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H S Scott

Showing results (1-10 of 84) with videos related to

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Genetic Engineering|September 26, 2001
Global transcript expression profiling by Serial Analysis of Gene Expression (SAGE)H S Scott, R Chrast
Human Molecular Genetics|August 1, 1993
Two novel mutations causing mucopolysaccharidosis type I detected by single strand conformational analysis of the alpha-L-iduronidase geneL A Clarke, H S Scott
Transgenic Research|September 11, 1999
Linearization and purification of BAC DNA for the development of transgenic miceR Chrast, H S Scott, S E Antonarakis
Nature Genetics|September 1, 1997
What is expanded in progressive myoclonus epilepsy?M D Lalioti, H S Scott, S E Antonarakis
Cytogenetic and Genome Research|October 4, 2003
The epilepsy, the protease inhibitor and the dodecamer: progressive myoclonus epilepsy, cystatin b and a 12-mer repeat expansionM D Lalioti, S E Antonarakis, H S Scott
Human Molecular Genetics|August 11, 1999
Altered spacing of promoter elements due to the dodecamer repeat expansion contributes to reduced expression of the cystatin B gene in EPM1M D Lalioti, H S Scott, S E Antonarakis
Brain Research. Brain Research Reviews|November 3, 2001
Differential gene expression studies to explore the molecular pathophysiology of Down syndromeS E Antonarakis, R Lyle, R Chrast, et al.
Human Genetics|September 1, 1997
Localization of a novel human RNA-editing deaminase (hRED2 or ADARB2) to chromosome 10p15L Mittaz, S E Antonarakis, M Higuchi, et al.
Human Mutation|January 1, 1992
A common mutation for mucopolysaccharidosis type I associated with a severe Hurler syndrome phenotypeH S Scott, T Litjens, J J Hopwood, et al.
Human Genetics|November 1, 1992
PCR detection of two RFLPs in exon I of the alpha-L-iduronidase (IDUA) geneH S Scott, T Litjens, J J Hopwood, et al.
Pageof 9

Showing results (1-10 of 84) with videos related to

Sort By:
Pageof 9
Genetic Engineering|September 26, 2001
Global transcript expression profiling by Serial Analysis of Gene Expression (SAGE)H S Scott, R Chrast
Human Molecular Genetics|August 1, 1993
Two novel mutations causing mucopolysaccharidosis type I detected by single strand conformational analysis of the alpha-L-iduronidase geneL A Clarke, H S Scott
Transgenic Research|September 11, 1999
Linearization and purification of BAC DNA for the development of transgenic miceR Chrast, H S Scott, S E Antonarakis
Nature Genetics|September 1, 1997
What is expanded in progressive myoclonus epilepsy?M D Lalioti, H S Scott, S E Antonarakis
Cytogenetic and Genome Research|October 4, 2003
The epilepsy, the protease inhibitor and the dodecamer: progressive myoclonus epilepsy, cystatin b and a 12-mer repeat expansionM D Lalioti, S E Antonarakis, H S Scott
Human Molecular Genetics|August 11, 1999
Altered spacing of promoter elements due to the dodecamer repeat expansion contributes to reduced expression of the cystatin B gene in EPM1M D Lalioti, H S Scott, S E Antonarakis
Brain Research. Brain Research Reviews|November 3, 2001
Differential gene expression studies to explore the molecular pathophysiology of Down syndromeS E Antonarakis, R Lyle, R Chrast, et al.
Human Genetics|September 1, 1997
Localization of a novel human RNA-editing deaminase (hRED2 or ADARB2) to chromosome 10p15L Mittaz, S E Antonarakis, M Higuchi, et al.
Human Mutation|January 1, 1992
A common mutation for mucopolysaccharidosis type I associated with a severe Hurler syndrome phenotypeH S Scott, T Litjens, J J Hopwood, et al.
Human Genetics|November 1, 1992
PCR detection of two RFLPs in exon I of the alpha-L-iduronidase (IDUA) geneH S Scott, T Litjens, J J Hopwood, et al.
Pageof 9