1 ous with unsegregated nucleoids or short and
anucleate.
2 ower and approximately 25% of the cells were
anucleate.
3 Because platelets are
anucleate and contain archetypal signal transduction mac
4 cleoids, approximately 10% of the cells were
anucleate,
and assembly of foci of the chromosome partit
5 Platelets are small
anucleate blood cells that aggregate to seal leaks at si
6 which are made in the liver, and platelets,
anucleate blood cells that are produced in the bone marr
7 Human platelets are
anucleate blood cells that retain cytoplasmic mRNA and m
8 ocytic clearance of intact effete platelets,
anucleated blood cells of critical importance in health
9 Platelets are
anucleated blood elements highly potent at generating ex
10 however, PSMs and SWs often also encapsulate
anucleate bodies both inside and outside of spores.
11 cytokinesis to produce one nucleated and one
anucleate cell (zoid).
12 Moreover, MksBEF can complement
anucleate cell formation in SMC-deficient cells.
13 s, nor did it suppress the high frequency of
anucleate cell formation.
14 Blood platelets are
anucleate cell fragments that play a critically importan
15 they suppressed temperature sensitivity and
anucleate cell production of cells containing null or po
16 ization in the regulatory repertoire of this
anucleate cell.
17 mechanisms that control endocytosis in this
anucleate cell.
18 l chromosome segregation, and an increase in
anucleated cell formation.
19 A significant population of
anucleate cells (zoids), apparently derived from kinetop
20 The chains included
anucleate cells and cells with aberrantly dense or diffu
21 This increase in production of
anucleate cells depended on recA, indicating that there
22 Blood platelets are functional
anucleate cells generated by specialized fragmentation o
23 ther examination of FtsZ ring positioning in
anucleate cells generated by the parC and mukB mutants:
24 mutation dramatically enhanced production of
anucleate cells in an smc null mutant.
25 in the production of approximately 0.9 to 3%
anucleate cells in prfA cultures grown at 30 or 37 degre
26 e ion channels are functional in these tiny,
anucleate cells is difficult to assess by direct electro
27 duces proinflammatory cytokine production in
anucleate cells lacking NF-kappaB is unknown.
28 ogressively lose organelles and convert into
anucleate cells or corneocytes.
29 also confirm that this is a feature of other
anucleate cells through transcriptome sequencing of matu
30 Human blood platelets are
anucleate cells whose response to extracellular stimuli
31 Conversely, in
anucleate cells, asters alone can support furrow inducti
32 segregation defects, including formation of
anucleate cells, compact nucleoids confined to one half
33 g aberrant nuclear division, as well as many
anucleate cells, demonstrating that the TRF4/5 function
34 ricted to low temperature with production of
anucleate cells, reflecting chromosome segregation defec
35 This, along with its expression in
anucleate cells, suggests that Bcl-3 has previously unre
36 s in protein oxidation have been reported in
anucleate cells, where no transcription occurs.
37 tivation leading to increased frequencies of
anucleate cells.
38 owth were impaired in viability and produced
anucleate cells.
39 tions nor, obviously, transcription by these
anucleate cells.
40 he temperature-sensitivity and production of
anucleate cells.
41 to a 100-fold increase in the production of
anucleate cells.
42 spoIIIE, led to an increase in production of
anucleate cells.
43 utants are temperature-sensitive and produce
anucleate cells.
44 segregation and divide frequently to produce
anucleate cells.
45 y closer to the cell extremities, whereas in
anucleated cells (deletion mutants for mukB), the Tsr cl
46 Consequently, polynucleated and
anucleated cells accumulated in these cultures.
47 Although they are
anucleated cells that lack a complex secretory apparatus
48 There is also an enhanced population of
anucleated cells, each containing a single kinetoplast k
49 (to our knowledge) that platelets, which are
anucleate cellular fragments, sense microenvironmental m
50 s were competent to express GFP, whereas the
anucleated central fiber cells were not.
51 Anucleate corneocytes contain keratin filaments bound to
52 Platelets are
anucleate cytoplasmic discs derived from megakaryocytes
53 Platelets are
anucleate cytoplasmic fragments that lack genomic DNA, b
54 that circulate as uniform small, disc-shaped
anucleate cytoplasmic fragments with critical roles in h
55 acute hemostasis and inflammation, but these
anucleate cytoplasts are not thought to synthesize prote
56 ostatic cells that circulate in the blood as
anucleate cytoplasts.
57 s can result in birth of multiple functional
anucleate daughter cells.
58 segregation of daughter nuclei, formation of
anucleated daughter cells, centrosomal amplification, an
59 ergo cytokinesis generating small numbers of
anucleated daughter cells, each containing a single kine
60 Preplatelets are
anucleate discoid particles 2-10 microm across that have
61 f beta-globin mRNA in the cytoplasm of their
anucleate erythroid progeny.
62 tiation of atherosclerosis and despite being
anucleate express nuclear receptors.
63 rse the direction of DNA transfer, producing
anucleate forespores.
64 ent, rhythmic protein modification shared in
anucleate human cells.
65 However, we observe that
anucleate human platelets, either maintained in suspensi
66 ganize cytoplasmic microtubules and actin in
anucleate hyphae.
67 Although the platelet is
anucleate,
it contains transcripts that may mirror disea
68 less, the lack of cell or tissue culture for
anucleate lens fibers and the insoluble state of catarac
69 Platelets are
anucleate mammalian blood cells that continuously circul
70 Platelets,
anucleated megakaryocyte (MK)-derived cells, play a majo
71 , first defined by a mutation giving rise to
anucleate minicells, has been cloned and characterized.
72 sulting in the formation of small, circular,
anucleate minicells.
73 Owing to their
anucleate nature, platelets have limited protein synthes
74 No increase in the number of
anucleate or multinucleate C377S mutant cells was found
75 sulfotransferase expressed in these discoid
anucleate particles.
76 in these evolutionarily critical roles, the
anucleate platelet is uniquely mammalian.
77 by functional transfer of RNA stored in the
anucleate platelet.
78 ng the multitude of events that occur in the
anucleate platelet.
79 nd CARMA/MALT1/Bcl10 complex) are present in
anucleate platelets and IkappaB is phosphorylated upon a
80 it is unknown whether DREAM is expressed in
anucleate platelets and plays a role in thrombogenesis.
81 ruous results point toward the complexity of
anucleate platelets and the need for more detailed studi
82 Dysfunction of
anucleate platelets is likely to be completely attributa
83 hich are capable of forming several thousand
anucleate platelets that circulate within blood vessels
84 diseases, but there is debate as to whether
anucleate platelets-the key cellular effector of thrombo
85 account for the presence of active PAI-1 in
anucleated platelets that have a mean life span of 9-12
86 ed PODXL expression correlated with abnormal
anucleated red cell representation in marrow.
87 enrichment at hyphal tips, branch points and
anucleate regions.
88 symmetrically positioned nucleoids and large
anucleate regions.
89 ion of late-stage nucleated erythroblasts to
anucleate reticulocytes.
90 The
anucleate sieve tube system of the angiosperm phloem del
91 Furthermore, we show that these
anucleate sperm induce both normal egg activation and an
92 Here we show that these
anucleate sperm not only differentiate into mature funct
93 In embryos fertilized with
anucleated sperm, only one centrosome was captured by sm
94 ned hyphal tips, misshaped aerial hyphae and
anucleate spores and demonstrates that cardiolipin synth
95 k, we show that an ftsK-null mutant produces
anucleate spores at the same frequency as the wild-type
96 gregation defect of the smc parB mutant (10%
anucleate spores).
97 both exacerbates the segregation defect (24%
anucleate spores).
98 a previously described parB-null mutant (12%
anucleate spores).
99 evelopmental segregation defects (7% and 15%
anucleate spores, respectively).
100 Despite their small size and
anucleate status, platelets have diverse roles in vascul
101 Although platelets are
anucleate,
they do contain coding or regulatory RNAs tha
102 owed by cleavage of host cells into numerous
anucleate vesicles in which virus replication continues
103 ed by cell cleavage, yielding numerous large
anucleate viral vesicles that continue to produce virion