1 a lower level of PSII proteins, as shown by
biochemical analyses.
2 appearance, weight changes, death, and blood
biochemical analyses.
3 re subjected to comprehensive behavioral and
biochemical analyses.
4 ; and validate results by genetic assays and
biochemical analyses.
5 ed reliably in a broad range of chemical and
biochemical analyses.
6 ing electron and atomic force microscopy and
biochemical analyses.
7 reverse-transcription PCR and histologic and
biochemical analyses.
8 A interaction, we carried out structural and
biochemical analyses.
9 o and subjected to a range of functional and
biochemical analyses.
10 means of electrophysiological, optical, and
biochemical analyses.
11 on was initiated following these genetic and
biochemical analyses.
12 in TIE-1 through genetic, physiological, and
biochemical analyses.
13 subject of intensive genetic, cellular, and
biochemical analyses.
14 ding viable specimens for CFTR bioelectrical/
biochemical analyses.
15 tissues were characterized by histologic and
biochemical analyses.
16 novel capsule types based on serological and
biochemical analyses.
17 l-forming dirigent protein based on in vitro
biochemical analyses.
18 cases were investigated by histochemical and
biochemical analyses.
19 patch clamp, fast substrate application, and
biochemical analyses.
20 ion of volatile metabolites by comprehensive
biochemical analyses.
21 stereology, morphometry, Sholl analysis, and
biochemical analyses.
22 tionally reconstituted in vitro for detailed
biochemical analyses.
23 ses we performed a battery of structural and
biochemical analyses.
24 electron microscopy, structural docking, and
biochemical analyses.
25 o MrkH function, we performed structural and
biochemical analyses.
26 ed neuroimaging, electroencephalography, and
biochemical analyses,
all of which were unremarkable exc
27 Recent
biochemical analyses also suggested roles for mixed or b
28 Here we use standard
biochemical analyses and Akt3-knockdown strategies to sh
29 are determined; these values are useful for
biochemical analyses and allow us to estimate the heme o
30 Biochemical analyses and cryo-electron microscopy reveal
31 tive approach combining crystal coordinates,
biochemical analyses and data from cross-linking mass-sp
32 Left ventricular tissue was used for
biochemical analyses and functional measurements (calciu
33 We used a combination of evolutionary and
biochemical analyses and homology modeling of the Galpha
34 Next, we used
biochemical analyses and immunoelectron microscopy to de
35 Biochemical analyses and immunohistochemical techniques
36 CTD variants using a combination of in vitro
biochemical analyses and in vivo binding experiments.
37 Through
biochemical analyses and loss-of-function in vivo studie
38 Biochemical analyses and mutational analyses indicate th
39 However,
biochemical analyses and recent experiments in mammalian
40 arify this issue, we use genetic, 2D gel and
biochemical analyses and show that a Rad5 helicase motif
41 Through
biochemical analyses and X-ray crystallographic structur
42 was cloned and expressed in Escherichia coli
Biochemical analyses and x-ray crystallography indicates
43 , by a combination of genetic manipulations,
biochemical analyses,
and a variety of imaging technique
44 We use molecular genetics,
biochemical analyses,
and experimental evolution to esta
45 crosslinking/mass spectrometry (CXMS) data,
biochemical analyses,
and previously published electron
46 le-cell microscopy methods and complementary
biochemical analyses are used to characterize receptor s
47 Cellular and
biochemical analyses as well as structural modelling rev
48 At the end of treatment, morphological and
biochemical analyses assessed the effects of these compo
49 confirms many features inferred by previous
biochemical analyses,
but adds unexpected insights.
50 Biochemical analyses characterized ISA activities in mut
51 in group 1 continued to have weight gain and
biochemical analyses comparable to wild-type pigs.
52 We carried out detailed genomic and
biochemical analyses comparing the white recessive with
53 Biochemical analyses confirm that His432Arg forms an obs
54 Biochemical analyses confirm the identification of the m
55 Biochemical analyses confirmed in silico predictions tha
56 Biochemical analyses confirmed that JMJD1A enhances c-My
57 Consistent with behavioral data,
biochemical analyses confirmed that Nep1 degrades dAbeta
58 Further mutational and
biochemical analyses confirmed that only one of the four
59 Structural, mutational, and
biochemical analyses confirmed the enzyme adopts a fold
60 y and atomic force microscopy, together with
biochemical analyses,
confirmed that collagen fiber degr
61 f phylogenetic analyses, gene silencing, and
biochemical analyses coupled with structural elucidation
62 Our functional and
biochemical analyses demonstrate McjD-dependent immunity
63 Furthermore,
biochemical analyses demonstrate that Daam2 associates w
64 Proximity ligation assays and
biochemical analyses demonstrate that MET-protein partne
65 Biochemical analyses demonstrate that Nmo forms a comple
66 Genetic and
biochemical analyses demonstrate that proper expression
67 Biochemical analyses demonstrate that Shp2 is required f
68 Biochemical analyses demonstrate that this protein plays
69 Biochemical analyses demonstrated an additional phosphor
70 d SHP2 phosphorylation; however, imaging and
biochemical analyses demonstrated CagA-mediated membrane
71 Biochemical analyses demonstrated direct interaction of
72 Single turnover flash experiments and
biochemical analyses demonstrated that cytochrome b6f fu
73 Cell-based and in vitro
biochemical analyses demonstrated that despite its inabi
74 Biochemical analyses demonstrated that loss of heparanas
75 Biochemical analyses demonstrated that recombinant IL-13
76 Genetic and
biochemical analyses demonstrated that SepA-related indu
77 Biochemical analyses demonstrated that SiaPg is an exo-a
78 Biochemical analyses demonstrated that the interaction b
79 Biochemical analyses demonstrated that translocon-target
80 Biochemical analyses demonstrated that Ub(G76V)-GFP-Syb2
81 Biochemical analyses demonstrated that while de novo myc
82 Although our previous
biochemical analyses demonstrated the ability of polymer
83 Biochemical analyses determined that the eB12 bridge con
84 Biochemical analyses documented variably reduced levels
85 utamate endopeptidase (ChiX), and subsequent
biochemical analyses established that both were required
86 Biochemical analyses established that the roots of AACT2
87 highlight the power of integrative omics and
biochemical analyses for annotating the functions of poo
88 Histopathologic and
biochemical analyses for MPO and myeloid cells confirmed
89 left ventricular myocardium was obtained for
biochemical analyses from explanted failing (n=18) and n
90 In contrast to recent suggestions, our
biochemical analyses further indicate that ObgE is neith
91 combination of structural, biophysical, and
biochemical analyses has revealed deep insights into the
92 s of Mga have been well characterized, basic
biochemical analyses have been limited due to difficulti
93 In summary, our quantitative proteomics and
biochemical analyses have identified Ptc6p as the primar
94 Furthermore, genetic screens and
biochemical analyses have revealed mechanisms that regul
95 Genetic and
biochemical analyses have revealed that glycerolipids pl
96 Initial genomic, proteomic, and
biochemical analyses have revealed the presence of "euka
97 Our genomic and
biochemical analyses identified candidate mediators of p
98 Although
biochemical analyses identified disaggregation machinery
99 Combined transcriptomic and
biochemical analyses identify target genes of GhHOX3 tha
100 Structural and
biochemical analyses illustrate that the nucleosides, pa
101 Based on a series of
biochemical analyses in combination with molecular docki
102 Based on a series of
biochemical analyses in combination with molecular docki
103 tion of whole-cell patch-clamp recording and
biochemical analyses in hippocampal slices from young ad
104 efore, we performed microscopy, genetic, and
biochemical analyses in vitro in order to understand thi
105 Biochemical analyses,
including density gradient sedimen
106 show synthetically enhanced phenotypes, and
biochemical analyses indicate that Ccr4-Not and TFIIS wo
107 Biochemical analyses indicate that CHD7 has characterist
108 Genetic and
biochemical analyses indicate that HBx interacts directl
109 Biochemical analyses indicate that PRL2 promotes Akt act
110 Microscopic and
biochemical analyses indicate that pzX co-forms during s
111 Biochemical analyses indicate that ROP18 and ROP17 have
112 Our genetic and
biochemical analyses indicate that SEDS proteins constit
113 Furthermore, our
biochemical analyses indicate that the BATS domain direc
114 Biochemical analyses indicate that the changes induced b
115 Both genetic and
biochemical analyses indicate that the Che7 system regul
116 Strikingly, structural and
biochemical analyses indicate that the dsRBD and N-termi
117 Biophysical, structural and
biochemical analyses indicate that the NTR is natively d
118 Importantly, our
biochemical analyses indicate that the nudA(F208V) mutat
119 Biochemical analyses indicate that the substrate prefere
120 Biochemical analyses indicate that USP9X binds directly
121 Proteomic and
biochemical analyses indicated a particular set of prote
122 Genetic and
biochemical analyses indicated that AmiB is regulated by
123 Immunohistochemical and
biochemical analyses indicated that JNK phosphorylation
124 Interestingly, our previous
biochemical analyses indicated that MED1 exists only in
125 immunotransmission electron microscopy, and
biochemical analyses indicated that NT-PGC-1alpha was lo
126 Here,
biochemical analyses indicated that RNA interaction inhi
127 Biochemical analyses indicated that RTA interacts with R
128 Various genetic and
biochemical analyses led us to propose a model in which
129 Specifically,
biochemical analyses of a construct of S6K1 lacking the
130 Biochemical analyses of a large panel of TRPV4-ARD mutat
131 Here, we present genetic and
biochemical analyses of a predicted PAS-GGDEF-EAL domain
132 To date, in vitro
biochemical analyses of adenosine deamination have been
133 However,
biochemical analyses of aggregated mutant huntingtin in
134 PANK3(G19V) cannot bind ATP, and
biochemical analyses of an engineered PANK3/PANK3(G19V)
135 e report on a series of crystallographic and
biochemical analyses of an evolutionarily conserved deub
136 Biochemical analyses of Bacillus subtilis Fur (BsFur) re
137 We present crystallographic and
biochemical analyses of Btk, which together reveal molec
138 Fourier transform infrared spectroscopy and
biochemical analyses of cell walls from aba1-6 and wild-
139 Here we present detailed functional and
biochemical analyses of Chlamydomonas DGTTs.
140 was processed for histologic examination or
biochemical analyses of chondrocyte cultures.
141 stion through comparative transcriptomic and
biochemical analyses of closely related C3, C3-C4, and C
142 Biochemical analyses of cortical tissue from these mice
143 Biochemical analyses of cultured cells revealed that PRL
144 Biochemical analyses of DnaK protein supported the forma
145 In addition,
biochemical analyses of dynein from one mutant strain sh
146 Biochemical analyses of each ADF protein confirmed the r
147 Genetic and
biochemical analyses of epsin in C. elegans and mammalia
148 Proteome and
biochemical analyses of ES-treated PCa cells further ind
149 In addition, we present
biochemical analyses of GTP-induced SAMHD1 full-length t
150 Microscopic and
biochemical analyses of HPV16 PsV determined that the an
151 We also carried out
biochemical analyses of human brain tissues and studied
152 Using transcriptomic and
biochemical analyses of human monocytes treated with a h
153 Herein we review the various structural and
biochemical analyses of influenza hemagglutinin-glycan r
154 Interestingly, our structural and
biochemical analyses of Kingella denitrificans and Neiss
155 Respirometry and survival assays and
biochemical analyses of lipids, proteins and carbohydrat
156 To facilitate high-throughput
biochemical analyses of membrane proteins, we have devel
157 Recent advances in molecular and
biochemical analyses of microalgae point toward interest
158 Biochemical analyses of NAEbeta mutants revealed slower
159 benthamiana leaves and, consistent with our
biochemical analyses of native grass tissues, shown to b
160 Crystal structures and
biochemical analyses of one of the inhibitors (CP2) with
161 The structural and
biochemical analyses of PenA and PenI provide key insigh
162 ntrary, prior results and our structural and
biochemical analyses of phosphate monoesterase PafA, fro
163 Through pharmacological treatments and
biochemical analyses of primary neuronal cultures expres
164 ckdown approach was used in conjunction with
biochemical analyses of protein subdomain structure and
165 Here, we report the crystal structures and
biochemical analyses of Rabphilin-3A C2B-SNAP25 and C2B-
166 Biochemical analyses of receptor mutants in the context
167 Biochemical analyses of recombinant plant SAT and OAS-TL
168 Biochemical analyses of recombinant protein variants lac
169 Genetic and
biochemical analyses of RNA interference (RNAi) and micr
170 ytochemical, immunoelectron microscopic, and
biochemical analyses of rodent neuronal cells showed tha
171 s by RuvC, we performed crystallographic and
biochemical analyses of RuvC from Thermus thermophilus (
172 Quantitative
biochemical analyses of selected AKAP79 complexes have d
173 Biochemical analyses of SynAPSK, SynAPSK H23C mutant, Sy
174 Altogether, structural and
biochemical analyses of T. gondii aldolase and aldolase-
175 The
biochemical analyses of TBX1 human mutations demonstrate
176 ort the mapping, cloning, and functional and
biochemical analyses of the bm2 gene.
177 Biochemical analyses of the N-glycan structure confirmed
178 A combination of the RNA-seq and
biochemical analyses of the positions for the errors rev
179 The
biochemical analyses of the protelomerase reactions furt
180 Here, we present crystallographic and
biochemical analyses of the TRIM coiled-coil and show th
181 Biochemical analyses of these analogues demonstrate thei
182 Bioinformatic and
biochemical analyses of these genes lead to a previously
183 Comparative bioinformatics and
biochemical analyses of these proteins with 2-epi-5-epi-
184 Biochemical analyses of three human missense mutations f
185 tasis were measured throughout the study and
biochemical analyses of white adipose tissue (WAT) and l
186 Biochemical analyses of WT and Casp1/11(-/-) BMDC indica
187 Our
biochemical analyses provide a mechanistic basis for the
188 Interestingly, in vitro
biochemical analyses provide novel evidence that LIL3 sh
189 Bioinformatic and
biochemical analyses provided additional support for the
190 ts, docking of partial X-ray structures, and
biochemical analyses resulted in comprehensive mapping o
191 Comparative evolutionary and
biochemical analyses reveal that a single, differently c
192 Our
biochemical analyses reveal that Baf200 forms at least t
193 Structural and
biochemical analyses reveal that GLMN adopts a HEAT-like
194 Biochemical analyses reveal that shelterin bridge assemb
195 Biochemical analyses reveal that the flavonoids function
196 s determined by cryo-electron microscopy and
biochemical analyses reveal that the NTD in these specie
197 Biochemical analyses reveal that the severe phenotype is
198 Biochemical analyses reveal that, in this context, Drosh
199 ed mutagenesis combined with biophysical and
biochemical analyses reveal the basis for normal functio
200 The structures, combined with
biochemical analyses,
reveal key features supporting the
201 Plasma metabolomics and
biochemical analyses revealed a marked global effect of
202 Molecular and
biochemical analyses revealed elevated insulin-related g
203 Biochemical analyses revealed increased activation of th
204 Microarray and
biochemical analyses revealed pfmdr1 amplification, elev
205 Biochemical analyses revealed significant inhibition of
206 Genetic and
biochemical analyses revealed that CaN adjusts the stren
207 Structural and
biochemical analyses revealed that DepH, in contrast to
208 Genetic and
biochemical analyses revealed that FLN90 is present surr
209 Biochemical analyses revealed that ForG is a rather weak
210 Immunofluorescence and
biochemical analyses revealed that H4K20me1 is present a
211 Molecular and
biochemical analyses revealed that increased expression
212 Structural and
biochemical analyses revealed that LIMD2 bound directly
213 Biochemical analyses revealed that LOXL2 readily promote
214 Bioinformatic and
biochemical analyses revealed that miR-431 directly inte
215 hylogenetic, bioinformatics, structural, and
biochemical analyses revealed that Rv2466c is a novel my
216 Biochemical analyses revealed that SPL, as well as the m
217 Comparative bioinformatics, mutagenesis, and
biochemical analyses revealed that the highly conserved
218 Immunocytochemical and
biochemical analyses revealed that the mutant AR aggrega
219 Biochemical analyses revealed that the PTP is a heterool
220 Electron microscopy and
biochemical analyses revealed that the RQC forms a stabl
221 Structural and
biochemical analyses revealed that UbVs specifically inh
222 Bioinformatic and
biochemical analyses revealed unexpected mechanisms by w
223 d GluN2A-mediated synaptic transmission, and
biochemical analyses show AIDA-1 cKO mice have low GluN2
224 Structural and
biochemical analyses show OsSWEET2b in an apparent inwar
225 Biochemical analyses show that a horizontally acquired p
226 Interspecies
biochemical analyses show that COQ8A and yeast Coq8p spe
227 Biochemical analyses show that in muscle cells of adult
228 Biochemical analyses show that PI5P4Kbeta preferentially
229 Biochemical analyses show that R79A and S83A mutant prot
230 Structural and
biochemical analyses show that tetrameric c-di-GMP links
231 Single-molecule and
biochemical analyses show that the N terminus plays an i
232 Biochemical analyses showed a physical association of Sh
233 Biochemical analyses showed enhanced generation of cycli
234 Biochemical analyses showed lower beta-hydroxyacyl coenz
235 Genetic and
biochemical analyses showed redundant enzymes for gamma-
236 Immunohistochemical and
biochemical analyses showed significant amounts of beta-
237 Further genetic and
biochemical analyses showed that an amphipathic helix at
238 Biochemical analyses showed that chronic excess glucocor
239 Biochemical analyses showed that Dcr1 dimers bind cooper
240 Biochemical analyses showed that peptide-induced alpha5b
241 Biochemical analyses showed that phenformin and PLX4720
242 Biochemical analyses showed that poly(dA-dT)-activated A
243 Accordingly, bioinformatic, functional, and
biochemical analyses showed that RB1-E2F complexes bind
244 Genetic and
biochemical analyses showed that SCD1 function is depend
245 Previous genetic and
biochemical analyses showed that SSIII also is required
246 Our
biochemical analyses showed that the conserved Y267 resi
247 Biochemical analyses showed that the tla2 strain was def
248 Biochemical analyses showed that the transition between
249 Biochemical analyses showed that the WR domain of TWIST
250 In addition, biomechanical and
biochemical analyses showed that Wnt1(sw/sw) mice exhibi
251 AP-1 in complex with Arf1-GTP, together with
biochemical analyses,
shows that Arf1 activates cargo bi
252 Biochemical analyses suggest a competition model in whic
253 expression of plastid-encoded PSI genes and
biochemical analyses suggest a posttranslational action
254 Biochemical analyses suggest a Shp2-TAO2-p38-p300-PPARga
255 Furthermore,
biochemical analyses suggest that DDL-1/2 negatively reg
256 However,
biochemical analyses suggest that isoeugenol inhibits TD
257 Genetic and
biochemical analyses suggested that Sec13p was required
258 Surprisingly, both modeling and
biochemical analyses suggested that SH2 domain overexpre
259 ether with molecular dynamics simulation and
biochemical analyses,
suggests Ub(B) restricts the flexi
260 We show by structural and
biochemical analyses that Prp3 contains a bipartite U4/U
261 and in solvated systems, informed downstream
biochemical analyses that tested key aspects of the hypo
262 Here, we show by transcriptome, genetic, and
biochemical analyses that the most common sialic acid, N
263 this study we demonstrate, using genetic and
biochemical analyses,
that in Escherichia coli, TnaC res
264 anscriptomics alongside immunohistologic and
biochemical analyses,
that neurons from thirteen-lined g
265 In combination with ultrastructural and
biochemical analyses,
these results demonstrate a role f
266 Through proteomic, structural, and
biochemical analyses,
this work shows that posttranslati
267 urrent study sought to use computational and
biochemical analyses to characterize decision-making pro
268 et of human osteosarcomas, we merged IHC and
biochemical analyses to characterize more fully the tumo
269 We combined detailed lipidomic and
biochemical analyses to characterize the functional role
270 s, combined with a suite of parallel NMR and
biochemical analyses to cross-validate their integrity,
271 Here, we use in vivo and in vitro
biochemical analyses to demonstrate that ATP-bound Rok1,
272 Here, we use structural and
biochemical analyses to establish how an antimicrobial p
273 e use electron cryo-tomography together with
biochemical analyses to investigate structures of indivi
274 or antiplasmid immunity and used genetic and
biochemical analyses to investigate the functions of pre
275 ography, molecular dynamics simulations, and
biochemical analyses to investigate the structural requi
276 Here, we use genetic and
biochemical analyses to show that this second DNA tether
277 Biochemical analyses uncover that the CD and AT-hook-lik
278 Histological, electron microscopic, and
biochemical analyses uncovered significant hypomyelinati
279 Biochemical analyses using (14)C-PA as a substrate demon
280 Consistently,
biochemical analyses using a phospho-synapsin-specific a
281 Biochemical analyses using Exo70 mutants and independent
282 tors that control RNA polymerase I activity,
biochemical analyses using purified transcription factor
283 Diagnostic
biochemical analyses using various m7G cap derivatives a
284 Biochemical analyses verify that MHF preferentially enga
285 itro pollen germination, immunolabeling, and
biochemical analyses was used on wild-type and Atpme48 m
286 Through
biochemical analyses we find that a proportion of p110al
287 Using a series of
biochemical analyses we found that TcdB from a hyperviru
288 Here, using structural, spectroscopic, and
biochemical analyses,
we found that this truncated varia
289 Here, using structural and
biochemical analyses,
we have identified FMDV 3D(pol) mu
290 ng phylogenetic, transcriptomic and in vitro
biochemical analyses,
we identified a single homotetrame
291 By combining electrophysiological and
biochemical analyses,
we identify subunit-specific struc
292 ing high-resolution behavioral, genetic, and
biochemical analyses,
we present evidence that excess mG
293 eles, live-cell spindle assays, and in vitro
biochemical analyses,
we show that She1 is required for
294 In vivo
biochemical analyses were conducted after UV-A1 irradiat
295 MPAR trafficking, pHluorin-GluA1 imaging and
biochemical analyses were performed on primary hippocamp
296 arative structural modeling, and genetic and
biochemical analyses were used to define the molecular a
297 mass spectrometry, together with genetic and
biochemical analyses,
were used to determine the molecul
298 Consistent with our
biochemical analyses,
whole-cell hCaV3.3 currents in cel
299 Future
biochemical analyses will be needed to determine whether
300 Here, we combine
biochemical analyses with a functional assay directly mo