ライフサイエンスコーパス: Y

1 Y chromosomes are typically viewed as genetic wastelands

2 Y-STR data were used to test different out-of-Africa mig

3 Y-STRs have emerged as important forensic and population

4 Y. pestis-infected Mefv(M680I/M680I) FMF knock-in mice e

5 m in spark plasma sintered Fe(48)Cr(15)Mo(14)Y(2)C(15)B(6) metallic glass is established by analyzing

6 eukaryotic translation initiation factor 1A Y-linked, together with its X-linked homolog EIF1AX Evol

7 can enter the hydrophobic cavity of alpha(3)Y and hydrogen bond to Y(32), as well as the possibility

8 g one pH- and redox-active tyrosine (alpha(3)Y and peptide A), and two proteins that contain multiple

9 l formation behavior of Y(32) in the alpha(3)Y model protein.

10 A clinical cohort study (N = 70) showed 40% Y-BOCS score improvement during DBS, and a prospective i

11 o higher burden for their child on the EQ-5D-Y and FAQLQ-PF dependent upon PA severity.

12 past 12 months significantly predicted EQ-5D-Y proxy utility (P < .01).

13 (86)Y-NM600 PET imaging was performed on female BALB/C mice

14 )Y complexes as radiopharmaceuticals and (86)Y tracers for positron emission tomography (PET) imaging

15 ing and rapid normal-tissue clearance of (86)Y-NM600 were noted in both 4T07 and 4T1 murine models.

16 e accuracy of the PET data and validated (86)Y-NM600 as a surrogate for (177)Lu-NM600.

17 Methods: NM600 was radiolabeled with (86)Y for PET imaging and (177)Lu for targeted radionuclide

18 genetic maps and Sanger sequences of over 90 Y chromosome BAC clones.

19 (90)Y bremsstrahlung SPECT images were transformed into dose

20 T) achieved before and after Yttrium-90 ((90)Y) administration and to evaluate additional benefits du

21 ble yttrium isotopes to enable roles for (90)Y complexes as radiopharmaceuticals and (86)Y tracers fo

22 tered activity for a therapy infusion of (90)Y-DOTA-BC8 were 0.35 +/- 0.20 cGy/MBq for red marrow, 0.

23 NET patients received up to 4 cycles of (90)Y-DOTATOC at 1.85 GBq/m(2)/cycle with a maximal kidney b

24 derived from mCRC cell lines exposed to (90)Y.

25 with glass microspheres were imaged with (90)Y PET/CT for voxel-level dosimetry to determine lesion a

26 bability (TCP) in radioembolization with (90)Y PET/CT-derived radiobiologic dose metrics.

27 ocrine tumor (NET) patients treated with (90)Y-DOTATOC in the setting of a prospective phase II trial

28 ter outcome in NET patients treated with (90)Y-DOTATOC.

29 tic cancer for follow-up to therapy with (90)Y-FAPI-46.

30 -Arg-Leu-Arg-Tyr-NH(2) (1), reported to be a Y(4)R partial agonist with high affinity (pK(i) Y(4)R: 8

31 etrapeptide (Arg-Leu-Arg-Tyr-NH(2)), being a Y(4)R partial agonist with unchanged Y(4)R affinity (pK(

32 olleagues report a micropeptide encoded by a Y chromosome-linked lncRNA that may explain the higher i

33 gulation of male sexual differentiation by a Y chromosome-linked male determining factor (M-factor) i

34 male sterility, while the upregulation of a Y allele of a cytokinin regulator (APRT3) may cause fema

35 linked homolog EIF1AX Evolutionary loss of a Y-linked microRNA target site enabled up-regulation of E

36 We used a Y-maze chamber to test whether reduced-pH seawater alter

37 ses may act in concert to further accelerate Y degeneration.

38 r findings demonstrate that self-adjuvanting Y. pestis OMVs provide a novel plague vaccine candidate

39 On day 14 after Y. enterocolitica infection (arthritis onset), we found

40 096 mg/L respectively) were observed against Y. enterocolitica.

41 inated BEA zeolite to produce Zn-DeAlBEA and Y-DeAlBEA.

42 ds, in the context SAY (where S = C or G and Y = C or T).

43 candidate for generation of tRNA halves and Y RNA fragments in biofluids.

44 cell-cycle-related cyclins A, B, D, G/I and Y, and transcriptional cyclin L, were identified in the

45 acteristic in-plane chemical order of Mo and Y/Sc and Kagome ordering of the Al atoms, as evident fro

46 othesis was that PS-induced changes in Q and Y would improve central and local mechanisms of Q contro

47 or control (meningococcal group A, C, W, and Y conjugate vaccine or saline).

48 to investigate this hypothesis, as the X and Y chromosomes are cytologically homomorphic and evolved

49 The human X and Y chromosomes evolved from a pair of autosomes approxima

50 Divergence between the X and Y Chromosomes in regulatory sequence can therefore lead

51 No such genes were identified on the X and Y chromosomes.

52 stically cue retrieval of task demands X and Y, respectively), and the role of the hippocampus and do

53 IATs), called Y. ruckeri invasin (YrInv) and Y. ruckeri invasin-like molecule (YrIlm).

54 S polymorphism (Y/S) and noncarrier animals (Y/Y).

55 ng genomic and historical data, we assembled Y. pestis genomes from nine individuals covering four Eu

56 with IMD caused by meningococci serogroup B, Y, or C, adjusting for age, gender, and comorbidities.

57 we show that a B6.Y (POS) colony bred and archived at the MRC Harwell Inst

58 Recently, a B6.Y (POS) colony was shown to carry a non-B6-derived regio

59 n of chromosome 11 that protected against B6.Y (POS) sex reversal.

60 us-type Y chromosome (Y (POS) ), known as B6.Y (POS) mice, commonly undergo gonadal sex reversal and

61 ity of hydrogen-bonding interactions between Y(32) and E(13), through structural fluctuations that re

62 re four tris- and one tetra-isomers for both Y(3)N@I(h)-C(80) and Gd(3)N@I(h)-C(80).

63 quences as they are homologous to the bovine Y chromosome.

64 eads that are properly aligned to the bovine Y sequence assembly accounted for 46.49%, indicating the

65 As in mice, an X-linked homolog of a bull Y-amplified gene has become testis-specific and amplifie

66 PA, the Ni bimetallic complexes supported by Y, Lu, and La form the Ni(eta(2)-alkyne) intermediate, (

67 (0.75> x <0.90) consistency, except for M1-C Y (0.73; examiner 1 to 2) and M1-M X (0.69; examiners 1

68 the inverse autotransporters (IATs), called Y. ruckeri invasin (YrInv) and Y. ruckeri invasin-like m

69 spheric retina, topological defects, called "Y-Junctions", form to maintain approximately constant ce

70 s dissipative orthogonal transitions to CDN "Y" and back or to CDN "Z" and back.

71 vates the reconfiguration of CDN "X" to CDN "Y" or CDN "X" to CDN "Z".

72 how a correlation between loss of chromosome Y and radioresistance.

73 a Mus musculus domesticus-type Y chromosome (Y (POS) ), known as B6.Y (POS) mice, commonly undergo go

74 The complementary Y-ions, generated under optimized low CE (soft) conditio

75 ditional functions, since the most conserved Y RNA contains a domain that is a close tRNA mimic and R

76 By contrast, Y-DeAlBEA was highly active for 1,3-butadiene formation

77 gene families, making it the most gene-dense Y Chromosome sequenced to date.

78 t years showed that tRNA halves and distinct Y RNA fragments are abundant in the extracellular space,

79 cate that GCP4, GCP5, and GCP6 form distinct Y-shaped assemblies that structurally mimic GCP2/GCP3 su

80 ys, K) and 3,4-Dihydroxyphenylalanine (DOPA, Y) residues in the mussel foot proteins (Mfps) has been

81 Information obtained using Rare Earths (Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, L

82 testis, we report many instances of elevated Y-Chromosome gene expression in a nonreproductive tissue

83 Roux-en-Y gastric bypass (RYGB) was associated with a higher rat

84 score for internal hernia (IH) after Roux-en-Y gastric bypass (RYGB).

85 the beneficial effect of bariatric (Roux-en-Y gastric bypass [RYGB]) surgery on insulin resistance.

86 sity Surgery Registry, 509 patients (Roux-en-Y gastric bypass n=465; sleeve gastrectomy n=44) could b

87 patients who underwent laparoscopic Roux-en-Y gastric bypass procedure, in which comprehensive video

88 and without T2D (n = 9) subjected to Roux-en-Y gastric bypass surgery (RYGB).

89 n morbidly obese subjects undergoing Roux-en-Y gastric bypass surgery compared to lean controls under

90 cancer and partial gastrectomy with Roux-en-Y reconstruction for nonhealing peptic ulcer presented t

91 es a direct HAT mechanism catalyzed by eosin Y.

92 the self-diffusion of a dye molecule (Eosin Y) in a series of polyacrylate networks with differing H

93 zing the visible-light absorptivity of Eosin Y for a reductive generation of alkyl radicals from N-(a

94 en; it was found that the diffusion of Eosin Y is significantly reduced in networks with H-bonding.

95 imethylsilyl)silane, and photocatalyst Eosin Y.

96 a typical 12-connected RE(6) cluster (RE=Eu, Y, Yb, Tb, Ce).

97 nappreciated epigenetic conflict on evolving Y chromosomes between transcription of essential genes a

98 Here, a root-specific nuclear factor Y (NF-Y) transcription factor PdNF-YB21 was isolated fro

99 nscription factors identifies nuclear factor Y subunit C10 (NF-YC10) as a GAPC-binding protein.

100 am dependent on nuclear transcription factor Y subunit alpha (NFYa) and nuclear factor erythroid 2-li

101 8)M(0.2)Ru(2)O(7-delta) (M = Cu, Co, Ni, Fe, Y) controls the concentration of surface oxygen vacancie

102 dy is considered to be a putative marker for Y cells forming a motion processing stream, we suggest t

103 o the noninflammatory environment needed for Y. pestis colonization and proliferation.

104 To identify roles for Y RNAs in mammals, we used CRISPR to generate mouse embr

105 (coded by GCX), aspartic acid (coded by GAY [Y = U or C]), glutamic acid (coded by GAZ [Z = A or G]),

106 mprising the complete mitochondrial genomes, Y-chromosome markers, and genotypes of a number of nucle

107 p turned Y(4)R agonism to antagonism, giving Y(4)R antagonists with pK(i) values <=7.57.

108 cly available human, chimpanzee, and gorilla Y assemblies.

109 omplete sequence assemblies of heteromorphic Y chromosomes have only been generated across a handful

110 probing a variety of color spaces (RGB, HSB, Y'UV, L*a*b*, etc.).

111 Little is known about how human Y-Chromosome gene expression directly contributes to dif

112 G-protein-coupled receptors like the human Y(1) receptor (hY(1)R) are promising targets in cancer t

113 olds of the cholinesterase inhibitor huprine Y and the antioxidant capsaicin results in compounds wit

114 )R partial agonist with high affinity (pK(i) Y(4)R: 8.43).

115 nce in situ hybridization directly implicate Y-specific genes that respectively suppress female (pist

116 Importantly, Y. ruckeri survives in the environment for long periods,

117 We propose that C-C bond coupling in Y-DeAlBEA proceeds via the reaction of coadsorbed acetal

118 The ratio was 2-fold higher in Y/S than in Y/Y cows for kynurenine.

119 The active sites in Y-DeAlBEA are 70 times more active than the Y sites supp

120 The Tyr-to-Phe substitution in Y(898)KAI reduced BRI1 internalization without affecting

121 The ratio was 2-fold higher in Y/S than in Y/Y cows for kynurenine.

122 , for which the Y site is similar to that in Y-SiO(2) but which lacks adjacent hydroxyl groups, and a

123 In the experiment, plants were trained in Y-shaped mazes for 3 days with fans and lights attached

124 eed to the Thoroughbred racehorse, including Y chromosome ancestry.

125 f bacteria in the footpad revealed increased Y. pestis-neutrophil interactions and increased neutroph

126 erize the arrangement of cones in individual Y-Junction cores as well as the spatial distribution of

127 Chronic treatment with Rho-kinase inhibitor Y-27632 after chronic social defeat stress reverses depr

128 Cluster chemistry involving Y, lanthanides (Ln, from La to Lu), actinides (An, from

129 on of CCD from one item (X) to another item (Y) was predicted by a decrease in alpha power following

130 ))(3) afforded the heteroleptic complex, [{L}Y(N(SiMe(3))(2))(2)] (1), by elimination of HN(SiMe(3))(

131 Twelve months of DBS resulted in a mean Y-BOCS score decrease of 13.5 points (SD=9.4) (40% reduc

132 Cells from Mecp2/Y mice have increased DSBs, so this finding suggests tha

133 mutations that improved phenotypes in Mecp2/Y mice after mutagenesis with N-ethyl-N-nitrosourea (ENU

134 ponse (DDR) also improve phenotypes in Mecp2/Y mice.

135 The glass microfluidic Y-system with planar immunocapture channel working in so

136 has an XY system and V. vinifera a modified Y haplotype (Yh) and that the sex locus is small, but it

137 and DNA-binding processes of the multidomain Y-family DNA polymerase IV (DPO4).

138 cells lacking one or both of the two murine Y RNAs.

139 tize OG in the nucleotide pool, and the MutM/Y system, which counteracts OG in chromosomal DNA.

140 with several distinct cases of neo-X and neo-Y formation, X-added regions, and conversion of autosome

141 Neuropeptide Y (NPY) and NPY receptors represent a highly conserved,

142 parvalbumin, somatostatin, and neuropeptide Y also show unique topographical distributions, suggesti

143 the basolateral amygdala (BLA), neuropeptide Y (NPY) is associated with buffering the neural stress r

144 ction of Caenorhabditis elegans neuropeptide Y/neuropeptide F and serotonin that could aid in our und

145 Endogenous neuropeptide Y (NPY) and corticotrophin-releasing factor (CRF) modula

146 uences IGL neurons that express neuropeptide Y (NPY) (hereafter, IGL(NPY) neurons), guiding the assem

147 er-modified microelectrodes for Neuropeptide Y measurement by electrochemical impedance spectroscopy

148 uropeptide receptors, including neuropeptide Y, gonadotropin inhibitory hormone (GnIH), pyroglutamyla

149 entral alpha-klotho to modulate neuropeptide Y/agouti-related peptide (NPY/AgRP)-expressing neurons,

150 cholinergic starburst ACs, NPY (neuropeptide Y)- and EBF1 (early B-cell factor 1)-positive ACs.

151 Within the family of neuropeptide Y (NPY) receptors, the Y(4) receptor (Y(4)R) is unique a

152 ed the evolutionary ortholog of neuropeptide Y/neuropeptide F in the nematode Caenorhabditis elegans,

153 We found that neuropeptide Y (NPY) expression identifies a class of GABAergic princ

154 ce of both sexes, we found that neuropeptide Y (NPY) expression identifies a major class of inhibitor

155 inding motifs of members of the neuropeptide Y and glucagon families modulate receptor activation pro

156 conformational dynamics of the neuropeptide Y receptor type 2 (Y2R) during activation was investigat

157 -regulated genes preferentially contained NF-Y-binding motifs in their proximal promoters, and notabl

158 Here, we knocked down NF-Y in two types of neuronal cells, neuro2a neuroblastoma

159 A heterotrimeric transcription factor NF-Y is crucial for cell-cycle progression in various types

160 ce was not correlated with DNA binding of NF-Y but with splicing of NF-YA.

161 However, whether NF-Y modulates a different transcriptome to mediate distinc

162 Here, a root-specific nuclear factor Y (NF-Y) transcription factor PdNF-YB21 was isolated from Popu

163 Three catalysts, Ni-Y, Ni-Lu, and Ni-Ga, showed nearly quantitative conversi

164 (M = Si, Ge, Sn, Pb, Ti, Al, Cr, Fe, Ni...; Y = O, NR, CH(2), S), i.e., substituted 5-azabicyclo[3.3

165 One is a duplication of a non-Y-linked, female-specifically expressed response regulat

166 We synthesized a series of peptidic NPY Y(4)R ligands, derived from the hexapeptide acetyl-Arg-T

167 nd Ai14 Cre-reporter mice, we found that NPY Y(1) receptor (Y(1)R)-expressing neurons are glutamaterg

168 he active centers for this process are =Si-O-Y(OH)-O-Si= or =Si-O-Zn-O-Si-O= groups closely associate

169 tem that oversynthesized the LcrV antigen of Y. pestis, raised the amounts of LcrV enclosed in OMVs b

170 anges in the overall genetic architecture of Y chromosomes.

171 Assemblies of Y'227C (or T'225C) with AgNCs/PMAA (PMAA = polymethyl ac

172 Assessment of Y chromosome in NSCLC tissue microarrays and expression

173 ve studied the radical formation behavior of Y(32) in the alpha(3)Y model protein.

174 ormed on Cr-soc-MOF-1 vs smaller cavities of Y-shp-MOF-5.

175 At pH > 8, the rate constant of Y(32)(*) formation (k(PCET)) increases by one order of m

176 cores as well as the spatial distribution of Y-junctions across entire retinae.

177 (AGMs) after challenge with a lethal dose of Y. pestis delivered as an aerosol, in 4 independent stud

178 istribution and local bonding environment of Y and Nd, as proxies for heavy and light REE, in the dep

179 Our results suggest that the fate of Y. pestis infection of the lung is decided extremely ear

180 Here we identify a group of Y chromosome-expressed long noncoding RNA (lncRNA) that

181 ate level could reflect the heterogeneity of Y cell subpopulations and the heterochrony of their post

182 ranscriptome analysis found that a number of Y chromosomal genes had altered expression patterns in t

183 gocytes in vitro and in vivo Opsonization of Y. pestis with polyclonal antiserum modestly increased p

184 Here, we show that the oxidation of Y(356) is regulated by proton release involving a specif

185 el ovine SNPs of the male-specific region of Y chromosome (MSY) by genome mapping.

186 d CD103(+)CD11b(+)) were found in the RLN of Y. enterocolitica-infected TNFRp55(-/-) mice.

187 lesions, which is a known biological role of Y-family polymerases.

188 ther, our data demonstrate that the roles of Y RNAs are intimately connected to that of their Ro60 pa

189 he alpha4-beta4 hinge and inward rotation of Y- or W106 with W58.

190 vitro FTY720 treatment downregulated CCR7 on Y. enterocolitica-infected bone marrow-derived DCs and p

191 we examine the effects of Ab opsonization on Y. pestis interactions with phagocytes in vitro and in v

192 sonizing Ab had a dramatic effect in vivo on Y. pestis-neutrophil interactions in the dermis and dLN

193 showed increased association of Ab-opsonized Y. pestis with neutrophils in the dermis in a mouse mode

194 The heptameric Nup84 or Y complex is an essential scaffolding component of the N

195 to exons 2 and 3 of POLG but also affect ORF-Y provides potential clinical significance to this findi

196 s 2 and 3 of POLG, herein referred to as ORF-Y that arose de novo in placental mammals.

197 on of the POLG ORF that is overlapped by ORF-Y.

198 de evidence for a novel coding sequence, ORF-Y, that overlaps the POLG ORF.

199 PhyloCSF and synplot2 analysis show that ORF-Y is subject to strong purifying selection.

200 Ribosome profiling data revealed that ORF-Y is translated and that initiation likely occurs at a C

201 nt of DNA polymerase eta (Pol eta) and other Y-family TLS polymerases to damaged DNA relies on prolif

202 The formation of 1,3-butadine over Y-DeAlBEA and Zn-DeAlBEA does not occur via aldol conden

203 46.49%, indicating the success in the ovine Y chromosome isolation and the high quality of the Y chr

204 encing, assembly and annotation of the ovine Y chromosome, but also provide a validated approach to o

205 cus on isolation and sequencing of the ovine Y chromosome.

206 ovel catalyst with improved OER performance, Y(1.8)Cu(0.2)Ru(2)O(7-delta), and provides general guide

207 cows carrying the ABCG2 Y581S polymorphism (Y/S) and noncarrier animals (Y/Y).

208 with somatostatin, glucagon, or polypeptide Y.

209 The multifunctional protein Y-box binding protein 1 (YBX1), is a critical regulator

210 n of methane to dimethyl ether (DME) over Pt/Y(2) O(3) .

211 substituent in yttrium ruthenium pyrochlores Y(1.8)M(0.2)Ru(2)O(7-delta) (M = Cu, Co, Ni, Fe, Y) cont

212 tyrosine produces a neutral tyrosyl radical (Y(*)) that is vital to many catalytic redox reactions.

213 This process causes rapid Y/W degeneration and simultaneous evolution of dosage co

214 S) effects on blood flow ( Q ), shear rate ( Y ), and vascular function in the feeding arteries of th

215 formation of new RE-MOFs, RE-ken-MOF-1 (RE: Y(3+), Ho(3+), Er(3+), Yb(3+)), that display an unpreced

216 orter mice, we found that NPY Y(1) receptor (Y(1)R)-expressing neurons are glutamatergic and were bro

217 eptide Y (NPY) receptors, the Y(4) receptor (Y(4)R) is unique as it prefers pancreatic polypeptide ov

218 genesis by increasing sex-determining region Y-box 2, nestin, and also enhances synaptic function thr

219 Global and regional Y-STR analysis demonstrated regional genetic continuity

220 The repeat-rich Y of D. miranda still contains many actively transcribed

221 ant than N input and RR(NUE) in improving RR(Y).

222 atment relative to the control) of yield (RR(Y)), WP (RR(WP)), and NUE (RR(NUE)), respectively.

223 lemental space of these borides with M = Sc, Y, Zr, Hf, and Nb, realizing an increased property tunin

224 ence (Yale-Brown Obsessive Compulsive Scale (Y-BOCS) score improved 37% during stimulation on), the o

225 ach to overcoming difficulties in sequencing Y chromosome in other mammalian species.

226 as responsible for the increase of serogroup Y IMD in Sweden.

227 Draft genomes of serogroup Y isolates in Sweden revealed that although the populati

228 hese isolates was similar to other serogroup Y isolates internationally, a distinct strain (YI) and m

229 These data suggest that the serogroup Y IMD increase in Sweden was most probably due to small

230 Extensive comparisons between the serogroup Y sublineages of all coding sequences, complex genomic r

231 The mammalian male-specific Y chromosome plays a critical role in sex determination

232 quence can therefore lead to tissue-specific Y-Chromosome-driven sex biases in expression of critical

233 and the disappearance of the trans-splicing Y structure intermediate, CRK9 is essential for the firs

234 to C1q and blocks its activity, and SRPX2(-/Y) mice show increased C3 deposition and microglial syna

235 C3(-/-);SRPX2(-/Y) double-knockout mice exhibit phenotypes associated wi

236 In the somatosensory cortex, SRPX2(-/Y) mice show decreased thalamocortical synapse numbers a

237 ciated with C3(-/-) mice rather than SRPX2(-/Y) mice, which indicates that C3 is necessary for the ef

238 The threespine stickleback Y shows convergence with more degenerate sex chromosomes

239 n identified an effector, with an N terminal Y/FxC motif, that induced a strong hypersensitive respon

240 Previous work established that Y. pestis uses the T3SS to inhibit neutrophil respirator

241 Studies in bacteria revealed that Y RNA tethers Ro60 to a ring-shaped exoribonuclease, for

242 Although it is often said that Y-Chromosome genes are lowly expressed outside the testi

243 Last, we show that Y RNAs tether Ro60 to diverse effector proteins to gener

244 The Y(trans)P conformation conformer can bind the HIV gp41 e

245 The Y-family DNA polymerase REV1 completes repair of the cro

246 non-recombining region between the X and the Y spans approximately 17.5 Mb on the X chromosome.

247 ghtly repressed throughout elongation by the Y-shaped DNA structure of replication forks.

248 In the complex, the Y(III) center was found to be tetracoordinate in a disto

249 super-resolution sequencing, we explore the Y Chromosome of Bos taurus (bull) and find it to be domi

250 ognize seven constituent nucleoporins of the Y and Nic96 complexes.

251 negative correlation between the loss of the Y chromosome or linc-SPRY3-2/3/4 and overall survival.

252 mosome isolation and the high quality of the Y chromosome sequences.

253 embly to generate a 15.87 Mb assembly of the Y chromosome.

254 owever, we lack comprehensive studies of the Y chromosomes of Denisovans and Neanderthals because the

255 ct accessible and obstructed surfaces of the Y complex and Nic96 within the NPC.

256 important details about the function of the Y complex that affect our understanding of NPC structure

257 NMR analyses of the Y(3)N@I(h)-C(80) adducts found that the tris-adducts wer

258 lies relative to females, and repeats on the Y chromosome are disproportionally mis-expressed during

259 amily of neuropeptide Y (NPY) receptors, the Y(4) receptor (Y(4)R) is unique as it prefers pancreatic

260 Y-DeAlBEA are 70 times more active than the Y sites supported on silica, for which the Y site is sim

261 uggest these forces are not exclusive to the Y chromosome, and chromosomal degeneration may have occu

262 e Y sites supported on silica, for which the Y site is similar to that in Y-SiO(2) but which lacks ad

263 mer can bind the HIV gp41 epitope, while the Y(cis)P is not binding competent and shows a higher aggr

264 t on the importance of neutrophils in AMI to Y. pestis and may provide a new correlate of protection

265 for this antibody-mediated immunity (AMI) to Y. pestis remain poorly understood.

266 bic cavity of alpha(3)Y and hydrogen bond to Y(32), as well as the possibility of hydrogen-bonding in

267 populations confer heightened resistance to Y. pestis.

268 ghtened IL-1beta specifically in response to Y. pestis.

269 s lends support to the idea that the 'toxic' Y chromosome can create a mutational burden in males whe

270 u in 1 and in derivatives of 1 by Trp turned Y(4)R agonism to antagonism, giving Y(4)R antagonists wi

271 ice harboring a Mus musculus domesticus-type Y chromosome (Y (POS) ), known as B6.Y (POS) mice, commo

272 Here, we identify amino acid Tyr (Y) 155 of the RLC as a novel regulatory site that spatia

273 We previously reported that tyrosine (Y) 138 of HPV-31 E2 is phosphorylated by the fibroblast

274 DYRK1A [dual specificity tyrosine-(Y)-phosphorylation-regulated kinase 1 A] is a high-confi

275 being a Y(4)R partial agonist with unchanged Y(4)R affinity (pK(i): 8.47).

276 This study describes previously unknown Y chromosome-expressed lncRNA regulators of radiation re

277 Untreated Y. pestis infection during pregnancy is associated with

278 K, Mn, Mo, Na, Ni, P, Pb, Th, Tl, Sb, U, V, Y and Zn) in 73 commercial products marketed in Spain.

279 It is shown that the R + G + B value (Y) of the reaction image and SBA concentration (X) are r

280 y input and induced dendritic hypotrophy via Y(5) receptor activation; conversely, CRF increased exci

281 ge and SBA concentration (X) are related via Y = -0.034 X +737.40, with a determination coefficient o

282 ates were also obtained against potato virus Y when targeting its cp gene.

283 We constructed six Env375 variants (M, H, W, Y, F, and S) for each SHIV, and we performed a pool comp

284 ere phenotypically female; however, 58% were Y chromosome-positive, resembling the phenotype of human

285 results indicated that 68.90% of reads were Y chromosome-related sequences as they are homologous to

286 Reaction of LH with Y(N(SiMe(3))(2))(3) afforded the heteroleptic complex, [

287 s a graded rather than a binary switch, with Y- or W106 side-chain burial correlated with increased F

288 Assembly of the full X, Y, and Yh haplotypes of V. sylvestris and V. vinifera se

289 e, we provide evidence that suppression of X-Y crossing-over unleashed a second dynamic: selfish X-Y

290 g-over unleashed a second dynamic: selfish X-Y arms races that reshaped the sex chromosomes in mammal

291 convergence implies that lineage-specific X-Y coevolution through gene amplification, and the selfis

292 ha power following the presentation of the X-Y pair.

293 Sets of azabicyclo[X.Y.0]alkanone amino acids have been effectively used to i

294 understanding of how flies with a typical X/Y heterogametic amphogeny (male and female offspring in

295 of E-selectin and ICAM-1, obtained at year (Y) 7 (Y7) and Y15 examinations, with cardiac function as

296 r, show that gene gain is prominent on young Y chromosomes.

297 poactive in distal CA3, compared with young (Y) rats.

298 Lau JY, Yu Y, Tang RS, et al.

299 Ford AC, Yuan Y, Moayyedi P.

300 Yang P, Zhang Y, Zhang L, et al.