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Y P Goldberg

Showing results (11-20 of 34) with videos related to

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Clinical Genetics|August 1, 2012
Human Mendelian pain disorders: a key to discovery and validation of novel analgesicsY P Goldberg, S N Pimstone, R Namdari, et al.
American Journal of Human Genetics|April 1, 1997
Different mechanisms underlie DNA instability in Huntington disease and colorectal cancerG M Goellner, D Tester, S Thibodeau, et al.
Journal of Medical Genetics|December 1, 1993
Molecular analysis of late onset Huntington's diseaseB Kremer, F Squitieri, H Telenius, et al.
Nucleic Acids Research|July 25, 1993
An Alu element retroposition in two families with Huntington disease defines a new active Alu subfamilyG B Hutchinson, S E Andrew, H McDonald, et al.
Journal of Medical Genetics|December 1, 1993
Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic casesY P Goldberg, S E Andrew, J Theilmann, et al.
American Journal of Human Genetics|May 1, 1994
Huntington disease without CAG expansion: phenocopies or errors in assignment?S E Andrew, Y P Goldberg, B Kremer, et al.
Human Molecular Genetics|December 1, 1994
DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalenceF Squitieri, S E Andrew, Y P Goldberg, et al.
Human Molecular Genetics|February 1, 1995
Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington diseaseE Almqvist, N Spence, K Nichol, et al.
Human Molecular Genetics|October 1, 1993
Differential 3' polyadenylation of the Huntington disease gene results in two mRNA species with variable tissue expressionB Lin, J M Rommens, R K Graham, et al.
Nature Genetics|August 1, 1993
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's diseaseS E Andrew, Y P Goldberg, B Kremer, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Clinical Genetics|August 1, 2012
Human Mendelian pain disorders: a key to discovery and validation of novel analgesicsY P Goldberg, S N Pimstone, R Namdari, et al.
American Journal of Human Genetics|April 1, 1997
Different mechanisms underlie DNA instability in Huntington disease and colorectal cancerG M Goellner, D Tester, S Thibodeau, et al.
Journal of Medical Genetics|December 1, 1993
Molecular analysis of late onset Huntington's diseaseB Kremer, F Squitieri, H Telenius, et al.
Nucleic Acids Research|July 25, 1993
An Alu element retroposition in two families with Huntington disease defines a new active Alu subfamilyG B Hutchinson, S E Andrew, H McDonald, et al.
Journal of Medical Genetics|December 1, 1993
Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic casesY P Goldberg, S E Andrew, J Theilmann, et al.
American Journal of Human Genetics|May 1, 1994
Huntington disease without CAG expansion: phenocopies or errors in assignment?S E Andrew, Y P Goldberg, B Kremer, et al.
Human Molecular Genetics|December 1, 1994
DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalenceF Squitieri, S E Andrew, Y P Goldberg, et al.
Human Molecular Genetics|February 1, 1995
Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington diseaseE Almqvist, N Spence, K Nichol, et al.
Human Molecular Genetics|October 1, 1993
Differential 3' polyadenylation of the Huntington disease gene results in two mRNA species with variable tissue expressionB Lin, J M Rommens, R K Graham, et al.
Nature Genetics|August 1, 1993
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's diseaseS E Andrew, Y P Goldberg, B Kremer, et al.
Pageof 4