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1 ine stem cells are controlled by the somatic distal tip cell.
2 igrations of two specific gonadal cells, the distal tip cells.
3 and the gonad, in the spermatheca and at the distal tip cells.
4 utants, we find defects in the generation of distal tip cells, anchor cells, and spermatheca; three o
5 an inductive interaction between the somatic distal tip cell and the germ line.
6 s mitotic relies on induction by the somatic distal tip cell and the glp-1 signal transduction pathwa
7 stress, including stress fibers in migratory distal tip cells and the proximal gonad sheath, where it
8      Septin mutants affect morphology of the distal tip cells, as well as their migration and guidanc
9 l-most cells-cells that directly contact the distal tip cell body-relative to cells further proximal,
10                                          The distal tip cell (DTC) caps a blind-ended tube; only the
11                                  Analysis of distal tip cell (DTC) migration during gonadogenesis in
12 LH) transcription factor required for proper distal tip cell (DTC) migration.
13             Notch pathway signaling from the distal tip cell (DTC) niche to the germline maintains th
14 e proliferative fate is specified by somatic distal tip cell (DTC) niche-germline GLP-1 Notch signali
15                   The Caenorhabditis elegans distal tip cell (DTC) provides a niche for germline stem
16 stem, a single-celled mesenchymal niche, the distal tip cell (DTC), employs GLP-1/Notch signaling and
17 in many neurons, vulval precursor cells, the distal tip cell (DTC), intestine, and the lateral hypode
18 -1/TGFbetaR signaling cascade in the gonadal distal tip cell (DTC), the germline stem cell niche, whe
19  fates: only its distal daughter generates a distal tip cell (DTC), which is required for stem cell m
20 ue-specific expression of HA-betatail in the distal tip cells (DTC), the cells that direct gonad morp
21 point in the gonadal lineage both to specify distal tip cells (DTCs) and in DTC differentiation and f
22               The two specialized C. elegans distal tip cells (DTCs) provide an in vivo model system
23 pression is found in the hypodermis, muscle, distal tip cells (DTCs), and in neurons.
24 tion, and the gonad arm migration led by the distal tip cells (DTCs).
25 onad arms are determined by migration of the distal tip cells (DTCs).
26               In Caenorhabditis elegans, the distal tip cell/germline interaction promotes a mitotic
27                            The hermaphrodite distal tip cell (hDTC) also provides "leader" function t
28                       The putative posterior distal tip cell is then eliminated in all but one specie
29                          Therefore, the male distal tip cell (mDTC) serves as a niche but not as a le
30 ON-1, an ADAMTS family protease required for distal tip cell migration in C. elegans.
31  Both functions are required for nuclear and distal tip cell migrations, but only one is required for
32                                   Third, the distal tip cell niche extends processes that nearly enci
33 l syncytium and in the migrations of the two distal tip cells of the gonad.
34 eporter gene are expressed in the sheath and distal tip cells of the somatic gonad, the gut and other
35                                        These distal tip cell processes are likely to play a critical
36 urprisingly, proper oocyte growth depends on distal tip cell signaling involving the redundant functi
37 icroscopy was used to directly visualize the distal tip cell which extends tentacle-like processes th
38                 Each first gives rise to one distal tip cell (which promotes arm growth and germ line
39  The septins are also expressed in migrating distal tip cells, which are leaders for gonad arm extens

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