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1 altered nuclear architecture in a postnatal, postmitotic cell.
2  are often expressed in both progenitors and postmitotic cells.
3 he terminal differentiation process of these postmitotic cells.
4 t embryonic day 13.5 (E13.5) in a cluster of postmitotic cells.
5 he dynamics of intracellular heteroplasmy in postmitotic cells.
6 ene expression was restricted to suprabasal, postmitotic cells.
7 lls were detected at the abembryonic pole in postmitotic cells.
8 hey arrest and terminally differentiate into postmitotic cells.
9 feasibility of Cre-mediated recombination in postmitotic cells.
10 ropism and an ability to infect quiescent or postmitotic cells.
11 k inhibitors, and thus its ability to act in postmitotic cells.
12 ore than a bystander role in SBMA-vulnerable postmitotic cells.
13 l networks that regulate rapid remodeling in postmitotic cells.
14                                  Neurons are postmitotic cells.
15 lular material is scarce and of non-cycling, postmitotic cells.
16 erent developmental stages, though mostly in postmitotic cells.
17 and cristae invagination in tissues with old postmitotic cells.
18 iched at the centrosome both in dividing and postmitotic cells.
19  proliferating cells but also in nondividing postmitotic cells.
20 been identified in extracellular matrices or postmitotic cells.
21  share protein derangements and attrition of postmitotic cells.
22 n the absence of Notch1 in mitotic and newly postmitotic cells.
23 igase that is active both in dividing and in postmitotic cells.
24 viewed as a highly stable epigenetic mark in postmitotic cells.
25 ed to block enucleation proper when added to postmitotic cells.
26   Cell columns form due to the properties of postmitotic cells.
27 ssociated with the initial migrations of the postmitotic cells.
28 erges at distinct embryonic ages and only in postmitotic cells.
29 be achieved by preventing apoptotic death of postmitotic cells.
30 itors that repeatedly divide to give rise to postmitotic cells.
31  is particularly crucial for interactions of postmitotic cells.
32 similarity in the regulation of apoptosis in postmitotic cells.
33 ic regional identity in late-differentiating/postmitotic cells.
34 hypothesize that CDK2 may have a function in postmitotic cells.
35  undiscovered physiological role for CDK2 in postmitotic cells.
36 provides a mechanism of estrogen delivery to postmitotic cells.
37 is, and induces an aberrant NE morphology in postmitotic cells.
38 d suggest an essential role for TRF2 even in postmitotic cells.
39 ool, whereas asymmetrical divisions generate postmitotic cells, although this remains to be proved.
40 H3K9me3/S10ph modification in differentiated postmitotic cells and also results in delocalisation of
41 ng telencephalon, p19(INK4d) is expressed by postmitotic cells and has a characteristic perinuclear d
42 de that LRCs in adult TECs are not senescent postmitotic cells and may represent the elusive progenit
43 ember of the cdk family, is active mainly in postmitotic cells and plays important roles in neuronal
44 vealed an underlying defect in the stream of postmitotic cells and secondary dentate progenitor cells
45  spinal cord, Dll1 and Dll3 are expressed by postmitotic cells and suggest that expression is sequent
46 hed in sensory components and coincided with postmitotic cells and the initiation of overt differenti
47 e boundary between the mantle layer of newly postmitotic cells and the posterior, epithelial region o
48 ding of NPC maintenance in proliferating and postmitotic cells, and how malfunction of nucleoporins (
49 e when neurons exit the cell cycle to become postmitotic cells, and it is generally accepted that, on
50 h transduction efficiency, ability to infect postmitotic cells, and large packaging capacity.
51 xit in cardiac muscle, induce hypertrophy in postmitotic cells, and promote cardiac myocyte survival.
52  (a small cluster of neuroepithelial cells), postmitotic cells appeared first in the ganglion cell la
53 nscription factors in neural progenitors and postmitotic cells are key regulators in this process.
54                      Long-lived proteins, in postmitotic cells, are particularly difficult to elimina
55                   Many adult tissues contain postmitotic cells as old as the host organism.
56 n to be a mix of neural progenitor cells and postmitotic cells at different stages of neural and glia
57 ific expression patterns emerge, however, as postmitotic cells become organized into layers.
58 ecruit stem cells to replace differentiated, postmitotic cells, but the capacity of an organ's differ
59 ogenitors at E10.5, it becomes restricted to postmitotic cells by E15.5.
60 s now established that fully differentiated, postmitotic cells can also acquire a senescence phenotyp
61 murine embryogenesis, Brn-3c is expressed in postmitotic cells committed to hair cell phenotype but n
62                       Thus, both mitotic and postmitotic cells decrease in size during spinal cord de
63 ater role than PAN1 in directing patterns of postmitotic cell expansion that determine the shapes of
64                           As a first step, a postmitotic cell extends its leading process, presumably
65 quence-binding protein 2 (Satb2), regulate a postmitotic cell fate choice between these subtypes.
66  the fate of postmitotic daughter cells, but postmitotic cell fate plasticity driven by extrinsic fac
67 or maintaining a balance between mitotic and postmitotic cell fates in development of the mammalian s
68  we present evidence that the progenitor and postmitotic cells flanking the pallial/subpallial bounda
69            Nucleoli continued to diminish in postmitotic cells following fate specification.
70 y have been linked to age-related decline in postmitotic cell function and degenerative diseases.
71 egeneration, and highlight the importance of postmitotic cell growth in gut epithelial repair.
72  types, a functional role for the complex in postmitotic cells has been elusive.
73 mely susceptible to apoptotic signals, while postmitotic cells have developed several strategies to p
74 ng methods that label both proliferative and postmitotic cells have found that cortical interneurons
75      It has been thought that differentiated postmitotic cells have their genomes hard wired, with li
76 be functional; appear most frequently within postmitotic cells; have diverse sequences; change with a
77 , although expression of p21 is increased in postmitotic cells immediately adjacent to the proliferat
78 uced efficiently in vivo in both mitotic and postmitotic cells in all tissues examined.
79           Math5 expression was restricted to postmitotic cells in developing retina, suggesting that
80                                      Because postmitotic cells in higher eukaryotes often do not star
81 present in the inner segment region of these postmitotic cells in several species, including mouse, t
82 s as a bilaterally symmetric condensation of postmitotic cells in the deep layers of the anterior reg
83 e II DNA topoisomerase normally expressed in postmitotic cells in the developing cortex, severely aff
84 ast, PACAP mRNA was localized exclusively in postmitotic cells in the dorsolateral parts of the rhomb
85 ear involvement of miRs in the physiology of postmitotic cells in vivo.
86                                   Excitable, postmitotic cells, in response to sublethal noxious stre
87 tand the protein composition of these unique postmitotic cells, in which irreversible protein degrada
88       Some ATR-sensitive expansion occurs in postmitotic cells including haploid gametes suggesting t
89 persistent stress, as occurs in ageing, both postmitotic cells - including neurons - and proliferativ
90 ively in males and localizes to telomeres in postmitotic cells, including mature sperm.
91 vivo studies and human tissue indicates that postmitotic cells, including neurons, may also become se
92 ly, provide long-term histone replacement in postmitotic cells, including neurons.
93 xpression of transgenes in both dividing and postmitotic cells, including preimplantation embryos.
94 s by a gene product expressed exclusively in postmitotic cells indicates a long-range effect of trans
95 clusively in a nonquiescent subpopulation of postmitotic cells, indicating an asymmetrical distributi
96                              We suggest that postmitotic cells influence progenitor cell fate decisio
97 ng that the growth of a key compartment of a postmitotic cell involves an extensive switch in gene ex
98                     Cell cycle withdrawal in postmitotic cells involves cyclin-dependent kinase (Cdk)
99 The efficient delivery of foreign genes into postmitotic cells is becoming very important for studies
100 in stem cell formation; however, its role in postmitotic cells is largely unknown.
101        However, the fate of nuclear pores in postmitotic cells is unknown.
102 espite a down-regulation of CDK2 activity in postmitotic cells, many cell types, including muscle cel
103  well as the expression of proliferative and postmitotic cell markers at E10.5-E11.5.
104        The first bromodeoxyuridine-negative (postmitotic) cells occupied the ganglion cell layer of v
105 ion in the cerebral wall is most abundant in postmitotic cells of the cortical plate and absent from
106 he outer external granule layer (EGL) and in postmitotic cells of the inner EGL, but not in mature gr
107 , the expression of which is enriched in the postmitotic cells of the intestinal epithelium.
108  hair growth cycle, PAI-2 was limited to the postmitotic cells of the outer root sheath directly abut
109 -lived proteins (ELLPs) did not turn over in postmitotic cells of the rat central nervous system.
110 how that Pk1 transcripts are detected in the postmitotic cells of the subplate and cortical plate dur
111 o that of extracts derived from the entirely postmitotic cells of young and senescent adults.
112 erative diseases by activating cell death in postmitotic cells or shifting the normal balance of mito
113 anoparticles may facilitate gene transfer in postmitotic cells, permitting nuclear uptake across the
114 take revealed that RA exerts its effect on a postmitotic cell population within the developing retina
115  different intervals postinjection to follow postmitotic cells' positional changes.
116                 Antagonizing miR-24 restores postmitotic cell proliferation and enhances fibroblast p
117 y of long-lived proteins (LLPs) in NPCs from postmitotic cells raises the exciting possibility that t
118 s, but their genomic targets and function in postmitotic cells remain poorly understood.
119 ion of proteins in an SDS-insoluble state in postmitotic cells represents a novel autophagic cargo pr
120 -induced Ngf gene expression was detected in postmitotic cells, required new protein synthesis and wa
121  associated with dysfunction and loss of the postmitotic cells residing within this tissue.
122 netoplasts and nuclei were misaligned in the postmitotic cells, resulting in partial cleavage furrow
123 own regarding the effect these drugs have on postmitotic cells such as neurons.
124 but little is known about their functions in postmitotic cells such as neurons.
125                                   RATIONALE: Postmitotic cells, such as cardiomyocytes, seem to be pa
126                         miRNAs also occur in postmitotic cells, such as neurons in the mammalian cent
127 monly observed in terminally differentiated, postmitotic cells, such as neurons.
128  implementing particular genetic programs in postmitotic cells, such as reelin expression in Cajal-Re
129 gh the presence of some of these isoforms in postmitotic cells suggests a role in controlling cell gr
130                                  Neurons are postmitotic cells that foster virus persistence.
131 essed at embryonic day 14 (E14), but only in postmitotic cells that have acquired a neuronal fate.
132          Neurons are electrically excitable, postmitotic cells that perform sensory, relaying, and mo
133 ular Tax1 on gene expression in NT2-N cells, postmitotic cells that share morphologic, phenotypic, an
134                     Adult cardiomyocytes are postmitotic cells that undergo very limited cell divisio
135 it nuclear activities of PML and PML/RARA in postmitotic cells through CyPN-dependent cytoplasmic seq
136 le in epidermis regulating the conversion of postmitotic cells to differentiating ones.
137 ore, TGFbeta and growth pathways interact in postmitotic cells to precisely coordinate cell-specific
138  that ZBTB20 acts both in progenitors and in postmitotic cells to regulate cell fate specification in
139  constitute the differentiation program of a postmitotic cell type.
140 e into neuronal, intestinal, and other known postmitotic cell types and are distributed throughout th
141 scripts accumulate in both proliferating and postmitotic cell types of Arabidopsis plants.
142 retina guide the genesis and distribution of postmitotic cell types, as well as their connectivity.
143  ventricular zones has commenced, individual postmitotic cells undergo directed migrations along the
144 ate regulator, Notch1, were studied in newly postmitotic cells using a conditional allele of Notch1 (
145 assified further by testing for an effect in postmitotic cells using the sev-GAL4 driver, by testing
146 meostasis and function, thus rendering these postmitotic cells vulnerable to premature death in retin
147 ifferentiation to hair cells of the normally postmitotic cells was restricted to the Lgr5-positive po
148                                    The first postmitotic cells were found in the retinal ganglion cel
149 BrdU analysis revealed that only a subset of postmitotic cells were induced to activate apoptosis.
150  and since no mitoses and only rare possible postmitotic cells were scored, postmitotic NE re-assembl
151         To investigate cohesin's function in postmitotic cells, where it is widely expressed, we have
152 es in turn specify the identity of any given postmitotic cell, which is evident by its cellular morph
153 ry persists within one cell generation or in postmitotic cells, while long-term memory can survive mu
154         Podocytes are highly differentiated, postmitotic cells, whose function is largely based on th
155 and misfolded proteins, which accumulates in postmitotic cells with advanced age.
156              Ectopic activation of Notch1 in postmitotic cells within the nail keratogenous zone resu
157  during the transition from proliferating to postmitotic cells within the zebrafish retina.
158 e kinetics, especially a rapid production of postmitotic cells, within a discrete portion of the tele

 
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