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Emily McFall

Showing results (1-10 of 7) with videos related to

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Human Molecular Genetics|February 8, 2017
Effect of genetic background on the phenotype of the Smn2B/- mouse model of spinal muscular atrophyMehdi Eshraghi, Emily McFall, Sabrina Gibeault, et al.
Environmental Science & Technology|May 31, 2012
Divalent base cations hamper Hg(II) uptakeValérie Daguené, Emily McFall, Emmanuel Yumvihoze, et al.
Human Molecular Genetics|January 22, 2017
Immune dysregulation may contribute to disease pathogenesis in spinal muscular atrophy miceMarc-Olivier Deguise, Yves De Repentigny, Emily McFall, et al.
Human Molecular Genetics|January 11, 2017
Oligodendrocyte development and CNS myelination are unaffected in a mouse model of severe spinal muscular atrophyRyan W O'Meara, Sarah E Cummings, Yves De Repentigny, et al.
Skeletal Muscle|July 28, 2022
Dysregulation of Tweak and Fn14 in skeletal muscle of spinal muscular atrophy miceKatharina E Meijboom, Emma R Sutton, Eve McCallion, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 25, 2013
Optimized tetramer analysis reveals Ly49 promiscuity for MHC ligandsEmily McFall, Megan M Tu, Nuha Al-Khattabi, et al.
Ebiomedicine|May 9, 2018
Interventions Targeting Glucocorticoid-Krüppel-like Factor 15-Branched-Chain Amino Acid Signaling Improve Disease Phenotypes in Spinal Muscular Atrophy MiceLisa M Walter, Marc-Olivier Deguise, Katharina E Meijboom, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Human Molecular Genetics|February 8, 2017
Effect of genetic background on the phenotype of the Smn2B/- mouse model of spinal muscular atrophyMehdi Eshraghi, Emily McFall, Sabrina Gibeault, et al.
Environmental Science & Technology|May 31, 2012
Divalent base cations hamper Hg(II) uptakeValérie Daguené, Emily McFall, Emmanuel Yumvihoze, et al.
Human Molecular Genetics|January 22, 2017
Immune dysregulation may contribute to disease pathogenesis in spinal muscular atrophy miceMarc-Olivier Deguise, Yves De Repentigny, Emily McFall, et al.
Human Molecular Genetics|January 11, 2017
Oligodendrocyte development and CNS myelination are unaffected in a mouse model of severe spinal muscular atrophyRyan W O'Meara, Sarah E Cummings, Yves De Repentigny, et al.
Skeletal Muscle|July 28, 2022
Dysregulation of Tweak and Fn14 in skeletal muscle of spinal muscular atrophy miceKatharina E Meijboom, Emma R Sutton, Eve McCallion, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 25, 2013
Optimized tetramer analysis reveals Ly49 promiscuity for MHC ligandsEmily McFall, Megan M Tu, Nuha Al-Khattabi, et al.
Ebiomedicine|May 9, 2018
Interventions Targeting Glucocorticoid-Krüppel-like Factor 15-Branched-Chain Amino Acid Signaling Improve Disease Phenotypes in Spinal Muscular Atrophy MiceLisa M Walter, Marc-Olivier Deguise, Katharina E Meijboom, et al.
Pageof 1