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N MACKAY

Showing results (41-50 of 52) with videos related to

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AIDS Research and Human Retroviruses|March 20, 1997
Comparative efficiency of feline immunodeficiency virus infection by DNA inoculationM A Rigby, M J Hosie, B J Willett, et al.
Human Molecular Genetics|April 18, 1998
Detection of a homozygous four base pair deletion in the protein X gene in a case of pyruvate dehydrogenase complex deficiencyM Ling, G McEachern, A Seyda, et al.
American Journal of Human Genetics|August 1, 1993
A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of QuebecF Merante, R Petrova-Benedict, N MacKay, et al.
Human Genetics|February 3, 2009
Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotypeJ M Cameron, M Maj, V Levandovskiy, et al.
Journal of Virology|September 23, 2000
Vaccination with inactivated virus but not viral DNA reduces virus load following challenge with a heterologous and virulent isolate of feline immunodeficiency virusM J Hosie, T Dunsford, D Klein, et al.
British Medical Journal|August 22, 1970
Treatment of hypertension with clonidineA I MacDougall, G J Addis, N MacKay, et al.
American Journal of Medical Genetics. Part A|March 3, 2004
Novel SCO2 mutation (G1521A) presenting as a spinal muscular atrophy type I phenotypeMark A Tarnopolsky, J M Bourgeois, M-H Fu, et al.
Journal of Cellular Biochemistry|November 22, 2016
Runx1 Orchestrates Sphingolipid Metabolism and Glucocorticoid Resistance in LymphomagenesisA Kilbey, A Terry, S Wotton, et al.
American Journal of Human Genetics|January 13, 2001
A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13A Seyda, R F Newbold, T J Hudson, et al.
Neuropediatrics|July 2, 2009
A novel mitochondrial DNA mutation in COX1 leads to strokes, seizures, and lactic acidosisE W Y Tam, A Feigenbaum, J B L Addis, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
AIDS Research and Human Retroviruses|March 20, 1997
Comparative efficiency of feline immunodeficiency virus infection by DNA inoculationM A Rigby, M J Hosie, B J Willett, et al.
Human Molecular Genetics|April 18, 1998
Detection of a homozygous four base pair deletion in the protein X gene in a case of pyruvate dehydrogenase complex deficiencyM Ling, G McEachern, A Seyda, et al.
American Journal of Human Genetics|August 1, 1993
A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of QuebecF Merante, R Petrova-Benedict, N MacKay, et al.
Human Genetics|February 3, 2009
Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotypeJ M Cameron, M Maj, V Levandovskiy, et al.
Journal of Virology|September 23, 2000
Vaccination with inactivated virus but not viral DNA reduces virus load following challenge with a heterologous and virulent isolate of feline immunodeficiency virusM J Hosie, T Dunsford, D Klein, et al.
British Medical Journal|August 22, 1970
Treatment of hypertension with clonidineA I MacDougall, G J Addis, N MacKay, et al.
American Journal of Medical Genetics. Part A|March 3, 2004
Novel SCO2 mutation (G1521A) presenting as a spinal muscular atrophy type I phenotypeMark A Tarnopolsky, J M Bourgeois, M-H Fu, et al.
Journal of Cellular Biochemistry|November 22, 2016
Runx1 Orchestrates Sphingolipid Metabolism and Glucocorticoid Resistance in LymphomagenesisA Kilbey, A Terry, S Wotton, et al.
American Journal of Human Genetics|January 13, 2001
A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13A Seyda, R F Newbold, T J Hudson, et al.
Neuropediatrics|July 2, 2009
A novel mitochondrial DNA mutation in COX1 leads to strokes, seizures, and lactic acidosisE W Y Tam, A Feigenbaum, J B L Addis, et al.
Pageof 6