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1 s a decrease in programmed cell death in the germarium.
2 cap cells located at the anterior tip of the germarium.
3 matic stem cell niche in the D. melanogaster germarium.
4 n may be distributed throughout the anterior germarium.
5 early germ cells correctly at the tip of the germarium.
6 distinguished when egg chambers bud from the germarium.
7 -beta (encoded by dpp) as such a molecule in germarium.
8 down may regulate germ cell divisions in the germarium.
9 omponents of the hh signaling pathway in the germarium.
10 ing of selective replication of mtDNA in the germarium.
11  hh affects somatic cells in region 2 of the germarium, 2-5 cells away from the cells in which Hh pro
12 fication of somatic cells in region 2 of the germarium, 2-5 cells away from the hh-expressing cells.
13                                          The germarium, a structure at the tip of the ovariole of a D
14 re expressed in somatic cells throughout the germarium and in developing egg chambers, with ptc expre
15  and in adult somatic cells of the posterior germarium and the follicular poles.
16 : (1) the region 2a/2b transition within the germarium, and (2) stage 8 egg chambers that are enterin
17 oth of these subgroups are determined in the germarium, and both cease division early in oogenesis.
18 of the presumptive oocyte in region 3 of the germarium, and the cell exits meiosis and becomes a nurs
19 in the differentiating follicle cells in the germarium, as determined by in situ hybridization.
20 C is expressed in proliferating cells in the germarium, as well as in the main body follicle cells.
21 resulted in reduced mtDNA replication in the germarium at the restrictive temperature.
22                                       In the germarium Bic-D is required for the organization of the
23          In the ovary, SYX is present in the germarium, but it is predominantly localized to nurse ce
24           These include an early role in the germarium for specification of stalk cells and a later r
25  cap cells (CpCs) at the anterior tip of the germarium form an environmental niche for germline stem
26 ormation, and postulate that it functions in germarium intercyst cells that are required for polar ce
27 tes in the pupal ovary, where the developing germarium is shaped by the basal stalk, a stack of cells
28            As meiotic cysts move through the germarium, microtubule minus ends progressively focus to
29 cells, impairs pFC differentiation, disrupts germarium morphology, and decreases fecundity.
30 follicle stem cells (FSCs) in the Drosophila germarium, necessitating careful control of signal gener
31                                       In the germarium of the Drosophila ovary, germline cysts are en
32                     Initially, somatic inner germarium sheath cells enter the empty niche, respond to
33  before oocyte determination during the late germarium stage and was dependent on mitochondrial fitne
34 naling from cells near the apical tip of the germarium stimulates the proliferation and specification
35 essed in additional somatic cells within the germarium, suggesting that Dpp protein may be distribute
36                     Gaps first appear in the germarium, suggesting that some nurse cells lack affinit
37 lation mechanisms explored in the Drosophila germarium through fluorescent immunohistochemistry.
38  non-autonomous role in somatic cells in the germarium to influence the differentiation of early germ
39  cyst flattens as it enters region 2b of the germarium to place the two pro-oocytes in the centre of
40     Using only published imaging data in the germarium, we first evaluated support for a published in
41 ne cysts at the region 2a/2b boundary of the germarium, while da overexpression leads to postmitotic
42 ngrailed (en) is co-expressed with hh in the germarium, while patched (ptc) and cubitus interruptus (

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