1 s in both native grass and wheat hosts using
biochemical analysis.
2 itamin was confirmed in final formulation by
biochemical analysis.
3 allowing long-term, storage and simplifying
biochemical analysis.
4 ed by dose response and subjected to further
biochemical analysis.
5 LacY-based crystal structures and refined by
biochemical analysis.
6 lymer) chains poses significant problems for
biochemical analysis.
7 The right donor kidneys were stored for
biochemical analysis.
8 tase-PCR (RT-PCR) and for haematological and
biochemical analysis.
9 l rods are converted to cone-like cells) for
biochemical analysis.
10 nism of action through extensive genetic and
biochemical analysis.
11 ver been isolated in an intact form to allow
biochemical analysis.
12 nd (31)P magnetic resonance spectroscopy and
biochemical analysis.
13 ng of information can be detrimental to pure
biochemical analysis.
14 Blood and urine were subjected to
biochemical analysis.
15 MS lipidomics as a vital tool for impactful
biochemical analysis.
16 8 eyeballs from healthy donors were used for
biochemical analysis.
17 rough the generation of deletion mutants and
biochemical analysis.
18 tions have utilized mostly simple methods of
biochemical analysis.
19 esis, cell-signaling assays, microscopy, and
biochemical analysis.
20 e specific to Arc eRNA before behavioral and
biochemical analysis.
21 increasingly important role in chemical and
biochemical analysis.
22 Biochemical analysis,
active site architecture molecular
23 tissues were collected for histological and
biochemical analysis after 16 weeks of diet exposure.
24 Biochemical analysis and comparative proteomics with 6Az
25 By combining
biochemical analysis and electron microscopy, we have st
26 hey have proven amenable to both genetic and
biochemical analysis and have recently been shown to exh
27 surfaces can be applied in water harvesting,
biochemical analysis and lab-on-chip devices.
28 dentify this ligand, we performed integrated
biochemical analysis and mass spectrometry studies of G-
29 Here, we use deep mutational scanning,
biochemical analysis and molecular simulations to unders
30 In addition, we employed
biochemical analysis and observed differential N-linked
31 repair has been limited to defined in vitro
biochemical analysis and prokaryotic cells.
32 ission that is amenable to both quantitative
biochemical analysis and real-time imaging by epifluores
33 of 23 years was measured using clinical and
biochemical analysis and set as the main exposure.
34 Biochemical analysis and structural modeling establish t
35 Detailed
biochemical analysis and targeted gene disruption studie
36 Collection, were grown in Stoneville, MS for
biochemical analysis and tofu texture and sensory qualit
37 Using a combination of bioinformatics,
biochemical analysis,
and cell-based assays, we identify
38 , a combination of cryo-electron microscopy,
biochemical analysis,
and crystal structure determinatio
39 t TERT in western blots, immunopurify it for
biochemical analysis,
and determine its subcellular loca
40 Nutrient deprivation,
biochemical analysis,
and metabolite quantification were
41 nt in the MyD88, TIRAP/MAL, or TRIF adaptor,
biochemical analysis,
and the use of specific small inte
42 t pathologists, ATR-FTIR spectroscopy, lipid
biochemical analysis,
and UPLC-ESI(+/-)TOFMS for lipidom
43 A fragment-based
biochemical analysis approach is used here to directly q
44 Topological mapping and
biochemical analysis brought experimental evidences that
45 We describe how 4-dimensional in vivo
biochemical analysis can be performed using photoacousti
46 prion protein deposition) were analysed and
biochemical analysis carried out.
47 Detailed
biochemical analysis,
carried out using chromatographic,
48 Biochemical analysis,
computational modeling, and single
49 Biochemical analysis confirmed that amino acid substitut
50 Biochemical analysis confirmed this interaction and mapp
51 Biochemical analysis confirms that Brd1 forms a HAT comp
52 s one of the most important technologies for
biochemical analysis critical for diagnosis and monitori
53 Genetic and
biochemical analysis demonstrated that AtICln is in the
54 Interestingly,
biochemical analysis demonstrated that both HupL and Nif
55 Biochemical analysis demonstrated that CNGA3 channels la
56 Biochemical analysis demonstrated that Spindly binds F-a
57 MS and
biochemical analysis demonstrated that TMC6 and TMC8 add
58 Biochemical analysis demonstrates that the substrate pre
59 Biochemical analysis determined that the mutant EPHB4 pr
60 Biochemical analysis established the role of C. trachoma
61 By contrast, confocal and protein
biochemical analysis failed to uncover substantial exo-
62 Serum
biochemical analysis following each procedure was compar
63 Biochemical analysis found that SufA bound and transferr
64 Biochemical analysis further shows that Ubx4 interacts w
65 Using immunolabeling,
biochemical analysis,
genetic approaches, microindentati
66 nd other bacteria over the past 15 years, no
biochemical analysis had been conducted on any FlgJ and
67 Structural and
biochemical analysis has led to the hypothesis that extr
68 Biochemical analysis has now identified the catalytic ac
69 Biochemical analysis has shown recently that the dual ph
70 Biochemical analysis,
histology, and immunohistochemistr
71 Biochemical analysis identified delta-toxin as the mast
72 Biochemical analysis identified that KLKB1 cleaves scuPA
73 Structural and
biochemical analysis identified the molecular determinan
74 enesis of this groove, coupled with detailed
biochemical analysis,
identified residues that did not i
75 A
biochemical analysis identifies key residues in the acti
76 udy, we have performed detailed clinical and
biochemical analysis in 34 genetically confirmed SPG5 ca
77 Based on pharmacological and
biochemical analysis in vitro and initial genetic analys
78 Through
biochemical analysis in Xenopus laevis egg extracts, we
79 Biochemical analysis including oxidative stress measurem
80 chniques that combine stain-free imaging and
biochemical analysis,
including Fourier transform infrar
81 Our structural and
biochemical analysis indicate that the enhanced potency
82 A
biochemical analysis indicated that Ca(2+) binding to th
83 Biochemical analysis indicated that Slr1796 is an integr
84 Our
biochemical analysis indicates that B. burgdorferi CheD
85 Biochemical analysis indicates that F, G, and TM interac
86 Yet,
biochemical analysis indicates that light-dependent rece
87 Biochemical analysis indicates that Prp5 has reduced aff
88 Homology modeling and
biochemical analysis indicates that the C-terminal domai
89 ation in clinical settings for point-of-care
biochemical analysis is discussed.
90 ently, and the requisite detachment prior to
biochemical analysis might induce chemical changes.
91 We conducted a
biochemical analysis of 29 092 participants in the ATBC
92 Furthermore,
biochemical analysis of 9-PAHSA biosynthesis and degrada
93 re, we report structural, computational, and
biochemical analysis of a CaM complex with GRK5, reveali
94 Here, we describe a thorough molecular and
biochemical analysis of a mutant FOS protein we identifi
95 uppressed by mutations in OKP1 and AME1, and
biochemical analysis of a mutant version of Okp1 showed
96 Finally, structural and
biochemical analysis of a ribosome particle depleted of
97 Here we perform a structural and
biochemical analysis of a ubiquitin-like modification pa
98 Biochemical analysis of AAV9-treated GM1 mice showed hig
99 paradigm, as well as immunohistological and
biochemical analysis of AD-related neuropathology.
100 ich is consistent with the structure and our
biochemical analysis of AgmNAT.
101 Biochemical analysis of AKAP220-null kidney extracts det
102 Through targeted gene disruption,
biochemical analysis of all predicted glycoside hydrolas
103 Furthermore,
biochemical analysis of an ACS5 mutant protein bearing a
104 Comparative genomics and
biochemical analysis of ASAT enzymes were combined with
105 Biochemical analysis of AtDEG15 deletion constructs in p
106 the crystal structure of B204 along with the
biochemical analysis of B204 mutants chosen based on str
107 each phase, the biofilms were collected for
biochemical analysis of biofilm wet weight (biomass), pr
108 Biochemical analysis of BiXyn10A demonstrated that such
109 Biochemical analysis of blood and urine samples.
110 We carried out a structural and
biochemical analysis of both the human and Xenopus laevi
111 , mouse embryonic stem cells, and Drosophila
Biochemical analysis of BRWD2 demonstrated an associatio
112 Biochemical analysis of C-RPS3 revealed that it comprise
113 Biochemical analysis of CD148-deficient ASM revealed hyp
114 Biochemical analysis of chimeric AIPL1-AIP proteins supp
115 Traditional
biochemical analysis of chromatin-associated complexes r
116 rotein levels was seen in both patients, and
biochemical analysis of Complex III revealed normal resp
117 cted the role of the flanking DNA segment by
biochemical analysis of complexes formed using DNAs with
118 Biochemical analysis of cortical extracts from behaviora
119 Biochemical analysis of D87H, V128I, H246Q and A243G pro
120 Biochemical analysis of de novo induced cultures indicat
121 To facilitate the
biochemical analysis of deadenylase enzymes, we have dev
122 Biochemical analysis of Destructin-1 showed that it medi
123 Biochemical analysis of detergent-soluble and detergent-
124 Gene expression, enzymatic activity and
biochemical analysis of developing cotton fibers was per
125 Ultrastructural, immunohistological, and
biochemical analysis of either sex revealed widespread a
126 c denervation/reinnervation changes, whereas
biochemical analysis of electron transport chain (ETC) e
127 Here, combining the
biochemical analysis of enzymatic and motile properties
128 Biochemical analysis of existing muscle biopsies was cor
129 sing a combination of structural imaging and
biochemical analysis of extracted waxes.
130 This report will facilitate protein
biochemical analysis of FFPE tumor samples and justifies
131 Using
biochemical analysis of fission-yeast cohesin, we find t
132 The structure and
biochemical analysis of five cohesin-dockerin complexes
133 Biochemical analysis of five representatives of these re
134 ased quantification of Abeta plaque load and
biochemical analysis of formic acid-extracted Abetax-40
135 Biochemical analysis of Galpha13 shows SR2 binds directl
136 Strategies combining
biochemical analysis of gene regulation, WGS analysis of
137 d inhibitor PF74 as a probe coupled with the
biochemical analysis of HIV-1 preintegration complexes (
138 Using comprehensive physiological and
biochemical analysis of intestinal and renal tissues fro
139 Following diet-induced obesity,
biochemical analysis of livers revealed that asparaginas
140 Biochemical analysis of multiple Fusobacterium strains r
141 Recent structural and
biochemical analysis of NAT proteins allows for a compar
142 Here,
biochemical analysis of NgR1 function uncovered a physic
143 Structural and
biochemical analysis of NolR reveals protein-DNA interac
144 detection of nuclear Abeta42 as follows: (i)
biochemical analysis of nuclear fractions; (ii) detectio
145 Structural and
biochemical analysis of Oryza sativa homolog FLO7 reveal
146 this study we provide a unique and detailed
biochemical analysis of Pch2.
147 A detailed
biochemical analysis of PhnF binding to its identified b
148 ethod for label-free, in vivo structural and
biochemical analysis of plant cuticles based on stimulat
149 Biochemical analysis of plasma cytokine levels and immun
150 The previous studies were carried out by
biochemical analysis of portions of the authentic viral
151 Biochemical analysis of prostate cancer cell lines revea
152 Biochemical analysis of PSII complexes further indicates
153 Biochemical analysis of purified avSGs showed interactio
154 In this study, we performed an in-depth
biochemical analysis of purified CHD6, CHD7, and CHD8 an
155 A
biochemical analysis of purified recombinant human Twink
156 Here we present the first
biochemical analysis of recombinant RecQ[Bs].
157 We used a combination of genome sequencing,
biochemical analysis of redox active components, and sho
158 nvolve additional surfaces as mutational and
biochemical analysis of residues within these surfaces 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 The X-ray crystal structure and
biochemical analysis of site-directed mutants identifies
162 xidation in the Sulfolobales is based on the
biochemical analysis of specific proteins from Acidianus
163 Histological and
biochemical analysis of STIM1 transgenic mice showed ful
164 Biochemical analysis of STM2215 determined that it is lo
165 The structures and
biochemical analysis of structure-inspired mutants showe
166 Here, we report a
biochemical analysis of the ASK1 kinase domain in conjun
167 These compounds may be useful tools for the
biochemical analysis of the Caf1/CNOT7 deadenylase subun
168 Biochemical analysis of the corresponding triphosphates
169 Biochemical analysis of the degron motif recognized by M
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 usion were recorded for 10 hours followed by
biochemical analysis of the kidney tissue.
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 Here we present a structural and
biochemical analysis of the more primitive ancestral for
178 Biochemical analysis of the mutations revealed that they
179 Preliminary
biochemical analysis of the N-terminal nonribosomal pept
180 Data from the
biochemical analysis of the nuclear and cytosolic fracti
181 Biochemical analysis of the pepsin-induced fibrils impli
182 Moreover, the structural and
biochemical analysis of the prefusion variants suggests
183 Here we provide results from a
biochemical analysis of the purified Escherichia coli Ye
184 However, there has been only basic
biochemical analysis of the role of TPP1 in the telomera
185 Here, we present a detailed structural and
biochemical analysis of the surface antigens of the viru
186 These assessments included
biochemical analysis of the TGFbeta and VEGF signaling a
187 ted importantly by definitive structural and
biochemical analysis of their activity.
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 Our structure and
biochemical analysis of this enzyme reveals its activati
192 PLA analysis of neurons in vitro and
biochemical analysis of tissue subsynaptic fractions con
193 evolved from naked DNA to chromatin, in the
biochemical analysis of transcription by RNA polymerase
194 Histology, haematology and
biochemical analysis of urine and plasma confirmed no to
195 ermination of the DivL crystal structure and
biochemical analysis of wild-type and site-specific DivL
196 Biochemical analysis of WRN protein purified from TT lym
197 the protein or enzyme that can be useful for
biochemical analysis or genome modifications.
198 -electron tomography with mass spectrometry,
biochemical analysis,
perturbation experiments and struc
199 We introduce a portable
biochemical analysis platform for rapid field deployment
200 To enable
biochemical analysis,
protein extraction from FFPE tissu
201 Biophysical/
biochemical analysis proved that two mutually exclusive
202 Structural comparisons, together with
biochemical analysis,
provide unforeseen details about h
203 Molecular dynamics, combined with
biochemical analysis,
reveal a lipid mediated dimer inte
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 Biochemical analysis revealed increased interaction of t
212 stry showed mitochondrial proliferation, and
biochemical analysis revealed severe complex I deficienc
213 The
biochemical analysis revealed that 41% of the patients p
214 Biochemical analysis revealed that carotenoids are absen
215 Biochemical analysis revealed that CD55 was associated w
216 Proteomic and
biochemical analysis revealed that cohesin complex membe
217 Biochemical analysis revealed that FAP163 is present in
218 Transcriptomic profiling and
biochemical analysis revealed that genetic or pharmacolo
219 Biochemical analysis revealed that his gammadelta and al
220 Biochemical analysis revealed that HSP60 knockdown incre
221 Biochemical analysis revealed that inhibiting AR resulte
222 maging, confocal imaging of cryosections and
biochemical analysis revealed that localization and traf
223 Behavioral and
biochemical analysis revealed that mice with conditional
224 Biochemical analysis revealed that multiple elements in
225 Biochemical analysis revealed that Nrf2 appeared in the
226 Biochemical analysis revealed that OeGLU is a homomultim
227 Biochemical analysis revealed that P466L mutation enhanc
228 Biochemical analysis revealed that PRR14, as a proline-r
229 Biochemical analysis revealed that the dimeric mutant al
230 This
biochemical analysis revealed that the DNA-binding activ
231 Biochemical analysis revealed that the nox mutant was sp
232 Quantitative mass spectrometry together with
biochemical analysis revealed that villin, an actin-modi
233 Further
biochemical analysis revealed that YAF2 bridges interact
234 Biochemical analysis revealed upregulation of proteins i
235 rate of recovery from desensitization, while
biochemical analysis reveals a large decrease in affinit
236 Biochemical analysis reveals a marked decrease in RYR1 p
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 detailed
biochemical analysis reveals the direct physical interac
246 Our structural and
biochemical analysis sheds new light on the molecular ba
247 In addition, structural and
biochemical analysis show that the C-terminal region of
248 Combined quantitative RT-PCR array and
biochemical analysis show that, upon the engagement of t
249 Biochemical analysis showed altered cutin and wax biosyn
250 Biochemical analysis showed ChF has strong ferroxidase a
251 In this study,
biochemical analysis showed dbToxRp to have a higher aff
252 ACOX2 expression in the patient's liver, and
biochemical analysis showed marked elevation of intermed
253 Biochemical analysis showed that AMSH1 is an active deub
254 Biochemical analysis showed that DC2 and KCP2 are respon
255 Biochemical analysis showed that FAM46C requires interac
256 Genetic and
biochemical analysis showed that inflammation was caused
257 using MCF-7 breast cancer cells, and further
biochemical analysis showed that it caused accumulation
258 Biochemical analysis showed that OsJAR1 encoded an enzym
259 Biochemical analysis showed that PLD deficiency affected
260 Previous genetic and
biochemical analysis showed that POLD3 may promote lesio
261 Unbiased phosphoproteomics and
biochemical analysis showed that SHP2 activates several
262 Our
biochemical analysis showed that the PTAP duplication, i
263 Supporting its direct involvement,
biochemical analysis shows that A2BP1 is part of the Sup
264 Our structural and
biochemical analysis shows that by decoupling the action
265 In vitro
biochemical analysis shows that C2c2 is guided by a sing
266 Structural and
biochemical analysis shows that the active site features
267 Biochemical analysis shows that the native CsTA and six
268 Biochemical analysis shows that the Ric8A C-terminal tai
269 structure has been recalcitrant to detailed
biochemical analysis,
so molecular details of how it ass
270 amples as low as 0.125 mug/ml prior to their
biochemical analysis such as in comparative proteomics.
271 in vitro mapping of protein-interactomes and
biochemical analysis suggest interactions between ZIKA-N
272 orescence microscopy, electrophysiology, and
biochemical analysis suggest METH exposure decreased the
273 Biochemical analysis suggested that the Acm1 D-box exten
274 mers together at the base of the trimer, and
biochemical analysis suggests that it neutralizes by inh
275 Biochemical analysis suggests that the activity of coppe
276 Biochemical analysis suggests that this defect is multil
277 Our
biochemical analysis supports a model in which the trans
278 re, of particular importance to chemical and
biochemical analysis systems such as chromatography and
279 Based on sequence alignment and further
biochemical analysis,
the amino acid residue substitutio
280 tudy, we combined X-ray crystallographic and
biochemical analysis to characterize the association of
281 es the development of new methods of in vivo
biochemical analysis to complement established in vitro
282 used structured illumination microscopy and
biochemical analysis to explore the asymmetric landscape
283 We used molecular modelling, mutagenesis and
biochemical analysis to identify amino acid residues imp
284 molecule FRET, single molecule pull-down and
biochemical analysis to investigate how the most common
285 re, we combined single-molecule and ensemble
biochemical analysis to show that FANCJ possesses a G4-s
286 Biochemical analysis using HP14 zymogen (proHP14), betaG
287 istration was assessed via histochemical and
biochemical analysis using markers of myelin, astrocytes
288 The
biochemical analysis using subfractionation studies show
289 Biochemical analysis verified double-mutant 3CLpro enzym
290 Biochemical analysis was conducted on purified PenA1 and
291 Here, using cryo-electron microscopy and
biochemical analysis,
we define the molecular basis of h
292 Combining proteomics and
biochemical analysis,
we demonstrate here that cells are
293 In line with our
biochemical analysis,
we find that the number of bleachi
294 fluorescence resonance energy transfer, and
biochemical analysis,
we observed that the EphB1 recepto
295 Together with
biochemical analysis,
we propose a structural model in w
296 By use of hydrogen/deuterium exchange and
biochemical analysis,
we show that the alpha8beta4 SiR h
297 Using quantitative FRET and
biochemical analysis,
we show that VEGFR-2 forms dimers
298 ex remains associated in conditions used for
biochemical analysis with a dissociation constant of 5 n
299 On
biochemical analysis with cellulosic substrates, seven o
300 We coupled
biochemical analysis with confocal imaging of both fixed