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S Seneca

Showing results (21-30 of 60) with videos related to

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Neurology|December 25, 2003
Patient homozygous for a recessive POLG mutation presents with features of MERRFG Van Goethem, R Mercelis, A Löfgren, et al.
Clinical Genetics|June 11, 2009
Clinical and biochemical spectrum of mitochondrial complex III deficiency caused by mutations in the BCS1L geneM A Ramos-Arroyo, J Hualde, A Ayechu, et al.
Prenatal Diagnosis|February 8, 2000
Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGGK Sermon, S Seneca, A Vanderfaeillie, et al.
Prenatal Diagnosis|February 9, 1999
Preimplantation diagnosis for Huntington's disease (HD): clinical application and analysis of the HD expansion in affected embryosK Sermon, V Goossens, S Seneca, et al.
Journal of Medical Genetics|December 1, 1998
Pitfalls in the diagnosis of mtDNA mutationsS Seneca, W Lissens, I Liebaers, et al.
Molecular Human Reproduction|March 2, 1999
Molecular analysis of the cystic fibrosis gene reveals a high frequency of the intron 8 splice variant 5T in Egyptian males with congenital bilateral absence of the vas deferensW Lissens, K Z Mahmoud, E El-Gindi, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|September 6, 2017
Tigecycline-induced inhibition of mitochondrial DNA translation may cause lethal mitochondrial dysfunction in humansS J Vandecasteele, S Seneca, J Smet, et al.
Archives of Neurology|August 2, 2001
A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndromeS Seneca, H Verhelst, L De Meirleir, et al.
Molecular Human Reproduction|June 26, 2008
CTG repeat instability in a human embryonic stem cell line carrying the myotonic dystrophy type 1 mutationN De Temmerman, S Seneca, A Van Steirteghem, et al.
Mitochondrion|July 28, 2022
Primary ovarian insufficiency in RMND1 mitochondrial diseaseE Boros, F Elilié Mawa Ongoth, C Heinrichs, et al.
Pageof 6

Showing results (21-30 of 60) with videos related to

Sort By:
Pageof 6
Neurology|December 25, 2003
Patient homozygous for a recessive POLG mutation presents with features of MERRFG Van Goethem, R Mercelis, A Löfgren, et al.
Clinical Genetics|June 11, 2009
Clinical and biochemical spectrum of mitochondrial complex III deficiency caused by mutations in the BCS1L geneM A Ramos-Arroyo, J Hualde, A Ayechu, et al.
Prenatal Diagnosis|February 8, 2000
Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGGK Sermon, S Seneca, A Vanderfaeillie, et al.
Prenatal Diagnosis|February 9, 1999
Preimplantation diagnosis for Huntington's disease (HD): clinical application and analysis of the HD expansion in affected embryosK Sermon, V Goossens, S Seneca, et al.
Journal of Medical Genetics|December 1, 1998
Pitfalls in the diagnosis of mtDNA mutationsS Seneca, W Lissens, I Liebaers, et al.
Molecular Human Reproduction|March 2, 1999
Molecular analysis of the cystic fibrosis gene reveals a high frequency of the intron 8 splice variant 5T in Egyptian males with congenital bilateral absence of the vas deferensW Lissens, K Z Mahmoud, E El-Gindi, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|September 6, 2017
Tigecycline-induced inhibition of mitochondrial DNA translation may cause lethal mitochondrial dysfunction in humansS J Vandecasteele, S Seneca, J Smet, et al.
Archives of Neurology|August 2, 2001
A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndromeS Seneca, H Verhelst, L De Meirleir, et al.
Molecular Human Reproduction|June 26, 2008
CTG repeat instability in a human embryonic stem cell line carrying the myotonic dystrophy type 1 mutationN De Temmerman, S Seneca, A Van Steirteghem, et al.
Mitochondrion|July 28, 2022
Primary ovarian insufficiency in RMND1 mitochondrial diseaseE Boros, F Elilié Mawa Ongoth, C Heinrichs, et al.
Pageof 6