戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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 can (homotypic adhesion, planar contraction, non-dividing boundaries, constant signaling and majority
9 in activity in the double mutant converted a non-dividing cell into a novel highly proliferating cell
10 ocytes of Xenopus laevis, as an example of a non-dividing cell, is exclusive to the nuclear pore comp
11 levels of DRAP1 expression in differentiated non dividing cells.
12 s, are capable of efficiently replicating in non-dividing cells (terminally differentiated macrophage
13 le sensitivity to study somatic mutations in non-dividing cells across several tissues, comparing ste
14               Hypotonic stress to flattened, non-dividing cells activated no additional current.
15  end joining-based methods, with activity in non-dividing cells and in vivo with fewer detectable off
16 been shown to improve knock-in efficiency in non-dividing cells and to harness HDR after direct injec
17 ar macrophages as terminally differentiated, non-dividing cells and underscores biological difference
18  other lentiviruses are capable of infecting non-dividing cells and, therefore, need to be imported i
19                                  In general, non-dividing cells are likely to have low cellular dNTP
20                               HIV can infect non-dividing cells because the viral capsid can overcome
21 llow dividing cells to be distinguished from non-dividing cells by a greater than two-fold increase i
22          Lentiviruses, such as HIV-1, infect non-dividing cells by traversing the nuclear pore comple
23 man immunodeficiency virus type 1 (HIV-1) in non-dividing cells critically depends on import of the v
24 man immunodeficiency virus type 1 (HIV-1) in non-dividing cells depends critically on import of the v
25 ral preintegration complex to the nucleus of non-dividing cells following virus entry.
26 hough H3.3-YFP deposition stably remained in non-dividing cells for days after IFN stimulation, it wa
27      The efficacy of in vivo transduction of non-dividing cells has been demonstrated in a wide varie
28   We transcriptionally profiled dividing and non-dividing cells in regenerating stump tissues, as wel
29                      Cilia are found on most non-dividing cells in the human body and, when faulty, c
30 iviral (HIV)-based vector that can transduce non-dividing cells in vitro and deliver genes in vivo.
31 for robust DNA knock-in in both dividing and non-dividing cells in vitro and, more importantly, in vi
32 irectional DNA knock-in in both dividing and non-dividing cells in vivo.
33      The data indicate that YycG activity in non-dividing cells is suppressed by its interaction with
34 s that could produce revertant phenotypes in non-dividing cells of both pro- and eukaryotes, we note
35 ortant mechanism for repairing DNA damage in non-dividing cells such as neurons.
36 iency virus type-1 (HIV-1) is able to infect non-dividing cells such as tissue macrophages productive
37 y type 1 (HIV-1) have the capacity to infect non-dividing cells such as tissue macrophages.
38 nctional proteins after cell division and in non-dividing cells that elongated.
39  other lentiviruses mediate the infection of non-dividing cells through the ability of the capsid pro
40 oliferation it is also strongly expressed in non-dividing cells undergoing DNA synthesis and repair.
41       Importantly, the rates of expansion in non-dividing cells were at least as high as those of pro
42 includes access of the pDNA to the nuclei of non-dividing cells where the presence of an intact nucle
43 ersistent HIV reservoir in both dividing and non-dividing cells while avoiding immunogenicity.
44                                           In non-dividing cells with lengths increased to 10 times no
45 3, (2) animals can recover from silencing in non-dividing cells, and (3) cleavage and tailing of mRNA
46 ion of DNA damage and apoptosis, activity in non-dividing cells, and bystander activity.
47                BRCA2 is not expressed in the non-dividing cells, and expression is cell cycle stage-d
48 tion of most mammalian cell types, including non-dividing cells, and features are included that give
49 ions reveal a role of heterochronic genes in non-dividing cells, and provide an example of cell-auton
50 thrin-coated vesicles occurs continuously in non-dividing cells, but is shut down during mitosis, whe
51 herefore, SAMHD1 expression, particularly in non-dividing cells, can restrict retroviral infections s
52 upport long-term expression of transgenes in non-dividing cells, exhibiting a decreased risk of inser
53 efined nucleotide edits in both dividing and non-dividing cells, offering potential for correcting pa
54 her somatic expansion of the repeat tract in non-dividing cells, particularly striatal neurons, haste
55 ve cells in the late embryonic brainstem are non-dividing cells, presumably immature oligodendrocytes
56  (HIV-1) contributes to viral replication in non-dividing cells, specifically those of the myeloid li
57 cargoes up to 12 kb for stable expression in non-dividing cells, stem cells and primary human T cells
58 iently deliver siRNAs into both dividing and non-dividing cells, stem cells, zygotes, and their diffe
59  with fewer byproducts in slowly dividing or non-dividing cells, such as those that make up most of t
60  that this metabolic adaptation can occur in non-dividing cells, suggesting a role for the Warburg ef
61 While RNAi therapies are highly effective in non-dividing cells, their efficacy in rapidly dividing c
62            Although expansions can accrue in non-dividing cells, we also show that cell cycle arrest
63 ting module for selective gene expression in non-dividing cells, which allows us to radically alter p
64 urrent tools are inefficient, especially for non-dividing cells, which compose most adult tissues.
65 ess programmable integration in dividing and non-dividing cells, with both research and therapeutic a
66 , possibly resulting in neurodegeneration in non-dividing cells.
67 or contains no viral genes and can transduce non-dividing cells.
68 upply the NLS(s) that enable HIV-1 to infect non-dividing cells.
69 rent disease conditions and the existence of non-dividing cells.
70 CF remains essential for TAD organization in non-dividing cells.
71  to genome stability especially in slowly or non-dividing cells.
72 ich highlights the utility of cRNAs in these non-dividing cells.
73 ently extended silencing duration, unlike in non-dividing cells.
74 istone turnover, discriminating dividing and non-dividing cells.
75 ved site-specific integration frequencies in non-dividing cells.
76  creating a therapeutic window compared with non-dividing cells.
77  of those prevailing either in cycling or in non-dividing cells.
78 g as replacement histone genes in long-lived non-dividing cells.
79 evelopment of gene-targeting applications in non-dividing cells.
80 tinuous accumulation of repeat expansions in non-dividing cells.
81 s of dGTP or GTP found in either dividing or non-dividing cells.
82  viability, homeostasis and DNA synthesis in non-dividing cells.
83 fficient long-term infection of dividing and non-dividing cells.
84  limitations, with good ability to transfect non-dividing cells.
85 (HIV-1), like other lentiviruses, can infect non-dividing cells.
86 tissues, the H2A-1 gene is expressed in many non-dividing cells.
87  is the ability of the virus to replicate in non-dividing cells.
88 eneration of mutant proteins in dividing and non-dividing cells.
89 nd the nuclear import of the viral genome in non-dividing cells.
90 % fewer secreted protein products than their non-dividing counterparts.
91 iability and accumulate small, nucleated and non-dividing daughter cells which remain attached to the
92  way as in mammals: the villi are lined with non-dividing differentiated cells, while cell division i
93 le the 'differentiation-tRNAs' are active in non-dividing, differentiated cells.
94 sly described InvEE transgenic mice in which non-dividing, differentiating epidermal cells express on
95 xpression is induced in an undifferentiated, non-dividing esophageal epithelial cell population in pa
96 proliferating wing disc cells but not in the non-dividing eye disc cells.
97 w that the siphon primordium arises within a non-dividing field of lateral-dorsal epidermis.
98 e a significant increase in gene transfer in non-dividing HeLa cells transiently transfected with pDN
99 duction of transient DNA repair signaling in non-dividing hepatocytes was responsible for enhancing A
100  a strategy to prolong silencing duration in non-dividing hepatocytes, had minimal impact on siRNA ef
101 used with human endothelial cells in stable, non-dividing, heterokaryons.
102                                 Dividing and non-dividing HSCs thus reside mainly in perisinusoidal n
103 ult to comprehensively localize dividing and non-dividing HSCs.
104 two H3K27Me3 demethylases, Jmjd3 and Utx, in non-dividing intrathymic CD4(+) T-cell precursors.
105 ltered during the formation of merozoites (a non-dividing, invasive, extracellular stage).
106      Most HSCs, both dividing (Ki-67(+)) and non-dividing (Ki-67(-)), were distant from arterioles, t
107 ranulosa cells to terminally differentiated, non-dividing luteal cells.
108                    However, Ddb1 deletion in non-dividing lymphocytes has no discernible phenotypes.
109 fective in nuclear import and replication in non-dividing macrophage cultures, even when functional V
110 target cell types: terminally differentiated/non-dividing macrophages and activated/dividing CD4(+) T
111                    Terminally differentiated/non-dividing macrophages contain extremely low cellular
112 HIV-1 reverse transcription, particularly in non-dividing macrophages.
113 ages replicating within red blood cells into non-dividing male and female gametocytes.
114             Infections of dividing PBMCs and non-dividing MDDCs were carried out with single-cycle an
115                                        These non-dividing, metabolically active cells are highly secr
116            We discovered that CD36-dependent non-dividing, metastasis-initiating tumour cells require
117 helia may use the same mechanism to generate non-dividing, motile cells for wound repair.
118 ing NC cells maintained position relative to non-dividing neighbors.
119  new cell types should occur in multipotent, non-dividing neoblast progeny cells.
120  affecting large, terminally differentiated, non-dividing neuronal cells.
121 n the metabolically demanding environment of non-dividing neuronal, cardiac and pancreatic beta cells
122 ous system including their ability to infect non-dividing neurones and establish asymptomatic latent
123  the DAN marker tyrosine hydroxylase (TH) in non-dividing neurons, which was associated with an incre
124 ocedure that efficiently introduces DNA into non-dividing normal human and murine T lymphocytes while
125 process in sexual reproduction, as a diploid non-dividing oocyte is transformed into a haploid fertil
126 mic and tightly regulated process in which a non-dividing oocyte is transformed into a rapidly dividi
127  find that FOXO1 is present in the nuclei of non-dividing pituitary cells during embryonic developmen
128 estes during a brief perinatal period in the non-dividing precursors of spermatogonial stem cells at
129 ey also steal a transcriptionally active but non-dividing prey nucleus, the kleptokaryon, from certai
130 in function in diverse cell types, including non-dividing primary cells where genome- and RNA-targeti
131  three human cell lines, primary T cells and non-dividing primary human hepatocytes.
132 nsduce a wide range of cell types, including non-dividing primary neurons and induced-pluripotent ste
133 ated in the more-internal domain of radially non-dividing procambial cells by the function of auxin,
134                                     However, non-dividing quiescent conidiospores of the Tyr15 mutant
135  changes are senescence-specific rather than non-dividing-related.
136  cyst lineage are anchored around the hub of non-dividing somatic cells located at the testis tip.
137 germination is a process in which quiescent, non-dividing spores become competent for mitotic cell di
138 d number of divisions in culture and enter a non-dividing state called replicative senescence.
139 in kinase involved in maintaining cells in a non-dividing state.
140    When stressed, bacteria can enter various non-dividing states, which are medically important.
141                                           In non-dividing stationary phase cells, Pol4-mediated non-h
142  of viral reverse transcription complexes in non-dividing target cells (e.g. terminally differentiate
143                                              Non-dividing terminally differentiated cells accumulate
144  In contrast, C. elegans PKC3 accumulates in non-dividing, terminally differentiated cells that will
145 pt recently has been shown to be enriched in non-dividing, terminally-differentiated cells.
146  While LLPC, by definition, are quiescent or non-dividing, the majority of blood ASC are thought to b
147 ote and mammalian amastigote stages) and the non-dividing trypomastigote stage.
148  between these organs is always bounded by a non-dividing vulval cell.
149 ge and promotes increased integrin levels in non-dividing vulval cells, stabilizing gap position.

 
Page Top