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1 le, is a specific target during aging of the housefly.
2 beetles and further refined from studies of houseflies.
3 tive and food odours in both male and female houseflies.
5 port that esc protein is highly conserved in housefly (72% identical to Drosophila esc), butterfly (5
7 gram-negative bacteria, as well as DNA from houseflies and feces from H. pylori-negative patients.
9 ess during chicken colonisation, survival in houseflies and under nutrient-rich and -poor conditions
10 e (kdr) to pyrethroids and DDT in aphids and houseflies, and gene amplification conferring metabolic
12 fully demonstrated for the identification of housefly arginine kinase, a cytosolic protein that is in
13 enerality of this phenomenon, using the male housefly as an insect model in which food intake can be
21 reted in feces from infected individuals and houseflies habitually develop and feed on excrement, we
27 drial membranes in the flight muscles of the housefly, manifested as carbonyl modifications, was dete
28 enced Drosophila species, medfly, blowflies, housefly, Megaselia scalaris, mosquitoes, butterfly, bee
30 ity of particulate matter on the antennae of houseflies (Musca domestica) collected from an urban env
32 nsecticide-resistant Cornell-R strain of the housefly (Musca domestica) produces an activity that deg
33 ter ant (Camponotus pennsylvanicus), and the housefly (Musca domestica), which use different modes of
36 has recently been reported that the domestic housefly, Musca domestica, when fed pure cultures of H.
37 and/or severe bottlenecks in the New World, houseflies (n = 14) display variation among populations
42 em to suggest the opposite, but we show that housefly Sc can substitute for fruit fly Sc in sex deter
44 less, in insects as diverse as honeybees and houseflies, Sxl seems not to determine sex or to be func