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Sara Seneca

Showing results (21-30 of 88) with videos related to

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European Journal of Pediatrics|July 11, 2014
Extremely high mutation load of the mitochondrial 8993 T>G mutation in a newborn: implications for prognosis and family planning decisionsClaudine De Praeter, Arnaud Vanlander, Piet Vanhaesebrouck, et al.
European Journal of Human Genetics : EJHG|September 20, 2012
EMQN/CMGS best practice guidelines for the molecular genetic testing of Huntington diseaseMonique Losekoot, Martine J van Belzen, Sara Seneca, et al.
The Biochemical Journal|January 16, 2015
Alteration of structure and function of ATP synthase and cytochrome c oxidase by lack of Fo-a and Cox3 subunits caused by mitochondrial DNA 9205delTA mutationKateřina Hejzlarová, Vilma Kaplanová, Hana Nůsková, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 16, 2004
Analysis of the mitochondrial encoded subunits of complex I in 20 patients with a complex I deficiencyAnn Meulemans, Willy Lissens, Rudy Van Coster, et al.
European Journal of Pediatrics|September 1, 2004
Early onset Huntington disease: a neuronal degeneration syndromeSara Seneca, Domique Fagnart, Kathelijn Keymolen, et al.
Journal of Inherited Metabolic Disease|April 13, 2011
Complex III staining in blue native polyacrylamide gelsJoél Smet, Boel De Paepe, Sara Seneca, et al.
American Journal of Human Genetics|June 9, 2004
Intergenerational instability of the expanded CTG repeat in the DMPK gene: studies in human gametes and preimplantation embryosNele De Temmerman, Karen Sermon, Sara Seneca, et al.
American Journal of Medical Genetics. Part A|February 16, 2006
Mitochondrial dysfunction in Brooks-Wisniewski-Brown syndromeEva Morava, Richard Rodenburg, Frans Hol, et al.
Archives of Neurology|August 16, 2006
A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failureAnn Meulemans, Sara Seneca, Lieven Lagae, et al.
Ophthalmic Genetics|April 16, 2021
Mild Leber hereditary optic neuropathy (LHON) in a Western European family due to the rare Asian m.14502T>C variant in the <i>MT-ND6</i> geneJustine Vandeputte, Mattias Van Heetvelde, Caroline Van Cauwenbergh, et al.
Pageof 9

Showing results (21-30 of 88) with videos related to

Sort By:
Pageof 9
European Journal of Pediatrics|July 11, 2014
Extremely high mutation load of the mitochondrial 8993 T>G mutation in a newborn: implications for prognosis and family planning decisionsClaudine De Praeter, Arnaud Vanlander, Piet Vanhaesebrouck, et al.
European Journal of Human Genetics : EJHG|September 20, 2012
EMQN/CMGS best practice guidelines for the molecular genetic testing of Huntington diseaseMonique Losekoot, Martine J van Belzen, Sara Seneca, et al.
The Biochemical Journal|January 16, 2015
Alteration of structure and function of ATP synthase and cytochrome c oxidase by lack of Fo-a and Cox3 subunits caused by mitochondrial DNA 9205delTA mutationKateřina Hejzlarová, Vilma Kaplanová, Hana Nůsková, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 16, 2004
Analysis of the mitochondrial encoded subunits of complex I in 20 patients with a complex I deficiencyAnn Meulemans, Willy Lissens, Rudy Van Coster, et al.
European Journal of Pediatrics|September 1, 2004
Early onset Huntington disease: a neuronal degeneration syndromeSara Seneca, Domique Fagnart, Kathelijn Keymolen, et al.
Journal of Inherited Metabolic Disease|April 13, 2011
Complex III staining in blue native polyacrylamide gelsJoél Smet, Boel De Paepe, Sara Seneca, et al.
American Journal of Human Genetics|June 9, 2004
Intergenerational instability of the expanded CTG repeat in the DMPK gene: studies in human gametes and preimplantation embryosNele De Temmerman, Karen Sermon, Sara Seneca, et al.
American Journal of Medical Genetics. Part A|February 16, 2006
Mitochondrial dysfunction in Brooks-Wisniewski-Brown syndromeEva Morava, Richard Rodenburg, Frans Hol, et al.
Archives of Neurology|August 16, 2006
A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failureAnn Meulemans, Sara Seneca, Lieven Lagae, et al.
Ophthalmic Genetics|April 16, 2021
Mild Leber hereditary optic neuropathy (LHON) in a Western European family due to the rare Asian m.14502T>C variant in the <i>MT-ND6</i> geneJustine Vandeputte, Mattias Van Heetvelde, Caroline Van Cauwenbergh, et al.
Pageof 9