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1 ct synergistically to modulate growth of the imaginal disk.
2 ssion of homeotic genes or reporter genes in imaginal disks.
3 o stimulate cell division and growth of wing imaginal disks.
6 analysis of ppan mutant clones in Drosophila imaginal disks and ovaries demonstrates that ppan is cel
7 n and the growth of internal organs, such as imaginal disks, and is required for the normal proportio
8 bovine ADA, also stimulates proliferation of imaginal disk cells, and addition of adenosine to this m
9 onstrate that in interphase cells in the eye imaginal disk cyclin A is present in both the nucleus an
10 ision and the duration of growth of the wing imaginal disks depend on the size of the body in which t
11 ression of an active form of Msn in the wing imaginal disk disrupted activation of endogenous MAD by
16 reparation for metamorphosis, the control of imaginal disk growth becomes feeding and nutrition-indep
21 arval feeding period, the growth of the wing imaginal disks of Lepidoptera is dependent on continuous
24 criptions from any type of tissue (e.g. wing imaginal disk, ovary) and at any stage of development.
25 ndages develop from precursor tissues called imaginal disks that grow after somatic growth has ceased
26 producing inositide messengers required for imaginal disk tissue maturation and subsequent formation
27 are that mutant larvae are almost devoid of imaginal disk tissue, have a reduction in brain size, an
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