ライフサイエンスコーパス: we report that

1 Here we report that 5-10% of malaria-exposed individuals, but

2 We report that 5-HT2 receptors can form homo- and hetero

3 Here, we report that a 0.1 Gy radiation dose reduces cancer pr

4 Here, we report that a 1 week delay between the lesion and tra

5 Here we report that a Fox family transcription factor, Foxc1,

6 We report that a novel emm32.2 genotype emerged in Liver

7 Here we report that a polyaromatic capsule acts as a supramol

8 In this study we report that a potent and specific small molecule anta

9 We report that a previously unknown, quorum-sensing-cont

10 Here, we report that a radical SAM protein, the heme chaperone

11 We report that a two week treatment of 3.5 month old 5XF

12 Here, we reported that a choline transporter gene, CTL1, contr

13 Here, we report that A3A is highly expressed in subsets of ped

14 Here, we report that abnormal embryonic development in aged fe

15 Here we report that abundant 6mA is associated with transcrip

16 titration calorimetry and NMR spectroscopy, we report that acidic residues in the BAZ2B PHD domain a

17 Here, we report that Actalpha, Actbeta, and Actgamma isoforms

18 We report that acute estrogen depletion rapidly disrupts

19 Here, we report that ADE13 encodes ADS lyase in C. neoformans.

20 We report that adhesion-induced eosinophil cytolysis tak

21 We report that, after a chemical lesion that ablates inn

22 We report that, after spinal cord contusion injury in ad

23 Here, we report that alpha-SYN present in dopaminergic nigral

24 In the present study we report that among PLK family members, PLK3 is also ab

25 Here we report that among the two PCS genes-OsPCS1 and OsPCS2

26 Here, we report that ancient fish-bone remains, despite being

27 Here we report that APE2 resection activity is regulated by D

28 Here we report that Arl4C functions with the actin regulator

29 Here, we report that ART treatment results in phosphorylation

30 We report that as a consequence AR variants lacking the

31 Here, we report that ASOs with specific backbone and sugar mod

32 We report that aspects of precipitation and potential ev

33 Here we report that Atf3-deficient (Atf3(-/-)) mice developed

34 Here we report that Aub promotes GSC self-renewal and GSC pro

35 Here, we report that autophagy is upregulated in HNSCC-associa

36 Finally, we report that BEC-1/BECN1/Beclin1 functions non-cell-au

37 We report that BH3-only proteins bind inactive full-leng

38 Here we report that bone marrow (BM) Gr-1(lo) immature myeloi

39 Here we report that bovine Rh, regenerated instead with a six

40 Here we report that breast cancer cells activate autophagy in

41 Here, we report that breast cancer patients with low MFN2 expr

42 Here, we report that C-type lectin dendritic cell (DC) immunor

43 Here we report that CaCCs coexist with BK and SK channels in

44 Here, we report that CAIII is highly expressed in osteocytes,

45 Furthermore, we report that calcium and integrin-binding protein 2 bi

46 Here, we report that cardiomyocyte-specific loss of SRC-2 (SRC

47 We report that CCRL2-deficient mice have a defect in neu

48 Herein, we report that CD10, also known as common acute lymphobl

49 Moreover, we report that CDK4 represses FAO through direct phospho

50 Here we report that CED-3 caspase and the Arg/N-end rule path

51 Here we report that cells with mutations in RFWD3, an E3 ubiq

52 Here, we report that certain RNA template structures and G-ric

53 Here, we report that cGAS localizes to micronuclei arising fro

54 In this study, we report that CGRP can act in both the brain and the pe

55 In the current paper, we report that CGRP-mAbs prevent the activation of Adelt

56 Here we report that CH4 is emitted from the stems of dominant

57 We report that CHD6 and CHD7 both bind with high affinit

58 We report that CheV1 and CheW have largely redundant abi

59 We report that chronic stress exposure in rodents produc

60 We report that CLYBL loss leads to a cell-autonomous def

61 Here we report that cold exposure in mice triggers a metaboli

62 Here we report that conserved GA repeat cis elements within t

63 Here, we report that constitutive Twf2a-deficient mice (Twf2a(

64 Herein, we report that crack formation can be effectively harnes

65 Here we report that cultures of expanded potential stem cells

66 Here, we report that Dbf4 is enriched at early origins through

67 Here, we report that DC migration from brain parenchyma is dep

68 th findings from repeated measures analysis, we reported that DEHP metabolites and BPA were significa

69 In this study, we report that deletion of intestinal nuclear receptor c

70 We report that deletion of Ric-8b in olfactory sensory n

71 We report that dietary Mn levels dictate the outcome of

72 Here, we report that diminished VGLL4 expression, but not VGLL

73 Here, we report that disruption of the Rasa1 gene in adult mic

74 Here, we report that dissociation of UNC5C and polymerized TUB

75 Here, we report that DPM-1001, an analog of the specific PTP1B

76 Here we report that Drosophila centrosomin (cnn) expresses tw

77 Here, we report that Drosophila melanogaster females but not m

78 Here, we report that dynamic changes in forebrain microRNA (mi

79 Here we report that EC lacking Cav-1 exhibit impaired LD form

80 Here we report that ectonucleotide pyrophosphatase/phosphodie

81 Here we report that endocytic recycling requires active mecha

82 Here we report that endogenous human p190A, but not its 50% i

83 We report that enterobactin (Ent), a catecholate siderop

84 Here we report that ErbB4 in midbrain DAergic axonal projecti

85 Here we report that ETH persists in adult Drosophila melanoga

86 Here we report that Ets-1 destruction is regulated by the deu

87 Here, we report that expression of the HBV entry receptor, hum

88 Herein, we report that extracellular Clusterin promoted epitheli

89 Here, we report that FA complementation group D2 protein (FANC

90 Here we report that FAF1 destabilizes TbetaRII on the cell su

91 Here we report that fasting alone robustly inhibits the initi

92 We report that fidelity of cholinergic SK responses requ

93 Here we report that formation of the pre-fusion Env-CD4-corec

94 We report that FOXC2 and GJC2 mutations are associated w

95 Here, we report that FOXP1-SHQ1 deletion cooperates with PTEN

96 Here we report that fully reduced HMGB1 orchestrates muscle a

97 In this study, we report that gamma interferon (IFN-gamma) treatment, b

98 Here we report that gamma networks desynchronize and theta ne

99 Here we report that GDNF-family receptor alpha-like (GFRAL),

100 Here, we report that genetic or pharmacological targeting of t

101 Previously, we reported that gestational carbofuran exposure has det

102 Here, we report that glutamine substitutions of these residues

103 We report that GSH is essential for T cell effector func

104 Here we report that hematopoietic-specific genetic inactivati

105 We report that high expression of the autophagy marker c

106 Here we report that high-level MDM2 but not MDM4 has a consis

107 Here we report that histone deacetylase 10 (HDAC10) is a robu

108 Here, we report that human microglial-like cells (iMGLs) can b

109 ne patients.SIGNIFICANCE STATEMENT Recently, we reported that humanized CGRP monoclonal antibodies (C

110 Here, we report that hypoxia-mediated downregulation of the du

111 We report that ICAM-1 augments myoblast adhesion to myob

112 In this study, we report that IFN regulatory factor 4 (Irf4) is highly

113 Here we report that IGF-1 level in blood and IGF-1 signaling

114 Here, we report that IL-10 was rapidly induced following intes

115 Here, we report that IL-15(-/-) mice developed enhanced allerg

116 In this study we report that IL-22 signals exclusively through the bas

117 Here, using Treg-specific Il27ra(-/-) mice, we report that IL-27 signaling in Foxp3(+) Tregs is esse

118 Here, we report that IL-33 (30 ng/mL), a member of the IL-1 fa

119 Collectively, we report that IL-33 expression is induced in an undiffe

120 Lastly, we report that ImaA directly affected the amount of host

121 Here, we report that in addition to the well-characterized mid

122 Here we report that in Cln1(-/-) mice, which mimic INCL, redu

123 Here, we report that in inflammatory lesions, a second barrier

124 Here, we report that in the Caenorhabditis elegans zygote, fee

125 Here we report that in the NTS of high-fat diet-induced obese

126 Herein, we report that in various cancer cells upon oxygen depri

127 Here, we report that, in addition to regulating CCND1, this en

128 We report that, in naive mouse ESCs (mESCs), p53 restric

129 We report that, in the absence of distal target organs,

130 We report that, in two organisms, the PBPs incorporate l

131 Here, we report that increased erythrocyte S1P binds to deoxyg

132 We report that increased vacancy diffusion barrier, whic

133 In this study, we report that individuals with orofacial neuropathic pa

134 Here we report that induced p53 loss in Krt8(+) mammary lumin

135 Here, we report that induction of neuronal autophagy enhances

136 We report that inflammation after SCI is dysregulated in

137 Here we report that lack of Trex2 results in the accumulation

138 Here we report that lal(-/-) ECs facilitated in vivo tumor an

139 Here, we report that Lamin B1 levels modulate the differentiat

140 Here, we report that LKB1 undergoes Aurora kinase A (AURKA)-me

141 Here, we report that low (0.1 mum) concentrations of Tg and Tg

142 Here we report that LT exposure rapidly reduces the levels of

143 Here, we report that LTM can be induced by partial training af

144 Here, we report that Lunatic fringe (Lfng), a key modifier of

145 Here, we report that lysine-specific demethylase 1 (LSD1) upre

146 Here, we report that Magnaporthe oryzae CKS1 encodes a cyclin-

147 In this study, we report that maintenance of human memory CD8 T cell ef

148 Here, we report that mammalian RNase H1 enriches in nucleoli a

149 Here, we report that manipulations of gonadal hormones do sign

150 We report that many members of the ykkC motif RNA, the l

151 Here, we report that MAPK signaling shows strong intratumoral

152 Here we report that MCPIP1 protein levels are decreased durin

153 Previously, we reported that membrane association of HIV-1 Gag, as w

154 -dependent memory-enhancement model in rats, we report that memory strengthens through activation of

155 We report that methionine substitution, but not leucine

156 Based on laboratory studies, we report that methyl benzoate (MB), a naturally-occurri

157 Here, we report that METTL14, a key component of the m(6)A met

158 Here, we report that mice lacking phospholipase Cgamma1 (PLCga

159 Here, we report that microstimulation in the prefrontal cortex

160 In summary, we report that miR-874 inhibits CCNE1 expression during

161 Previously, we reported that mitochondrial membrane potential regula

162 Here, we report that mitophagy, the selective removal of mitoc

163 Here, we report that MLH1, a key protein involved in mismatch

164 We report that mohawk homeobox (Mkx), a tendon-specific

165 We report that monoamine oxidase A (MAOA) is a clinicall

166 Herein, we report that MoS2 films with vertically-aligned 2D lay

167 Here we report that mTORC1 signaling suppresses endogenous DN

168 Here, we report that mutagenizing MELK with CRISPR/Cas9 has no

169 Here, we report that MYC stimulates the transcription of DANCR

170 Here we report that myometrial cells from human and mouse exp

171 Here, we report that nanoparticle-drug conjugates (NDCs) of mo

172 Here we report that NatD promotes the migratory and invasive

173 Here we report that NCEH-1 protects dopaminergic neurons from

174 Here we report that Nck is required for the growth and vascul

175 We report that nearly 80% of detected mutations have no

176 Here, we report that Necdin deletion disturbs the migration of

177 Here we report that neural representations within the mouse h

178 Here we report that neural-specific inactivation of two murin

179 In this study, we report that noble gases are hosted by two major sites

180 Here we report that Nuclear receptor-related 1 (Nurr1):Retino

181 We report that nuclei display spontaneous calcium transi

182 Here we report that oncogenic kinase and growth-factor signal

183 Here we report that one of the K-Ras splice variants, K-Ras4a

184 We report that Ophn1 deficiency in the mouse generated s

185 Here, we report that optimization of caloric loading in B6 mic

186 In this study, we report that oral administration of a selective ROCK2

187 Here we report that P450s derived from a thermophilic organis

188 Here we report that patching an eye is unnecessary for produc

189 Here, we report that peripheral nerve injury increases express

190 Here, we report that Peromyscus polionotus is strikingly preco

191 Here we report that PI3K signaling is critical for the contro

192 We report that PIAS2 promotes SUMOylation of alpha-synuc

193 Here, we report that PIPKIgamma is highly expressed in lung ca

194 Here we report that PIPs, predominantly <3,000 p53 immunoposi

195 However, we report that PL inactivation after training attenuates

196 Here, we report that plasma OT concentrations increased within

197 Here we report that platelet-derived growth factor receptor a

198 In addition, we report that PM with a negative surface charge can ads

199 In this paper, we report that primary fibroblasts that have been isolat

200 In this study, we report that PSY is a substrate of the Clp protease.

201 Here we report that PTCL are sensitive to transcription-targe

202 Here we report that RA95.5-8 variants catalyze the asymmetric

203 We report that RAC1(P29S) evokes a Rasopathy-like phenot

204 Here we report that recombinant HSV-1 with a mutation in the

205 Here, we report that reduced SMN function impacts the action o

206 Finally, we report that resting levels of long-chain triacylglyce

207 We report that RFRP-3 immunofluorescence expression patt

208 In this study, we report that RGC-32 is preferentially upregulated duri

209 In this article, we report that rhAPC binds to human neutrophils via inte

210 Here we report that RIN1 controls the plasticity of cultured

211 Additionally, we report that RIPK1 kinase-dependent IFN-beta productio

212 Here, we report that RNF145, a previously uncharacterized ER m

213 Herein, we report that (S)P(MeAN) can be activated to generate O

214 Here we report that serine-arginine protein kinase 2 (SRPK2)

215 In this study, we report that shifting hPSC-CMs from glucose-containing

216 Here, we report that silencing or inhibition of endogenous TAK

217 In this article, we report that silencing the INSR in inducible knockdown

218 Here we report that SIRT6 depletion in cardiac as well as ske

219 Here we report that six out of a sample of seven 'jellyfish'

220 In this study, we report that spatiotemporal enrichment of actin monome

221 Here, we report that specific protein synthesis inhibitors cou

222 Here we report that Src family kinases (SFK) and focal adhesi

223 Here we report that SRC-3 supports the TIC/CSC state and indu

224 Here we report that steady states of systems with non-equilib

225 Here we report that Stx3 undergoes monoubiquitination in a co

226 Here, we report that super-enhancers drive the biogenesis of m

227 Here, we report that T cells activated in such a context are m

228 Here, we report that the active intracellular portion of NOTCH

229 Here we report that the addition of peracetic acid, a strong

230 Here, we report that the AR-repressed gene CCN3/NOV inhibits A

231 Here, we report that the architecture of the secondary root sy

232 In this study, we report that the bud cortex is a landmark that signals

233 Here, we report that the conserved lysine residue 714 in the E

234 We report that the cVLPs induced significantly higher an

235 Here we report that the deprotonation of ureas generates a cl

236 from the aneuploid Drosophila S2 cell line, we report that the dose effect of aneuploidy can be furt

237 We report that the efficiency of subcutaneous islet tran

238 Here we report that the endoplasmic reticulum (ER) is asymmet

239 We report that the environmental stress of carbon dioxid

240 We report that the FGF13 locus, comprising FGF13 and miR

241 Here, we report that the fowlpox virus prosurvival protein FPV

242 Here, we report that the fungal nitrooxidative stress response

243 We report that the Gm7068 (CatSpere) and Tex40 (CatSperz

244 Here, we report that the host E3-ubiquitin ligase TRIM6 promot

245 Here, we report that the human skin odour profile is affected

246 Here, we report that the hydrophilic N-terminal domain of Bras

247 We report that the inclusion of nonaromatic 5,5-dimethyl

248 Here we report that the inducible nuclear dual-specificity MA

249 Here we report that the interplay between reversible disulfid

250 Here we report that the intragenic DNA methylation-mediated b

251 Here we report that the isoform characterized by the presence

252 Here we report that the KCNE2 potassium channel transmembrane

253 Here we report that the KDM3 family of histone demethylases p

254 Herein, we report that the live-attenuated herpes simplex virus

255 Herein we report that the matrikine acetylated Pro-Gly-Pro (PGP

256 Here, we report that the myeloid differentiation-related trans

257 We report that the oxidation state of PEG-thiol is key t

258 In this study, we report that the P. falciparum translation enhancing f

259 Here, we report that the parasite-encoded RhopH complex contri

260 Here we report that the passive compliance of the cochlear pa

261 Here we report that the pharmacokinetics and clearance of ren

262 Here, we report that the PML-NB protein Speckled 110 kDa (Sp11

263 Here we report that the radio light curve of GW170817 has no

264 Here, we report that the rainbow enhancers activate RGB cone-s

265 We report that the reduction of 7,16-heptacenequinone pr

266 Here, we report that the remaining members of the RVE8 clade,

267 We report that the RR inhibitor 3-AP actively induces PE

268 In the current study, we report that the SaeRS TCRS also governs fermentative

269 Here, we report that the sensing of IAV RNA by retinoic acid i

270 We report that the single-molecule junction conductance

271 Here we report that the splicing of AR variants AR-V7 as well

272 Here, we report that the stress-inducible 78-kDa glucose-regul

273 Here, we report that the transfer of diverse, task-rule inform

274 Here, we report that the translational activity in the primord

275 Here we report that the tumor microenvironment creates an imm

276 We report that the volume of white matter (WM) is dispro

277 Also, we reported that the absence of CX3CR1-mediated sampling

278 Herein, we report that these conformational changes can also dis

279 We report that these dsRBD homodimers display structural

280 Here we report that these membrane-bound structures derive fr

281 Here, we report that these seed phenotypes can be traced back

282 We report that this degradation gives rise to strong vis

283 Here, we report that this diminution correlates with alteratio

284 Here we report that this strong binding enables a quark-rearr

285 Here, we report that this virus activates caspase-8 in macroph

286 Previously, we reported that this splicing event is highly dysregula

287 Here, we report that TIGIT expression increased over time desp

288 Using the mature calyx of Held (P16-20), we report that tissue-specific ablation of dynamin-1 (cK

289 We report that transcriptional and phenotypic responses

290 We report that transgenic FOXC1 overexpression suppresse

291 We report that transgenic mice expressing endogenous lev

292 However, we report that treatment efficacy has a clear impact on

293 Here, using fluorescence anisotropy, we report that TRIP8b binding to the CNBD of HCN2 channe