1 mponents in ETI was confirmed by genetic and
biochemical analyses.
2 ing electron and atomic force microscopy and
biochemical analyses.
3 means of electrophysiological, optical, and
biochemical analyses.
4 novel capsule types based on serological and
biochemical analyses.
5 cases were investigated by histochemical and
biochemical analyses.
6 electron microscopy alongside structural and
biochemical analyses.
7 patch clamp, fast substrate application, and
biochemical analyses.
8 ion of volatile metabolites by comprehensive
biochemical analyses.
9 stereology, morphometry, Sholl analysis, and
biochemical analyses.
10 tionally reconstituted in vitro for detailed
biochemical analyses.
11 ses we performed a battery of structural and
biochemical analyses.
12 electron microscopy, structural docking, and
biochemical analyses.
13 o MrkH function, we performed structural and
biochemical analyses.
14 a lower level of PSII proteins, as shown by
biochemical analyses.
15 appearance, weight changes, death, and blood
biochemical analyses.
16 re subjected to comprehensive behavioral and
biochemical analyses.
17 ; and validate results by genetic assays and
biochemical analyses.
18 ed reliably in a broad range of chemical and
biochemical analyses.
19 reverse-transcription PCR and histologic and
biochemical analyses.
20 A interaction, we carried out structural and
biochemical analyses.
21 o and subjected to a range of functional and
biochemical analyses.
22 on was initiated following these genetic and
biochemical analyses.
23 ther Na(+)-dependent, which was validated by
biochemical analyses.
24 hich was validated by immunofluorescence and
biochemical analyses.
25 ed neuroimaging, electroencephalography, and
biochemical analyses,
all of which were unremarkable exc
26 Our genetic, molecular, and
biochemical analyses allowed us to characterize rootstoc
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 Biochemical analyses and cryo-electron microscopy reveal
30 tive approach combining crystal coordinates,
biochemical analyses and data from cross-linking mass-sp
31 Left ventricular tissue was used for
biochemical analyses and functional measurements (calciu
32 Histopathological studies, serum
biochemical analyses and hepatic TNF-alpha level were ev
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 This has been elaborated by
biochemical analyses and immunohistochemistry of long bo
37 Through
biochemical analyses and in silico modeling using prefer
38 CTD variants using a combination of in vitro
biochemical analyses and in vivo binding experiments.
39 Through
biochemical analyses and loss-of-function in vivo studie
40 ound ribose 5-phosphate (R5P), combined with
biochemical analyses and molecular dynamic simulations,
41 Biochemical analyses and mutational analyses indicate th
42 arify this issue, we use genetic, 2D gel and
biochemical analyses and show that a Rad5 helicase motif
43 Biochemical analyses and studies in cultured cells have
44 Through
biochemical analyses and X-ray crystallographic structur
45 was cloned and expressed in Escherichia coli
Biochemical analyses and x-ray crystallography indicates
46 , by a combination of genetic manipulations,
biochemical analyses,
and a variety of imaging technique
47 Using a combination of confocal microscopy,
biochemical analyses,
and behavioral testing, we show th
48 bination of high-resolution structural work,
biochemical analyses,
and computational modeling indicat
49 We use molecular genetics,
biochemical analyses,
and experimental evolution to esta
50 Here, using cellular fractionation,
biochemical analyses,
and histological assays, we show t
51 crosslinking/mass spectrometry (CXMS) data,
biochemical analyses,
and previously published electron
52 Cellular and
biochemical analyses as well as structural modelling rev
53 At the end of treatment, morphological and
biochemical analyses assessed the effects of these compo
54 Electrophysiological and
biochemical analyses at corticostriatal synapses of EAAT
55 confirms many features inferred by previous
biochemical analyses,
but adds unexpected insights.
56 d to participate in HIV-1 membrane fusion in
biochemical analyses,
but its role in viral entry and in
57 in group 1 continued to have weight gain and
biochemical analyses comparable to wild-type pigs.
58 We carried out detailed genomic and
biochemical analyses comparing the white recessive with
59 Biochemical analyses confirmed that JMJD1A enhances c-My
60 Consistent with behavioral data,
biochemical analyses confirmed that Nep1 degrades dAbeta
61 Further mutational and
biochemical analyses confirmed that only one of the four
62 Biochemical analyses confirmed that the Cas10 Palm domai
63 Structural, mutational, and
biochemical analyses confirmed the enzyme adopts a fold
64 y and atomic force microscopy, together with
biochemical analyses,
confirmed that collagen fiber degr
65 f phylogenetic analyses, gene silencing, and
biochemical analyses coupled with structural elucidation
66 Our functional and
biochemical analyses demonstrate McjD-dependent immunity
67 Furthermore,
biochemical analyses demonstrate that Daam2 associates w
68 Proximity ligation assays and
biochemical analyses demonstrate that MET-protein partne
69 Biochemical analyses demonstrate that Shp2 is required f
70 Instead, mass spectrometry and in vitro
biochemical analyses demonstrate that SidJ modifies anot
71 Biochemical analyses demonstrate that this protein plays
72 Biochemical analyses demonstrated an additional phosphor
73 d SHP2 phosphorylation; however, imaging and
biochemical analyses demonstrated CagA-mediated membrane
74 Biochemical analyses demonstrated direct interaction of
75 Biochemical analyses demonstrated lower Ser23 5-HT(2C)R
76 Cell-based and in vitro
biochemical analyses demonstrated that despite its inabi
77 Biochemical analyses demonstrated that loss of heparanas
78 Biochemical analyses demonstrated that recombinant IL-13
79 Genetic and
biochemical analyses demonstrated that SepA-related indu
80 red in the N-terminal domain of the protein;
biochemical analyses demonstrated that SERPINA1 binds ph
81 SAXS and
biochemical analyses demonstrated that the "A" shape is
82 Combined structural and
biochemical analyses demonstrated that the unusual dimer
83 Biochemical analyses demonstrated that translocon-target
84 Biochemical analyses demonstrated that Ub(G76V)-GFP-Syb2
85 Biochemical analyses demonstrated that while de novo myc
86 Although our previous
biochemical analyses demonstrated the ability of polymer
87 Biochemical analyses determine that these two enzymes ca
88 Biochemical analyses determined that the eB12 bridge con
89 Further mutational and
biochemical analyses dissected the modifiable selectivit
90 Biochemical analyses documented variably reduced levels
91 utamate endopeptidase (ChiX), and subsequent
biochemical analyses established that both were required
92 highlight the power of integrative omics and
biochemical analyses for annotating the functions of poo
93 left ventricular myocardium was obtained for
biochemical analyses from explanted failing (n=18) and n
94 In contrast to recent suggestions, our
biochemical analyses further indicate that ObgE is neith
95 Mass spectrometry and phylogeny-guided
biochemical analyses further reveal that similar rules o
96 combination of structural, biophysical, and
biochemical analyses has revealed deep insights into the
97 In summary, our quantitative proteomics and
biochemical analyses have identified Ptc6p as the primar
98 Furthermore, genetic screens and
biochemical analyses have revealed mechanisms that regul
99 Initial genomic, proteomic, and
biochemical analyses have revealed the presence of "euka
100 Our genomic and
biochemical analyses identified candidate mediators of p
101 Combined transcriptomic and
biochemical analyses identify target genes of GhHOX3 tha
102 Structural and
biochemical analyses illustrate that the nucleosides, pa
103 Based on a series of
biochemical analyses in combination with molecular docki
104 Based on a series of
biochemical analyses in combination with molecular docki
105 tion of whole-cell patch-clamp recording and
biochemical analyses in hippocampal slices from young ad
106 efore, we performed microscopy, genetic, and
biochemical analyses in vitro in order to understand thi
107 show synthetically enhanced phenotypes, and
biochemical analyses indicate that Ccr4-Not and TFIIS wo
108 Microscopic and
biochemical analyses indicate that pzX co-forms during s
109 Biochemical analyses indicate that ROP18 and ROP17 have
110 Our genetic and
biochemical analyses indicate that SEDS proteins constit
111 Both genetic and
biochemical analyses indicate that the Che7 system regul
112 Strikingly, structural and
biochemical analyses indicate that the dsRBD and N-termi
113 Biochemical analyses indicate that the internal loop seq
114 Biophysical, structural and
biochemical analyses indicate that the NTR is natively d
115 Biochemical analyses indicate that the substrate prefere
116 Biochemical analyses indicate that USP9X binds directly
117 Proteomic and
biochemical analyses indicated a particular set of prote
118 Genetic and
biochemical analyses indicated that AmiB is regulated by
119 Biochemical analyses indicated that CsTFL1 interacts wit
120 Biochemical analyses indicated that CsWUS directly bound
121 immunotransmission electron microscopy, and
biochemical analyses indicated that NT-PGC-1alpha was lo
122 Here,
biochemical analyses indicated that RNA interaction inhi
123 ndria from plant cells for physiological and
biochemical analyses is a lengthy and tedious process.
124 t, anthropometric measurements and objective
biochemical analyses is essential for evaluation, follow
125 Using protease inhibitor screening and
biochemical analyses,
matriptase, a member of the membra
126 Finally, we use a combination of
biochemical analyses,
mutagenesis, and molecular simulat
127 Biochemical analyses of aged CFH mice after HFC diet rev
128 PANK3(G19V) cannot bind ATP, and
biochemical analyses of an engineered PANK3/PANK3(G19V)
129 e report on a series of crystallographic and
biochemical analyses of an evolutionarily conserved deub
130 We present crystallographic and
biochemical analyses of Btk, which together reveal molec
131 Here we present detailed functional and
biochemical analyses of Chlamydomonas DGTTs.
132 Biochemical analyses of clinical samples reveal that a u
133 stion through comparative transcriptomic and
biochemical analyses of closely related C3, C3-C4, and C
134 ein from Pseudomonas aeruginosa Results from
biochemical analyses of CopG purified under aerobic cond
135 Biochemical analyses of cultured cells revealed that PRL
136 Biochemical analyses of DnaK protein supported the forma
137 Biochemical analyses of each ADF protein confirmed the r
138 Proteome and
biochemical analyses of ES-treated PCa cells further ind
139 In addition, we present
biochemical analyses of GTP-induced SAMHD1 full-length t
140 Microscopic and
biochemical analyses of HPV16 PsV determined that the an
141 We also carried out
biochemical analyses of human brain tissues and studied
142 Using transcriptomic and
biochemical analyses of human monocytes treated with a h
143 Herein we review the various structural and
biochemical analyses of influenza hemagglutinin-glycan r
144 We performed histologic and
biochemical analyses of intestinal tissues from C57BL/6
145 Interestingly, our structural and
biochemical analyses of Kingella denitrificans and Neiss
146 benthamiana leaves and, consistent with our
biochemical analyses of native grass tissues, shown to b
147 Crystal structures and
biochemical analyses of one of the inhibitors (CP2) with
148 Here, structural and
biochemical analyses of ostreolysin A (OlyA), a protein
149 ntrary, prior results and our structural and
biochemical analyses of phosphate monoesterase PafA, fro
150 Through pharmacological treatments and
biochemical analyses of primary neuronal cultures expres
151 Using biolayer interferometry and
biochemical analyses of purified mutant V(1)-ATPase and
152 Here, we report the crystal structures and
biochemical analyses of Rabphilin-3A C2B-SNAP25 and C2B-
153 the corpus callosum, while histochemical and
biochemical analyses of skeletal muscle revealed signs o
154 Biochemical analyses of SynAPSK, SynAPSK H23C mutant, Sy
155 Altogether, structural and
biochemical analyses of T. gondii aldolase and aldolase-
156 The
biochemical analyses of TBX1 human mutations demonstrate
157 ort the mapping, cloning, and functional and
biochemical analyses of the bm2 gene.
158 Biochemical analyses of the N-glycan structure confirmed
159 ce microscopy and spectroscopy combined with
biochemical analyses of the receptor in primary lymphati
160 Here, we present crystallographic and
biochemical analyses of the TRIM coiled-coil and show th
161 Biochemical analyses of the WT enzyme and active site va
162 Biochemical analyses of these analogues demonstrate thei
163 Bioinformatic and
biochemical analyses of these genes lead to a previously
164 However, in vivo
biochemical analyses of these processes are challenging,
165 Cryo-EM and
biochemical analyses of this subcomplex shows that ARP b
166 Biochemical analyses of three human missense mutations f
167 Biochemical analyses of variants as part of the human Na
168 tasis were measured throughout the study and
biochemical analyses of white adipose tissue (WAT) and l
169 Biochemical analyses of WT and Casp1/11(-/-) BMDC indica
170 Here, using comparative crystallographic and
biochemical analyses of WT human CYP51 (CYP51A1) and its
171 Complemented by structural-guided
biochemical analyses,
our studies reveal the substrate b
172 Our
biochemical analyses provide a mechanistic basis for the
173 Our structural data and
biochemical analyses provide a physical model to explain
174 Interestingly, in vitro
biochemical analyses provide novel evidence that LIL3 sh
175 In conclusion, the AFF-CHD structure and
biochemical analyses reported here reveal the molecular
176 ts, docking of partial X-ray structures, and
biochemical analyses resulted in comprehensive mapping o
177 Biochemical analyses reveal a conserved arginine on FLCN
178 Comparative evolutionary and
biochemical analyses reveal that a single, differently c
179 Genetic and
biochemical analyses reveal that Apn2 resolves phosphoty
180 Our
biochemical analyses reveal that Baf200 forms at least t
181 Here, results of MS and
biochemical analyses reveal that dAKAP1 anchors addition
182 Genetic, molecular, and
biochemical analyses reveal that PNPase promotes crRNA m
183 Detailed genomic and
biochemical analyses reveal that PRDM10 functions as a s
184 Biochemical analyses reveal that shelterin bridge assemb
185 Biochemical analyses reveal that the flavonoids function
186 Genetic and
biochemical analyses reveal that the PBL13 receptor-like
187 Biochemical analyses reveal that, in this context, Drosh
188 ed mutagenesis combined with biophysical and
biochemical analyses reveal the basis for normal functio
189 The structures, combined with
biochemical analyses,
reveal key features supporting the
190 Biochemical analyses revealed a defect in Met-tRNAiMet b
191 Plasma metabolomics and
biochemical analyses revealed a marked global effect of
192 slinking immunoprecipitation (HITS-CLIP) and
biochemical analyses revealed direct binding between end
193 Biochemical analyses revealed dysregulated brain mTOR an
194 Molecular and
biochemical analyses revealed elevated insulin-related g
195 Biochemical analyses revealed increased activation of th
196 Hematological and
biochemical analyses revealed no undesired NP-induced ch
197 Transcriptional and
biochemical analyses revealed that aggressive meningioma
198 Genetic and
biochemical analyses revealed that CaN adjusts the stren
199 Structural and
biochemical analyses revealed that DepH, in contrast to
200 Genetic and
biochemical analyses revealed that FLN90 is present surr
201 Biochemical analyses revealed that ForG is a rather weak
202 Immunofluorescence and
biochemical analyses revealed that H4K20me1 is present a
203 Structural and
biochemical analyses revealed that LIMD2 bound directly
204 Biochemical analyses revealed that LOXL2 readily promote
205 Bioinformatic and
biochemical analyses revealed that miR-431 directly inte
206 Biochemical analyses revealed that organic or synthetic
207 ic analysis of suppressor mutants as well as
biochemical analyses revealed that rapid degradation of
208 hylogenetic, bioinformatics, structural, and
biochemical analyses revealed that Rv2466c is a novel my
209 Biochemical analyses revealed that SPL, as well as the m
210 The structure along with
biochemical analyses revealed that the cIAP1 RING domain
211 Biochemical analyses revealed that the deglycosylation d
212 romatin with high-throughput sequencing) and
biochemical analyses revealed that the effects of ROCK2
213 Comparative bioinformatics, mutagenesis, and
biochemical analyses revealed that the highly conserved
214 Immunocytochemical and
biochemical analyses revealed that the mutant AR aggrega
215 Biochemical analyses revealed that the PTP is a heterool
216 Our integrated bioinformatic and
biochemical analyses revealed that these passenger hotsp
217 Structural and
biochemical analyses revealed that UbVs specifically inh
218 Biochemical analyses revealed that WKS1 phosphorylates P
219 Bioinformatic and
biochemical analyses revealed unexpected mechanisms by w
220 d GluN2A-mediated synaptic transmission, and
biochemical analyses show AIDA-1 cKO mice have low GluN2
221 Biochemical analyses show high phyB protein levels in ME
222 Structural and
biochemical analyses show OsSWEET2b in an apparent inwar
223 Biochemical analyses show that a horizontally acquired p
224 Structural and
biochemical analyses show that BB0270 has a similar stru
225 Our expression studies and
biochemical analyses show that biliary abnormalities in
226 The structures and
biochemical analyses show that CENP-H and CENP-K form a
227 Interspecies
biochemical analyses show that COQ8A and yeast Coq8p spe
228 Enzymatic, NMR, mutational, and
biochemical analyses show that in the autoinhibited, off
229 Tracing and
biochemical analyses show that MFSD12 is necessary for t
230 Biochemical analyses show that PI5P4Kbeta preferentially
231 Biochemical analyses show that R79A and S83A mutant prot
232 Subsequent genetic and
biochemical analyses show that RNA G-quadruplex folding
233 Structural and
biochemical analyses show that tetrameric c-di-GMP links
234 Single-molecule and
biochemical analyses show that the N terminus plays an i
235 Biochemical analyses showed enhanced generation of cycli
236 Immunohistochemical and
biochemical analyses showed significant amounts of beta-
237 Biochemical analyses showed that chronic excess glucocor
238 Biochemical analyses showed that peptide-induced alpha5b
239 Biochemical analyses showed that poly(dA-dT)-activated A
240 Accordingly, bioinformatic, functional, and
biochemical analyses showed that RB1-E2F complexes bind
241 Our
biochemical analyses showed that the conserved Y267 resi
242 Biochemical analyses showed that the transition between
243 Biochemical analyses showed that the WR domain of TWIST
244 In addition, biomechanical and
biochemical analyses showed that Wnt1(sw/sw) mice exhibi
245 Our
biochemical analyses suggest a mechanism in coral which
246 However,
biochemical analyses suggest that isoeugenol inhibits TD
247 The
biochemical analyses suggest that the lactose-free formu
248 Surprisingly, both modeling and
biochemical analyses suggested that SH2 domain overexpre
249 More importantly, the
biochemical analyses suggested that this novel binding s
250 ether with molecular dynamics simulation and
biochemical analyses,
suggests Ub(B) restricts the flexi
251 Biochemical analyses support shoot-to-root transport of
252 We show by structural and
biochemical analyses that Prp3 contains a bipartite U4/U
253 and in solvated systems, informed downstream
biochemical analyses that tested key aspects of the hypo
254 this study we demonstrate, using genetic and
biochemical analyses,
that in Escherichia coli, TnaC res
255 anscriptomics alongside immunohistologic and
biochemical analyses,
that neurons from thirteen-lined g
256 Based on structural, mutational, and
biochemical analyses,
the cofactor channel and the subst
257 Through proteomic, structural, and
biochemical analyses,
this work shows that posttranslati
258 combines in silico, molecular genetics, and
biochemical analyses to characterize both the structure
259 urrent study sought to use computational and
biochemical analyses to characterize decision-making pro
260 We combined detailed lipidomic and
biochemical analyses to characterize the functional role
261 s, combined with a suite of parallel NMR and
biochemical analyses to cross-validate their integrity,
262 ulations using recent cryo-EM structures and
biochemical analyses to delineate an optimal free energy
263 Here, we use in vivo and in vitro
biochemical analyses to demonstrate that ATP-bound Rok1,
264 , we undertake physiological, structural and
biochemical analyses to elucidate the catalytic mechanis
265 Here, we use structural and
biochemical analyses to establish how an antimicrobial p
266 med bioinformatics, immunohistochemical, and
biochemical analyses to examine if collagen cross-linkin
267 Here, we use bioinformatic and
biochemical analyses to explore this largely uncharacter
268 e use electron cryo-tomography together with
biochemical analyses to investigate structures of indivi
269 ography, molecular dynamics simulations, and
biochemical analyses to investigate the structural requi
270 ata set, we used quantitative microscopy and
biochemical analyses to show that 1 novel hit, TMEM41B,
271 Here, we use genetic and
biochemical analyses to show that this second DNA tether
272 Our
biochemical analyses uncover CEP83 as a bona fide TTBK2
273 Biochemical analyses uncover that the CD and AT-hook-lik
274 Histological, electron microscopic, and
biochemical analyses uncovered significant hypomyelinati
275 Biochemical analyses using (14)C-PA as a substrate demon
276 Consistently,
biochemical analyses using a phospho-synapsin-specific a
277 Diagnostic
biochemical analyses using various m7G cap derivatives a
278 Biochemical analyses verify that MHF preferentially enga
279 itro pollen germination, immunolabeling, and
biochemical analyses was used on wild-type and Atpme48 m
280 Through
biochemical analyses we find that a proportion of p110al
281 Using
biochemical analyses,
we found that BcelPL6 initially re
282 osphatase activity assays along with various
biochemical analyses,
we found that Pho8 is active when
283 Here, using structural, spectroscopic, and
biochemical analyses,
we found that this truncated varia
284 Using
biochemical analyses,
we further document a direct inter
285 Using complexome profiling and
biochemical analyses,
we have explored the structural re
286 Here, using structural and
biochemical analyses,
we have identified FMDV 3D(pol) mu
287 redundancy-circumventing genetic screen and
biochemical analyses,
we have identified functionally-re
288 ng phylogenetic, transcriptomic and in vitro
biochemical analyses,
we identified a single homotetrame
289 Here, using bioinformatics and
biochemical analyses,
we identified an enzyme, Jd1381 fr
290 By combining electrophysiological and
biochemical analyses,
we identify subunit-specific struc
291 eles, live-cell spindle assays, and in vitro
biochemical analyses,
we show that She1 is required for
292 In vivo
biochemical analyses were conducted after UV-A1 irradiat
293 e blood cell differential counts, and plasma
biochemical analyses were conducted to evaluate tissue d
294 MPAR trafficking, pHluorin-GluA1 imaging and
biochemical analyses were performed on primary hippocamp
295 In addition, a number of
biochemical analyses were performed to determine the int
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 SAD in human HEK293T cells, here we combined
biochemical analyses with NMR spectroscopy.