HRM) profilingSteven F Dobrowolski, Alexandra T M Hendrickx, Bianca J C van den Bosch, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 12, 2017
A comprehensive strategy for exome-based preconception carrier screeningSuzanne C E H Sallevelt, Bart de Koning, Radek Szklarczyk, et al.
International Journal of Molecular Sciences|February 13, 2026
Fusion Between Control Mesoangioblasts and mtDNA-Mutant Myotubes Preserves Myotube Morphology and Mitochondrial Network OrganizationSomaieh Ahmadian, Patrick J Lindsey, Monique Ummelen, et al.
Brain Communications|February 21, 2022
Neurodegenerative and functional signatures of the cerebellar cortex in m.3243A > G patientsRoy A M Haast, Irenaeus F M De Coo, Dimo Ivanov, et al.
Frontiers in Cell and Developmental Biology|June 30, 2020
<i>Tfam</i> Knockdown Results in Reduction of mtDNA Copy Number, OXPHOS Deficiency and Abnormalities in Zebrafish EmbryosAuke B C Otten, Rick Kamps, Patrick Lindsey, et al.
Annals of the New York Academy of Sciences|August 28, 2015
Preventing the transmission of mitochondrial DNA disorders using prenatal or preimplantation genetic diagnosisHubert J M Smeets, Suzanne C E H Sallevelt, Jos C F M Dreesen, et al.
Alcoholism, Clinical and Experimental Research|January 9, 2007
A functional polymorphism of the mu-opioid receptor gene (OPRM1) influences cue-induced craving for alcohol in male heavy drinkersEsther van den Wildenberg, Reinout W Wiers, Joelle Dessers, et al.
European Journal of Human Genetics : EJHG|July 23, 2015
Pathogenic CWF19L1 variants as a novel cause of autosomal recessive cerebellar ataxia and atrophyMinh Nguyen, Iris Boesten, Debby M E I Hellebrekers, et al.
Pageof 8