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Marcy E MacDonald

Showing results (11-20 of 150) with videos related to

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Human Molecular Genetics|February 14, 2004
Striatal cells from mutant huntingtin knock-in mice are selectively vulnerable to mitochondrial complex II inhibitor-induced cell death through a non-apoptotic pathwayQingmin Ruan, Mathieu Lesort, Marcy E MacDonald, et al.
Developmental Neuroscience|October 10, 2006
Characterization of mouse striatal precursor cell lines expressing functional dopamine receptorsKiyomi Y Araki, Satoshi Fujimura, Marcy E MacDonald, et al.
Neurobiology of Disease|July 12, 2005
Thalamocortical neuron loss and localized astrocytosis in the Cln3Deltaex7/8 knock-in mouse model of Batten diseaseCharlie C Pontikis, Susan L Cotman, Marcy E MacDonald, et al.
Journal of Huntington'S Disease|October 11, 2014
Huntingtin Supplies a csaA-Independent Function Essential for EDTA-Resistant Homotypic Cell Adhesion in Dictyostelium discoideumMorgan N Thompson, Marcy E MacDonald, James F Gusella, et al.
Brain Pathology (Zurich, Switzerland)|December 21, 2007
Systematic assessment of BDNF and its receptor levels in human cortices affected by Huntington's diseaseChiara Zuccato, Manuela Marullo, Paola Conforti, et al.
The Journal of Biological Chemistry|October 3, 2003
Enhanced Akt signaling is an early pro-survival response that reflects N-methyl-D-aspartate receptor activation in Huntington's disease knock-in striatal cellsSilvia Gines, Elena Ivanova, Ihn-Sik Seong, et al.
Current Protocols in Human Genetics|January 12, 2017
Highly Expandable Human iPS Cell-Derived Neural Progenitor Cells (NPC) and Neurons for Central Nervous System Disease Modeling and High-Throughput ScreeningChialin Cheng, Daniel M Fass, Kat Folz-Donahue, et al.
The European Journal of Neuroscience|January 17, 2004
The serum- and glucocorticoid-induced kinase SGK inhibits mutant huntingtin-induced toxicity by phosphorylating serine 421 of huntingtinHélène Rangone, Ghislaine Poizat, Juan Troncoso, et al.
Human Molecular Genetics|January 30, 2003
Mismatch repair gene Msh2 modifies the timing of early disease in Hdh(Q111) striatumVanessa C Wheeler, Lori-Anne Lebel, Vladimir Vrbanac, et al.
Neurology|August 29, 2012
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashionN Ahmad Aziz, Raymund A C Roos, James F Gusella, et al.
Pageof 15

Showing results (11-20 of 150) with videos related to

Sort By:
Pageof 15
Human Molecular Genetics|February 14, 2004
Striatal cells from mutant huntingtin knock-in mice are selectively vulnerable to mitochondrial complex II inhibitor-induced cell death through a non-apoptotic pathwayQingmin Ruan, Mathieu Lesort, Marcy E MacDonald, et al.
Developmental Neuroscience|October 10, 2006
Characterization of mouse striatal precursor cell lines expressing functional dopamine receptorsKiyomi Y Araki, Satoshi Fujimura, Marcy E MacDonald, et al.
Neurobiology of Disease|July 12, 2005
Thalamocortical neuron loss and localized astrocytosis in the Cln3Deltaex7/8 knock-in mouse model of Batten diseaseCharlie C Pontikis, Susan L Cotman, Marcy E MacDonald, et al.
Journal of Huntington'S Disease|October 11, 2014
Huntingtin Supplies a csaA-Independent Function Essential for EDTA-Resistant Homotypic Cell Adhesion in Dictyostelium discoideumMorgan N Thompson, Marcy E MacDonald, James F Gusella, et al.
Brain Pathology (Zurich, Switzerland)|December 21, 2007
Systematic assessment of BDNF and its receptor levels in human cortices affected by Huntington's diseaseChiara Zuccato, Manuela Marullo, Paola Conforti, et al.
The Journal of Biological Chemistry|October 3, 2003
Enhanced Akt signaling is an early pro-survival response that reflects N-methyl-D-aspartate receptor activation in Huntington's disease knock-in striatal cellsSilvia Gines, Elena Ivanova, Ihn-Sik Seong, et al.
Current Protocols in Human Genetics|January 12, 2017
Highly Expandable Human iPS Cell-Derived Neural Progenitor Cells (NPC) and Neurons for Central Nervous System Disease Modeling and High-Throughput ScreeningChialin Cheng, Daniel M Fass, Kat Folz-Donahue, et al.
The European Journal of Neuroscience|January 17, 2004
The serum- and glucocorticoid-induced kinase SGK inhibits mutant huntingtin-induced toxicity by phosphorylating serine 421 of huntingtinHélène Rangone, Ghislaine Poizat, Juan Troncoso, et al.
Human Molecular Genetics|January 30, 2003
Mismatch repair gene Msh2 modifies the timing of early disease in Hdh(Q111) striatumVanessa C Wheeler, Lori-Anne Lebel, Vladimir Vrbanac, et al.
Neurology|August 29, 2012
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashionN Ahmad Aziz, Raymund A C Roos, James F Gusella, et al.
Pageof 15