ライフサイエンスコーパス: postmitotic cell

1 t embryonic day 13.5 (E13.5) in a cluster of postmitotic cells.

2 he dynamics of intracellular heteroplasmy in postmitotic cells.

3 ene expression was restricted to suprabasal, postmitotic cells.

4 lls were detected at the abembryonic pole in postmitotic cells.

5 iched at the centrosome both in dividing and postmitotic cells.

6 hey arrest and terminally differentiate into postmitotic cells.

7 feasibility of Cre-mediated recombination in postmitotic cells.

8 ropism and an ability to infect quiescent or postmitotic cells.

9 k inhibitors, and thus its ability to act in postmitotic cells.

10 proliferating cells but also in nondividing postmitotic cells.

11 been identified in extracellular matrices or postmitotic cells.

12 share protein derangements and attrition of postmitotic cells.

13 n the absence of Notch1 in mitotic and newly postmitotic cells.

14 igase that is active both in dividing and in postmitotic cells.

15 viewed as a highly stable epigenetic mark in postmitotic cells.

16 ed to block enucleation proper when added to postmitotic cells.

17 Cell columns form due to the properties of postmitotic cells.

18 ssociated with the initial migrations of the postmitotic cells.

19 be achieved by preventing apoptotic death of postmitotic cells.

20 itors that repeatedly divide to give rise to postmitotic cells.

21 erges at distinct embryonic ages and only in postmitotic cells.

22 similarity in the regulation of apoptosis in postmitotic cells.

23 ic regional identity in late-differentiating/postmitotic cells.

24 hypothesize that CDK2 may have a function in postmitotic cells.

25 undiscovered physiological role for CDK2 in postmitotic cells.

26 provides a mechanism of estrogen delivery to postmitotic cells.

27 d suggest an essential role for TRF2 even in postmitotic cells.

28 he terminal differentiation process of these postmitotic cells.

29 ool, whereas asymmetrical divisions generate postmitotic cells, although this remains to be proved.

30 H3K9me3/S10ph modification in differentiated postmitotic cells and also results in delocalisation of

31 ng telencephalon, p19(INK4d) is expressed by postmitotic cells and has a characteristic perinuclear d

32 de that LRCs in adult TECs are not senescent postmitotic cells and may represent the elusive progenit

33 ember of the cdk family, is active mainly in postmitotic cells and plays important roles in neuronal

34 vealed an underlying defect in the stream of postmitotic cells and secondary dentate progenitor cells

35 spinal cord, Dll1 and Dll3 are expressed by postmitotic cells and suggest that expression is sequent

36 hed in sensory components and coincided with postmitotic cells and the initiation of overt differenti

37 e boundary between the mantle layer of newly postmitotic cells and the posterior, epithelial region o

38 e when neurons exit the cell cycle to become postmitotic cells, and it is generally accepted that, on

39 h transduction efficiency, ability to infect postmitotic cells, and large packaging capacity.

40 xit in cardiac muscle, induce hypertrophy in postmitotic cells, and promote cardiac myocyte survival.

41 (a small cluster of neuroepithelial cells), postmitotic cells appeared first in the ganglion cell la

42 nscription factors in neural progenitors and postmitotic cells are key regulators in this process.

43 n to be a mix of neural progenitor cells and postmitotic cells at different stages of neural and glia

44 ific expression patterns emerge, however, as postmitotic cells become organized into layers.

45 ecruit stem cells to replace differentiated, postmitotic cells, but the capacity of an organ's differ

46 ogenitors at E10.5, it becomes restricted to postmitotic cells by E15.5.

47 murine embryogenesis, Brn-3c is expressed in postmitotic cells committed to hair cell phenotype but n

48 Thus, both mitotic and postmitotic cells decrease in size during spinal cord de

49 ater role than PAN1 in directing patterns of postmitotic cell expansion that determine the shapes of

50 As a first step, a postmitotic cell extends its leading process, presumably

51 quence-binding protein 2 (Satb2), regulate a postmitotic cell fate choice between these subtypes.

52 or maintaining a balance between mitotic and postmitotic cell fates in development of the mammalian s

53 we present evidence that the progenitor and postmitotic cells flanking the pallial/subpallial bounda

54 Nucleoli continued to diminish in postmitotic cells following fate specification.

55 egeneration, and highlight the importance of postmitotic cell growth in gut epithelial repair.

56 types, a functional role for the complex in postmitotic cells has been elusive.

57 mely susceptible to apoptotic signals, while postmitotic cells have developed several strategies to p

58 ng methods that label both proliferative and postmitotic cells have found that cortical interneurons

59 It has been thought that differentiated postmitotic cells have their genomes hard wired, with li

60 , although expression of p21 is increased in postmitotic cells immediately adjacent to the proliferat

61 uced efficiently in vivo in both mitotic and postmitotic cells in all tissues examined.

62 Math5 expression was restricted to postmitotic cells in developing retina, suggesting that

63 Because postmitotic cells in higher eukaryotes often do not star

64 s as a bilaterally symmetric condensation of postmitotic cells in the deep layers of the anterior reg

65 e II DNA topoisomerase normally expressed in postmitotic cells in the developing cortex, severely aff

66 ast, PACAP mRNA was localized exclusively in postmitotic cells in the dorsolateral parts of the rhomb

67 ear involvement of miRs in the physiology of postmitotic cells in vivo.

68 Excitable, postmitotic cells, in response to sublethal noxious stre

69 tand the protein composition of these unique postmitotic cells, in which irreversible protein degrada

70 Some ATR-sensitive expansion occurs in postmitotic cells including haploid gametes suggesting t

71 ively in males and localizes to telomeres in postmitotic cells, including mature sperm.

72 xpression of transgenes in both dividing and postmitotic cells, including preimplantation embryos.

73 s by a gene product expressed exclusively in postmitotic cells indicates a long-range effect of trans

74 clusively in a nonquiescent subpopulation of postmitotic cells, indicating an asymmetrical distributi

75 We suggest that postmitotic cells influence progenitor cell fate decisio

76 ng that the growth of a key compartment of a postmitotic cell involves an extensive switch in gene ex

77 Cell cycle withdrawal in postmitotic cells involves cyclin-dependent kinase (Cdk)

78 The efficient delivery of foreign genes into postmitotic cells is becoming very important for studies

79 in stem cell formation; however, its role in postmitotic cells is largely unknown.

80 However, the fate of nuclear pores in postmitotic cells is unknown.

81 espite a down-regulation of CDK2 activity in postmitotic cells, many cell types, including muscle cel

82 well as the expression of proliferative and postmitotic cell markers at E10.5-E11.5.

83 The first bromodeoxyuridine-negative (postmitotic) cells occupied the ganglion cell layer of v

84 ion in the cerebral wall is most abundant in postmitotic cells of the cortical plate and absent from

85 he outer external granule layer (EGL) and in postmitotic cells of the inner EGL, but not in mature gr

86 , the expression of which is enriched in the postmitotic cells of the intestinal epithelium.

87 hair growth cycle, PAI-2 was limited to the postmitotic cells of the outer root sheath directly abut

88 -lived proteins (ELLPs) did not turn over in postmitotic cells of the rat central nervous system.

89 how that Pk1 transcripts are detected in the postmitotic cells of the subplate and cortical plate dur

90 o that of extracts derived from the entirely postmitotic cells of young and senescent adults.

91 erative diseases by activating cell death in postmitotic cells or shifting the normal balance of mito

92 anoparticles may facilitate gene transfer in postmitotic cells, permitting nuclear uptake across the

93 take revealed that RA exerts its effect on a postmitotic cell population within the developing retina

94 different intervals postinjection to follow postmitotic cells' positional changes.

95 Antagonizing miR-24 restores postmitotic cell proliferation and enhances fibroblast p

96 s, but their genomic targets and function in postmitotic cells remain poorly understood.

97 ion of proteins in an SDS-insoluble state in postmitotic cells represents a novel autophagic cargo pr

98 -induced Ngf gene expression was detected in postmitotic cells, required new protein synthesis and wa

99 associated with dysfunction and loss of the postmitotic cells residing within this tissue.

100 netoplasts and nuclei were misaligned in the postmitotic cells, resulting in partial cleavage furrow

101 own regarding the effect these drugs have on postmitotic cells such as neurons.

102 but little is known about their functions in postmitotic cells such as neurons.

103 RATIONALE: Postmitotic cells, such as cardiomyocytes, seem to be pa

104 miRNAs also occur in postmitotic cells, such as neurons in the mammalian cent

105 implementing particular genetic programs in postmitotic cells, such as reelin expression in Cajal-Re

106 gh the presence of some of these isoforms in postmitotic cells suggests a role in controlling cell gr

107 Neurons are postmitotic cells that foster virus persistence.

108 essed at embryonic day 14 (E14), but only in postmitotic cells that have acquired a neuronal fate.

109 ular Tax1 on gene expression in NT2-N cells, postmitotic cells that share morphologic, phenotypic, an

110 it nuclear activities of PML and PML/RARA in postmitotic cells through CyPN-dependent cytoplasmic seq

111 le in epidermis regulating the conversion of postmitotic cells to differentiating ones.

112 ore, TGFbeta and growth pathways interact in postmitotic cells to precisely coordinate cell-specific

113 constitute the differentiation program of a postmitotic cell type.

114 e into neuronal, intestinal, and other known postmitotic cell types and are distributed throughout th

115 scripts accumulate in both proliferating and postmitotic cell types of Arabidopsis plants.

116 retina guide the genesis and distribution of postmitotic cell types, as well as their connectivity.

117 ventricular zones has commenced, individual postmitotic cells undergo directed migrations along the

118 ate regulator, Notch1, were studied in newly postmitotic cells using a conditional allele of Notch1 (

119 assified further by testing for an effect in postmitotic cells using the sev-GAL4 driver, by testing

120 meostasis and function, thus rendering these postmitotic cells vulnerable to premature death in retin

121 ifferentiation to hair cells of the normally postmitotic cells was restricted to the Lgr5-positive po

122 The first postmitotic cells were found in the retinal ganglion cel

123 BrdU analysis revealed that only a subset of postmitotic cells were induced to activate apoptosis.

124 and since no mitoses and only rare possible postmitotic cells were scored, postmitotic NE re-assembl

125 To investigate cohesin's function in postmitotic cells, where it is widely expressed, we have

126 es in turn specify the identity of any given postmitotic cell, which is evident by its cellular morph

127 ry persists within one cell generation or in postmitotic cells, while long-term memory can survive mu

128 Podocytes are highly differentiated, postmitotic cells, whose function is largely based on th

129 Ectopic activation of Notch1 in postmitotic cells within the nail keratogenous zone resu

130 during the transition from proliferating to postmitotic cells within the zebrafish retina.

131 e kinetics, especially a rapid production of postmitotic cells, within a discrete portion of the tele