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The Journal of Clinical Investigation|March 1, 1990
Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteinsS G Young, S T Hubl, R S Smith, et al.The American Journal of Physiology|December 22, 1999
Chronic run training suppresses alpha-adrenergic response of rat cardiomyocytes and isovolumic left ventricleB M Palmer, M C Olsson, J M Lynch, et al.Journal of Lipid Research|March 1, 1993
Four new mutations in the apolipoprotein B gene causing hypobetalipoproteinemia, including two different frameshift mutations that yield truncated apolipoprotein B proteins of identical lengthS G Young, C R Pullinger, B R Zysow, et al.Pageof 3