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921.
922.
923.
DNA methylation profiling of human chromosomes 6, 20 and 22 总被引:24,自引:0,他引:24
924.
Recent experience with several high-profile drugs demonstrates the great challenges in developing effective and safe therapeutics. A complementary approach to the popular paradigm of disease genetics is based on inherited factors that reduce the incidence and severity of disease among individuals who are genetically predisposed to disease. We propose testing specifically for modifier genes and protective alleles among at-risk individuals and studying the efficacy of therapeutics based on the genetics of health. 相似文献
925.
Aggressive behavior is pervasive throughout the animal kingdom, and yet very little is known about its molecular underpinnings. To address this problem, we have developed a population-based selection procedure to increase aggression in Drosophila melanogaster. We measured changes in aggressive behavior in the selected subpopulations with a new two-male arena assay. In only ten generations of selection, the aggressive lines became markedly more aggressive than the neutral lines. After 21 generations, the fighting index increased more than 30-fold. Using microarray analysis, we identified genes with differing expression levels in the aggressive and neutral lines as candidates for this strong behavioral selection response. We tested a small set of these genes through mutant analysis and found that one significantly increased fighting frequency. These results suggest that selection for increases in aggression can be used to molecularly dissect this behavior. 相似文献
926.
The mammalian olfactory system is not uniformly organized but consists of several subsystems each of which probably serves
distinct functions. Not only are the two major nasal chemosensory systems, the vomeronasal organ and the main olfactory epithelium,
structurally and functionally separate entities, but the latter is further subcompartimentalized into overlapping expression
zones and projection-related subzones. Moreover, the populations of ‘OR37’ neurons not only express a unique type of olfactory
receptors but also are segregated in a cluster-like manner and generally project to only one receptor-specific glomerulus.
The septal organ is an island of sensory epithelium on the nasal septum positioned at the nasoplatine duct; it is considered
as a ‘mini-nose’ with dual function. A specific chemosensory function of the most recently discovered subsystem, the so-called
Grueneberg ganglion, is based on the expression of olfactory marker protein and the axonal projections to defined glomeruli
within the olfactory bulb. This complexity of distinct olfactory subsystems may be one of the features determining the enormous
chemosensory capacity of the sense of smell. 相似文献
927.
Glycogen synthase kinase 3β and Alzheimer’s disease: pathophysiological and therapeutic significance 总被引:3,自引:0,他引:3
Balaraman Y Limaye AR Levey AI Srinivasan S 《Cellular and molecular life sciences : CMLS》2006,63(11):1226-1235
Alzheimer’s disease (AD) is a neurodegenerative disorder associated with cognitive and behavioral dysfunction and is the leading
cause of dementia in the elderly. Several studies have implicated molecular and cellular signaling cascades involving the
serine-threonine kinase, glycogen synthase kinase β(GSK-3β) in the pathogenesis of AD. GSK-3β may play an important role in
the formation of neurofibrillary tangles and senile plaques, the two classical pathological hallmarks of AD. In this review,
we discuss the interaction between GSK-3β and several key molecules involved in AD, including the presenilins, amyloid precursor
protein, tau, and β-amyloid. We identify the signal transduction pathways involved in the pathogenesis of AD, including Wnt,
Notch, and the PI3 kinase/Akt pathway. These may be potential therapeutic targets in AD.
Received 19 December 2005; received after revision 24 January 2006; accepted 6 February 2006 相似文献
928.
929.
Relation between total and exchangeable sodium in the body 总被引:1,自引:0,他引:1
930.
Ethanol, 3 g/kg i.p., did not significantly alter the acute toxicity of amphetamine in the mouse. However, the urinary metabolite pattern was changed, suggesting that ethanol suppressed metabolism of the stimulant during the initial 6 h period. After 24 h, the mouse metabolized the same fraction of a given dose of amphetamine, whether it was given as amphetamine alone or amphetamine mixed with 2,3 or 4 g/kg ethanol. 相似文献