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S Harper

Showing results (721-730 of 1,225) with videos related to

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Journal of Medical Genetics|September 1, 1991
Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17M C Koch, K Ricker, M Otto, et al.
Human Genetics|November 1, 1991
Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17M C Koch, K Ricker, M Otto, et al.
EXS|January 1, 1996
The pH paradox in ischemia-reperfusion injury to cardiac myocytesJ J Lemasters, J M Bond, E Chacon, et al.
Journal of Medical Genetics|December 1, 1985
Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales familiesP S Harper, S Youngman, M A Anderson, et al.
BMJ (Clinical Research Ed.)|April 1, 1995
Genetic testing for familial hypertrophic cardiomyopathy in newborn infantsM P Ryan, J French, S al-Mahdawi, et al.
Emergency Medicine Journal : EMJ|December 24, 2009
Google governance: increasing the effectiveness of critical care physicians through the use of an online usergroupC Reid, S Harper, A Tzannes, et al.
Nature|February 6, 1992
Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophyH G Harley, J D Brook, S A Rundle, et al.
Virology|June 4, 2013
Ribonuclease L is not critical for innate restriction and adaptive immunity against Friend retrovirus infectionSam X Li, Bradley S Barrett, Michael S Harper, et al.
Human Genetics|May 1, 1991
Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19qH G Harley, K V Walsh, S Rundle, et al.
Lancet (London, England)|October 16, 1993
Molecular analysis and clinical correlations of the Huntington's disease mutationJ C MacMillan, R G Snell, A Tyler, et al.
Pageof 123

Showing results (721-730 of 1,225) with videos related to

Sort By:
Pageof 123
Journal of Medical Genetics|September 1, 1991
Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17M C Koch, K Ricker, M Otto, et al.
Human Genetics|November 1, 1991
Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17M C Koch, K Ricker, M Otto, et al.
EXS|January 1, 1996
The pH paradox in ischemia-reperfusion injury to cardiac myocytesJ J Lemasters, J M Bond, E Chacon, et al.
Journal of Medical Genetics|December 1, 1985
Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales familiesP S Harper, S Youngman, M A Anderson, et al.
BMJ (Clinical Research Ed.)|April 1, 1995
Genetic testing for familial hypertrophic cardiomyopathy in newborn infantsM P Ryan, J French, S al-Mahdawi, et al.
Emergency Medicine Journal : EMJ|December 24, 2009
Google governance: increasing the effectiveness of critical care physicians through the use of an online usergroupC Reid, S Harper, A Tzannes, et al.
Nature|February 6, 1992
Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophyH G Harley, J D Brook, S A Rundle, et al.
Virology|June 4, 2013
Ribonuclease L is not critical for innate restriction and adaptive immunity against Friend retrovirus infectionSam X Li, Bradley S Barrett, Michael S Harper, et al.
Human Genetics|May 1, 1991
Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19qH G Harley, K V Walsh, S Rundle, et al.
Lancet (London, England)|October 16, 1993
Molecular analysis and clinical correlations of the Huntington's disease mutationJ C MacMillan, R G Snell, A Tyler, et al.
Pageof 123