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M E MacDonald

Showing results (101-110 of 118) with videos related to

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Genomics|September 1, 1987
A somatic cell hybrid panel for localizing DNA segments near the Huntington's disease geneM E MacDonald, M A Anderson, T C Gilliam, et al.
Human Molecular Genetics|February 5, 1999
Analysis of germline mutation spectra at the Huntington's disease locus supports a mitotic mutation mechanismE P Leeflang, S Tavaré, P Marjoram, et al.
Genomics|April 1, 1989
Synteny on mouse chromosome 5 of homologs for human DNA loci linked to the Huntington disease geneS V Cheng, G R Martin, J H Nadeau, et al.
American Journal of Human Genetics|August 1, 1992
A recombination event that redefines the Huntington disease regionR G Snell, L M Thompson, D A Tagle, et al.
Human Molecular Genetics|January 15, 1999
Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouseV C Wheeler, W Auerbach, J K White, et al.
Cell|August 14, 1987
Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomereT C Gilliam, R E Tanzi, J L Haines, et al.
Science (New York, N.Y.)|June 16, 2001
Loss of huntingtin-mediated BDNF gene transcription in Huntington's diseaseC Zuccato, A Ciammola, D Rigamonti, et al.
Human Molecular Genetics|March 1, 1993
The isolation of cDNAs within the Huntington disease region by hybridisation of yeast artificial chromosomes to a cDNA libraryR G Snell, L A Doucette-Stamm, K M Gillespie, et al.
Neurology|August 28, 2002
Clinical and genetic heterogeneity in benign hereditary choreaG J Breedveld, A K Percy, M E MacDonald, et al.
Journal of Medical Genetics|August 3, 2005
Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1H G Kim, S R Herrick, E Lemyre, et al.
Pageof 12

Showing results (101-110 of 118) with videos related to

Sort By:
Pageof 12
Genomics|September 1, 1987
A somatic cell hybrid panel for localizing DNA segments near the Huntington's disease geneM E MacDonald, M A Anderson, T C Gilliam, et al.
Human Molecular Genetics|February 5, 1999
Analysis of germline mutation spectra at the Huntington's disease locus supports a mitotic mutation mechanismE P Leeflang, S Tavaré, P Marjoram, et al.
Genomics|April 1, 1989
Synteny on mouse chromosome 5 of homologs for human DNA loci linked to the Huntington disease geneS V Cheng, G R Martin, J H Nadeau, et al.
American Journal of Human Genetics|August 1, 1992
A recombination event that redefines the Huntington disease regionR G Snell, L M Thompson, D A Tagle, et al.
Human Molecular Genetics|January 15, 1999
Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouseV C Wheeler, W Auerbach, J K White, et al.
Cell|August 14, 1987
Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomereT C Gilliam, R E Tanzi, J L Haines, et al.
Science (New York, N.Y.)|June 16, 2001
Loss of huntingtin-mediated BDNF gene transcription in Huntington's diseaseC Zuccato, A Ciammola, D Rigamonti, et al.
Human Molecular Genetics|March 1, 1993
The isolation of cDNAs within the Huntington disease region by hybridisation of yeast artificial chromosomes to a cDNA libraryR G Snell, L A Doucette-Stamm, K M Gillespie, et al.
Neurology|August 28, 2002
Clinical and genetic heterogeneity in benign hereditary choreaG J Breedveld, A K Percy, M E MacDonald, et al.
Journal of Medical Genetics|August 3, 2005
Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1H G Kim, S R Herrick, E Lemyre, et al.
Pageof 12