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Science (New York, N.Y.)|March 27, 1992
An amino acid mutation in a potassium channel that prevents inhibition by protein kinase CA E Busch, M D Varnum, R A North, et al.
Investigative Ophthalmology & Visual Science|February 1, 1989
Calpain II in human lensL L David, M D Varnum, K J Lampi, et al.
Nature Genetics|March 4, 2000
Analysing complex genetic traits with chromosome substitution strainsJ H Nadeau, J B Singer, A Matin, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Mapping of the murine and rat Facc genes and assessment of flexed-tail as a candidate mouse homolog of Fanconi anemia group CR Wevrick, J E Barker, J H Nadeau, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1991
Loss of heterozygosity and mitotic linkage maps in the mouseV Henson, L Palmer, S Banks, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
Close linkage of retinoic acid receptor genes with homeobox- and keratin-encoding genes on paralogous segments of mouse chromosomes 11 and 15J H Nadeau, J G Compton, V Giguère, et al.
International Journal of Andrology|June 10, 2011
Spontaneous metastasis in mouse models of testicular germ-cell tumoursJ L Zechel, G T MacLennan, J D Heaney, et al.
Mechanisms of Development|May 1, 1992
Disorganization is a completely dominant gain-of-function mouse mutation causing sporadic developmental defectsJ L Crosby, D S Varnum, L L Washburn, et al.
Clinical Pharmacology and Therapeutics|December 1, 1988
Alpha-adrenergic blockade makes minimal contribution to ketanserin's hypotensive effectT C Naslund, W J Merrell, J H Nadeau, et al.
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