ライフサイエンスコーパス: symmetric division

1 division, or an ISC becoming two EEs through symmetric division.

2 are kept firmly within this plane to give a symmetric division.

3 whose expression accumulates just before the symmetric division.

4 ated concurrently by asymmetric and terminal symmetric divisions.

5 s were present and replaced through periodic symmetric divisions.

6 top hierarchical HSCs preferentially undergo symmetric divisions.

7 , glioblasts underwent a prolonged series of symmetric divisions.

8 press neurog1 inside the placode, and apical symmetric divisions amplify the specified pool.

9 e-assisted laser inactivation created a more symmetric division and allowed the survival and differen

10 he adult SVZ, and the transient increases in symmetric division and neuronal differentiation may resu

11 Intestinal stem cells (ISCs) undergo symmetric division and neutral drift dynamics to renew t

12 divisions where loss of TOE-2 led to a more symmetric division and to survival of the smaller Q.a da

13 An initial amplification occurs through symmetric divisions and is followed by a switch to asymm

14 In mes-1 embryos, P(2) and P(3) undergo symmetric divisions and partition germ granules to both

15 the capacity to propagate themselves through symmetric divisions and to divide asymmetrically to enge

16 limited tumor-propagating capacity, undergo symmetric division, and are sensitive to castration.

17 ular zone, differentiated astrocytes undergo symmetric division, and their progeny integrate function

18 xpansion in number and have reduced rates of symmetric division as well as reduced insulin signaling.

19 These precursors undergo nonapical symmetric division at the laminar location where mature

20 precursor cell identity that leads to extra symmetric divisions at the end of the cell lineage.

21 matal patterning by permitting only a single symmetric division before stomata differentiate.

22 re that, contrarily to other eukaryotes with symmetric division, budding yeast keeps the nascent tran

23 showing TuJ1 immunoreactivity in cells with symmetric division but not cells with asymmetric divisio

24 olon stem cells (ISCs) predominantly undergo symmetric division but turn on asymmetric division to cu

25 A;1, with medium levels being sufficient for symmetric divisions but high levels being required for f

26 We demonstrate how symmetric divisions can work to stabilize paw epidermis

27 rsity and epithelial stratification, whereas symmetric divisions contribute to tissue growth, spreadi

28 quiring mutations that permit asymmetric and symmetric division, converting the host immune attack to

29 cell precursors (GCPs) undergo predominantly symmetric division during postnatal development; (2) clo

30 Thus, control of symmetric division, essential for neuroepithelial stem c

31 that superficial cells renew their number by symmetric division, express mesenchymal stem cell marker

32 celerated division rates and predominance of symmetric division fates.

33 rating zone of the Arabidopsis root, regular symmetric divisions give rise to patterns of parallel fi

34 These mirror-symmetric divisions have powerful morphogenetic influenc

35 Furthermore, these mirror-symmetric divisions have powerful morphogenetic influenc

36 testinal progenitor cells and promotes their symmetric division in response to nutrients, defining a

37 growth in the heart, decreased proliferative symmetric divisions in brain neural progenitors, and inc

38 e TONNEAU1a (TON1a) gene display misoriented symmetric divisions in the epidermis and have no divisio

39 itiated cell capable of clonal expansion via symmetric division is predicted to occur with a frequenc

40 ell is reduced coincident with the number of symmetric divisions it must perform.

41 rd cells of a stoma are produced by a single symmetric division just before terminal differentiation.

42 orientation is orthogonal to cell polarity, symmetric division occurs.

43 fferentiating stem cells are replaced by the symmetric division of adjacent stem cells.

44 C5aR1 inhibition reducing proliferation and symmetric division of apical neural progenitors in human

45 We show limited, life-long, symmetric division of cardiomyocytes as a rare event tha

46 toreceptors of the same type are produced by symmetric division of dedicated precursors.

47 , we found that loss of Neur activity causes symmetric division of GMC-1 into two RP2s.

48 te GMC-1 causes mis-localization of Insc and symmetric division of GMC-1 to generate two RP2s.

49 central position of the spindle and ensures symmetric division of mouse zygotes.

50 ic division at both poles of the cell and by symmetric division of the endospores at an early stage o

51 raction with the SCMC and their roles in the symmetric division of the zygote in early mouse developm

52 h-frequency stimulation of the ATN increases symmetric divisions of a defined class of neural progeni

53 ike cells in the dentate gyrus but increases symmetric divisions of an early progenitor cell class.

54 cell cycle duration in the cortex and during symmetric divisions of epidermal cells was constant and

55 its adult body plan through the bilaterally symmetric divisions of mesodermal proteloblast DM'' and

56 and NUMB(+) cells, indicating an increase in symmetric divisions of putative cancer stem cells.

57 In contrast, in symmetric divisions, old and young centrosomes are thoug

58 radioresistance, a shift from asymmetric to symmetric division or a fast cycle of GSCs following fra

59 n how they respond to the signals that guide symmetric division orientation during patterning might p

60 , defining the abembryonic pole, forms where symmetric divisions predominate.

61 nd notable regional differences, in terms of symmetric division ratio, have been noted-higher in thic

62 cleavage orientations produce asymmetric and symmetric divisions, respectively.

63 ed that less than 10% of radial glia undergo symmetric divisions resulting in two radial glia, wherea

64 NE cells undergoing proliferative, symmetric divisions retract their basal processes, and b

65 In addition to multiple, synchronous, and symmetric divisions, single-sorted CD34(+)/CD38(-) cells

66 ible explanation is that daughter cells of a symmetric division subsequently adopt differing cell fat

67 ng divisions but were more likely to undergo symmetric divisions that expanded the oRG population, as

68 x2 levels in individual blastomeres promotes symmetric divisions, thereby allocating more cells to th

69 maize leaf epidermis, without affecting the symmetric divisions through which most epidermal cells a

70 Stem cells switch between asymmetric and symmetric division to expand in number as tissues grow d

71 upted epithelial cell polarity, and enhanced symmetric division to expand the stem cell population.

72 is, guard mother cells undergo a stereotyped symmetric division to form the guard cells of stomata.

73 Neural progenitors can undergo symmetric divisions to expand cell population or asymmet

74 However, stem cells are also capable of symmetric division where both daughters remain stem cell

75 After an initial phase of symmetric divisions which causes an increase in their ow

76 ropose that this dynamic mechanism maintains symmetric divisions while allowing the quick adjustment

77 visions of MGE progenitor cells, followed by symmetric divisions within the subventricular zone.