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1 tial cell divisions, and fail to undergo the intercalary and stacking behaviors essential for normal
2 and adherens junction proteins and polarized intercalary behavior is disrupted in baz mutants.
3 ion of FGF signaling is sufficient to induce intercalary behaviors in cells that have not received No
4 ries: (i) at or near to the centromere, (ii) intercalary between markers UL-Thin5 and Xgwm1130 and (i
5                                           In intercalary growing cells, the normal actin organization
6                                              Intercalary growth (epimorphic regeneration), which prev
7                                         This intercalary growth in a restricted space results in the
8  mutants as well as for the relative lack of intercalary heterocysts in patA mutants.
9 which is necessary for the formation of most intercalary heterocysts, or hetF resulted in an increase
10 R fusion does not result in the formation of intercalary heterocysts.
11 nderstanding of growth and exocytosis during intercalary hyphal extension, subapical branch initiatio
12 rns that are consistent with the presence of intercalary inversions.
13 B is also required for proper development of intercalary, labral and mandibular structures.
14 s more slowly, when the repeats are found at intercalary locations.
15     RPA1 mRNA levels increase rapidly in the intercalary meristem during submergence and treatment wi
16 ed a number of genes whose expression in the intercalary meristem is regulated by GA.
17 nes that are differentially expressed in the intercalary meristem of deepwater rice (Oryza sativa L.)
18 e primary target tissue for GA action is the intercalary meristem of the internode.
19 hich all contained MLG) and in E. fluviatile intercalary meristems and callus (which lacked MLG).
20 aging experiments show that FGF controls the intercalary movements of ventral neural progenitors, whe
21 sults indicate that the development of these intercalary neuromasts occurs principally because of the
22 rmally make only a minor contribution to the intercalary regenerate, but if transplanted cells are ex
23 ied polar coordinate model, and the rules of intercalary regeneration, as defined by French et al. Th
24 ibular identity, and labial is necessary for intercalary segment identity.
25  domain in crustaceans and in the homologous intercalary segment of insects suggests that the lab gen
26 o the filament ends, a process which we term intercalary subunit exchange.

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