1 lymer) chains poses significant problems for
biochemical analysis.
2 The right donor kidneys were stored for
biochemical analysis.
3 tase-PCR (RT-PCR) and for haematological and
biochemical analysis.
4 l rods are converted to cone-like cells) for
biochemical analysis.
5 nism of action through extensive genetic and
biochemical analysis.
6 ver been isolated in an intact form to allow
biochemical analysis.
7 nd (31)P magnetic resonance spectroscopy and
biochemical analysis.
8 increasingly important role in chemical and
biochemical analysis.
9 ng of information can be detrimental to pure
biochemical analysis.
10 uid samples were taken for microbiologic and
biochemical analysis.
11 r(428) as revealed by mass spectrometric and
biochemical analysis.
12 s in both native grass and wheat hosts using
biochemical analysis.
13 20 strains, 20alpha and 20beta, by extensive
biochemical analysis.
14 ous morphological, molecular biological, and
biochemical analysis.
15 itamin was confirmed in final formulation by
biochemical analysis.
16 ed by dose response and subjected to further
biochemical analysis.
17 LacY-based crystal structures and refined by
biochemical analysis.
18 Biochemical analysis,
active site architecture molecular
19 tissues were collected for histological and
biochemical analysis after 16 weeks of diet exposure.
20 on of these two subunits by a combination of
biochemical analysis and cellular assays.
21 Biochemical analysis and comparative proteomics with 6Az
22 By combining
biochemical analysis and electron microscopy, we have st
23 Biochemical analysis and five crystal structures of OTU
24 hey have proven amenable to both genetic and
biochemical analysis and have recently been shown to exh
25 We have used a combination of
biochemical analysis and knockdown replacement studies i
26 surfaces can be applied in water harvesting,
biochemical analysis and lab-on-chip devices.
27 dentify this ligand, we performed integrated
biochemical analysis and mass spectrometry studies of G-
28 Here, we use deep mutational scanning,
biochemical analysis and molecular simulations to unders
29 repair has been limited to defined in vitro
biochemical analysis and prokaryotic cells.
30 ission that is amenable to both quantitative
biochemical analysis and real-time imaging by epifluores
31 Detailed
biochemical analysis and targeted gene disruption studie
32 Collection, were grown in Stoneville, MS for
biochemical analysis and tofu texture and sensory qualit
33 Biochemical analysis and whole-exome sequencing identifi
34 Using a combination of bioinformatics,
biochemical analysis,
and cell-based assays, we identify
35 , a combination of cryo-electron microscopy,
biochemical analysis,
and crystal structure determinatio
36 t TERT in western blots, immunopurify it for
biochemical analysis,
and determine its subcellular loca
37 Nutrient deprivation,
biochemical analysis,
and metabolite quantification were
38 nt in the MyD88, TIRAP/MAL, or TRIF adaptor,
biochemical analysis,
and the use of specific small inte
39 P-gp not only is compatible with decades of
biochemical analysis,
but also helps to explain perplexi
40 Detailed
biochemical analysis,
carried out using chromatographic,
41 Biochemical analysis,
computational modeling, and single
42 Biochemical analysis confirmed that amino acid substitut
43 Biochemical analysis confirmed this interaction and mapp
44 Biochemical analysis confirms that Brd1 forms a HAT comp
45 s one of the most important technologies for
biochemical analysis critical for diagnosis and monitori
46 These structures, combined with
biochemical analysis,
define features for the conjugatio
47 Biochemical analysis delineates ZirT into an N-terminal
48 Genetic and
biochemical analysis demonstrated that AtICln is in the
49 Interestingly,
biochemical analysis demonstrated that both HupL and Nif
50 Biochemical analysis demonstrated that CNGA3 channels la
51 Biochemical analysis demonstrated that the mutation abol
52 Biochemical analysis demonstrated that these five putati
53 Consistently,
biochemical analysis demonstrates that the compound abat
54 Biochemical analysis demonstrates that the substrate pre
55 Biochemical analysis determined that the mutant EPHB4 pr
56 als with presumed cblC based on cellular and
biochemical analysis do not have mutations in MMACHC.
57 Biochemical analysis established the role of C. trachoma
58 By contrast, confocal and protein
biochemical analysis failed to uncover substantial exo-
59 Biochemical analysis found that SufA bound and transferr
60 Biochemical analysis further shows that Ubx4 interacts w
61 nd other bacteria over the past 15 years, no
biochemical analysis had been conducted on any FlgJ and
62 Biochemical analysis has been combined with isothermal t
63 Structural and
biochemical analysis has led to the hypothesis that extr
64 Biochemical analysis has shown recently that the dual ph
65 Forty years of classical
biochemical analysis have identified the molecular playe
66 A wealth of genetic information and some
biochemical analysis have made the GAL regulon of the ye
67 Using mutational and
biochemical analysis,
here we identify Asp-46 and His-14
68 Biochemical analysis,
histology, and immunohistochemistr
69 Biochemical analysis identified delta-toxin as the mast
70 Biochemical analysis identified that KLKB1 cleaves scuPA
71 Structural and
biochemical analysis identified the molecular determinan
72 enesis of this groove, coupled with detailed
biochemical analysis,
identified residues that did not i
73 A
biochemical analysis identifies key residues in the acti
74 udy, we have performed detailed clinical and
biochemical analysis in 34 genetically confirmed SPG5 ca
75 Biochemical analysis in Chlamydomonas revealed that the
76 Based on pharmacological and
biochemical analysis in vitro and initial genetic analys
77 Through
biochemical analysis in Xenopus laevis egg extracts, we
78 Biochemical analysis including oxidative stress measurem
79 chniques that combine stain-free imaging and
biochemical analysis,
including Fourier transform infrar
80 Our structural and
biochemical analysis indicate that the enhanced potency
81 Previous
biochemical analysis indicated that Cas10, Csm2, Csm3, C
82 Biochemical analysis indicated that Slr1796 is an integr
83 Our
biochemical analysis indicates that B. burgdorferi CheD
84 Biochemical analysis indicates that F, G, and TM interac
85 Yet,
biochemical analysis indicates that light-dependent rece
86 Biochemical analysis indicates that Prp5 has reduced aff
87 Homology modeling and
biochemical analysis indicates that the C-terminal domai
88 ty of this system to direct live imaging and
biochemical analysis makes it ideal for the modeling and
89 ently, and the requisite detachment prior to
biochemical analysis might induce chemical changes.
90 Furthermore,
biochemical analysis of 9-PAHSA biosynthesis and degrada
91 Here, we describe a thorough molecular and
biochemical analysis of a mutant FOS protein we identifi
92 Finally, structural and
biochemical analysis of a ribosome particle depleted of
93 Our
biochemical analysis of a SOCS-family regulator from a l
94 Here, we used a
biochemical analysis of a tomato introgression line with
95 Here we perform a structural and
biochemical analysis of a ubiquitin-like modification pa
96 Biochemical analysis of AAV9-treated GM1 mice showed hig
97 paradigm, as well as immunohistological and
biochemical analysis of AD-related neuropathology.
98 ich is consistent with the structure and our
biochemical analysis of AgmNAT.
99 Biochemical analysis of AKAP220-null kidney extracts det
100 [(18)F]fluorothymidine (FLT)-uptake, and by
biochemical analysis of ALK-induced signaling.
101 Through targeted gene disruption,
biochemical analysis of all predicted glycoside hydrolas
102 Here, we present a detailed
biochemical analysis of an archaeal transcriptional acti
103 Comparative genomics and
biochemical analysis of ASAT enzymes were combined with
104 Biochemical analysis of AtDEG15 deletion constructs in p
105 the crystal structure of B204 along with the
biochemical analysis of B204 mutants chosen based on str
106 Biochemical analysis of BiXyn10A demonstrated that such
107 Biochemical analysis of blood and urine samples.
108 We carried out a structural and
biochemical analysis of both the human and Xenopus laevi
109 Finally, biologic and
biochemical analysis of BRAF(V600E)/PIK3CA(H1047R)-expre
110 , mouse embryonic stem cells, and Drosophila
Biochemical analysis of BRWD2 demonstrated an associatio
111 Biochemical analysis of C-RPS3 revealed that it comprise
112 X-ray structures and
biochemical analysis of C6orf130 suggest a mechanism of
113 Biochemical analysis of candidate mutations revealed tha
114 Biochemical analysis of CD148-deficient ASM revealed hyp
115 Traditional
biochemical analysis of chromatin-associated complexes r
116 cted the role of the flanking DNA segment by
biochemical analysis of complexes formed using DNAs with
117 Biochemical analysis of cortical extracts from behaviora
118 Biochemical analysis of de novo induced cultures indicat
119 To facilitate the
biochemical analysis of deadenylase enzymes, we have dev
120 Biochemical analysis of Destructin-1 showed that it medi
121 Biochemical analysis of detergent-soluble and detergent-
122 Gene expression, enzymatic activity and
biochemical analysis of developing cotton fibers was per
123 Our
biochemical analysis of E1 helicase demonstrates that a
124 Here, combining the
biochemical analysis of enzymatic and motile properties
125 his study we exploited recent structural and
biochemical analysis of ERAP1 and ERAP2 to design and de
126 Biochemical analysis of existing muscle biopsies was cor
127 sing a combination of structural imaging and
biochemical analysis of extracted waxes.
128 Using
biochemical analysis of fission-yeast cohesin, we find t
129 The structure and
biochemical analysis of five cohesin-dockerin complexes
130 Biochemical analysis of five representatives of these re
131 ased quantification of Abeta plaque load and
biochemical analysis of formic acid-extracted Abetax-40
132 Biochemical analysis of Galpha13 shows SR2 binds directl
133 Biochemical analysis of hearts from Lmna(H222P/H222P) mi
134 Biochemical analysis of heterodimers between wild-type a
135 Biochemical analysis of Hrq1 reveals a DEAH box- and ATP
136 Using comprehensive physiological and
biochemical analysis of intestinal and renal tissues fro
137 ch to stable isotope tracing facilitates the
biochemical analysis of known pathways and yields rapid
138 nces in recent years have revolutionized the
biochemical analysis of lipids in plants, and made possi
139 Following diet-induced obesity,
biochemical analysis of livers revealed that asparaginas
140 Biochemical analysis of multiple Fusobacterium strains r
141 Structural and
biochemical analysis of NolR reveals protein-DNA interac
142 detection of nuclear Abeta42 as follows: (i)
biochemical analysis of nuclear fractions; (ii) detectio
143 anisms, and possible therapies will hinge on
biochemical analysis of patient-derived materials and an
144 this study we provide a unique and detailed
biochemical analysis of Pch2.
145 A detailed
biochemical analysis of PhnF binding to its identified b
146 ethod for label-free, in vivo structural and
biochemical analysis of plant cuticles based on stimulat
147 Biochemical analysis of plasma cytokine levels and immun
148 The previous studies were carried out by
biochemical analysis of portions of the authentic viral
149 Biochemical analysis of prostate cancer cell lines revea
150 Biochemical analysis of PSII complexes further indicates
151 Notwithstanding the speed of the process,
biochemical analysis of purified aggregates showed the p
152 In this study, we performed an in-depth
biochemical analysis of purified CHD6, CHD7, and CHD8 an
153 A
biochemical analysis of purified recombinant human Twink
154 Here, we report a detailed
biochemical analysis of RbgA and its interaction with th
155 Here we present the first
biochemical analysis of recombinant RecQ[Bs].
156 Biochemical analysis of recombinant zebrafish Papp-a dem
157 We used a combination of genome sequencing,
biochemical analysis of redox active components, and sho
158 Biochemical analysis of ribosomal initiation complexes a
159 Since
biochemical analysis of SAD6 in yeast (Saccharomyces cer
160 The resulting energy profiles, supported by
biochemical analysis of site-directed mutants disturbing
161 Histological and
biochemical analysis of STIM1 transgenic mice showed ful
162 Biochemical analysis of STM2215 determined that it is lo
163 The structures and
biochemical analysis of structure-inspired mutants showe
164 Biochemical analysis of TgASH1 indicated that this enzym
165 Here, we report a
biochemical analysis of the ASK1 kinase domain in conjun
166 These compounds may be useful tools for the
biochemical analysis of the Caf1/CNOT7 deadenylase subun
167 Biochemical analysis of the corresponding triphosphates
168 Biochemical analysis of the DCL1 suppressor variants rev
169 Here, we have carried out a
biochemical analysis of the different NC populations upo
170 r fluorescent receptor-based probes and from
biochemical analysis of the effect of sigma2 selective l
171 Biochemical analysis of the encoded proteins, a cobalami
172 ubstrate, and lay the foundation for further
biochemical analysis of the enzyme.substrate complex and
173 The
biochemical analysis of the interacting regions provides
174 imbine-induced impulsivity on the 5CSRTT and
biochemical analysis of the lateral orbital frontal cort
175 d to nonantigenic lipids, followed by direct
biochemical analysis of the lipid antigens trapped at th
176 Nevertheless,
biochemical analysis of the lipid profile in blood in vi
177 Biochemical analysis of the lipoglycans obtained in the
178 Here we present a structural and
biochemical analysis of the more primitive ancestral for
179 Biochemical analysis of the mutations revealed that they
180 Preliminary
biochemical analysis of the N-terminal nonribosomal pept
181 Data from the
biochemical analysis of the nuclear and cytosolic fracti
182 Biochemical analysis of the pepsin-induced fibrils impli
183 Moreover, the structural and
biochemical analysis of the prefusion variants suggests
184 However, there has been only basic
biochemical analysis of the role of TPP1 in the telomera
185 Structural and
biochemical analysis of the SopB GTPase binding domain i
186 Here, we present a detailed structural and
biochemical analysis of the surface antigens of the viru
187 These assessments included
biochemical analysis of the TGFbeta and VEGF signaling a
188 Here we report a
biochemical analysis of these mutations based on rapid s
189 Here, we present a
biochemical analysis of these pathways.
190 Biochemical analysis of this C3 cleavage fragment reveal
191 Biochemical analysis of this enzyme provides insight int
192 Our structure and
biochemical analysis of this enzyme reveals its activati
193 Biochemical analysis of three B. pseudomallei CdiA-CTs r
194 PLA analysis of neurons in vitro and
biochemical analysis of tissue subsynaptic fractions con
195 Biochemical analysis of TOP3beta revealed that this topo
196 Systematic cell biology and
biochemical analysis of two markers (GRP78, sXBP-1) in t
197 The X-ray crystallographic and
biochemical analysis of two proteins encoded by this PUL
198 ermination of the DivL crystal structure and
biochemical analysis of wild-type and site-specific DivL
199 Biochemical analysis of WRN protein purified from TT lym
200 the protein or enzyme that can be useful for
biochemical analysis or genome modifications.
201 -electron tomography with mass spectrometry,
biochemical analysis,
perturbation experiments and struc
202 We introduce a portable
biochemical analysis platform for rapid field deployment
203 Biophysical/
biochemical analysis proved that two mutually exclusive
204 Biochemical analysis revealed a relatively high perchlor
205 fic changes at high stoichiometry sites, and
biochemical analysis revealed altered acetyl-CoA metabol
206 Phosphoproteomic and
biochemical analysis revealed an association between CTL
207 Moreover, proteomics and
biochemical analysis revealed CORO1C, another F-actin bi
208 Biochemical analysis revealed decreased beta-catenin pho
209 Biochemical analysis revealed defective mitochondrial fu
210 A
biochemical analysis revealed deficiencies in the activi
211 stry showed mitochondrial proliferation, and
biochemical analysis revealed severe complex I deficienc
212 The
biochemical analysis revealed that 41% of the patients p
213 Biochemical analysis revealed that as-APF increased p53
214 Biochemical analysis revealed that carotenoids are absen
215 Biochemical analysis revealed that CD55 was associated w
216 Biochemical analysis revealed that FAP163 is present in
217 Biochemical analysis revealed that his gammadelta and al
218 Biochemical analysis revealed that HSP60 knockdown incre
219 Biochemical analysis revealed that inhibiting AR resulte
220 Biochemical analysis revealed that its catalytic rate wa
221 maging, confocal imaging of cryosections and
biochemical analysis revealed that localization and traf
222 Biochemical analysis revealed that MEK/ERK reactivation
223 Biochemical analysis revealed that multiple elements in
224 Biochemical analysis revealed that Nrf2 appeared in the
225 Biochemical analysis revealed that OeGLU is a homomultim
226 Biochemical analysis revealed that PRR14, as a proline-r
227 Biochemical analysis revealed that the dimeric mutant al
228 Biochemical analysis revealed that the hexose monophosph
229 Biochemical analysis revealed that the nox mutant was sp
230 Quantitative mass spectrometry together with
biochemical analysis revealed that villin, an actin-modi
231 Biochemical analysis revealed that VT/GG substitutions d
232 Further
biochemical analysis revealed that YAF2 bridges interact
233 Biochemical analysis revealed this transformation is dep
234 Biochemical analysis revealed upregulation of proteins i
235 rate of recovery from desensitization, while
biochemical analysis reveals a large decrease in affinit
236 Structure-guided
biochemical analysis reveals that a second Arf1-GTP mole
237 Biochemical analysis reveals that ATP hydrolysis-fueled
238 d for their actions, but further genetic and
biochemical analysis reveals that beta-secretase activit
239 Biochemical analysis reveals that omega6 binds to beta'
240 Biochemical analysis reveals that PKCiota directly phosp
241 In addition,
biochemical analysis reveals that RPA serves to stimulat
242 Biochemical analysis reveals that Sesn3 interacts with a
243 Biochemical analysis reveals that the PTAP duplication r
244 Our
biochemical analysis reveals that the sequence-specific
245 Our structural and
biochemical analysis sheds new light on the molecular ba
246 Combined quantitative RT-PCR array and
biochemical analysis show that, upon the engagement of t
247 Biochemical analysis showed ChF has strong ferroxidase a
248 Biochemical analysis showed increased levels of protein
249 ACOX2 expression in the patient's liver, and
biochemical analysis showed marked elevation of intermed
250 Biochemical analysis showed that AMSH1 is an active deub
251 Biochemical analysis showed that DC2 and KCP2 are respon
252 Biochemical analysis showed that EhC2PK is an unusual Mn
253 Immunofluorescent and
biochemical analysis showed that H(2)O(2) led to increas
254 Genetic and
biochemical analysis showed that inflammation was caused
255 using MCF-7 breast cancer cells, and further
biochemical analysis showed that it caused accumulation
256 Biochemical analysis showed that low levels of PrP-res w
257 Biochemical analysis showed that OsJAR1 encoded an enzym
258 Biochemical analysis showed that PLD deficiency affected
259 Previous genetic and
biochemical analysis showed that POLD3 may promote lesio
260 Unbiased phosphoproteomics and
biochemical analysis showed that SHP2 activates several
261 Our
biochemical analysis showed that the PTAP duplication, i
262 Supporting its direct involvement,
biochemical analysis shows that A2BP1 is part of the Sup
263 Our structural and
biochemical analysis shows that by decoupling the action
264 In vitro
biochemical analysis shows that C2c2 is guided by a sing
265 Structural and
biochemical analysis shows that the active site features
266 structure has been recalcitrant to detailed
biochemical analysis,
so molecular details of how it ass
267 amples as low as 0.125 mug/ml prior to their
biochemical analysis such as in comparative proteomics.
268 in vitro mapping of protein-interactomes and
biochemical analysis suggest interactions between ZIKA-N
269 orescence microscopy, electrophysiology, and
biochemical analysis suggest METH exposure decreased the
270 Biochemical analysis suggests that both types of contact
271 mers together at the base of the trimer, and
biochemical analysis suggests that it neutralizes by inh
272 Informatic and
biochemical analysis suggests that large portions of the
273 Biochemical analysis suggests that the activity of coppe
274 Biochemical analysis suggests that this defect is multil
275 Our
biochemical analysis supports a model in which the trans
276 re, of particular importance to chemical and
biochemical analysis systems such as chromatography and
277 Based on sequence alignment and further
biochemical analysis,
the amino acid residue substitutio
278 tudy, we combined X-ray crystallographic and
biochemical analysis to characterize the association of
279 es the development of new methods of in vivo
biochemical analysis to complement established in vitro
280 molecule FRET, single molecule pull-down and
biochemical analysis to investigate how the most common
281 ined a genome-wide expression profiling with
biochemical analysis to reveal the molecular basis for i
282 re, we combined single-molecule and ensemble
biochemical analysis to show that FANCJ possesses a G4-s
283 re of the dimer, (alpha7)2, was confirmed by
biochemical analysis,
transmission electron microscopy a
284 Biochemical analysis using HP14 zymogen (proHP14), betaG
285 Biochemical analysis using NMR, fluorescence spectroscop
286 The
biochemical analysis using subfractionation studies show
287 Biochemical analysis using substrate and flavin analogs,
288 Biochemical analysis verified double-mutant 3CLpro enzym
289 Here, using cryo-electron microscopy and
biochemical analysis,
we define the molecular basis of h
290 Combining proteomics and
biochemical analysis,
we demonstrate here that cells are
291 In line with our
biochemical analysis,
we find that the number of bleachi
292 Along with a
biochemical analysis,
we show that P3 is catalytically i
293 By use of hydrogen/deuterium exchange and
biochemical analysis,
we show that the alpha8beta4 SiR h
294 Through crystallographic and
biochemical analysis,
we show that the RNF146 WWE domain
295 Using quantitative FRET and
biochemical analysis,
we show that VEGFR-2 forms dimers
296 ex remains associated in conditions used for
biochemical analysis with a dissociation constant of 5 n
297 On
biochemical analysis with cellulosic substrates, seven o
298 We coupled
biochemical analysis with confocal imaging of both fixed
299 Biochemical analysis with three biomarkers revealed that
300 Here, we combined
biochemical analysis with whole-exome sequencing (WES) t