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R L Margolis

Showing results (141-150 of 153) with videos related to

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Nature Genetics|May 13, 1999
Synphilin-1 associates with alpha-synuclein and promotes the formation of cytosolic inclusionsS Engelender, Z Kaminsky, X Guo, et al.
The Journal of Biological Chemistry|March 20, 1999
Cleavage of atrophin-1 at caspase site aspartic acid 109 modulates cytotoxicityL M Ellerby, R L Andrusiak, C L Wellington, et al.
Neuron|February 17, 2000
Nuclear accumulation of truncated atrophin-1 fragments in a transgenic mouse model of DRPLAG Schilling, J D Wood, K Duan, et al.
Neurology|July 23, 1998
Patients with features similar to Huntington's disease, without CAG expansion in huntingtinA Rosenblatt, N G Ranen, D C Rubinsztein, et al.
Neurology|April 13, 2005
The clinical and genetic spectrum of spinocerebellar ataxia 14D-H Chen, P J Cimino, L P W Ranum, et al.
Human Molecular Genetics|September 25, 1997
A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1T S Breschel, M G McInnis, R L Margolis, et al.
Molecular Psychiatry|July 13, 2000
Allelic distribution of CTG18.1 in Caucasian populations: association studies in bipolar disorder, schizophrenia, and ataxiaM G McInnis, T Swift-Scanlanl, A T Mahoney, et al.
The Journal of Biological Chemistry|May 16, 1998
Caspase cleavage of gene products associated with triplet expansion disorders generates truncated fragments containing the polyglutamine tractC L Wellington, L M Ellerby, A S Hackam, et al.
Archives of Neurology|April 10, 2002
Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locusI Silveira, C Miranda, L Guimarães, et al.
Nature Genetics|December 2, 1999
Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12S E Holmes, E E O'Hearn, M G McInnis, et al.
Pageof 16

Showing results (141-150 of 153) with videos related to

Sort By:
Pageof 16
Nature Genetics|May 13, 1999
Synphilin-1 associates with alpha-synuclein and promotes the formation of cytosolic inclusionsS Engelender, Z Kaminsky, X Guo, et al.
The Journal of Biological Chemistry|March 20, 1999
Cleavage of atrophin-1 at caspase site aspartic acid 109 modulates cytotoxicityL M Ellerby, R L Andrusiak, C L Wellington, et al.
Neuron|February 17, 2000
Nuclear accumulation of truncated atrophin-1 fragments in a transgenic mouse model of DRPLAG Schilling, J D Wood, K Duan, et al.
Neurology|July 23, 1998
Patients with features similar to Huntington's disease, without CAG expansion in huntingtinA Rosenblatt, N G Ranen, D C Rubinsztein, et al.
Neurology|April 13, 2005
The clinical and genetic spectrum of spinocerebellar ataxia 14D-H Chen, P J Cimino, L P W Ranum, et al.
Human Molecular Genetics|September 25, 1997
A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1T S Breschel, M G McInnis, R L Margolis, et al.
Molecular Psychiatry|July 13, 2000
Allelic distribution of CTG18.1 in Caucasian populations: association studies in bipolar disorder, schizophrenia, and ataxiaM G McInnis, T Swift-Scanlanl, A T Mahoney, et al.
The Journal of Biological Chemistry|May 16, 1998
Caspase cleavage of gene products associated with triplet expansion disorders generates truncated fragments containing the polyglutamine tractC L Wellington, L M Ellerby, A S Hackam, et al.
Archives of Neurology|April 10, 2002
Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locusI Silveira, C Miranda, L Guimarães, et al.
Nature Genetics|December 2, 1999
Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12S E Holmes, E E O'Hearn, M G McInnis, et al.
Pageof 16