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C J Cummings

Showing results (1-10 of 13) with videos related to

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Annual Review of Genomics and Human Genetics|November 10, 2001
Trinucleotide repeats: mechanisms and pathophysiologyC J Cummings, H Y Zoghbi
Human Molecular Genetics|April 18, 2000
Fourteen and counting: unraveling trinucleotide repeat diseasesC J Cummings, H Y Zoghbi
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 6, 1999
Progress in pathogenesis studies of spinocerebellar ataxia type 1C J Cummings, H T Orr, H Y Zoghbi
American Journal of Medical Genetics|July 23, 1998
Analysis of the genomic structure of the human glycine receptor alpha2 subunit gene and exclusion of this gene as a candidate for Rett syndromeC J Cummings, E J Dahle, H Y Zoghbi
Nature|November 14, 1997
The cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1A Matilla, B T Koshy, C J Cummings, et al.
Nature Genetics|June 10, 1998
Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1C J Cummings, M A Mancini, B Antalffy, et al.
American Journal of Respiratory and Critical Care Medicine|August 1, 1997
Soluble E-selectin levels in sepsis and critical illness. Correlation with infection and hemodynamic dysfunctionC J Cummings, C N Sessler, L D Beall, et al.
Human Molecular Genetics|July 13, 2001
Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 miceC J Cummings, Y Sun, P Opal, et al.
Nature|November 14, 1997
Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structuresP J Skinner, B T Koshy, C J Cummings, et al.
Neuron|January 7, 2000
Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 miceC J Cummings, E Reinstein, Y Sun, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Annual Review of Genomics and Human Genetics|November 10, 2001
Trinucleotide repeats: mechanisms and pathophysiologyC J Cummings, H Y Zoghbi
Human Molecular Genetics|April 18, 2000
Fourteen and counting: unraveling trinucleotide repeat diseasesC J Cummings, H Y Zoghbi
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 6, 1999
Progress in pathogenesis studies of spinocerebellar ataxia type 1C J Cummings, H T Orr, H Y Zoghbi
American Journal of Medical Genetics|July 23, 1998
Analysis of the genomic structure of the human glycine receptor alpha2 subunit gene and exclusion of this gene as a candidate for Rett syndromeC J Cummings, E J Dahle, H Y Zoghbi
Nature|November 14, 1997
The cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1A Matilla, B T Koshy, C J Cummings, et al.
Nature Genetics|June 10, 1998
Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1C J Cummings, M A Mancini, B Antalffy, et al.
American Journal of Respiratory and Critical Care Medicine|August 1, 1997
Soluble E-selectin levels in sepsis and critical illness. Correlation with infection and hemodynamic dysfunctionC J Cummings, C N Sessler, L D Beall, et al.
Human Molecular Genetics|July 13, 2001
Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 miceC J Cummings, Y Sun, P Opal, et al.
Nature|November 14, 1997
Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structuresP J Skinner, B T Koshy, C J Cummings, et al.
Neuron|January 7, 2000
Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 miceC J Cummings, E Reinstein, Y Sun, et al.
Pageof 2