1 As in Drosophila ovaries, murine testes, and
Xenopus eggs.
2 ating kinase in extracts of M phase-arrested
Xenopus eggs.
3 incubation in extracts of metaphase-arrested
Xenopus eggs.
4 ves in various tissues, and mitotic waves in
Xenopus eggs.
5 sis signaling using cytoplasmic extract from
Xenopus eggs.
6 ent upon the binding of Xic1 to PCNA in both
Xenopus egg and gastrulation stage extracts.
7 ntly formed high molecular mass complexes in
Xenopus egg and HeLa extracts.
8 he rapid synchronous cell division cycles of
Xenopus eggs and cell-free systems derived from them.
9 tosis and G1 in somatic cells, is missing in
Xenopus eggs and early embryos.
10 When
Xenopus eggs and egg extracts replicate DNA, replication
11 loped a system to encapsulate cytoplasm from
Xenopus eggs and embryos inside cell-like compartments o
12 ere, we purify an activator of Aurora A from
Xenopus eggs and identify it as TPX2.
13 ecific ICL in cell-free extract derived from
Xenopus eggs and in mammalian cells.
14 t exogenous Emi1 is unstable in CSF-arrested
Xenopus eggs and is destroyed by the SCF(betaTrCP) ubiqu
15 i, a Xenopus Piwi homologue, and piRNAs from
Xenopus eggs and oocytes.
16 xpression reduces cyclin B levels in cycling
Xenopus eggs and reduces levels of the cyclin B ortholog
17 NP, and survivin are present in a complex in
Xenopus eggs and Saccharomyces cerevisiae.
18 used concentrated cytoplasmic extracts from
Xenopus eggs as a model cytoplasm, and visualized metabo
19 Here, we report that in the early
Xenopus egg cell cycles, phosphorylation of endogenous c
20 In
Xenopus egg cell-free extracts, Xkid and Xklp1 are essen
21 In
Xenopus eggs,
compensatory endocytosis is driven by dyna
22 immunohistochemistry analysis indicates that
Xenopus eggs contain a maternal supply of serotonin that
23 ochemical reconstitution of Wnt signaling in
Xenopus egg cytoplasmic extracts.
24 nuclei in cell-free reactions dependent upon
Xenopus egg cytosol or HeLa cell-derived cytosol.
25 In activated
Xenopus eggs,
exocytosing cortical granules (CGs) are su
26 te assembly of spindle and spindle matrix in
Xenopus egg extract and in mammalian cells.
27 We describe an in vitro system using
Xenopus egg extract and purified centrioles in which bot
28 ICH complex was purified to homogeneity from
Xenopus egg extract and was found to contain only WSTF a
29 In
Xenopus egg extract assays, we showed that poly(ADP-ribo
30 suppress initiation of DNA replication in a
Xenopus egg extract based cell-free system, leading to t
31 r resizing assay wherein nuclei assembled in
Xenopus egg extract become smaller in the presence of cy
32 B pathway is suppressed in the cytoplasm of
Xenopus egg extract by phosphatases, but that it becomes
33 to 70% of XlORC-dependent DNA replication in
Xenopus egg extract by preventing XlORC from binding to
34 We also devised a cell-free assay using
Xenopus egg extract containing fluorescent actin to foll
35 the Tetrahymena group I ribozyme embedded in
Xenopus egg extract demonstrate the ability of M2-seq to
36 itation analysis using human DR-GFP cells or
Xenopus egg extract demonstrated that MCM8 and MCM9 prot
37 assembly, 4.1 domain peptides were added to
Xenopus egg extract nuclear reconstitution reactions.
38 Imaging of single filaments in
Xenopus egg extract provided evidence that disassembly b
39 microtubule plus-end dynamic instability in
Xenopus egg extract spindles.
40 subsequent degradation both in vivo and in a
Xenopus egg extract system in vitro.
41 In this study, we took advantage of the
Xenopus egg extract system to address these questions.
42 Using the
Xenopus egg extract system, we have investigated regulat
43 Using the
Xenopus egg extract system, we investigated the involvem
44 Using the
Xenopus egg extract system, we show that lesions induced
45 MBT regulators, we developed an assay using
Xenopus egg extract that recapitulates the activation of
46 o caspase activation, and supplementation of
Xenopus egg extract with glucose-6-phosphate, which prom
47 Using
Xenopus egg extract, we show that direct, cell-cycle-reg
48 atenin stabilization and Axin degradation in
Xenopus egg extract.
49 n interaction partner of SUMOylated PARP1 in
Xenopus egg extract.
50 ed in a cell-free system based on interphase
Xenopus egg extract.
51 n established in Drosophila, C. elegans, and
Xenopus egg extracts .
52 Additional experiments in
Xenopus egg extracts and artificially crowded in vitro s
53 complexes associate with B-Raf at mitosis in
Xenopus egg extracts and contribute to its phosphorylati
54 rphase nuclei and metaphase spindles both in
Xenopus egg extracts and cultured cells.
55 support the initiation of DNA replication in
Xenopus egg extracts and during early embryonic developm
56 We previously studied this process in
Xenopus egg extracts and established Greatwall (Gwl) as
57 the sperm-mediated spindle assembly assay in
Xenopus egg extracts and extensive mutagenesis studies,
58 phatase that acts on model CDK substrates in
Xenopus egg extracts and has antimitotic activity.
59 ch is related to S. pombe Cdt2, functions in
Xenopus egg extracts and human cells to destroy the repl
60 Using
Xenopus egg extracts and human cells, we show that the t
61 ctivation of ATR-dependent signaling in both
Xenopus egg extracts and human cells.
62 acks RPA1N is unable to support resection in
Xenopus egg extracts and human cells.
63 Depletion of PP1 impairs NHEJ in both
Xenopus egg extracts and human cells.
64 Here, using
Xenopus egg extracts and human somatic cells, we show th
65 suppress DSB-induced ATM activation in both
Xenopus egg extracts and human tumor cell lines.
66 d MEK-activating protein kinase from mitotic
Xenopus egg extracts and identified it as the Mos protoo
67 ified the xNdc80 complex to homogeneity from
Xenopus egg extracts and identified two novel interactin
68 odel 5' adducts were efficiently resected in
Xenopus egg extracts and immunodepletion of Xenopus DNA2
69 omatid separation have recently been made in
Xenopus egg extracts and in HeLa cells.
70 Using
Xenopus egg extracts and in vitro assays, we show that t
71 osphorylation decreases severing activity in
Xenopus egg extracts and is involved in controlling spin
72 amage-induced S-phase checkpoint response in
Xenopus egg extracts and mammalian cells.
73 Here, using
Xenopus egg extracts and mass spectrometry, we identify
74 ecipitation from both interphase and mitotic
Xenopus egg extracts and mass spectrometry.
75 Biochemical studies in
Xenopus egg extracts and microinjection studies in human
76 hat modifies chromosomal proteins in mitotic
Xenopus egg extracts and plays an essential role in mito
77 nction as MTOCs in the presence of RanGTP in
Xenopus egg extracts and RanGTP stimulates AurA to recru
78 titive loci or a single chromosomal locus in
Xenopus egg extracts and show that a complex library can
79 ivator of the MAPK cascade during mitosis in
Xenopus egg extracts and showed that B-Raf activation is
80 We have studied assembly of chromatin using
Xenopus egg extracts and single DNA molecules held at co
81 is recruited to a DSB-mimicking substrate in
Xenopus egg extracts and sites of laser microirradiation
82 a direct role in mitotic spindle assembly in
Xenopus egg extracts and that this role is independent o
83 optical reconstruction microscopy (STORM) to
Xenopus egg extracts and tissue culture cells, we report
84 treatment with either mitotic or interphase
Xenopus egg extracts and to identify the single function
85 osis, however, has been demonstrated only in
Xenopus egg extracts and via ectopic Cdk1 activation .
86 In
Xenopus egg extracts And-1 is loaded on the chromatin af
87 roscopy reveals that microtubule dynamics in
Xenopus egg extracts are unaffected by maskin depletion.
88 his mitotic activation, using cyclin-treated
Xenopus egg extracts as a model system, and presented ev
89 Using
Xenopus egg extracts as a vertebrate model system, we sh
90 We have used
Xenopus egg extracts as an in vitro system to study the
91 Using
Xenopus egg extracts as the model system, we found that
92 We find that the APC/C from
Xenopus egg extracts binds to the D-box of cyclin B, whe
93 multiple rounds of centrosome duplication in
Xenopus egg extracts but not for the initial round of re
94 yclin E is imported into nuclei assembled in
Xenopus egg extracts by a pathway that requires importin
95 on was reconstituted in phosphatase-depleted
Xenopus egg extracts by PP2A, but not PP1.
96 this hypothesis, the induction of mitosis in
Xenopus egg extracts by the addition of cyclin B was blo
97 of Aurora B in cultured cells and in cycling
Xenopus egg extracts caused escape from the spindle chec
98 Xenopus egg extracts containing a mutant of TopBP1 that
99 Furthermore,
Xenopus egg extracts containing a version of TopBP1 with
100 for the ATR-dependent activation of Chk1 in
Xenopus egg extracts containing aphidicolin-induced DNA
101 1 displays increased binding to ATR-ATRIP in
Xenopus egg extracts containing checkpoint-inducing DNA
102 for the ATR-dependent activation of Chk1 in
Xenopus egg extracts containing incompletely replicated
103 for the ATR-dependent activation of Chk1 in
Xenopus egg extracts containing incompletely replicated
104 for the ATR-dependent activation of Chk1 in
Xenopus egg extracts containing incompletely replicated
105 for the ATR-dependent activation of Chk1 in
Xenopus egg extracts containing incompletely replicated
106 otrimeric RCC1/Ran/RanBP1 complex in M phase
Xenopus egg extracts controls both RCC1's enzymatic acti
107 Studies in
Xenopus egg extracts demonstrate that Repo-Man interacts
108 Further characterization of Pontin in
Xenopus egg extracts demonstrates that Pontin interacts
109 EB1 from cytostatic factor-arrested M-phase
Xenopus egg extracts dramatically reduced microtubule le
110 both biochemical and morphological events in
Xenopus egg extracts during mitosis.
111 e actin inhibitor latrunculin A was added to
Xenopus egg extracts during nuclear assembly.
112 Soluble
Xenopus egg extracts efficiently replicate added plasmid
113 perm pronuclear expansion, in Dppa2-depleted
Xenopus egg extracts excess microtubules cause pronuclea
114 immunodepletion of Greatwall kinase prevents
Xenopus egg extracts from entering or maintaining M phas
115 Xenopus egg extracts have distinct Cdk-active and Cdk-in
116 data with human cells and in vitro data with
Xenopus egg extracts have led to the conclusion that the
117 Studies in
Xenopus egg extracts have shown that the major MT destab
118 Immunodepletion of DDK from
Xenopus egg extracts impairs chromatin association of Sc
119 Immunodepletion from
Xenopus egg extracts indicated that both proteins are on
120 Overexpression of Pnuts in
Xenopus egg extracts inhibited both mitotic and meiotic
121 in response to stalled replication forks in
Xenopus egg extracts involves a complex pathway containi
122 Recombinant geminin that is added to
Xenopus egg extracts is efficiently degraded upon exit f
123 However, removal of geminin from
Xenopus egg extracts is insufficient to cause rereplicat
124 Mitotic spindle assembly in
Xenopus egg extracts is regulated at least in part by im
125 Depletion from human cells or
Xenopus egg extracts is used to demonstrate that the ZW1
126 ication of an activating enzyme from mitotic
Xenopus egg extracts led to cloning and characterization
127 We now demonstrate that in
Xenopus egg extracts Mad1 and Mad2 form a stable complex
128 Addition of alpha-p-S196 antibodies to
Xenopus egg extracts or injection of alpha-p-S196 antibo
129 Addition of purified Ddk to
Xenopus egg extracts or overexpression of Dbf4 in HeLa c
130 t both recombinant RSK and endogenous RSK in
Xenopus egg extracts phosphorylate all three isoforms of
131 und to ATM and Aven overexpressed in cycling
Xenopus egg extracts prevented mitotic entry and induced
132 e of p97-Ufd1-Npl4 function, microtubules in
Xenopus egg extracts remain as monopolar spindles attach
133 regulator of mitotic entry, and new work in
Xenopus egg extracts shows that Greatwall is required fo
134 howed that only monopolar spindles formed in
Xenopus egg extracts supplemented with recombinant Plx1N
135 wo distinct steps during spindle assembly in
Xenopus egg extracts that can be distinguished by their
136 esence of a checkpoint adaptation pathway in
Xenopus egg extracts that displays interesting molecular
137 ized on magnetic beads and then incubated in
Xenopus egg extracts that provide a source for centromer
138 ped a model system using ssDNA templates and
Xenopus egg extracts that recapitulates eukaryotic G4 re
139 ere, we describe a cell-free system based on
Xenopus egg extracts that supports ICL repair.
140 We combined microfluidic technology with
Xenopus egg extracts to characterize spindle assembly wi
141 In this study, we used
Xenopus egg extracts to form spindles in the absence of
142 rom metaphase hamster cells and incubated in
Xenopus egg extracts to initiate DNA replication.
143 Here, we have used
Xenopus egg extracts to investigate Aur-A's contribution
144 We have used
Xenopus egg extracts to investigate the functional inter
145 Here, we use
Xenopus egg extracts to investigate the roles of MCM7 an
146 ere, we have used an activity-based assay in
Xenopus egg extracts to purify the mRNA export protein R
147 We use
Xenopus egg extracts to recapitulate DPC repair in vitro
148 tely soluble replication system derived from
Xenopus egg extracts to show that Cdk1/cyclin B also can
149 ein binding assays and functional studies in
Xenopus egg extracts to show that TopBP1 makes a direct
150 ere, we use repair of a site-specific ICL in
Xenopus egg extracts to study the mechanism of lesion by
151 Cdk2, but not full-length cyclin A2-Cdk2, to
Xenopus egg extracts triggers apoptotic DNA fragmentatio
152 otubule assembly in tissue culture cells and
Xenopus egg extracts using two-photon microscopy with FL
153 id-based DSB templates that were repaired in
Xenopus egg extracts via the canonical, Ku-dependent NHE
154 Using
Xenopus egg extracts we show that although each origin c
155 When
Xenopus egg extracts were immunodepleted of Xenopus Hbo1
156 ylated and destroyed in Fizzy/Cdc20-depleted
Xenopus egg extracts when only the N-terminal domain of
157 Our results show that in
Xenopus egg extracts, aggregation of multiple replicatio
158 the membranous spindle matrix isolated from
Xenopus egg extracts, and it is required for proper spin
159 also prevents the activation of APCCdc20 in
Xenopus egg extracts, and restores the mitotic arrest in
160 ial for RIR of a site-specific ICL lesion in
Xenopus egg extracts, and that both its catalytic activi
161 results in continuous spindle elongation in
Xenopus egg extracts, and we quantitatively correlate th
162 In
Xenopus egg extracts, ATM associates with TopBP1 and the
163 re we show that, in both mammalian cells and
Xenopus egg extracts, BRCA1/BARD1 is required for mitoti
164 Here, we report that in
Xenopus egg extracts, Cdc7-Drf1 is far more abundant tha
165 N-APC interacts with Mad2 in
Xenopus egg extracts, colon cancer cells, and in vitro w
166 In
Xenopus egg extracts, condensin I function is predominan
167 During replication in
Xenopus egg extracts, DUE-B and Cdc45 bind to chromatin
168 two other MEK-activating kinases present in
Xenopus egg extracts, had little effect on cyclin-stimul
169 In
Xenopus egg extracts, ICL repair is initiated when two r
170 Consistently, in
Xenopus egg extracts, Idas-Geminin is less active in lic
171 of caspase-2, the initiator of apoptosis in
Xenopus egg extracts, is associated with an accumulation
172 Using
Xenopus egg extracts, nuclei have been assembled and the
173 The data suggest that in
Xenopus egg extracts, origins of replication contain mul
174 ternal reflection fluorescent microscopy and
Xenopus egg extracts, Petry et al. demonstrate that new
175 a B, is critical for H3T3 phosphorylation in
Xenopus egg extracts, Plk1 and Aurora B both promote thi
176 lly restores DNA replication to ORC-depleted
Xenopus egg extracts, providing strong evidence for its
177 In
Xenopus egg extracts, recombinant L also inhibits mitoti
178 e were stimulated to initiate replication in
Xenopus egg extracts, replication initiated without any
179 abrogate the spindle assembly checkpoint in
Xenopus egg extracts, restore APC/C activity, and disrup
180 In
Xenopus egg extracts, the C terminus of Nbs1 recruits AT
181 Here, we show that in mitotic
Xenopus egg extracts, the carboxyl-terminus of APC can a
182 In
Xenopus egg extracts, the embryonic linker histone H1M d
183 Using purified components and
Xenopus egg extracts, the kinetochore-associated microtu
184 In mitotic
Xenopus egg extracts, the Nup107-160 complex localized t
185 ve attempted to reconstitute this process in
Xenopus egg extracts, the only eukaryotic in vitro syste
186 Upon exposure to
Xenopus egg extracts, this DNA underwent extensive repli
187 Using
Xenopus egg extracts, we analyzed the functions of FANCM
188 Using
Xenopus egg extracts, we demonstrate that high CDC2 acti
189 Using
Xenopus egg extracts, we describe here a replication-cou
190 Using
Xenopus egg extracts, we find that degradation of Xic1,
191 Using different assays in
Xenopus egg extracts, we found that depleting lamin B ca
192 sing immunodepletion/add-back experiments in
Xenopus egg extracts, we have determined that both Walke
193 Using
Xenopus egg extracts, we have identified a metazoan-spec
194 Using
Xenopus egg extracts, we have studied Xenopus BLM (Xblm)
195 Using a proteomic screen in
Xenopus egg extracts, we identified factors that are enr
196 icating nuclei from transcriptionally silent
Xenopus egg extracts, we identified numerous actin regul
197 Using
Xenopus egg extracts, we identify an acidic residue in P
198 Using
Xenopus egg extracts, we identify two sequence elements
199 Using
Xenopus egg extracts, we now report an additional pathwa
200 g the GST-Cdc25C phosphorylating activity in
Xenopus egg extracts, we previously defined roles of MAP
201 In
Xenopus egg extracts, we replaced endogenous Eg5 with re
202 Using
Xenopus egg extracts, we show that DNA replication at hi
203 Working in
Xenopus egg extracts, we show that Nudel/NudE facilitate
204 Using
Xenopus egg extracts, we show that ultraviolet radiation
205 Here, using
Xenopus egg extracts, we show that while the somatic H1s
206 Depletion of MTBP from
Xenopus egg extracts, which also removes Treslin, abolis
207 nts for their effects on nuclear assembly in
Xenopus egg extracts, which contain approximately 12 mic
208 Using
Xenopus egg extracts, which support replication-coupled
209 domain are defective for DNA replication in
Xenopus egg extracts.
210 dle manipulation of preassembled spindles in
Xenopus egg extracts.
211 s (DSBs) depends upon ATM in human cells and
Xenopus egg extracts.
212 equired for M phase entry and maintenance in
Xenopus egg extracts.
213 envelope fusion and nuclear pore assembly in
Xenopus egg extracts.
214 the vertebrate meiotic spindle assembled in
Xenopus egg extracts.
215 R pathway in response to oxidative stress in
Xenopus egg extracts.
216 pecific for a model mitotic CDK substrate in
Xenopus egg extracts.
217 ndles at interaction zones between asters in
Xenopus egg extracts.
218 ons of the model were tested and verified in
Xenopus egg extracts.
219 , a mitochondrial enzyme, from HeLa cell and
Xenopus egg extracts.
220 lly to the Rad9-Hus1-Rad1 (9-1-1) complex in
Xenopus egg extracts.
221 n of the ATR-dependent checkpoint pathway in
Xenopus egg extracts.
222 this hypothesis with model DNA substrates in
Xenopus egg extracts.
223 ts ATM and ATR in a DNA damage checkpoint in
Xenopus egg extracts.
224 ate that MAPK phosphorylates Mps1 at S844 in
Xenopus egg extracts.
225 itotic function, we examined its behavior in
Xenopus egg extracts.
226 matin to induce Op18 hyperphosphorylation in
Xenopus egg extracts.
227 pindle localization, and spindle assembly in
Xenopus egg extracts.
228 response to stalled DNA replication forks in
Xenopus egg extracts.
229 opus oocyte maturation and during mitosis in
Xenopus egg extracts.
230 equence-specific replication fork pausing in
Xenopus egg extracts.
231 not translation, leads to spindle defects in
Xenopus egg extracts.
232 of Topoisomerase-II by SUMO-2 conjugation in
Xenopus egg extracts.
233 rse of the first round of DNA replication in
Xenopus egg extracts.
234 between bipolarity and poleward flux, using
Xenopus egg extracts.
235 itant with cohesin during DNA replication in
Xenopus egg extracts.
236 mage and replication checkpoint responses in
Xenopus egg extracts.
237 ATRIP bound well to various DNA templates in
Xenopus egg extracts.
238 zed microtubule asters in metaphase-arrested
Xenopus egg extracts.
239 Mad2 to inhibit APC/C(Cdc20) in vitro and in
Xenopus egg extracts.
240 phopeptide triggered actin tail formation in
Xenopus egg extracts.
241 on protein Mcm2 as an ATM-binding protein in
Xenopus egg extracts.
242 re microtubules for chromosomal targeting in
Xenopus egg extracts.
243 g replisomes with a site-specific barrier in
Xenopus egg extracts.
244 itotic activation of the p42 MAPK pathway in
Xenopus egg extracts.
245 e examine here how licensing is regulated in
Xenopus egg extracts.
246 le-strand DNA gaps affect DNA replication in
Xenopus egg extracts.
247 Drf1 and characterized this protein by using
Xenopus egg extracts.
248 -conjugated species during the cell cycle in
Xenopus egg extracts.
249 e in buffer but are rapidly depolymerized in
Xenopus egg extracts.
250 lear envelope breakdown and mitotic entry in
Xenopus egg extracts.
251 kinase was required for spindle assembly in
Xenopus egg extracts.
252 of microtubule behavior around chromatin in
Xenopus egg extracts.
253 during G1 phase initiate DNA replication in
Xenopus egg extracts.
254 ase (Plx1), are simultaneously depleted from
Xenopus egg extracts.
255 ISWI exists in two major complexes in
Xenopus egg extracts.
256 dynamics during perturbed DNA replication in
Xenopus egg extracts.
257 teins to immobilized linear DNA fragments in
Xenopus egg extracts.
258 1 is important for the spindle checkpoint in
Xenopus egg extracts.
259 erated cargoes around chromosomes in mitotic
Xenopus egg extracts.
260 onstituted the checkpoint response to MMS in
Xenopus egg extracts.
261 CKI abrogated beta-catenin degradation in
Xenopus egg extracts.
262 ) and studied the function of the protein in
Xenopus egg extracts.
263 ve psoralen- and abasic site-induced ICLs in
Xenopus egg extracts.
264 5 in vivo, and loads Cdc45 onto chromatin in
Xenopus egg extracts.
265 in metaphase chromosome alignment defects in
Xenopus egg extracts.
266 ted]-dependent but ATM-independent manner in
Xenopus egg extracts.
267 ors in kinetochore-microtubule attachment in
Xenopus egg extracts.
268 ing defined ATR-activating DNA structures in
Xenopus egg extracts.
269 from mitotic chromosomes in human cells and
Xenopus egg extracts.
270 he sides of existing microtubules in meiotic
Xenopus egg extracts.
271 NA in buffer or during chromatin assembly in
Xenopus egg extracts.
272 sidues (S50/T64/T68/T79/S114/S165) by CDK in
Xenopus egg extracts.
273 chromatin-coated beads after introduction of
Xenopus egg extracts.
274 ization using Ran-mediated asters in meiotic
Xenopus egg extracts.
275 onted with strand-specific DNA roadblocks in
Xenopus egg extracts.
276 y a 1-fold increase of Lis1 concentration in
Xenopus egg extracts.
277 es features of meiotic spindles assembled in
Xenopus egg extracts.
278 but is essential for mitotic SUMOylation in
Xenopus egg extracts.
279 microtubules, to support spindle assembly in
Xenopus egg extracts.
280 alled Treslin that associates with TopBP1 in
Xenopus egg extracts.
281 omplex containing Cdc7, Drf1, and Claspin in
Xenopus egg extracts.
282 -1 with the ATR-activating protein TopBP1 in
Xenopus egg extracts.
283 nd to be necessary for spindle bipolarity in
Xenopus egg extracts.
284 quired for mitotic activation of p42 MAPK in
Xenopus egg extracts; however, the identity of the kinas
285 vitro and prevents the assembly of nuclei in
Xenopus egg interphase extracts.
286 As shown by a new study, a
Xenopus egg model system has great promise to illuminate
287 We used the
Xenopus egg/
oocyte system to examine the hypothesis that
288 At fertilization,
Xenopus eggs produce a cytoplasmic Ca(2+) (Ca(2+)(cyt))
289 In a
Xenopus egg replication system, the origin recognition c
290 Unfertilized
Xenopus eggs,
similar to other metazoan cells, contain t
291 By the use of a cell-free system from
Xenopus eggs that reproduces the mitotic checkpoint, we
292 methylosome protein 50 (Mep50) isolated from
Xenopus eggs that specifically methylates predeposition
293 We used the large size of
Xenopus eggs to analyze small RNAs at the single cell le
294 iled model of the fertilization Ca2+ wave in
Xenopus eggs to explore the hypothesis that IP3 is produ
295 used a soluble cell-free system derived from
Xenopus eggs to investigate the role of protein phosphat
296 As the fertilized
Xenopus egg undergoes sequential cell divisions to form
297 soluble DNA replication system derived from
Xenopus eggs,
we demonstrate that immunodepletion of pro
298 Using replicating extracts from
Xenopus eggs,
we developed cell-free assays for FA prote
299 Using mouse and
Xenopus eggs,
we show that IP3R1 is phosphorylated durin
300 Here, we have used extracts of
Xenopus eggs,
which normally proceed through the early e