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B J Scrimshaw

Showing results (1-10 of 7) with videos related to

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Biotechniques|August 1, 1992
A simple nonradioactive procedure for visualization of (dC-dA)n dinucleotide repeat length polymorphismsB J Scrimshaw
Journal of Human Genetics|November 26, 1999
Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicityB J Scrimshaw, J M Faed, W P Tate, et al.
The New Zealand Medical Journal|July 22, 1999
The frequency in New Zealand of a mitochondrial DNA mutation (1555 A to G) associated with aminoglycoside-induced hearing lossB J Scrimshaw, J M Faed, W P Tate, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 22, 1998
Testing migration patterns and estimating founding population size in Polynesia by using human mtDNA sequencesR P Murray-McIntosh, B J Scrimshaw, P J Hatfield, et al.
Australian and New Zealand Journal of Medicine|August 1, 1993
Concurrent hepatitis B and C infection treated successfully with alpha interferonM J Burt, B A Chapman, B J Scrimshaw, et al.
Thyroid : Official Journal of the American Thyroid Association|January 1, 1992
A novel variant of transthyretin (prealbumin), Thr119 to Met, associated with increased thyroxine bindingB J Scrimshaw, A P Fellowes, B N Palmer, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1994
Thyroxine binding by human transthyretin variants: mutations at position 119, but not position 54, increase thyroxine binding affinityA J Curtis, B J Scrimshaw, D J Topliss, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Biotechniques|August 1, 1992
A simple nonradioactive procedure for visualization of (dC-dA)n dinucleotide repeat length polymorphismsB J Scrimshaw
Journal of Human Genetics|November 26, 1999
Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicityB J Scrimshaw, J M Faed, W P Tate, et al.
The New Zealand Medical Journal|July 22, 1999
The frequency in New Zealand of a mitochondrial DNA mutation (1555 A to G) associated with aminoglycoside-induced hearing lossB J Scrimshaw, J M Faed, W P Tate, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 22, 1998
Testing migration patterns and estimating founding population size in Polynesia by using human mtDNA sequencesR P Murray-McIntosh, B J Scrimshaw, P J Hatfield, et al.
Australian and New Zealand Journal of Medicine|August 1, 1993
Concurrent hepatitis B and C infection treated successfully with alpha interferonM J Burt, B A Chapman, B J Scrimshaw, et al.
Thyroid : Official Journal of the American Thyroid Association|January 1, 1992
A novel variant of transthyretin (prealbumin), Thr119 to Met, associated with increased thyroxine bindingB J Scrimshaw, A P Fellowes, B N Palmer, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1994
Thyroxine binding by human transthyretin variants: mutations at position 119, but not position 54, increase thyroxine binding affinityA J Curtis, B J Scrimshaw, D J Topliss, et al.
Pageof 1