1 han that of wild-type fortilin as shown by a
pulse-chase experiment.
2 cells when compared with control cells in a
pulse-chase experiment.
3 life ~7-10 h), which we confirmed by in vivo
pulse-chase experiments.
4 reaction amplitudes between pulse-quench and
pulse-chase experiments.
5 tect replicase intermediates and products in
pulse-chase experiments.
6 7 +/- 17 and 245 +/- 29 min as determined by
pulse-chase experiments.
7 e observed processivity in pregnenolone/DHEA
pulse-chase experiments.
8 pressed in the absence of virE1, as shown by
pulse-chase experiments.
9 ylated mutant (N259Q,N263Q) were compared in
pulse-chase experiments.
10 immunohistochemistry, and bromodeoxyuridine
pulse-chase experiments.
11 rmed delayed pulse, pulse-chase, and delayed
pulse-chase experiments.
12 hemical approach, human islets were used for
pulse-chase experiments.
13 other within 30 min of their synthesis with
pulse-chase experiments.
14 detectably alter the stability of sigmaE in
pulse-chase experiments.
15 of newly synthesized apo(a) was analyzed in
pulse-chase experiments.
16 ines, as well as with BrdU incorporation and
pulse-chase experiments.
17 cells and analyzed by immunofluorescence and
pulse-chase experiments.
18 r rates of cleavage in vivo as determined by
pulse-chase experiments.
19 mmunoprecipitation in the context of in vivo
pulse-chase experiments.
20 n of protein synthesis with puromycin and by
pulse-chase experiments.
21 cinal plant Pentalinon andrieuxii by (13)CO2
pulse-chase experiments.
22 ociation of the intermediates as revealed by
pulse-chase experiments.
23 r Abeta levels and hasten its degradation in
pulse-chase experiments.
24 ar behavior of these mutants was assessed in
pulse-chase experiments.
25 lesterol lead to increased apoE secretion in
pulse/chase experiments.
26 In
pulse-chase experiments,
14-3-3beta increased the synthe
27 oteins was determined by chemical detection,
pulse-chase experiments,[
3H]mannose labeling, and altera
28 In
pulse-chase experiments,
addition of LPL during the chas
29 Pulse-chase experiments after transferrin uptake showed
30 Second,
pulse-chase experiments also establish that tREs are the
31 In vivo
pulse chase experiments and immunoelectronmicroscopy hav
32 tail loss, we performed a bromodeoxyuridine
pulse-chase experiment and found that a subset of ependy
33 Using nucleoside
pulse-chase experiments and clonal analysis, we determin
34 cell fractionation in the context of in vivo
pulse-chase experiments and immunoblot analysis.
35 EdU
pulse-chase experiments and in vivo tracking of individu
36 Here we performed
pulse-chase experiments and showed that the C29/C30 ster
37 degradation of the molecule were analyzed by
pulse-chase experiments and then by immunoprecipitation
38 Pulse-chase experiments and treatment of cells with bref
39 nce are based upon monoclonal antibodies and
pulse-chase experiments,
and there have been no reports
40 e results of serial transplantation and BrdU
pulse-chase experiments are most consistent with the con
41 The study shows that (13)CO2
pulse-chase experiments are powerful in elucidating, und
42 Lipid turnover rates were studied by
pulse-chase experiments at the single cell level.
43 In
pulse-chase experiments, [
Cl-] in Tf-labeled early/recyc
44 Pulse chase experiments conducted in the presence of BFA
45 Isotope
pulse-chase experiments confirm that all intermediates o
46 Pulse-chase experiments confirm that LRAD3 expression si
47 Pulse-chase experiments confirm these results.
48 (14)CO2
pulse-chase experiments confirmed that water deficit enh
49 Pulse-chase experiments confirmed the stress-dependent M
50 Pulse-chase experiments could not detect newly assembled
51 rrest of tumour cell proliferation with TMZ,
pulse-chase experiments demonstrate a tumour re-growth c
52 Last,
pulse-chase experiments demonstrate that Hsp70 preferent
53 Pulse-chase experiments demonstrate that in cells expres
54 Pulse-chase experiments demonstrate that PFK-M associate
55 Pulse-chase experiments demonstrate that the bulk popula
56 Examination of selected mutants during a
pulse-chase experiment demonstrated an increase in F pro
57 EdU
pulse-chase experiments demonstrated a perivascular canc
58 Pulse-chase experiments demonstrated similar levels of n
59 Western immunoblots and
pulse-chase experiments demonstrated that EsaR is stable
60 Pulse-chase experiments demonstrated that in the presenc
61 BrdU
pulse-chase experiments demonstrated that LRCs were dist
62 Pulse-chase experiments demonstrated that NGF treatment
63 Pulse-chase experiments demonstrated that SpoIVFA synthe
64 Western blotting and
pulse-chase experiments demonstrated that the D319E prot
65 Radioactive
pulse-chase experiments demonstrated that the defect lie
66 Pulse-chase experiments demonstrated that the down-regul
67 Pulse-chase experiments demonstrated that the loss of Si
68 Metabolic
pulse-chase experiments demonstrated that the two mutati
69 BrdU
pulse-chase experiments demonstrated the longevity of th
70 Pulse-chase experiments demonstrated the reduced rate of
71 hese results were consistent with those from
pulse-chase experiments demonstrating the conversion of
72 peptide-bond/ubiquitin-like conjugation) and
pulse-chase experiments detected subtle protein maturati
73 In fact, as directly demonstrated by
pulse-chase experiments,
EECs in the vascularized, but n
74 In
pulse-chase experiments,
either miR-33 overexpression or
75 Pulse chase experiments established that the reaction in
76 biosynthesis of both proteins were similar,
pulse-chase experiments established that the apparent ha
77 rodimer formation in the ER was confirmed by
pulse-chase experiment followed by coimmunoprecipitation
78 The 5-ethynyl-2'-deoxyuridine
pulse-chase experiments further reveal that this stem ce
79 Additional rapid-quench and
pulse-chase experiments have documented this stoichiomet
80 In organello, pulse labelling and
pulse-chase experiments have enabled us to track the mit
81 Pulse-chase experiments have shown that the increased N-
82 Pulse-chase experiments identified sites of cell surface
83 Pulse chase experiments in 293 T cells expressing rhGAA
84 Pulse chase experiments in cells labeled with 35S-methio
85 Pulse-chase experiments in combination with endoglycosid
86 Pulse-chase experiments in COS-7 cells show that there i
87 Pulse-chase experiments in gonococci demonstrated that L
88 In [35S]methionine
pulse-chase experiments in transiently transfected CHO c
89 Pulse-chase experiments in transiently transfected COS-7
90 Pulse-chase experiments in transiently transfected cultu
91 Single-molecule tracking and
pulse-chase experiments in vivo confirmed that LHX2 and
92 to the rate of loss of palmitate observed in
pulse-chase experiments in vivo.
93 d a HaloTag-Gpsm2 mouse strain and performed
pulse-chase experiments in vivo.
94 Pulse-chase experiments in which we utilized the transpo
95 Moreover,
pulse/chase experiments in HepG2 cells treated with AvRB
96 In
pulse-chase experiments,
in which (64)Cu-TETA-OC was inc
97 Pulse chase experiments indicate that the newly-generate
98 f the elemental effect using dNTPalphaS, and
pulse-chase experiments indicate that a rapid phosphodie
99 ted by cycling through the endosomal system,
pulse-chase experiments indicate that cleavage at Gly-91
100 Pulse-chase experiments indicate that DBMsignal/PHMs tur
101 Pulse-chase experiments indicate that the probe turns ov
102 Pulse-chase experiments indicate that translation of tru
103 Finally,
pulse/chase experiments indicate that the half-life of E
104 Pulse chase experiments indicated that A1PiZ was stabili
105 Pulse-chase experiments indicated decreased protein turn
106 Radiolabel
pulse-chase experiments indicated that all of the cell l
107 Finally, results of
pulse-chase experiments indicated that an increase in fu
108 Pulse-chase experiments indicated that early steps in DB
109 Pulse-chase experiments indicated that EGF stimulated th
110 Pulse-chase experiments indicated that HDC isoforms are
111 However,
pulse-chase experiments indicated that p53 protein degra
112 Pulse-chase experiments indicated that the G protein of
113 Pulse-chase experiments indicated that the increased p53
114 Pulse-chase experiments indicated that the rates of hist
115 For instance, radiolabel
pulse-chase experiments indicated that the transport rat
116 Pulse/chase experiments indicated that RA affects FN bio
117 A modified
pulse-chase experiment is applied to determine if the na
118 The half-life of bundlin as detected by
pulse-chase experiments is dramatically reduced in a dsb
119 In a control
pulse-chase experiment,
levels of (64)Cu from [(64)Cu]cu
120 y of PDI is sufficient for wild-type growth,
pulse-chase experiments monitoring the maturation of car
121 ks the starting point for a crystallographic
pulse-chase experiment of the active site during turnove
122 Optical
pulse-chase experiments of Dendra2-tau demonstrate that
123 Pulse-chase experiments of lens organ cultures with [35S
124 Pulse-chase experiments of up to 6 months revealed that
125 A
pulse-chase experiment on living cells showed that the r
126 They enable regional optical marking in
pulse-chase experiments on live cells and tissues, and t
127 Pulse/chase experiments on HepG2 cells treated with AvRB
128 Pulse-chase experiments or addition of the proteasome in
129 Pulse-chase experiments over extended chase periods show
130 Pulse-chase experiments performed in COS-1 cells indicat
131 Results from
pulse-chase experiments performed with infected macropha
132 Furthermore,
pulse-chase experiments previously demonstrated that the
133 By
pulse-chase experiments,
RanC/d proteins are more resist
134 In
pulse-chase experiments,
recycled peptidoglycan was not
135 Pulse-chase experiments reveal a 4-5-fold increase in th
136 Pulse-chase experiments reveal a delay in rRNA processin
137 First, BrdU
pulse-chase experiments reveal that CD44(+) cells coloca
138 Pulse-chase experiments reveal that Hsp70 does not regul
139 Cycloheximide and [(35)S]methionine pulse/
pulse-chase experiments reveal that mevalonate depletion
140 Pulse-chase experiments reveal that newly synthesized en
141 Immunofluorescence microscopy and
pulse-chase experiments reveal that stabilization of ORF
142 Pulse-chase experiments reveal that TCDD shortens the ha
143 Pulse-chase experiments reveal that the p53 upregulation
144 Pulse-chase experiments reveal that, at a subsaturating
145 Finally,
pulse-chase experiments reveal the spatiotemporal coordi
146 nding occurred at 2.1 muM(-1) s(-1), and the
pulse-chase experiments revealed an ATP-promoted isomeri
147 sis of polyadenylated RNA stability via 5-EU
pulse-chase experiments revealed RNAs with shorter half-
148 In contrast,
pulse-chase experiments revealed significantly shorter d
149 Pulse-chase experiments revealed that A774wt and avirule
150 Metabolic
pulse-chase experiments revealed that after core glycosy
151 Fourth,
pulse-chase experiments revealed that cholesterol enrich
152 Pulse-chase experiments revealed that CPAF was initially
153 Pulse-chase experiments revealed that cytoplasmic WHx ha
154 Pulse-chase experiments revealed that IE2-86 but not IE1
155 Pulse-chase experiments revealed that Msh2-Msh6 binds AT
156 Pulse-chase experiments revealed that newly made protein
157 nously expressing PC1, both steady-state and
pulse-chase experiments revealed that peptides derived f
158 Fate mapping using BrdU
pulse-chase experiments revealed that such deficits may
159 In fact,
pulse-chase experiments revealed that synthesis of p53 i
160 Furthermore,
pulse-chase experiments revealed that the binding of QPD
161 Pulse-chase experiments revealed that the DeltaMAM and a
162 Pulse-chase experiments revealed that the half-life of t
163 y-state levels of the mMCP-2 transcript, and
pulse-chase experiments revealed that the half-life of t
164 A series of
pulse-chase experiments revealed that the origin of aort
165 Pulse-chase experiments revealed that the t(1/2) of scFv
166 HO cells stably expressing the hKOR-N25/39Q,
pulse-chase experiments revealed that the turnover rate
167 Pulse-chase experiments revealed that the turnover rate
168 Pulse-chase experiments revealed that transferrin accumu
169 Pulse chase experiments show that Tap/NXT significantly
170 Pulse-chase experiments show that although the viral gly
171 Pulse-chase experiments show that approximately 35% of t
172 Rather,
pulse-chase experiments show that decreases in steady st
173 Bromodeoxyuridine
pulse-chase experiments show that distal and proximal bl
174 Pulse-label and
pulse-chase experiments show that GPA is not incorporate
175 Pulse and
pulse-chase experiments show that IL-2 stimulation resul
176 lferrin is also found in the cytoplasm where
pulse-chase experiments show that it, in turn, releases
177 Pulse-chase experiments show that one of the splice vari
178 Metabolic
pulse-chase experiments show that TC10 did not affect CF
179 Interestingly, both Western blotting and a
pulse-chase experiment showed co-immunoprecipitation of
180 In addition, a
pulse-chase experiment showed that the depletion of MCL1
181 A
pulse-chase experiment showed that, at 37 degrees C but
182 Pulse-chase experiments showed a monophasic degradation
183 Pulse-chase experiments showed an enhanced degradation a
184 Pulse-chase experiments showed CLIP dissociated more rap
185 affinity of the aldehydes for P450 2A6, but
pulse-chase experiments showed only limited exchange wit
186 Furthermore,
pulse-chase experiments showed PKCdelta is stabilized in
187 Pulse-chase experiments showed that a fraction of gO rem
188 Pulse-chase experiments showed that a portion of newly s
189 Pulse-chase experiments showed that BIN1 was short-lived
190 Pulse-chase experiments showed that both mutant and wild
191 Pulse-chase experiments showed that caveolin-1 palmitoyl
192 Pulse-chase experiments showed that collagen type I secr
193 Significantly,
pulse-chase experiments showed that cotransfection of Nr
194 Metabolic labeling and
pulse-chase experiments showed that ectopic hBH expressi
195 Pulse-chase experiments showed that G protein folding in
196 Pulse-chase experiments showed that p150 is rapidly gene
197 Pulse-chase experiments showed that PreGN C-terminal cle
198 Pulse-chase experiments showed that secretion of rVWFR27
199 Pulse-chase experiments showed that sMR production in cu
200 Pulse-chase experiments showed that SR-BII rapidly inter
201 Pulse-chase experiments showed that the astrovirus capsi
202 Metabolic
pulse-chase experiments showed that the CD3 gamma-chain
203 Pulse-chase experiments showed that the contribution of
204 Pulse-chase experiments showed that the induced form of
205 Pulse-chase experiments showed that the interaction betw
206 Long-term
pulse-chase experiments showed that the mature DeltaRI/D
207 Pulse-chase experiments showed that the sulfated complex
208 Pulse-chase experiments showed that these fragments were
209 Pre-steady-state
pulse-chase experiments showed that three ATPs were tigh
210 Pulse-chase experiments showed that UT-A1 half-life is r
211 Pulse/chase experiments showed that the newly synthesize
212 In
pulse-chase experiments,
stellate-shaped NCMs with rando
213 In
pulse-chase experiments,
stretch in parallel with the MF
214 ckdown, REGgamma-deficient MEF analysis, and
pulse-chase experiments substantiate that REGgamma promo
215 Our previous in organello
pulse-chase experiments suggest that poly(A) tails stimu
216 Cell synchronization and
pulse-chase experiments suggest that the timing of Chs2p
217 cell medium very early during the course of
pulse-chase experiments suggested that natural Abeta oli
218 Here, we report genetic
pulse-chase experiments that define osteoblastic cells a
219 We demonstrate, using [35S]methionine
pulse-chase experiments,
that native eNOS in adult rat v
220 During a brief
pulse-chase experiment,
the fluorescent lipid accumulate
221 In
pulse-chase experiments,
the mutant islets incorporate l
222 In
pulse-chase experiments,
the newly synthesized type I pr
223 In
pulse-chase experiments,
the primary Vhs translation pro
224 In
pulse-chase experiments,
the two pools of calnuc had dif
225 We employed a carbon-13
pulse-chase experiment to investigate how a temperate es
226 Application of the modified
pulse-chase experiment to the study of rapidly formed fo
227 rd commitment to catalysis was determined by
pulse-chase experiments to be 0.70%.
228 To overcome this difficulty, we used Mg(2+)
pulse-chase experiments to differentiate each reaction i
229 echniques to follow formation of NR by using
pulse-chase experiments to examine protein and lipid del
230 In
pulse-chase experiments to examine the effects of Ad-Acs
231 r organ culture and bromodeoxyuridine (BrdU)
pulse-chase experiments to identify and evaluate stem ce
232 By combining
pulse-chase experiments to measure the rate at which the
233 We performed
pulse-chase experiments to monitor the fate of endogenou
234 ng, molecular imaging, and [(35)S]methionine
pulse-chase experiments,
together with lysosome (chloroq
235 Pulse-chase experiments unambiguously demonstrate that a
236 In
pulse chase experiments using a deconvolved, confocal li
237 A
pulse-chase experiment using [35S]methionine labeling of
238 Here we describe a new
pulse-chase experiment using long-term enrichment with 1
239 Finally,
pulse-chase experiments using [(14)C]serine revealed tha
240 Pulse-chase experiments using [(35)S]methionine metaboli
241 Pulse-chase experiments using [35S]methionine demonstrat
242 Rev protein in living cells was evaluated by
pulse-chase experiments using a transient Rev expression
243 Pulse-chase experiments using hepatocytes isolated from
244 From the results of
pulse-chase experiments using radiolabeled intact yeast
245 Pulse-chase experiments using transiently transfected CO
246 In
pulse chase experiments,
using metabolically 35S-labeled
247 In
pulse-chase experiments,
vacuoles labeled with the lumen
248 In
pulse-chase experiments,
various chase periods decreased
249 A
pulse-chase experiment was used to demonstrate that even
250 nucleocapsids into virions as determined in
pulse-chase experiments was dependent on the activity of
251 Here, using a (13)C
pulse-chase experiment,
we demonstrate how trophic struc
252 Using
pulse-chase experiments,
we also discovered that the pec
253 Using
pulse-chase experiments,
we found that at equivalent dos
254 By
pulse-chase experiments,
we found that the half-lives of
255 lizing in vivo imaging and bromodeoxyuridine
pulse-chase experiments,
we have analyzed growth and reg
256 Using
pulse-chase experiments,
we have demonstrated that wild-
257 es to different parts of the molecule and in
pulse-chase experiments,
we showed that the C terminus o
258 ed cells to assemble the tripartite complex,
pulse-chase experiments were performed.
259 action time courses, substrate trapping, and
pulse-chase experiments were used to assess folate relea
260 Pulse-chase experiments were used to examine the uptake
261 NMR
pulse-chase experiments were used to show that 13C-enric
262 of these mutant enzymes was also studied by
pulse-chase experiments which produced results consisten
263 sults are further supported by proteome-wide
pulse-chase experiments,
which show that the loss of UCH
264 Pulse-chase experiments with (14)CO(2) show that transpo
265 Pulse-chase experiments with 5-EU allowed us to determin
266 In studies with cycloheximide or in
pulse-chase experiments with [(35)S]methionine, we demon
267 lation of sarcolemmal eNOS, as determined by
pulse-chase experiments with [3H]palmitate.
268 of protein degradation kinetics obtained in
pulse-chase experiments with Bayesian data fitting using
269 inetic lags were observed in acid formation;
pulse-chase experiments with carrier aldehydes showed on
270 Optical
pulse-chase experiments with Dendra2-tagged aSyn version
271 Pulse-chase experiments with dialkylindocarbocyanine low
272 Through
pulse-chase experiments with halogenated thymidine analo
273 By
pulse-chase experiments with in vivo L-[methyl-(3)H]meth
274 Pulse-chase experiments with labeled fatty acids in all
275 Pulse-chase experiments with radiolabeled sugars and ami
276 Bromodeoxyuridine
pulse-chase experiments with short survival times sugges
277 Pulse and
pulse/chase experiments with BrdU confirmed the germinal