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1 average, half of the follicle cells in each ovariole.
2 em to conclude that there are 15-16 FSCs per ovariole.
3 thelial sheath cells, the muscle surrounding ovarioles.
4 d allows the formation of normally patterned ovarioles.
5 t the conclusion that there are two FSCs per ovariole, a recent study used a novel clonal marking sys
6 ired for FSC daughters to migrate across the ovariole and on occasion to replace the opposite stem ce
16 o somatic follicle stem cells (FSCs) in each ovariole give rise to all polar cells, stalk cells, and
18 ingle cells, cell monolayers, and Drosophila ovarioles highlights the NMBS's ability to dynamically t
21 tion was due to a reduction in the number of ovarioles in D. sechellia relative to its sister species
22 ssed at the extreme apical end of Drosophila ovarioles in terminal filament cells and a newly identif
26 an cell number that regulate D. melanogaster ovariole number also regulate ovariole number in Hawaiia
29 stigated the genetic basis for plasticity of ovariole number and body size, as well the genetic basis
34 While previously mapped factors affecting ovariole number appear to impact the rate of egg product
37 gy on the developmental processes underlying ovariole number evolution among Hawaiian Drosophila, a l
48 genetic changes underlying species-specific ovariole number may alter the total number of TFCs avail
49 t in these Drosophila lineages, reduction in ovariole number occurs primarily through variations in o
53 tively large within-population variation for ovariole number suggest that substantial microhabitat va
54 independently evolved a significantly lower ovariole number than the D. melanogaster Oregon R strain
55 major groups of Hawaiian Drosophila, wherein ovariole number variation is best explained by adaptatio
57 ontrast, temperature-dependent plasticity in ovariole number was due to changes in cell-cell sorting
59 and used to identify 34 candidate genes for ovariole number, a quantitative trait, in Drosophila mel
60 ophila melanogaster, ovary size, measured as ovariole number, and body size, measured as thorax lengt
61 of recombinant inbred lines were assayed for ovariole number, and QTL analyses for this trait identif
62 dependent evolution of a reproductive trait, ovariole number, has resulted from changes in distinct d
63 To study the genetic architecture of worker ovariole number, we performed a series of crosses betwee
71 stinct developmental processes that regulate ovariole number: establishment of total TFC number, and
72 ogenetic modeling to an expanded sampling of ovariole numbers and substrate types and show support fo
73 discuss how the phenotype of extreme worker ovariole numbers and the underlying genetic factors we i
74 ive radiation wherein the highest and lowest ovariole numbers of the family have evolved within 25 mi
75 transgressive worker phenotypes with extreme ovariole numbers that were sensitive to the social envir
77 The germarium, a structure at the tip of the ovariole of a Drosophila ovary, contains two follicle st
78 tifying micrometastasis formation within the ovarioles of adult hosts after transplantation and deter
80 susceptibility to I. fumosorosea, number of ovarioles, or ovipostioning were seen between any of the
81 ific mapping between Drosophila sechellia (8 ovarioles/ovary) and D. simulans (15 ovarioles/ovary) id
82 llia (8 ovarioles/ovary) and D. simulans (15 ovarioles/ovary) identified a major QTL on chromosome 3
83 insect reproductive organs and the number of ovarioles per ovary strongly influences egg-laying rate
84 ition, Cct1 mutants display a novel branched ovariole phenotype, demonstrating a requirement for this
85 g (Hh) at the extreme anterior of Drosophila ovarioles suggests that it might provide an asymmetric c
86 acity is largely determined by the number of ovarioles, the egg-producing subunits of the ovary [e.g.
87 that there are typically two active FSCs per ovariole, though they are consistent with up to four FSC
89 oducing structures of insect ovaries, called ovarioles, to deduce systems-level gene regulatory relat
90 ce a range of phenotypes, including agametic ovarioles, tumorous egg chambers, and late stage oogenic
92 one site) that differed by an average of 4.6 ovarioles were used to generate F1, F2 and backcross gen
93 ries are composed of functional units called ovarioles, which contain sequentially developing egg cha
94 ted by stem cell loss, we studied Drosophila ovarioles, which maintain two to three germ-line stem ce
95 lls in the follicle cell layer of developing ovarioles with down-regulated expression of the major mi