1 sufficient to confer STI-571 resistance in a
reconstitution experiment.
2 or the assembly of the NLRP3 inflammasome in
reconstitution experiment.
3 es, human hepatoma cell lines and telomerase
reconstitution experiments.
4 ild-type and mutant proteins in inflammasome
reconstitution experiments.
5 ough a methodological series of knockout and
reconstitution experiments.
6 sh multilineage hematopoiesis in competitive
reconstitution experiments.
7 subjected the purified monomers to in vitro
reconstitution experiments.
8 on of chlamydial protective antigens through
reconstitution experiments.
9 ral CoQ10 content, were chosen for depletion/
reconstitution experiments.
10 aches: antibody interception experiments and
reconstitution experiments.
11 ultured tracheal SMC and verified by in vivo
reconstitution experiments.
12 topoietic cells were excluded by bone marrow
reconstitution experiments.
13 rrent interpretation of the classic omission-
reconstitution experiments.
14 the tubulin-blocked state in single-channel
reconstitution experiments.
15 ctivation by InsP(3) in planar lipid bilayer
reconstitution experiments.
16 d MPK substrates were validated by in planta
reconstitution experiments.
17 nstability (CIN) in vivo using hematopoietic
reconstitution experiments.
18 r was Pol epsilon able to extend a D-loop in
reconstitution experiments.
19 mi1 subunit also stimulates Top3 activity in
reconstitution experiments.
20 In in vitro
reconstitution experiments,
acetylation was sufficient t
21 Here we use biochemical
reconstitution experiments alongside genetic and structu
22 In vitro
reconstitution experiments also indicated that sequences
23 In vitro
reconstitution experiments also show that the associatio
24 In vitro
reconstitution experiments also support that TLR2 mediat
25 id composition used for bilayer formation in
reconstitution experiments and increases with the increa
26 ) pathogenic T cells (CD4(+Path) T cells) in
reconstitution experiments and most efficiently ablated
27 diolipin stabilizes UCP1, as demonstrated by
reconstitution experiments and thermostability assays, i
28 Reconstitution experiments antagonized IGF-I-mediated MA
29 es of protein binding inferred from omission-
reconstitution experiments are thought to preclude certa
30 ngeability with hTERT in in vitro telomerase
reconstitution experiments,
as mTERT produces strong tel
31 In vitro
reconstitution experiments,
as well as analysis of CRISP
32 Crossed bone marrow
reconstitution experiments between A/J and MHC congenic
33 In biochemical
reconstitution experiments,
both response elements are a
34 In p53-
reconstitution experiments,
cell-cycle arrest, apoptosis
35 In marrow
reconstitution experiments,
coexpression of both genes p
36 By reciprocal
reconstitution experiments,
comparing wild-type versus P
37 t are consistent with this location and with
reconstitution experiments conducted with isolated perip
38 Biochemical in vitro
reconstitution experiments confirmed electron transport
39 Serum-free
reconstitution experiments confirmed the involvement of
40 In vitro
reconstitution experiments confirmed the requirement for
41 In
reconstitution experiments,
CRAF R391W, but not CRAF WT,
42 Reconstitution experiments demonstrate linearity of ASE
43 Lastly,
reconstitution experiments demonstrate that Jak2 is not
44 Reconstitution experiments demonstrate that Ppr covalent
45 Remarkably, in vitro
reconstitution experiments demonstrate that Wapl forms a
46 entified and immunoneutralizing antibody and
reconstitution experiments demonstrated IL-8 is a critic
47 In vitro
reconstitution experiments demonstrated that CENP-E-depe
48 Interestingly, in vitro
reconstitution experiments demonstrated that NIK was act
49 Medium
reconstitution experiments demonstrated that spent mediu
50 In vitro
reconstitution experiments demonstrated that the 53-kDa
51 Reconstitution experiments demonstrated that the additio
52 Soluble
reconstitution experiments demonstrated that the chimeri
53 Moreover,
reconstitution experiments demonstrated that the peptide
54 Fetal liver
reconstitution experiments demonstrated that the require
55 Competitive
reconstitution experiments demonstrated that Zfp36l2 KO
56 ctivity of Spo0A in vivo and, using in vitro
reconstitution experiments,
determine that they stimulat
57 sponsible for inhibition of LH1 formation in
reconstitution experiments,
different regions (N-terminu
58 In
reconstitution experiments,
either whole splenocytes, T
59 for AP release; however, immunodepletion and
reconstitution experiments establish that it is necessar
60 In vitro
reconstitution experiments established that the soluble
61 Metal
reconstitution experiments examining the reaction kineti
62 Taken together, these microbial
reconstitution experiments formally establish that a def
63 Bone marrow
reconstitution experiments further mapped the effect of
64 Reconstitution experiments further reveal that ApoER2-R9
65 Competitive
reconstitution experiments further showed that fetal liv
66 Bone marrow
reconstitution experiments further supported an intrinsi
67 arrow transplantation and platelet depletion/
reconstitution experiments generating mice with selectiv
68 way for eukaryotic RNA polymerases, in vitro
reconstitution experiments have been carried out with re
69 inhibit Ca(2+) uptake in imaging assays, and
reconstitution experiments have been equivocal.
70 marrow (BM) have been described, irradiation-
reconstitution experiments have failed to reveal defects
71 Reconstitution experiments have suggested that N-ethylma
72 Holoenzyme
reconstitution experiments identified a new sigma factor
73 Bone marrow
reconstitution experiments identified that many of the h
74 d optical tweezers to observe in a cell-free
reconstitution experiment in real time a long-sought SNA
75 Cell depletion and
reconstitution experiments in a DSS-induced colitis mode
76 s as shown by overexpression, knockdown, and
reconstitution experiments in cell culture models.
77 In this report, we conducted nucleosome
reconstitution experiments in conjunction with high-thro
78 examine this question, we have used genetic
reconstitution experiments in mice.
79 Knockdown and
reconstitution experiments in mouse and human breast can
80 Reconstitution experiments in non-hematopoietic cells sh
81 ant of HP68 in mammalian cells and depletion-
reconstitution experiments in the cell-free system, we d
82 Reconstitution experiments in the JAK1-deficient cells d
83 In
reconstitution experiments in the same cell line all fou
84 Further,
reconstitution experiments in total head homogenates sho
85 However, in heterologous
reconstitution experiments in vitro with RNase P subunit
86 Reconstitution experiments in which LDLR variants were i
87 Reconstitution experiments in which non-polysomal mRNA-b
88 We performed in vivo
reconstitution experiments in which ST8Sia IV(-/-) proge
89 Depletion-
reconstitution experiments in Xenopus laevis egg extract
90 Reconstitution experiments in yeast demonstrated that LG
91 Our in vitro
reconstitution experiments indeed identified a 5' nick-d
92 Reconstitution experiments indicate that both STG-1 and
93 Reconstitution experiments indicate that MPN/MDS and mye
94 Direct
reconstitution experiments indicate that NK cytotoxic ac
95 Reconstitution experiments indicate that nucleotide and
96 Recent
reconstitution experiments indicate that one of these, R
97 Mixed bone marrow
reconstitution experiments indicate that sbb2(a) is expr
98 Reconstitution experiments indicate that specific functi
99 4Fe-4S and 3Fe-4S clusters, and the in vitro
reconstitution experiment indicated an iron-sulfur scaff
100 Reconstitution experiments indicated that CCND1 and p53
101 Bone marrow
reconstitution experiments indicated that the mechanism
102 In planar lipid bilayer
reconstitution experiments,
InsP3R1 activation by InsP3
103 In
reconstitution experiments,
lysophosphatidic acid comple
104 In in vitro
reconstitution experiments,
NiV particles provided time-
105 Using bone marrow
reconstitution experiments of lethally irradiated hosts,
106 NMR, and resonance Raman spectroscopies with
reconstitution experiments of the apoprotein with protoh
107 Combined with in vitro
reconstitution experiments,
our data show that the polym
108 In vitro
reconstitution experiment proves that MMP-13, but not it
109 dings, together with the results of previous
reconstitution experiments,
reduce the number of possibl
110 Competitive
reconstitution experiments reveal that fucoidan also eli
111 Data obtained in bone marrow
reconstitution experiments reveal that interleukin-1beta
112 Reconstitution experiments reveal that symplekin, previo
113 Reconstitution experiments revealed an important role fo
114 from infected HeLa cell lysates and in vitro
reconstitution experiments revealed evidence for ubiquit
115 t for T-bet in these subsets and competitive
reconstitution experiments revealed roles for T-bet in m
116 Reconstitution experiments revealed that Hunk is suffici
117 ith recombinant kinase, and kinase depletion-
reconstitution experiments revealed that Ser1232 in eIF4
118 However,
reconstitution experiments revealed that the catalytic a
119 urther mechanistic studies using bone marrow
reconstitution experiments revealed that the increased d
120 Biochemical
reconstitution experiments revealed that the polyubiquit
121 In this work, 30S ribosomal subunit kinetic
reconstitution experiments revealed that thermodynamic d
122 The results from both in vivo and in vitro
reconstitution experiments show increased activity level
123 Competitive
reconstitution experiments show that average levels of 0
124 In vivo
reconstitution experiments show that CLPs and CMPs can r
125 Bone marrow
reconstitution experiments show that Nlrp3 gene expressi
126 Bone marrow
reconstitution experiments show that Nogo in myeloid cel
127 Finally,
reconstitution experiments show that the association of
128 Reconstitution experiments show that the binding pocket
129 Reconstitution experiments show that the helicase activi
130 Bone marrow
reconstitution experiments show that the PC defect is B-
131 Bone marrow (BM)
reconstitution experiments showed monocyte-dependent qua
132 The results from
reconstitution experiments showed that aged bone marrow
133 Enzyme
reconstitution experiments showed that both microsomal a
134 Bone marrow
reconstitution experiments showed that gammadelta T cell
135 In vitro
reconstitution experiments showed that like AV, but in c
136 Pharmacological and lipid
reconstitution experiments showed that new synapses form
137 ilateral inhibition of suckling and hormonal
reconstitution experiments showed that TGFbeta3 inductio
138 Reconstitution experiments showed that the formation of
139 Biochemical
reconstitution experiments showed that the two intronic
140 Promoter
reconstitution experiments showed that this novel elemen
141 Reconstitution experiments showed that, for the Sir2/Sir
142 Reconstitution experiments showed tight interactions bet
143 yond the nucleolus, consistent with in vitro
reconstitution experiments showing that SRP19 must bind
144 Reconstitution experiments suggest that EP2 receptors pr
145 Reconstitution experiments suggest that the discrepancy
146 Our in vitro
reconstitution experiments suggest that the Z-ring consi
147 Reconstitution experiments suggest that, although OB-R m
148 Results of depletion/
reconstitution experiments suggested that KuAg does not
149 In the
reconstitution experiments,
SV40 DNA was allowed to inte
150 Here, we show using functional GFP
reconstitution experiments that Kenyon cells and dopamin
151 llular source for this mediator, we find via
reconstitution experiments that mast cells are a dispens
152 as cell autonomous, because in a competitive
reconstitution experiment the knockout-derived cells pro
153 de RNAi screening approaches and biochemical
reconstitution experiments,
the basic machinery of FGF2
154 In
reconstitution experiments,
the mitochondrial cytochrome
155 whole frequency range accessible in channel
reconstitution experiments,
the noise power spectrum is
156 vivo fluorescence spectroscopy, and in vitro
reconstitution experiments,
this study demonstrates that
157 e have used structural probing and molecular
reconstitution experiments to examine the structures for
158 Dyn2 KO cell line and performed knockout and
reconstitution experiments to explore the isoform- and s
159 We have now used fractionation and
reconstitution experiments to functionally identify cell
160 cipitation-coupled western blot and in vitro
reconstitution experiments to show that HSP70-2 interact
161 We performed BAC mutagenesis and
reconstitution experiments to test the hypothesis that t
162 Reconstitution experiments to unravel essential componen
163 mpaired in the LTalpha-/- mice, we performed
reconstitution experiments using a hapten/carrier system
164 In
reconstitution experiments using purified proteasomes an
165 Reconstitution experiments using recombinant proteins an
166 e was essential in promoting angiogenesis as
reconstitution experiments using Src-transformed FAK-nul
167 Reconstitution experiments utilizing exogenous recombina
168 Through
reconstitution experiments,
we demonstrate here that TIN
169 lusions based on nonphysiological nucleosome
reconstitution experiments,
we find that the histone ami
170 Through
reconstitution experiments,
we have defined more precise
171 Through live cell and in vitro
reconstitution experiments,
we have discovered a major s
172 Using depletion and
reconstitution experiments,
we showed that IL-4-responsi
173 Depletion and
reconstitution experiments were consistent with a suppre
174 In this study, biochemical
reconstitution experiments were used to gain insight int
175 tional activity in an in vitro transcription
reconstitution experiment,
whereas the L protein in peak
176 Reconstitution experiments with a chemically synthesized
177 onstructs, coimmunoprecipitation, functional
reconstitution experiments with deletion mutants, and pe
178 Reconstitution experiments with different fusion assays
179 Reconstitution experiments with different RIP mutants fu
180 We perform in vitro motility
reconstitution experiments with high-resolution particle
181 Reconstitution experiments with mutant MAP65-1 proteins
182 Reconstitution experiments with pertussis toxin-insensit
183 In vitro
reconstitution experiments with proteins from both M. ca
184 In vitro
reconstitution experiments with purified cyt b6f and rec
185 Using bone marrow
reconstitution experiments with purified PIGA(-) cells w
186 Reconstitution experiments with purified proteins indica
187 Reconstitution experiments with recombinant interleukin
188 In
reconstitution experiments with recombinantly expressed
189 Reconstitution experiments with the individual genes dem
190 A combination of knockdown and
reconstitution experiments with wild type and a PDZ doma
191 trated in vitro using blocking antibody, and
reconstitution experiments with wild-type and mutant Fcg
192 Affinity chromatography and biochemical
reconstitution experiments with Xenopus egg extracts ide
193 Renaturation and
reconstitution experiments with Zn(2+) ions failed to pr