ライフサイエンスコーパス: X

1 X-linked Retinoschisis (XLRS) is one of the most common

2 X-ray absorption spectra indicated that U(IV) in both he

3 X-ray absorption spectroscopy and high-energy X-ray scat

4 X-ray absorption spectroscopy and X-ray photoelectron sp

5 X-ray computed tomography (CT) is a powerful noninvasive

6 X-ray crystal structures were obtained for five of the d

7 X-ray crystallography confirms they have the fluorite st

8 X-ray diffraction analysis showed that calcium carbonate

9 X-ray diffraction of precipitates showed that Mnt interl

10 X-ray fluorescence (XRF) microscopy, quantified with ele

11 X-ray photoelectron spectroscopy reveals that, at pH </=

12 Here we report the 2.1 A X-ray structure and molecular function of ClbS, a gene p

13 Here we report the 2.7-A X-ray crystal structure of MazF-mt6.

14 O into CH3CN solutions of the salts afforded X-ray quality crystals of five compounds with hydroxyl g

15 An X-chromosome exome screen identified a missense mutation

16 An X-ray crystallography study of the rabbit muscle GPb inh

17 An X-ray structural investigation of the cerium imido compl

18 re competitive with acetyl coenzyme A and an X-ray cocrystal structure reveals that binding is biased

19 ared by a templated clipping reaction and an X-ray crystal structure shows that the squaraine gem-dim

20 the highly organized capsules is shown by an X-ray crystal structure which features the assembly of t

21 -cell line panel and allowed us to obtain an X-ray co-crystal structure of the synthetic secondary me

22 Moreover, we show that Rnf12, an X-encoded ubiquitin ligase important for initiation of X

23 nic bands surrounding the Gamma = (0, 0) and X = (pi/aFe, 0) points of FeSe and to measure the corres

24 sonance (EPR), SQUID, UV-vis absorption, and X-ray absorption spectroscopy (XAS)) coupled with advanc

25 across Diptera from ordinary autosomes, and X-chromosomes mostly conserve their ancestral genes.

26 cterized by UV, circular dichroism (CD), and X-ray photoelectron spectroscopy (XPS).

27 Through X-ray diffraction and X-ray photoelectron spectroscopy, the as-grown tungsten(

28 d EDA2, that bind to EDA receptor (EDAR) and X-linked EDA receptor (XEDAR/EDA2R), respectively.

29 ogress in imaging defects using electron and X-ray techniques, in situ three-dimensional imaging of d

30 orption, resonance Raman, (1)H NMR, EPR, and X-ray absorption (near-edge) spectroscopy, ESI mass spec

31 Mechanistic and X-ray evidence is presented that supports that the react

32 bioinformatic, biochemical, mutational, and X-ray crystallographic studies on the unicellular alga C

33 Here we present NMR and X-ray characterization for the two classes of these inhi

34 ton emission computed tomography (SPECT) and X-ray computed tomography (CT) for investigating transpo

35 electron microscopy, UV-Visible spectra and X-ray diffraction pattern.

36 fully characterized by NMR spectroscopy and X-ray crystallography.

37 roposed on the basis of NMR spectroscopy and X-ray crystallography.

38 X-ray absorption spectroscopy and X-ray photoelectron spectroscopy studies of SNNO/LSMO he

39 elerators to produce compact ultraviolet and X-ray sources, has attracted considerable interest for a

40 Small angle X-ray scattering and ensemble modeling yielded models of

41 Biophysical analysis, using small angle X-ray scattering and multi-angle light scattering experi

42 Small angle X-ray scattering studies show that the 'Open' form of th

43 ical microscopy, calorimetry and small angle X-ray scattering studies.

44 ape of the dimerization curve in small-angle X-ray scattering (SAXS) experiments using isolated GluA2

45 ation spectroscopy (XPCS) in the small-angle X-ray scattering (SAXS) geometry to probe both the struc

46 APE2 Zf-GRF X-ray structure and small-angle X-ray scattering analyses show that the Zf-GRF fold is t

47 presence of NEIL1 and DNA, while small-angle X-ray scattering analysis confirmed the NEIL1 mediated P

48 ied by in situ grazing-incidence small-angle X-ray scattering and complementary scanning tunneling mi

49 ysed by simultaneous synchrotron small-angle X-ray scattering and Raman spectroscopy in a controlled

50 the complex was calculated from small-angle X-ray scattering data and was in good agreement with a m

51 e-tetrameric form, combined with small-angle X-ray scattering data, allows the localisation of the B

52 secondary structure information, small-angle X-ray scattering data, and any readily available tertiar

53 Small-angle X-ray scattering showed that certain sequences can form

54 Through small-angle X-ray scattering studies of sTie2 dimers in solution and

55 ermal titration calorimetry, and small-angle X-ray scattering, we show that in the homodimeric state,

56 g in situ synchrotron-based small/wide angle X-ray scattering and photoluminescence (PL) probes, the

57 Here we combine wide-angle X-ray scattering (WAXS) with X-ray photon-correlation sp

58 In situ small/wide-angle X-ray scattering and electron microscopic measurements s

59 nts for N-glycosylation have yielded the Asn-X-Ser/Thr (NXS/T) sequon and the enhanced aromatic sequo

60 and the enhanced aromatic sequons (Phe-X-Asn-X-Thr and Phe-X-X-Asn-X-Thr), which can be efficiently N

61 tic sequons (Phe-X-Asn-X-Thr and Phe-X-X-Asn-X-Thr), which can be efficiently N-glycosylated.

62 A combination of synchrotron based X-ray microprobe and bulk techniques was used to study t

63 d by in situ time-resolved synchrotron-based X-ray diffraction, remarkably agreeing with the sorption

64 turies were analyzed using synchrotron-based X-ray diffraction.

65 Remarkably, BoNT/X is the only toxin that also cleaves non-canonical subs

66 cromolecular structure determination at both X-ray free electron lasers (XFELs) and, more recently, s

67 amily of 16 literature ligands, known as bpp(X,Y) [X,Y-substituted 2,6-(pyrazol-1-yl)pyridines], whic

68 hich have produced 16 SCO-active [Fe(II)(bpp(X,Y))2](Z)2 complexes (Z = BF4 or in one case PF6) in (C

69 degrees that was unambiguously confirmed by X-ray crystallographic analysis.

70 Structures of 1 and 2 are confirmed by X-ray crystallography.

71 ious gating voltage regions, as confirmed by X-ray photoelectron spectroscopy and atomic force micros

72 eochemistry was unequivocally established by X-ray analysis of precursor trans-(+)-5a as camphorsulfo

73 ized, and its stereochemistry established by X-ray crystallography.

74 and the IgG1 CH3 homodimer was evidenced by X-ray crystallography and used to engineer examples of b

75 ere shown to possess a novel binding mode by X-ray crystallography, in which the triazolo N1 atom coo

76 percolation of metallic melt is provided by X-ray microtomography of primitive achondrite Northwest

77 r|glassy carbon electrode (GCE), as shown by X-ray photoelectron spectroscopy (XPS) measurements.

78 dynamic regions that proved unresolvable by X-ray crystallography in homologous receptors.

79 (SIV)-specific CD8 T cells express CXCR5 (C-X-C chemokine receptor type 5, a chemokine receptor requ

80 s are isomorphous, with slightly different C-X...NR3 (X = I, Br) distances and packing interactions.

81 e and human germ cells exhibit non-canonical X dosage states that differ from the soma and between th

82 family (B)2(A)n-1PbnX3n+1 (B and A= cations; X= halide).

83 sure follows loss of X inactivation, causing X dosage excess.

84 comprehensive structural characterizations (X-ray diffraction, electron microscopy, Raman, and UV-vi

85 Here, we combine X-ray crystallography, native mass spectrometry, single-

86 ife stage, the latter through micro-computed X-ray tomography.

87 and 38.2%, 51.9%, and 36.3% of which contain X-ray, computed tomography (CT) scan, and genomic data,

88 Functional groups containing X-X bonds are found in all major classes of natural prod

89 ed regression of the postnatal fetal cortex (X-zone) were detected in both the SUMOylation-deficient-

90 first time an InGaP (GaInP) photon counting X-ray photodiode has been developed and shown to be suit

91 and shown to be suitable for photon counting X-ray spectroscopy when coupled to a low-noise charge-se

92 ation of the effects of cyclopentadienyl (Cp(X)) ligand structure on reaction rate and selectivity ha

93 7)Fe Mossbauer, magnetometry, single crystal X-ray diffraction, XAS, and EXAFS for 6.

94 rized by multinuclear NMR and single-crystal X-ray diffraction analysis.

95 Single-crystal X-ray diffraction confirmed structures that resemble a s

96 ctroscopy and low-temperature single-crystal X-ray diffraction, and in the gas phase by quantum-chemi

97 Knowledge of their single-crystal X-ray structures has been instrumental to enable advance

98 This article describes X-ray crystallographic and solution-state NMR studies of

99 roscopy, grazing incident X-ray diffraction, X-ray photoelectron spectroscopy, and Fourier transform

100 ectron microscopy (HRTEM), energy dispersive X-ray analysis (EDX), atomic force microscopy (AFM), sca

101 ere chemically analysed by energy dispersive X-ray spectroscopy (EDX), inductively coupled plasma mas

102 tron microscopy (STEM) and energy dispersive X-ray spectroscopy in STEM (EDX-STEM).

103 copy, Raman and wavelength/energy dispersive X-ray spectroscopy.

104 an, 7.7 years) using anthropometric and dual X-ray absorptiometry (DXA) measurements.

105 ary and sufficient for Xist spreading during X-chromosome inactivation.

106 al was probed using state of the art dynamic X-ray radiography.

107 t higher Mo loadings, indicated by Mo K-edge X-ray absorption spectra.

108 g the co-localization results to iron K-edge X-ray absorption spectroscopy fitting results allowed to

109 dipolar contributions in the uranium L3-edge X-ray absorption cross section to provide unique informa

110 line-shape of the measured resonant elastic X-ray response can be explained with the "site-selective

111 s that clinical criteria (National Emergency X-Radiography Utilization Study [NEXUS] Head CT decision

112 Grazing incidence and grazing emission X-ray fluorescence spectroscopy (GI/GE-XRF) are techniqu

113 s Hg(II) biouptake pathway, we have employed X-ray absorption spectroscopy (XAS) to investigate the r

114 Hepatitis B virus (HBV)-encoded X protein (HBx) plays a critical role in HBV-related hep

115 Measures of dual-energy X-ray absorptiometry-derived fat mass included the limb-

116 -ray absorption spectroscopy and high-energy X-ray scattering demonstrate a correlation between the d

117 Extended X-ray absorption fine-structure spectroscopy showed red

118 Linear combination fitting of extended X-ray absorption fine structure (EXAFS) data using refer

119 (SR-AI) as a receptor for coagulation factor X (FX), mediating the formation of an FX reservoir at th

120 Deficiency of factor X (F10) in humans is a rare bleeding disorder with a het

121 e enzyme factor IXa and the substrate factor X.

122 ies of the hepatic TR, NR1H4 (FXR; farnesoid X receptor), as our model system to tackle this question

123 hibition induced the expression of farnesoid X receptor alpha, a transcription factor that upregulate

124 activated nuclear hormone receptor farnesoid X receptor (FXR) and G protein-coupled membrane receptor

125 In this study, we present the first X-ray structures of barbiturates bound to GLIC, a cation

126 This first X-ray crystallographic study of a single human CCT subun

127 High-flux X-ray tomography enabled us to observe both growth and m

128 e of Xist, the noncoding RNA responsible for X inactivation.

129 The most severe form, X-linked CNM, is caused by myotubularin 1 (MTM1) loss-of

130 Fragile X related protein 1 (FXR1P) is a member of the fragile X

131 Fragile X Syndrome (FX) is generally considered a developmental

132 Fragile X syndrome (FXS), caused by the loss of functional FMRP,

133 Fragile X syndrome, the most common known monogenic cause of aut

134 ion disorders (Friedreich ataxia and fragile X syndrome), and cancer.

135 otrophic lateral sclerosis (ALS) and fragile X syndrome, is challenging for short-read whole-genome s

136 enotypes displayed by the Drosophila fragile X model, and thus reveal a metabolic pathway that can be

137 oral and anatomical deficits seen in fragile X syndrome (FXS) are widely believed to result from imba

138 es of abnormal sensory processing in Fragile X syndrome (FXS).

139 n that disrupts the transcription of Fragile X Mental Retardation Protein (FMRP).

140 xes results in the identification of fragile X protein family (FMRP, Fxr1 and Fxr2) as binding partne

141 1 knock-out mice, the mouse model of fragile X syndrome (FXS).

142 ficits in FXS.SIGNIFICANCE STATEMENT Fragile X Syndrome (FXS) is the most common inheritable form of

143 protein 1 (FXR1P) is a member of the fragile X family of RNA-binding proteins, which includes FMRP an

144 icits and sensory dysfunction in the fragile X syndrome (FXS).

145 and already approved drugs to treat fragile X patients.

146 havioural phenotypes associated with fragile X syndrome.

147 Fmr1 knock-out (KO) mice, a model of Fragile-X Syndrome, to test the E/I imbalance theory.

148 ansfer maximizes the XRS signal at the given X-ray energy and enhances nondipole contributions compar

149 s for therapeutic intervention, however GPCR X-ray structures are mostly restricted to their inactive

150 Moreover, an APE2 Zf-GRF X-ray structure and small-angle X-ray scattering analyse

151 Here we combine operando hard X-ray spectroscopic imaging and phase-field modeling to

152 therefore, the house fly is expected to have X and Y Chromosomes with different gene content.

153 Here, X-ray absorption spectroscopy (XAS) and rR studies have

154 presses transcription from the hermaphrodite X chromosomes.

155 However, X-ray crystallography of these intermediates is severely

156 lage, with chondromodulin, collagen types II/X downregulated, deiodinase II and netrin-1 upregulated.

157 fectiveness which exceeds 38.4 or 47.5 dB in X-band at 1.6 mm, while the density is merely 0.0058 or

158 that a three order of magnitude increase in X-ray brightness and over an order of magnitude increase

159 s and over an order of magnitude increase in X-ray photon energy is achieved by passing a 3 GeV elect

160 the epigenome and the enhancer landscape in X. tropicalis x X. laevis hybrid embryos.

161 +) value strongly predicts infection risk in X-linked CGD carriers, and the carrier state itself is a

162 as previously shown to have diverse roles in X-chromosome inactivation, imprinting and double-strand

163 riptional and chromatin features of inactive X-linked genes in WT and Eed (-/-) TSCs suggests that PR

164 Here, we show that the inactive X chromosome (Xi) of primed hESCs was reactivated in nai

165 including at genes silenced on the inactive X chromosome in females.

166 duction of transcribed genes on the inactive X chromosome, a mode of PRC2 function that may apply bro

167 r active chromatin hallmarks on the inactive-X, including RNA PolII, H3K27ac, and H3K36me3, but not t

168 including synchrotron-based grazing incident X-ray diffraction to observe crystal structure and chemi

169 by atomic force microscopy, grazing incident X-ray diffraction, X-ray photoelectron spectroscopy, and

170 Here we use resonant inelastic X-ray scattering over a wide temperature range across th

171 optical spectroscopy and resonant inelastic X-ray scattering.

172 ethod for protein structure determination is X-ray crystallography which relies on the availability o

173 E-selectin binding determinant sialyl Lewis X (sLe(X)) and display markedly greater adhesive interac

174 states and bearing different anionic ligands X revealed that the nature of anion influences the react

175 ammatory signaling and derepression of liver X receptor activity.

176 positions, were designed as potential liver X receptor (LXR) agonists.

177 ulation of the miR-155 target gene the liver X receptor (LXR)alpha in lung fibroblasts and macrophage

178 Low X-ray absorption contrast in non-mineralised tissue can

179 a contained abundant mCH similar to the male X chromosome and the autosomes.

180 oton NMR relaxation dispersion measurements, X-ray crystallography, and structure-based chemical shif

181 s included transmission electron microscopy, X-ray diffraction and asymmetrical flow field-flow fract

182 e composition of autosomal as well as mtDNA, X chromosome, and Y chromosome ancestries.

183 Synchrotron mu-X-ray based techniques combined with mu-Raman spectrosco

184 ocalizes at the tip of filopodia like myosin-X full-length (M10(Full)).

185 lected asparagine residues in the sequence N-X-S/T (X not equal P), a motif known as an N-glycosylati

186 severe, progressive, and rare neuromuscular, X-linked recessive disease.

187 morphous, with slightly different C-X...NR3 (X = I, Br) distances and packing interactions.

188 Comparison of reactivities of [(PyTACN)Fe(O)(X)](+) generated in different spin states and bearing di

189 ]pyrrole-5-carboxamide for which we obtained X-ray structures of the most potent hit (compound 19, IC

190 , by taking advantage of naturally occurring X-linked somatic PIGA mutations in hematopoietic stem an

191 aphy of biological objects-an application of X-ray free-electron lasers that greatly enhances our abi

192 We also monitored the behaviors of X-linked non-coding transcripts before and after XCI.

193 By combination of X-ray crystallography, SAXS and EM, together with bioche

194 The results show that erosion of X. laevis genes and functional regulatory elements is as

195 the X chromosome to upregulate expression of X-linked genes in male flies.

196 tation in Eda, which caused a milder form of X-linked HED (XLHED), contained low levels of EDA capabl

197 ubiquitin ligase important for initiation of X-chromosome inactivation and XIST transcription in ES c

198 In females, erasure follows loss of X inactivation, causing X dosage excess.

199 ween 5f and 6d electronic states by means of X-ray magnetic circular dichroism.

200 e 123 (DHR) oxidation data for percentage of X-chromosome inactivation.

201 viding ultra-short high-brightness pulses of X-ray radiation have great potential for a wide impact o

202 Each of those panels contains a series of X-Y plots depicting expression levels of subsystems of t

203 icipants (71%) who completed the 24 weeks of X-82 treatment, all except 1 maintained or improved thei

204 ations, one of which is most likely the open-X structure which has unpaired bases at the junction.

205 ssion electron microscopy (TEM) and operando X-ray absorption spectroscopy showed that oxygen species

206 Co(II) to Co(III), as evidenced by operando X-ray absorption spectroscopy at the Co K-edge.

207 In operando X-ray absorption spectroscopy identified reduced Pt cove

208 Conventional optical, X-ray and photoelectron probes often fail to provide int

209 AM beams in the extreme ultraviolet (XUV) or X-ray, and controlling the OAM on these beams remains ch

210 mplemented using C# and run on Linux, Mac OS X & Windows operating systems.

211 P-X cross-linked to NPC1 when added to intact cells.

212 Six of 783 non-pseudoautosomal region (PAR) X-chromosome genes (ATRX, CNKSR2, DDX3X, KDM5C, KDM6A, a

213 ersely, in males, erasure leads to permanent X dosage decompensation.

214 ed aromatic sequons (Phe-X-Asn-X-Thr and Phe-X-X-Asn-X-Thr), which can be efficiently N-glycosylated.

215 equon and the enhanced aromatic sequons (Phe-X-Asn-X-Thr and Phe-X-X-Asn-X-Thr), which can be efficie

216 the postnatal 20alphaHSD-positive postnatal X-zone cells.

217 lowed by in situ variable temperature powder X-ray diffraction.

218 analysis (fwhm) was performed on the powder X-ray diffraction traces and showed that the higher conc

219 n was analyzed for polymorphism using powder X-ray diffraction, solid fat content by pulsed nuclear m

220 ucture and purity were verified using powder X-ray diffraction, transmission electron microscopy, Ram

221 Cumulatively, these loci also predicted X chromosome loss in women (n = 96,123; P = 4 x 10(-6)).

222 Pregnane X receptor (PXR) is a xenobiotic receptor that regulates

223 ny drugs bind to and activate human pregnane X receptor (hPXR) to upregulate drug-metabolizing enzyme

224 Using near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) we show that

225 n, synchrotron radiation-based high-pressure X-ray diffraction is used to quantify the influence of d

226 Protein X-ray crystallography established that 3-unsubstituted 2

227 n analyzing dynamics of crystalline proteins.X-ray crystallography is the main method for protein str

228 in situ high-pressure synchrotron radiation X-ray diffraction, we reveal a polymorphic transition fr

229 in the positive concordance group (log rank: X(2)=80.96; P=0.001) and lowest in the negative concorda

230 n with a low power benchtop total reflection X-ray fluorescence (TXRF) system has been developed for

231 dentify human-specific mechanisms regulating X chromosome activity in early embryonic development.

232 We report a 3.4-A resolution X-ray crystal structure of a sigma(N) fragment in comple

233 sed on previously published 3.8-A resolution X-ray data.

234 changes were detected in the high-resolution X-ray reflectivity data with monotonic increase in rough

235 haliana Alpha Thalassemia-mental Retardation X-linked (ATRX) ortholog and show that ATRX is involved

236 of the retinoic acid receptor beta-retinoic X receptor alpha (RARbeta-RXRalpha) heterodimer bound to

237 neuronally directed effects of the retinoid X receptor agonist bexarotene in an aggressive model of

238 odimers to active heterodimers with retinoid X receptor alpha (RXRalpha), and phosphorylation of the

239 ere mechanics and micrometer-nanometer-scale X-ray diffraction from synchrotron light in intact ventr

240 lyzed by Scanning Electron Microscopy (SEM), X-ray-tomography and Fourier-Transform Infrared spectros

241 Serial X-ray crystallography allows macromolecular structure de

242 catalyst during the reaction, quasi in situ X-ray photoelectron spectroscopy showed that the surface

243 Furthermore, skewed X chromosome inactivation has been found in the thyroid

244 ctin binding determinant sialyl Lewis X (sLe(X)) and display markedly greater adhesive interactions w

245 oit the element and site selectivity of soft X-ray absorption to sensitively follow the ultrafast pip

246 solved elemental depth profiling in the soft X-ray range with a laboratory source, opening, for examp

247 ption edges of matter, which lie in the soft X-ray regime above 200 eV, permit the probing of electro

248 Key steps were a palladium-catalyzed C(sp3)X-C(sp3)ZnX Negishi cross-coupling affording an omega-hy

249 ctron microscopy (SEM), UV-Vis spectroscopy, X-ray diffraction (XRD) analysis and Fourier transform i

250 Synchrotron X-ray nanofluorescence was applied to map the trace elem

251 llulose were detected by NMR and synchrotron X-ray diffraction.

252 c visualization study using fast synchrotron X-ray micro-tomography to provide new insights into thes

253 Here, utilizing the synchrotron X-ray diffraction technique, we for the first time, expe

254 l is investigated here using the synchrotron X-ray microdiffraction.

255 In this work, synchrotron X-ray reflectivity measurements, accompanied by large-sc

256 asparagine residues in the sequence N-X-S/T (X not equal P), a motif known as an N-glycosylation'sequ

257 advances in free electron laser technology, X-rays with small enough bandwidth have become available

258 The X-chromosome harbors hundreds of disease genes whose ass

259 The X-ray data show how Tyr34 maintains solvent exclusion an

260 Here, we determined the X-ray crystallographic structures of two catalytically i

261 influence of temperature by determining the X-ray structure of Aqy1 at room temperature (RT) at 1.3

262 Here we explore the X chromosome behavior in female and hermaphrodite meiose

263 inary selectivity of the MSL complex for the X chromosome has never been explained.

264 We present here the X-ray crystal structure of the ADAM10 ectodomain, which,

265 Mutations in the X-linked gene Protocadherin-19 (Pcdh19) cause female-lim

266 ic C-F...H-C interaction was observed in the X-ray crystal structure of a fluorinated triterpenoid.

267 to our knowledge, the first analysis of the X chromosome.

268 that reactivation of gene expression on the X chromosome depends on gene chromosomal position.

269 otein like 1 (IL1RAPL1) gene, located on the X chromosome, are associated with intellectual disabilit

270 Deletion of a recruitment site on the X results in reduced DCC binding across several megabase

271 Here, we have solved the X-ray crystal structure of an EBNA1 DNA-binding domain (

272 male-specific lethal (MSL) complexes to the X chromosome to upregulate expression of X-linked genes

273 nd 6 is described and rationalized using the X-ray crystal structure of 6 bound to human IDO-1, which

274 larger than 1 mum(3) in volume, whereas the X-ray beam is often attenuated to protect the detector f

275 Through X-ray diffraction and X-ray photoelectron spectroscopy,

276 of the male-specific lethal (MSL) complex to X-linked genes and modification of chromatin to increase

277 exation and extraction (pH, DDTC, and Triton X-100 concentration, vortex agitation time and complexat

278 temperature of non-ionic surfactant, Triton X-100 occurred and complex was entrapped in surfactant a

279 Schmid (MCDS) is linked to mutations in type X collagen, which increase ER stress by inducing misfold

280 We used X-ray absorption spectroscopy to characterize the struct

281 of structural analysis of drug binding using X-ray structures obtained at 100 K.

282 contrary to formulation, was confirmed using X-ray absorption near edge spectroscopy, suggesting subs

283 the CL40 and CL59 complexes with gHgL using X-ray crystallography and EM to identify their epitope l

284 al distribution of PLAG1 in the testis using X-gal staining; (ii) transcriptomic consequences of PLAG

285 f the compounds were measured using variable X-ray energies in the vicinity of the U L3 edge in the T

286 near dependence of two continuous variables (X and Y).

287 atitis B virus deploys the hepatitis B virus X protein (HBx) as a suppressor of host defenses consist

288 self is able to abstract H-atoms from weaker X-H bonds such as TEMPO-H to re-form 2.

289 However, when X=Cl, only one equivalent of methane is lost with concom

290 While X-ray crystallography and nuclear magnetic resonance spe

291 membranes that could easily be analyzed with X-ray techniques.

292 g the transcriptomes of tomato infected with X. gardneri vs. XgDeltaavrHah1 revealed the differential

293 OGT (759G>T (p.L254F)) that segregates with X-linked intellectual disability (XLID) in an affected f

294 bine wide-angle X-ray scattering (WAXS) with X-ray photon-correlation spectroscopy (XPCS) in the smal

295 nd the enhancer landscape in X. tropicalis x X. laevis hybrid embryos.

296 eficiency, B cell-specific CD79a-Cre x XBP1 (X-box binding protein-1) floxed mice (XBP1-conditional k

297 ries of oligomers d(XGiXC5X) and d(XC5XGiX) (X = A, T or none; i < 5) are designed to study the impac

298 of 16 literature ligands, known as bpp(X,Y) [X,Y-substituted 2,6-(pyrazol-1-yl)pyridines], which have

299 leading to normal hydrogen bonds of type YH-X analogous to secondary bonding.

300 Strikingly, young X. tropicalis DNA transposons are derepressed and recrui