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

Sara Seneca

Showing results (1-10 of 88) with videos related to

Pageof 9
Sort By:
Annales D'Endocrinologie|April 29, 2014
Genetic causes of male infertilityKatrien Stouffs, Sara Seneca, Willy Lissens
European Journal of Human Genetics : EJHG|February 25, 2010
Consensus and controversies in best practices for molecular genetic testing of spinocerebellar ataxiasJorge Sequeiros, Sara Seneca, Joanne Martindale
Case Reports in Ophthalmology|May 27, 2026
Progressive Visual Recovery in a Patient with Leber Hereditary Optic Neuropathy Harboring a Rare Heteroplasmic (MT-ND5):m.13042G>A, p(Ala236Thr) Variant with Low Mutant Load: A Case ReportTom Buelens, Audrey Meunier, Sara Seneca, et al.
Human Mutation|July 4, 2012
Spinocerebellar ataxias: an example of the challenges associated with genetic databases for dynamic mutationsJoanne E Martindale, Sara Seneca, Stefan Wieczorek, et al.
European Heart Journal. Cardiovascular Imaging|September 3, 2016
Severe biventricular hypertrophy in MELAS mitochondrial diseaseLiesbeth Rosseel, Jeroen Breckpot, Jan Debrauwere, et al.
Thrombosis and Haemostasis|June 5, 2025
Diagnostic Performance of Commercial Antithrombin Activity Assays: Do We Get What We Expect?Christelle Orlando, Céline Drèze, Anton Evenepoel, et al.
European Journal of Human Genetics : EJHG|February 28, 2008
Experience and outcome of 3 years of a European EQA scheme for genetic testing of the spinocerebellar ataxiasSara Seneca, Michael A Morris, Simon Patton, et al.
Nature Biotechnology|January 11, 2013
Human embryonic stem cells commonly display large mitochondrial DNA deletionsLindsey Van Haute, Claudia Spits, Mieke Geens, et al.
Human Molecular Genetics|October 31, 2021
Translation of MT-ATP6 pathogenic variants reveals distinct regulatory consequences from the co-translational quality control of mitochondrial protein synthesisKah Ying Ng, Uwe Richter, Christopher B Jackson, et al.
Human Reproduction (Oxford, England)|October 31, 2002
Preimplantation genetic diagnosis for fragile Xa syndrome: difficult but not impossiblePeter Platteau, Karen Sermon, Sara Seneca, et al.
Pageof 9

Showing results (1-10 of 88) with videos related to

Sort By:
Pageof 9
Annales D'Endocrinologie|April 29, 2014
Genetic causes of male infertilityKatrien Stouffs, Sara Seneca, Willy Lissens
European Journal of Human Genetics : EJHG|February 25, 2010
Consensus and controversies in best practices for molecular genetic testing of spinocerebellar ataxiasJorge Sequeiros, Sara Seneca, Joanne Martindale
Case Reports in Ophthalmology|May 27, 2026
Progressive Visual Recovery in a Patient with Leber Hereditary Optic Neuropathy Harboring a Rare Heteroplasmic (MT-ND5):m.13042G>A, p(Ala236Thr) Variant with Low Mutant Load: A Case ReportTom Buelens, Audrey Meunier, Sara Seneca, et al.
Human Mutation|July 4, 2012
Spinocerebellar ataxias: an example of the challenges associated with genetic databases for dynamic mutationsJoanne E Martindale, Sara Seneca, Stefan Wieczorek, et al.
European Heart Journal. Cardiovascular Imaging|September 3, 2016
Severe biventricular hypertrophy in MELAS mitochondrial diseaseLiesbeth Rosseel, Jeroen Breckpot, Jan Debrauwere, et al.
Thrombosis and Haemostasis|June 5, 2025
Diagnostic Performance of Commercial Antithrombin Activity Assays: Do We Get What We Expect?Christelle Orlando, Céline Drèze, Anton Evenepoel, et al.
European Journal of Human Genetics : EJHG|February 28, 2008
Experience and outcome of 3 years of a European EQA scheme for genetic testing of the spinocerebellar ataxiasSara Seneca, Michael A Morris, Simon Patton, et al.
Nature Biotechnology|January 11, 2013
Human embryonic stem cells commonly display large mitochondrial DNA deletionsLindsey Van Haute, Claudia Spits, Mieke Geens, et al.
Human Molecular Genetics|October 31, 2021
Translation of MT-ATP6 pathogenic variants reveals distinct regulatory consequences from the co-translational quality control of mitochondrial protein synthesisKah Ying Ng, Uwe Richter, Christopher B Jackson, et al.
Human Reproduction (Oxford, England)|October 31, 2002
Preimplantation genetic diagnosis for fragile Xa syndrome: difficult but not impossiblePeter Platteau, Karen Sermon, Sara Seneca, et al.
Pageof 9