共查询到20条相似文献,搜索用时 31 毫秒
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Jean W. MacCluer 《American journal of human genetics》1977,29(2):216-217
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McClearn GE 《Trends in genetics : TIG》2006,22(6):314-319
Complex phenotypes result from multiple inputs from genetic and environmental sources, with intricate subsystems mediating the influence of both sources on the phenotype. Experiments that attempt to describe the influence of a particular gene involve partial isolation of the sub-system in which that gene is an element from other components of the total system influencing the phenotype. Any interactions that exist between the controlled variables and the processes downstream of the gene in the normally operating total system become undetectable; therefore, the results of the experiment can be restricted to the particular configuration of the controlled variables. The inescapable price of the precision of knowledge generated by experiment is a reduction in the generalizability of the results beyond the constrained circumstances of the particular experimental situation. Integrative research, permitting the influence of related subsystems, is required to provide a comprehensive assessment of the influence of a gene. 相似文献
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Lynn R. Goldin 《American journal of human genetics》1982,34(2):360-361
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Genetics and pharmacology can elicit surprisingly different phenotypes despite targeting the same protein. This Essay explores these unexpected differences and their implications for biology and medicine. 相似文献
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Alexander G. Bearn 《American journal of human genetics》1974,26(6):777-778
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Louise A. Paquin 《American journal of human genetics》1989,44(1):168-169
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Beal B. Hyde 《American journal of human genetics》1956,8(2):128-129
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Georg Michaelis Eric Petrochilo Piotr P. Slonimski 《Molecular & general genetics : MGG》1973,123(1):51-65
Summary Cytoplasmic petite mutants of Saccharomyces cerevisiae carrying the gene conferring the resistance to chloramphenicol on one hand and the gene conferring the resistance to erythromycin on the other, have been crossed with each other. The two types of petites differed in the buoyant densities of their mitochondrial DNA. A novel type of evidence has been adduced, that the two genes are indeed located on mitochondrial DNA. Diploid petite recombinants were found, carrying both genes and containing not a mixture of the two parental DNAs but a new species of mitochondrial DNA of intermediate buoyant density. Recombination of mitochondrial genes involves therefore breakage and reunion of DNA molecules. New suppressiveness, different from the two parental ones, can result from the recombination of mitochondrial DNA. Recombination between petite mutants implies that the mitochondrial recombination enzymes have to be synthesized on cytosol ribosomes. 相似文献
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