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   1 thelial sheath cells, the muscle surrounding ovarioles.                                              
     2 d allows the formation of normally patterned ovarioles.                                              
     3 ired for FSC daughters to migrate across the ovariole and on occasion to replace the opposite stem ce
  
  
  
  
  
  
  
  
    12 o somatic follicle stem cells (FSCs) in each ovariole give rise to all polar cells, stalk cells, and 
  
  
    15 tion was due to a reduction in the number of ovarioles in D. sechellia relative to its sister species
    16 ssed at the extreme apical end of Drosophila ovarioles in terminal filament cells and a newly identif
  
  
  
  
    21 stigated the genetic basis for plasticity of ovariole number and body size, as well the genetic basis
  
  
  
    25    While previously mapped factors affecting ovariole number appear to impact the rate of egg product
  
  
  
  
  
  
  
  
  
    35  genetic changes underlying species-specific ovariole number may alter the total number of TFCs avail
    36 t in these Drosophila lineages, reduction in ovariole number occurs primarily through variations in o
  
  
    39 tively large within-population variation for ovariole number suggest that substantial microhabitat va
    40  independently evolved a significantly lower ovariole number than the D. melanogaster Oregon R strain
  
    42 ontrast, temperature-dependent plasticity in ovariole number was due to changes in cell-cell sorting 
  
    44  and used to identify 34 candidate genes for ovariole number, a quantitative trait, in Drosophila mel
    45 ophila melanogaster, ovary size, measured as ovariole number, and body size, measured as thorax lengt
    46 of recombinant inbred lines were assayed for ovariole number, and QTL analyses for this trait identif
    47 dependent evolution of a reproductive trait, ovariole number, has resulted from changes in distinct d
    48  To study the genetic architecture of worker ovariole number, we performed a series of crosses betwee
  
  
  
  
  
    54 stinct developmental processes that regulate ovariole number: establishment of total TFC number, and 
    55  discuss how the phenotype of extreme worker ovariole numbers and the underlying genetic factors we i
    56 transgressive worker phenotypes with extreme ovariole numbers that were sensitive to the social envir
  
    58 The germarium, a structure at the tip of the ovariole of a Drosophila ovary, contains two follicle st
    59 tifying micrometastasis formation within the ovarioles of adult hosts after transplantation and deter
  
    61  susceptibility to I. fumosorosea, number of ovarioles, or ovipostioning were seen between any of the
    62 ific mapping between Drosophila sechellia (8 ovarioles/ovary) and D. simulans (15 ovarioles/ovary) id
    63 llia (8 ovarioles/ovary) and D. simulans (15 ovarioles/ovary) identified a major QTL on chromosome 3 
    64 insect reproductive organs and the number of ovarioles per ovary strongly influences egg-laying rate 
    65 ition, Cct1 mutants display a novel branched ovariole phenotype, demonstrating a requirement for this
    66 g (Hh) at the extreme anterior of Drosophila ovarioles suggests that it might provide an asymmetric c
  
    68 ce a range of phenotypes, including agametic ovarioles, tumorous egg chambers, and late stage oogenic
  
    70 one site) that differed by an average of 4.6 ovarioles were used to generate F1, F2 and backcross gen
    71 ries are composed of functional units called ovarioles, which contain sequentially developing egg cha
    72 ted by stem cell loss, we studied Drosophila ovarioles, which maintain two to three germ-line stem ce
    73 lls in the follicle cell layer of developing ovarioles with down-regulated expression of the major mi
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