ライフサイエンスコーパス: tapetal cell

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1 arietal cells then predominantly to daughter tapetal cells.

2 ollen coat and premature degeneration of the tapetal cells.

3 lationship between the development of ml and tapetal cells.

4 densely stained cytoplasm typical of normal tapetal cells.

5 within the large cytoplasmic lipid bodies of tapetal cells.

6 ) are contributed by surrounding sporophytic tapetal cells.

7 localized to endoplasmic reticulum of anther tapetal cells.

8 me genes may be expressed in the sporophytic tapetal cells and in gametophytic tissues, they are regu

9 Transgenic plants exhibited GUS activity in tapetal cells and pollen of the developing anthers indic

10 that produces excess microsporocytes, lacks tapetal cells, and abnormally maintains middle layer cel

11 Unusually for plants, tapetal cells are specified very early in development, a

12 ly from the mitochondria into the cytosol of tapetal cells before the gross morphological changes ass

13 mal and 24-nt meiotic phasiRNAs dependent on tapetal cell differentiation.

14 These lipids are released following tapetal cell disintegration and are relocated to form th

15 indicated that the protein is secreted from tapetal cells during the early microspore stage.

16 is targeted to the endoplasmic reticulum in tapetal cells in vivo.

17 The ablation of tapetal cells interferes with pollen production and resu

18 to suppress trans-differentiation of somatic tapetal cells into meiocytes, we find that mac1 anthers

19 tion and inhibits periclinal division once a tapetal cell is specified.

20 equence of the premature degeneration of the tapetal cell layer during microspore development.

21 e 6 anthers and are more concentrated in the tapetal cell layer later.

22 ouble mutant anthers lack development of the tapetal cell layer, which accounts for the microspore ab

23 not RF2B, accumulates to high levels in the tapetal cells of anthers.

24 ese vacuolar inclusions were not observed in tapetal cells of double mutants of abcg26 and genes enco

25 accumulate to high levels in rapidly growing tapetal cells of pea anthers.

26 microspores/ pollen grains (gametophyte) and tapetal cells (sporophyte) of B. napus.

27 e differentiation of the microsporocytes and tapetal cells, suggesting that EMS1 mediates signals tha

28 morphology beginning at anther stage 4, with tapetal cells that have excess and/or enlarged vacuoles

29 ail to elongate, and there are fewer, larger tapetal cells that retain, rather than secrete, their co

30 ere ABCG26-exported polyketides traffic from tapetal cells to form the sporopollenin backbone, in coo

31 nsport and assembly of exine components from tapetal cells to microspores in the intact anthers of Ar

32 asm in sunflower causes premature PCD of the tapetal cells, which then extends to other anther tissue

33 ned by biphasic protein expression in anther tapetal cells, with an initial peak around pollen meiosi

34 n, accumulated large fluorescent vacuoles in tapetal cells, with corresponding loss of fluorescence o

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