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D Sternberg

Showing results (61-70 of 94) with videos related to

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American Journal of Human Genetics|July 27, 1999
Evaluation of parental mitochondrial inheritance in neonates born after intracytoplasmic sperm injectionC Danan, D Sternberg, A Van Steirteghem, et al.
International Journal of Cell Cloning|September 1, 1992
Dynamic changes in cytokine secretion by stromal cells during prolonged maintenance under protein-free conditionsA Kadouri, R Kompier, J Honigwachs-Sha'anani, et al.
Ecology and Evolution|October 17, 2025
Species Richness of Freshwater Fish Trophic Guilds Increases With Tropical River Discharge and Decreases With VariabilityC N Perna, D Sternberg, M J Kennard, et al.
Brain : a Journal of Neurology|May 4, 2001
Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disordersD Sternberg, E Chatzoglou, P Laforêt, et al.
Trends in Parasitology|July 3, 2017
Priorities for Broadening the Malaria Vector Control Tool KitPriscille Barreaux, Antoine M G Barreaux, Eleanore D Sternberg, et al.
Malaria Journal|October 24, 2018
Screening and field performance of powder-formulated insecticides on eave tube inserts against pyrethroid resistant Anopheles gambiae s.l.: an investigation into 'actives' prior to a randomized controlled trial in Côte d'IvoireWelbeck A Oumbouke, Innocent Z Tia, Antoine M G Barreaux, et al.
Evolution; International Journal of Organic Evolution|October 31, 2012
Food plant derived disease tolerance and resistance in a natural butterfly-plant-parasite interactionsEleanore D Sternberg, Thierry Lefèvre, James Li, et al.
Brain : a Journal of Neurology|May 17, 2001
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4AD Sternberg, T Maisonobe, K Jurkat-Rott, et al.
American Journal of Physiology. Cell Physiology|July 3, 2009
Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubesS Sacconi, D Simkin, N Arrighi, et al.
Neuromuscular Disorders : NMD|August 5, 2014
Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotoniaA Furby, S Vicart, J P Camdessanché, et al.
Pageof 10

Showing results (61-70 of 94) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|July 27, 1999
Evaluation of parental mitochondrial inheritance in neonates born after intracytoplasmic sperm injectionC Danan, D Sternberg, A Van Steirteghem, et al.
International Journal of Cell Cloning|September 1, 1992
Dynamic changes in cytokine secretion by stromal cells during prolonged maintenance under protein-free conditionsA Kadouri, R Kompier, J Honigwachs-Sha'anani, et al.
Ecology and Evolution|October 17, 2025
Species Richness of Freshwater Fish Trophic Guilds Increases With Tropical River Discharge and Decreases With VariabilityC N Perna, D Sternberg, M J Kennard, et al.
Brain : a Journal of Neurology|May 4, 2001
Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disordersD Sternberg, E Chatzoglou, P Laforêt, et al.
Trends in Parasitology|July 3, 2017
Priorities for Broadening the Malaria Vector Control Tool KitPriscille Barreaux, Antoine M G Barreaux, Eleanore D Sternberg, et al.
Malaria Journal|October 24, 2018
Screening and field performance of powder-formulated insecticides on eave tube inserts against pyrethroid resistant Anopheles gambiae s.l.: an investigation into 'actives' prior to a randomized controlled trial in Côte d'IvoireWelbeck A Oumbouke, Innocent Z Tia, Antoine M G Barreaux, et al.
Evolution; International Journal of Organic Evolution|October 31, 2012
Food plant derived disease tolerance and resistance in a natural butterfly-plant-parasite interactionsEleanore D Sternberg, Thierry Lefèvre, James Li, et al.
Brain : a Journal of Neurology|May 17, 2001
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4AD Sternberg, T Maisonobe, K Jurkat-Rott, et al.
American Journal of Physiology. Cell Physiology|July 3, 2009
Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubesS Sacconi, D Simkin, N Arrighi, et al.
Neuromuscular Disorders : NMD|August 5, 2014
Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotoniaA Furby, S Vicart, J P Camdessanché, et al.
Pageof 10