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O C Stine

Showing results (41-50 of 69) with videos related to

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Neurology|February 1, 1997
Longitudinal change in basal ganglia volume in patients with Huntington's diseaseE H Aylward, Q Li, O C Stine, et al.
Cancer Research|August 17, 2001
Instabilotyping: comprehensive identification of frameshift mutations caused by coding region microsatellite instabilityY Mori, J Yin, A Rashid, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 1, 2000
Rate of caudate atrophy in presymptomatic and symptomatic stages of Huntington's diseaseE H Aylward, A M Codori, A Rosenblatt, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Adrenoleukodystrophy: phenotypic variability and implications for therapyH W Moser, A B Moser, K D Smith, et al.
Brain Research. Molecular Brain Research|March 1, 1996
DRPLA gene (atrophin-1) sequence and mRNA expression in human brainR L Margolis, S H Li, W S Young, et al.
Journal of Medical Genetics|February 9, 1999
Unstable expansion of the CAG trinucleotide repeat in MAB21L1: report of a second pedigree and effect on protein expressionR L Margolis, O C Stine, C M Ward, et al.
American Journal of Human Genetics|September 1, 1995
Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington diseaseN G Ranen, O C Stine, M H Abbott, et al.
Pediatric Research|November 1, 1990
Heteroplasmy in chronic external ophthalmoplegia: clinical and molecular observationsO Hurko, D R Johns, S L Rutledge, et al.
Human Genetics|July 1, 1997
cDNAs with long CAG trinucleotide repeats from human brainR L Margolis, M R Abraham, S B Gatchell, et al.
Neuron|November 1, 1993
Huntington's disease gene (IT15) is widely expressed in human and rat tissuesS H Li, G Schilling, W S Young, et al.
Pageof 7

Showing results (41-50 of 69) with videos related to

Sort By:
Pageof 7
Neurology|February 1, 1997
Longitudinal change in basal ganglia volume in patients with Huntington's diseaseE H Aylward, Q Li, O C Stine, et al.
Cancer Research|August 17, 2001
Instabilotyping: comprehensive identification of frameshift mutations caused by coding region microsatellite instabilityY Mori, J Yin, A Rashid, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 1, 2000
Rate of caudate atrophy in presymptomatic and symptomatic stages of Huntington's diseaseE H Aylward, A M Codori, A Rosenblatt, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Adrenoleukodystrophy: phenotypic variability and implications for therapyH W Moser, A B Moser, K D Smith, et al.
Brain Research. Molecular Brain Research|March 1, 1996
DRPLA gene (atrophin-1) sequence and mRNA expression in human brainR L Margolis, S H Li, W S Young, et al.
Journal of Medical Genetics|February 9, 1999
Unstable expansion of the CAG trinucleotide repeat in MAB21L1: report of a second pedigree and effect on protein expressionR L Margolis, O C Stine, C M Ward, et al.
American Journal of Human Genetics|September 1, 1995
Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington diseaseN G Ranen, O C Stine, M H Abbott, et al.
Pediatric Research|November 1, 1990
Heteroplasmy in chronic external ophthalmoplegia: clinical and molecular observationsO Hurko, D R Johns, S L Rutledge, et al.
Human Genetics|July 1, 1997
cDNAs with long CAG trinucleotide repeats from human brainR L Margolis, M R Abraham, S B Gatchell, et al.
Neuron|November 1, 1993
Huntington's disease gene (IT15) is widely expressed in human and rat tissuesS H Li, G Schilling, W S Young, et al.
Pageof 7