ライフサイエンスコーパス: non-dividing

1 beta genes were expressed, gonadotropes were non-dividing.

2 crophage-tropic viral isolate in cultures of non-dividing and dividing cells.

3 Replication of HIV-1 in non-dividing and slowly proliferating cell populations d

4 cts YAP/TAZ activity to establish a group of non-dividing and specialized cells that constitute a sig

5 Moreover, the presence of non-dividing bacteria in vivo does not necessarily lead

6 y metabolism and identify a strategy to kill non-dividing bacteria.

7 r, SKu2-YFP foci formed in response to IR in non-dividing bacteroids, indicating that NHEJ system is

8 in activity in the double mutant converted a non-dividing cell into a novel highly proliferating cell

9 ocytes of Xenopus laevis, as an example of a non-dividing cell, is exclusive to the nuclear pore comp

10 levels of DRAP1 expression in differentiated non dividing cells.

11 s, are capable of efficiently replicating in non-dividing cells (terminally differentiated macrophage

12 Hypotonic stress to flattened, non-dividing cells activated no additional current.

13 ar macrophages as terminally differentiated, non-dividing cells and underscores biological difference

14 other lentiviruses are capable of infecting non-dividing cells and, therefore, need to be imported i

15 In general, non-dividing cells are likely to have low cellular dNTP

16 llow dividing cells to be distinguished from non-dividing cells by a greater than two-fold increase i

17 man immunodeficiency virus type 1 (HIV-1) in non-dividing cells critically depends on import of the v

18 man immunodeficiency virus type 1 (HIV-1) in non-dividing cells depends critically on import of the v

19 ral preintegration complex to the nucleus of non-dividing cells following virus entry.

20 hough H3.3-YFP deposition stably remained in non-dividing cells for days after IFN stimulation, it wa

21 The efficacy of in vivo transduction of non-dividing cells has been demonstrated in a wide varie

22 Cilia are found on most non-dividing cells in the human body and, when faulty, c

23 iviral (HIV)-based vector that can transduce non-dividing cells in vitro and deliver genes in vivo.

24 for robust DNA knock-in in both dividing and non-dividing cells in vitro and, more importantly, in vi

25 The data indicate that YycG activity in non-dividing cells is suppressed by its interaction with

26 s that could produce revertant phenotypes in non-dividing cells of both pro- and eukaryotes, we note

27 ortant mechanism for repairing DNA damage in non-dividing cells such as neurons.

28 iency virus type-1 (HIV-1) is able to infect non-dividing cells such as tissue macrophages productive

29 y type 1 (HIV-1) have the capacity to infect non-dividing cells such as tissue macrophages.

30 oliferation it is also strongly expressed in non-dividing cells undergoing DNA synthesis and repair.

31 Importantly, the rates of expansion in non-dividing cells were at least as high as those of pro

32 includes access of the pDNA to the nuclei of non-dividing cells where the presence of an intact nucle

33 BRCA2 is not expressed in the non-dividing cells, and expression is cell cycle stage-d

34 tion of most mammalian cell types, including non-dividing cells, and features are included that give

35 ions reveal a role of heterochronic genes in non-dividing cells, and provide an example of cell-auton

36 thrin-coated vesicles occurs continuously in non-dividing cells, but is shut down during mitosis, whe

37 herefore, SAMHD1 expression, particularly in non-dividing cells, can restrict retroviral infections s

38 upport long-term expression of transgenes in non-dividing cells, exhibiting a decreased risk of inser

39 ve cells in the late embryonic brainstem are non-dividing cells, presumably immature oligodendrocytes

40 (HIV-1) contributes to viral replication in non-dividing cells, specifically those of the myeloid li

41 iently deliver siRNAs into both dividing and non-dividing cells, stem cells, zygotes, and their diffe

42 Although expansions can accrue in non-dividing cells, we also show that cell cycle arrest

43 urrent tools are inefficient, especially for non-dividing cells, which compose most adult tissues.

44 of those prevailing either in cycling or in non-dividing cells.

45 g as replacement histone genes in long-lived non-dividing cells.

46 evelopment of gene-targeting applications in non-dividing cells.

47 tinuous accumulation of repeat expansions in non-dividing cells.

48 s of dGTP or GTP found in either dividing or non-dividing cells.

49 viability, homeostasis and DNA synthesis in non-dividing cells.

50 CF remains essential for TAD organization in non-dividing cells.

51 fficient long-term infection of dividing and non-dividing cells.

52 limitations, with good ability to transfect non-dividing cells.

53 (HIV-1), like other lentiviruses, can infect non-dividing cells.

54 tissues, the H2A-1 gene is expressed in many non-dividing cells.

55 is the ability of the virus to replicate in non-dividing cells.

56 eneration of mutant proteins in dividing and non-dividing cells.

57 nd the nuclear import of the viral genome in non-dividing cells.

58 or contains no viral genes and can transduce non-dividing cells.

59 upply the NLS(s) that enable HIV-1 to infect non-dividing cells.

60 % fewer secreted protein products than their non-dividing counterparts.

61 iability and accumulate small, nucleated and non-dividing daughter cells which remain attached to the

62 way as in mammals: the villi are lined with non-dividing differentiated cells, while cell division i

63 sly described InvEE transgenic mice in which non-dividing, differentiating epidermal cells express on

64 xpression is induced in an undifferentiated, non-dividing esophageal epithelial cell population in pa

65 proliferating wing disc cells but not in the non-dividing eye disc cells.

66 w that the siphon primordium arises within a non-dividing field of lateral-dorsal epidermis.

67 e a significant increase in gene transfer in non-dividing HeLa cells transiently transfected with pDN

68 used with human endothelial cells in stable, non-dividing, heterokaryons.

69 Dividing and non-dividing HSCs thus reside mainly in perisinusoidal n

70 ult to comprehensively localize dividing and non-dividing HSCs.

71 two H3K27Me3 demethylases, Jmjd3 and Utx, in non-dividing intrathymic CD4(+) T-cell precursors.

72 ltered during the formation of merozoites (a non-dividing, invasive, extracellular stage).

73 Most HSCs, both dividing (Ki-67(+)) and non-dividing (Ki-67(-)), were distant from arterioles, t

74 ranulosa cells to terminally differentiated, non-dividing luteal cells.

75 However, Ddb1 deletion in non-dividing lymphocytes has no discernible phenotypes.

76 fective in nuclear import and replication in non-dividing macrophage cultures, even when functional V

77 target cell types: terminally differentiated/non-dividing macrophages and activated/dividing CD4(+) T

78 Terminally differentiated/non-dividing macrophages contain extremely low cellular

79 HIV-1 reverse transcription, particularly in non-dividing macrophages.

80 ages replicating within red blood cells into non-dividing male and female gametocytes.

81 Infections of dividing PBMCs and non-dividing MDDCs were carried out with single-cycle an

82 These non-dividing, metabolically active cells are highly secr

83 helia may use the same mechanism to generate non-dividing, motile cells for wound repair.

84 ing NC cells maintained position relative to non-dividing neighbors.

85 new cell types should occur in multipotent, non-dividing neoblast progeny cells.

86 affecting large, terminally differentiated, non-dividing neuronal cells.

87 n the metabolically demanding environment of non-dividing neuronal, cardiac and pancreatic beta cells

88 ous system including their ability to infect non-dividing neurones and establish asymptomatic latent

89 ocedure that efficiently introduces DNA into non-dividing normal human and murine T lymphocytes while

90 mic and tightly regulated process in which a non-dividing oocyte is transformed into a rapidly dividi

91 find that FOXO1 is present in the nuclei of non-dividing pituitary cells during embryonic developmen

92 estes during a brief perinatal period in the non-dividing precursors of spermatogonial stem cells at

93 in function in diverse cell types, including non-dividing primary cells where genome- and RNA-targeti

94 nsduce a wide range of cell types, including non-dividing primary neurons and induced-pluripotent ste

95 However, non-dividing quiescent conidiospores of the Tyr15 mutant

96 changes are senescence-specific rather than non-dividing-related.

97 cyst lineage are anchored around the hub of non-dividing somatic cells located at the testis tip.

98 germination is a process in which quiescent, non-dividing spores become competent for mitotic cell di

99 d number of divisions in culture and enter a non-dividing state called replicative senescence.

100 in kinase involved in maintaining cells in a non-dividing state.

101 When stressed, bacteria can enter various non-dividing states, which are medically important.

102 of viral reverse transcription complexes in non-dividing target cells (e.g. terminally differentiate

103 Non-dividing terminally differentiated cells accumulate

104 In contrast, C. elegans PKC3 accumulates in non-dividing, terminally differentiated cells that will

105 pt recently has been shown to be enriched in non-dividing, terminally-differentiated cells.

106 ote and mammalian amastigote stages) and the non-dividing trypomastigote stage.

107 between these organs is always bounded by a non-dividing vulval cell.

108 ge and promotes increased integrin levels in non-dividing vulval cells, stabilizing gap position.