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