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D C Rubinsztein

Showing results (41-50 of 125) with videos related to

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Journal of Medical Genetics|October 21, 1999
Subclinical cognitive impairment in autosomal dominant "pure" hereditary spastic paraplegiaE Reid, C Grayson, D C Rubinsztein, et al.
American Journal of Human Genetics|March 21, 2000
A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13E Reid, A M Dearlove, O Osborn, et al.
Journal of Medical Genetics|May 19, 2001
The spastic paraplegia SPG10 locus: narrowing of critical region and exclusion of sodium channel gene SCN8A as a candidateE Reid, A Escayg, A M Dearlove, et al.
Journal of Medical Genetics|May 20, 2009
Wild-type but not mutant huntingtin modulates the transcriptional activity of liver X receptorsM Futter, H Diekmann, E Schoenmakers, et al.
Journal of Medical Genetics|March 1, 1997
Mild myotonic dystrophy is associated with memory impairment in the context of normal general intelligenceJ S Rubinsztein, D C Rubinsztein, P J McKenna, et al.
Human Molecular Genetics|June 1, 1996
Genetic association between monoamine oxidase A microsatellite and RFLP alleles and bipolar affective disorder: analysis and meta-analysisD C Rubinsztein, J Leggo, S Goodburn, et al.
Psychological Medicine|February 24, 2001
The molecular biology of Huntington's diseaseL W Ho, J Carmichael, J Swartz, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 2000
Bacterial and yeast chaperones reduce both aggregate formation and cell death in mammalian cell models of Huntington's diseaseJ Carmichael, J Chatellier, A Woolfson, et al.
American Journal of Medical Genetics|April 24, 1995
Normal CAG and CCG repeats in the Huntington's disease genes of Parkinson's disease patientsD C Rubinsztein, J Leggo, S Goodburn, et al.
Human Molecular Genetics|February 1, 1995
Haplotype analysis of the delta 2642 and (CAG)n polymorphisms in the Huntington's disease (HD) gene provides an explanation for an apparent 'founder' HD haplotypeD C Rubinsztein, J Leggo, S Goodburn, et al.
Pageof 13

Showing results (41-50 of 125) with videos related to

Sort By:
Pageof 13
Journal of Medical Genetics|October 21, 1999
Subclinical cognitive impairment in autosomal dominant "pure" hereditary spastic paraplegiaE Reid, C Grayson, D C Rubinsztein, et al.
American Journal of Human Genetics|March 21, 2000
A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13E Reid, A M Dearlove, O Osborn, et al.
Journal of Medical Genetics|May 19, 2001
The spastic paraplegia SPG10 locus: narrowing of critical region and exclusion of sodium channel gene SCN8A as a candidateE Reid, A Escayg, A M Dearlove, et al.
Journal of Medical Genetics|May 20, 2009
Wild-type but not mutant huntingtin modulates the transcriptional activity of liver X receptorsM Futter, H Diekmann, E Schoenmakers, et al.
Journal of Medical Genetics|March 1, 1997
Mild myotonic dystrophy is associated with memory impairment in the context of normal general intelligenceJ S Rubinsztein, D C Rubinsztein, P J McKenna, et al.
Human Molecular Genetics|June 1, 1996
Genetic association between monoamine oxidase A microsatellite and RFLP alleles and bipolar affective disorder: analysis and meta-analysisD C Rubinsztein, J Leggo, S Goodburn, et al.
Psychological Medicine|February 24, 2001
The molecular biology of Huntington's diseaseL W Ho, J Carmichael, J Swartz, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 2000
Bacterial and yeast chaperones reduce both aggregate formation and cell death in mammalian cell models of Huntington's diseaseJ Carmichael, J Chatellier, A Woolfson, et al.
American Journal of Medical Genetics|April 24, 1995
Normal CAG and CCG repeats in the Huntington's disease genes of Parkinson's disease patientsD C Rubinsztein, J Leggo, S Goodburn, et al.
Human Molecular Genetics|February 1, 1995
Haplotype analysis of the delta 2642 and (CAG)n polymorphisms in the Huntington's disease (HD) gene provides an explanation for an apparent 'founder' HD haplotypeD C Rubinsztein, J Leggo, S Goodburn, et al.
Pageof 13