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American Journal of Human Genetics
|
July 27, 1999
Evaluation of parental mitochondrial inheritance in neonates born after intracytoplasmic sperm injection
C 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 conditions
A 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 Variability
C 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 disorders
D Sternberg, E Chatzoglou, P Laforêt, et al.
Trends in Parasitology
|
July 3, 2017
Priorities for Broadening the Malaria Vector Control Tool Kit
Priscille 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'Ivoire
Welbeck 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 interactions
Eleanore 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 SCN4A
D 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 myotubes
S Sacconi, D Simkin, N Arrighi, et al.
Neuromuscular Disorders : NMD
|
August 5, 2014
Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotonia
A Furby, S Vicart, J P Camdessanché, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 94) with videos related to
Sort By:
Page
of 10
American Journal of Human Genetics
|
July 27, 1999
Evaluation of parental mitochondrial inheritance in neonates born after intracytoplasmic sperm injection
C 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 conditions
A 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 Variability
C 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 disorders
D Sternberg, E Chatzoglou, P Laforêt, et al.
Trends in Parasitology
|
July 3, 2017
Priorities for Broadening the Malaria Vector Control Tool Kit
Priscille 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'Ivoire
Welbeck 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 interactions
Eleanore 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 SCN4A
D 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 myotubes
S Sacconi, D Simkin, N Arrighi, et al.
Neuromuscular Disorders : NMD
|
August 5, 2014
Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotonia
A Furby, S Vicart, J P Camdessanché, et al.
Page
of 10