ライフサイエンスコーパス: axis

1 ve activation of an integrin/reactive oxygen axis.

2 along the antero-posterior and dorso-ventral axis.

3 erent positions along the anterior-posterior axis.

4 to engage an MTSS1-Src-cortactin inhibitory axis.

5 s activates HSC by modulating the SOCS-STAT3 axis.

6 ral axons along the anterior-posterior (A-P) axis.

7 ed in the longitudinal (or planar-polarized) axis.

8 skeletal patterning along a proximal-distal axis.

9 ssic RAS Ang II/Ang II Type 1 (AT1) receptor axis.

10 nsversely modulated orientation of the optic axis.

11 of the hypothalamic-pituitary-adrenal (HPA) axis.

12 ndodermal derivatives along the primary body axis.

13 regulating key elements in the EMT signaling axis.

14 can develop anywhere along the craniospinal axis.

15 rray of electrodes positioned along the flow axis.

16 each species' niche in at least one isotopic axis.

17 along the interaural and naso-occipital head axis.

18 death via the RIG-I-MAVS-IFN-beta signaling axis.

19 droplet and/or oscillation along the vortex axis.

20 (MDSC) infiltration in tumors via chemokine axis.

21 e embryo, suggesting that they develop an AP axis.

22 eddy generation on the two sides of Kuroshio axis.

23 through the highly interconnected gut-brain axis.

24 ered Drosophila free to rotate about the yaw axis.

25 in a high degree of twisting along the long axis.

26 ngement of the IF network along the polarity axis.

27 wnstream of the ROCK-LIMK-cofilin signalling axis.

28 pectively, after zeroing at the phlebostatic axis.

29 naling during establishment of the embryonic axis.

30 th the side chains perpendicular to the long axis.

31 outgrowth along the proximal to distal (PD) axis.

32 rotate 180 degrees about their longitudinal axis.

33 d cells divide along their long apical-basal axis.

34 ascribed to the ACE2/angiotensin-(1-7)/MasR axis.

35 ignment and orientation to the cell's growth axis.

36 essential for normal functioning of the HPI axis.

37 essential role in the oncogenic AR signaling axis.

38 s are injected orthogonally to the interface axis.

39 to support the outgrowth of LRs along a new axis.

40 (HR1) coiled coil is assembled at the trimer axis.

41 spectrally opponent responses along the S-M axis.

42 ng growth of the primary shoot (gametophore) axis.

43 input is organized across the rostral-caudal axis.

44 y axis, and a channel at the 5-fold symmetry axis.

45 morphology along the benthic-limnetic trait axis.

46 ar fibres, oriented along the medial-lateral axis.

47 infinite metal-ligand chain along the fibril axis.

48 n of behavior with the hormonal reproductive axis.

49 onstrating a distinct role for the R-Ras-Akt axis.

50 e processes along a posterior-anterior vmPFC axis.

51 protein 88 (MyD88)-IRAK-dependent signaling axis.

52 unctions as an organizer of the dorsoventral axis.

53 is mediated by a FOXO1 induced TGFbeta1/CTGF axis.

54 anipulate sound along a continuous frequency axis.

55 lass-specific traits expressed along the A-P axis.

56 and the alignment of nanofibers along fiber axis.

57 and the hypothalamus-pituitary-adrenal (HPA) axis.

58 egulate spindle orientation and the division axis [1, 2].

59 a local twofold noncrystallographic symmetry axis, a conformation clearly distinct from that of actin

60 and one oriented with the medio-lateral hand axis (Across orientation).

61 This feedforward ACh-NGF axis activates the gastric cancer niche and offers a com

62 ects on hypothalamic pituitary-adrenal (HPA) axis activation, aversive conditioning, or insulin secre

63 limbic-hypothalamic-pituitary-adrenal (LHPA) axis activity in the offspring.

64 r exacerbated hypothalamic-pituitary-adrenal axis activity.

65 The first axis allows for coexistence of different shade tolerance

66 l lithium iron phosphate microrods with long-axis along the [010] direction.

67 e leads to a radial variation of the optical axis along the plane of the film.

68 asurements identify a uniaxial magnetic easy axis along the rips.

69 , one oriented with the proximal-distal hand axis (Along orientation) and one oriented with the medio

70 ine series shows that the crystallographic a-axis, along the channel, can be varied in increments les

71 y soften the short Na-O bond along the polar axis - an effect that is proposed to facilitate reorient

72 Principal axis analysis revealed a four-factorial structure of the

73 Cu gradient along the duodenal crypt-villus axis and buffers Cu levels in the cytosol of enterocytes

74 role for thrombin, the thrombospondin-1/CD36 axis and cyclooxygenase 1 in subsequent platelet activat

75 reased HIF-1alpha activates the JAK1/2-STAT3 axis and enhances tumor stem-like cell self-renewal.

76 ing promoted activation of the PI3K/Akt/mTOR axis and FoxO1 nuclear exclusion in DCs, leading to decr

77 rnal rhythmicity of the RBP4/STRA6 signaling axis and investigated whether STRA6 is necessary for diu

78 ar switch that controls the cardiac TGF-beta axis and its early transcriptional effects that lead to

79 ed the LA and RA of all subjects using short axis and long axis slices by steady-state free precessio

80 pressions at the icosahedral 2-fold symmetry axis and surrounding the 5-fold symmetry axis, protrusio

81 mplicate CK2 as a regulator of the Th17/Treg axis and Th17 cell maturation and suggest that CK2 could

82 s the activation of the Shp1-STAT5 signaling axis and the composition of the c-Kit/STAT signalosome.

83 st integrate each component of the brain-gut axis and the influence of biological sex, early-life str

84 le oriented with respect to the illumination axis and the second being a sphere made of dendrites of

85 protrusions surrounding the 3-fold symmetry axis, and a channel at the 5-fold symmetry axis.

86 optic vibrations of Tl-rattlers along the c-axis, and acoustic phonons that likely causes the low la

87 injury directly via the interferon-beta/IRF1 axis, and by modulating properties of NPCs.

88 ity through the inhibition of c-Met-Ras-HO-1 axis; and it can have significant therapeutic potential

89 ent of a TN-alpha2beta1-JAG1-NOTCH signaling axis as a candidate therapeutic target in glioma patient

90 uminated a novel STRAP-NOTCH1-HES1 molecular axis as a CSC regulator in colorectal cancer, with poten

91 ect the importance of the vertical (gravity) axis as a reference frame.

92 ify the evolutionarily conserved SIRT1-FoxO1 axis as a regulator of resting CD8(+) memory T cell meta

93 cation approach has identified the AID/RAD51 axis as a target for a potentially clinically translatab

94 over, these results underline the ILC2/IL-13 axis as a targetable pathway to curtail the M-MDSC compa

95 ll, our results identify the CXCL2/MIF-CXCR2 axis as an important mediator in MDSC recruitment and as

96 ich defines the MHC class I-LILRB1 signaling axis as an important regulator of the effector function

97 ation-53BP1 nuclear body formation-G1 arrest axis as an unanticipated outcome of homologous recombina

98 suggests an alternative Ang 1-7/Mas receptor axis as counter-regulatory to the classic RAS Ang II/Ang

99 s with preexisting dysfunction in at least 1 axis at baseline was also significantly lower in the SCR

100 Inhibition of this adaptive axis at multiple nodes rendered glioma cells with primar

101 establishment of the stem niche at the bract axis but, after the reproductive transition, it is antag

102 nal AMPK signalling or the mTORC1-HIF-1alpha axis, but contributed to the activation of beta-catenin

103 ated the locations of clumps along the trait axis by creating niches that promoted the growth of spec

104 M seems to play a crucial role in the BTB-BM axis by modulating BTB dynamics during spermatogenesis.

105 ith different thickness and an in-plane easy axis (c-axis) of magnetization were grown on a-plane sin

106 fundamental to the establishment of the body axis, cell migration, synaptic plasticity, and a vast ra

107 ivation and disrupts the p53/MDM2 regulatory axis, conferring resistance to various chemotherapeutics

108 -specific executable models of the signaling axis, connecting genetic aberrations in FLT3, tyrosine k

109 We propose that a SMYD2-H4K20me1-L3MBTL1 axis contributes to HIV-1 latency and can be targeted wi

110 ransition to the adult form, in which the AP axis converges on a molecular architecture similar to th

111 processes because the neuroendocrine stress axis coordinates developmental remodelling, immune funct

112 manipulating the EPO/EPO receptor signaling axis could be exploited to prevent and/or treat T cell-m

113 Targeting the CXCL12-CXCR4/CXCR7 axis could lead to novel approaches for offsetting the e

114 Together, the CAMKIIgamma:c-Myc axis critically influences the development and maintenan

115 .77 at 200 K, with an unchanged polarisation axis determined by the material crystallography.

116 (crh) neurons, key regulators of the stress axis, develop abnormally, and rx3-derived pomc+ neurons

117 -signal regulatory protein alpha (SIRPalpha) axis dictates the fate of ingested DNA in DCs for immune

118 at two of its opposing faces along the same axis, different stiffness (i.e., soft on one face and ha

119 argeting of the gut microbiota for brain-gut axis disorders, opening new avenues in the field of nutr

120 Our findings reveal a new signaling axis downstream of the cytosolic DNA pathway and suggest

121 ional significance of the SPL-IKKepsilon-IFN axis during host innate immunity against viral infection

122 ends to form the complete anterior-posterior axis during the somite-forming stages.

123 = .01) while developing a new neuroendocrine axis dysfunction in patients with preexisting dysfunctio

124 promote hypothalamic-pituitary-adrenal (HPA) axis dysregulation, a key feature of affective disorders

125 In fixed ventricular myocardium, dual-axis electron tomography was used for three-dimensional

126 ically engineered mouse models, the WDR4/PML axis elevates intratumoral Tregs and M2-like macrophages

127 quantify the tissue-specific contribution to axis elongation using 3D volumetric techniques, then qua

128 astrocytes closely follows the dorsoventral axis, especially posteriorly from cortex/hippocampus to

129 and5 expression pattern and left-right (L-R) axis establishment.

130 During Drosophila embryonic axis extension, actomyosin has a specific planar-polaris

131 als extensive sliding between tissues during axis extension.

132 rather than the orientation of the division axis, facilitates the onset of this motion.

133 device coupled with the application of hard-axis field aids the velocity enhancement by preventing W

134 lanocyrtes hyper-activation of the PGC1alpha axis, finalized to counteract the energy defect.

135 P-selectin/P-selectin glycoprotein ligand 1 axis, followed by (2) firm platelet adhesion to the endo

136 potential of targeting YAP-BCAR4-glycolysis axis for breast cancer treatment.

137 of different shade tolerances and the second axis for coexistence among species with the same shade t

138 lymphoid cells (ILC2s) provide an essential axis for rapid immune responses and tissue homeostasis.

139 Collectively, we define a new axis for thymic emigration involving stimulation of the

140 alyzing enhancers during dorsal-ventral (DV) axis formation in the Drosophila embryo, we find that th

141 BPTF is required for anterior-posterior axis formation of the mouse embryo and was shown to prom

142 ity that defines the anterior-posterior body axis frequently fails.

143 HPA axis genetic variation and activity were important predi

144 ults suggest that the HSPA1L/HIF-1alpha/GP78 axis has a crucial role in PrP(C) accumulation during tu

145 motions from translational motions in the z-axis has been a long-standing challenge.

146 skeletal patterning along a proximal-distal axis has been an area of intense inquiry.

147 hin the hypothalamic-pituitary-adrenal (HPA) axis has been linked to risk for depression and antidepr

148 microbiota in lung diseases by the gut-lung axis has been widely observed, but the underlying mechan

149 molecular control of patterning across this axis has important functional implications.

150 Salivary cortisol (hypothalamic pituitary axis), heart rate variability (sympathetic adrenal medul

151 Off-axis high speed imaging confirms a technically relevant

152 targeting the FGFBP1 and TGF-beta1 signaling axis holds promise for slowing age- and disease-related

153 15 that compared activation in patients with axis I disorders and matched healthy control participant

154 y disorders (n=60) or no lifetime history of Axis I psychopathology (ie, healthy controls; n=26).

155 onse was always aligned with the inter-aural axis (i.e. craniocentric).

156 trol force transmission along this molecular axis (i.e. modulating integrin activation and controllin

157 tide inhibitors of the CXCL1-CXCR2 signaling axis identified HIF-2alpha-dependent neutrophil recruitm

158 es a potential role for the IL-17A signaling axis in AD pathogenesis.

159 CSF (GM-CSF) enhanced the KDR/ID2 signaling axis in BMDCs.

160 consequently, the role of MTA1-DNMT3a-IGFBP3 axis in breast cancer progression.

161 e, we reveal a role for the GUCY2C paracrine axis in compensatory mechanisms opposing RIGS.

162 p27T187A KI activated an E2F1-p73-apoptosis axis in DKO prostate tumorigenesis, slowed disease progr

163 ntaining G protein-coupled receptor 4 (LGR4) axis in driving aberrant Wnt/beta-catenin signaling in M

164 ablish an important role for the Tet2-Foxo3a axis in epigenetically regulating critical genes in aNSC

165 Differential role of pannexin-1/ATP/P2X7 axis in IL-1beta release by human monocytes.

166 ults unveil a novel stromal PTEN-to-JAGGED-1 axis in maintaining the MaSC niche, and subsequently inh

167 rapeutic efficacy of targeting the MALT1-MYC axis in MCL patients.

168 known as Akt) signaling pathway is a central axis in mediating proximal signaling events of TCR and C

169 emonstrated a critical role of the p53-CXCR2 axis in mediating RSV-induced senescence.

170 determine whether a deficient CNP signaling axis in mice causes accelerated progression of aortic va

171 thways involved in the regulation of the HPA axis in mice.

172 ts reveal the SPI1-METTL14-MYB/MYC signaling axis in myelopoiesis and leukemogenesis and highlight th

173 s metabolic functions along the portocentral axis in normal liver.

174 of its inhibitory action on the reproductive axis in other vertebrates, we investigated the role of R

175 se data reveal a key role for the IL-6/STAT3 axis in potentiating FGF19-driven HCC in mice, a finding

176 prosurvival function of a p53/PINCR/Matrin 3 axis in response to DNA damage in CRC cells.

177 t role for the adipose PPARgamma-adiponectin axis in susceptibility to stress and negative emotion-re

178 tion of a potentially targetable fractalkine axis in the formation and the development of advanced an

179 n and siloxane contraction along the pulling axis in the respective rate-determining transition state

180 ion of spermatogenesis by a local functional axis in the testis: role of the basement membrane-derive

181 y Maf as a downstream target of the CIC-ETV5 axis in this process.

182 -eukaryotic translation initiation factor 4E axis in TNF production downstream of NOD1.

183 The critical role of the CCL1-CCR8 axis in Treg cells was further dissected through adoptiv

184 Differences in the RANKL/OPG Axis in vivo, and RANKL-induced maturation of osteoclast

185 to bacterial infection and suggest that the axis in which these kinases operate may represent a targ

186 largely compromises the LKB1/AMPK signaling axis, in turn leading to the elevation of NSCLC cell pro

187 However, structures downstream of the MHb-IP axis, including the median (MnR) and caudal dorsal raphe

188 t inhibitors (ICIs) targeting the PD-1/PD-L1 axis induce sustained clinical responses in a sizable mi

189 eterotroph, densely colonizing the mesogleal axis inside the gastric filaments.

190 periodic segmentation of the vertebrate body axis into somites, and later vertebrae, relies on a gene

191 The previously unidentified Gut-Liver-Bone Axis intriguingly implies the normal gut microbiota's os

192 We conclude that the Nrf-2/HO-1 axis is a critical pathway in the hyperglucidic-mediated

193 he establishment of the anteroposterior (AP) axis is a crucial step during animal embryo development.

194 Elongation of the body axis is a key aspect of body plan development.

195 ver, the extent to which the TIGIT/CD226/PVR-axis is affected by HIV-infection has not been character

196 ipoxygenase/leukotriene-B4 (PLA2/5-LOX/LTB4) axis is an important inflammatory signaling pathway.

197 ntribution to expansion along the orthogonal axis is cancelled by cell rearrangements and cell shape

198 gulation of MMP7 by FOXC1 and the WNT5A-MMP7 axis is essential for FOXC1-induced invasiveness of TNBC

199 Also, the CXCR4-CXCL12 axis is involved in the interaction between hematopoieti

200 rmation to the hypothalamo-pituitary-gonadal axis is mediated by leptin receptors on AgRP neurons.

201 er synaptic strength along the proximodistal axis is mirrored by an increasing gradient of direct syn

202 e impact of diet on the metabolism-epigenome axis is poorly understood but could alter gene expressio

203 direct signature of the afterglow of an off-axis jet.

204 Addition of this second axis leads to communities with a high diversity of shade

205 B-cell receptor signalling and PI3K-AKT-mTOR axis leads to release of MCL cells from TME, reversal of

206 aminergic and hypothalamic-pituitary-adrenal axis leads to splenic atrophy and contraction of NK cell

207 Activation of the 16:4(n-3)-GPR120 axis led to enhanced cPLA2 activity in these splenic mac

208 tionality is achieved by application of hard-axis magnetic field favoring and opposing the Dzyloshins

209 Targeting the GnRH/GnRHR1/miR-200b axis may be key for the management of hepatic fibrosis d

210 rance mechanisms and the BCL9L/caspase-2/BID axis may limit cancer diversity and evolution.

211 al miRNA downregulation, the miR-140-5p/Pin1 axis may play a major role in tumorigenesis and offer pr

212 Accordingly, the IL-17-IL-17R axis may provide an attractive target for the management

213 nd suggest that the holo-RBP/STRA6 signaling axis may represent a novel therapeutic target in type II

214 in multiple TLR pathways, and this signaling axis may serve as a pharmacologically tractable target d

215 ed expression of CDKN2A, and this regulatory axis may therefore represent a potential therapeutic tar

216 l component of field along the magnetic easy-axis melts long-range order, revealing a bistable, stron

217 eal that the microbiota-inosine-A2A receptor axis might represent a potential avenue for combatting a

218 lateral plate, ectoderm, endoderm) to drive axis morphogenesis remain largely unknown.

219 he functional implication of this regulatory axis next showed the proangiogenic activity of ZO-1 in b

220 grative fashion, rather than focusing on one axis of community structure at a time, will improve our

221 htly packed linear arrays oriented along the axis of constriction and restricted to a narrow zone wit

222 ymorphism loci, and population density as an axis of environmental variation.

223 chanism for how sustained activation of PERK axis of ER-stress during chronic HCV infection activates

224 ntensity profiles measured along the optical axis of human eye lenses with age-related nuclear catara

225 disorders, and that dynamics are a critical axis of manipulation for causal optogenetic studies.

226 ing cell poles, PlpA reinforces the polarity axis of MglA and thus stabilizes the direction of motili

227 The c-axis of non-cross-linked C-(A-)S-H is more deformable du

228 is primed, in part, by the PI3K/AKT effector axis of oncogenic RAS signalling.

229 eceptor pair that defines the neuroendocrine axis of serotonergic body fat loss in Caenorhabditis ele

230 two Cas2 domains form a central hub (twofold axis of symmetry) flanked by two Cas1 lobes and two Cas3

231 e molecule displacements only along the long axis of the cell, where molecules experience the least c

232 ing zone components along the inner-to-outer axis of the ciliary gating zone.

233 d-polymer chains are extended along the long axis of the crystal with the side chains perpendicular t

234 lobal gene expression along the dorsoventral axis of the developing arches.

235 The main axis of the DWBC, characterized by a low temperature cor

236 electron donor perylene is aligned along the axis of the electric field vector with respect to the CT

237 contralaterally, and along the longitudinal axis of the hippocampus, thereby establishing an associa

238 O atom positioned on the three-fold symmetry axis of the NH3(+) group (angle C(epsilon)-N(zeta)-O clo

239 erent thickness and an in-plane easy axis (c-axis) of magnetization were grown on a-plane single-crys

240 significant effect of the IL-23/PI3K/mTORC1 axis on regulating IL-22 production and also identify a

241 Our data provide evidence that the 5-LO/LTB4 axis orchestrates GVHD development and suggest it could

242 rium hexaferrite (BaM) films with in-plane c-axis orientation are promising and technically important

243 lattice misorientation with respect to the c-axis orientation in the center of the crystal.

244 generate single-crystal joints with their c-axis orientation tailored to best combat a selected fail

245 m for the study of evolution, development of axis pattern formation, venom production, haplo-diploid

246 k and left inferior (n=12) or superior (n=2) axis pattern with the presence of a notch in the middle

247 molecules are rotated by 23 degrees along an axis perpendicular to their pi systems.

248 cillatory activity across the septo-temporal axis, phasing the firing of specific CA3 interneurons, t

249 ynchrony of Golgi cells along the transverse axis, powerfully regulating granule cell firing by impos

250 Thus, the PGE2/Ep3 axis promotes cardiac healing after MI by activating rep

251 try axis and surrounding the 5-fold symmetry axis, protrusions surrounding the 3-fold symmetry axis,

252 Targeting this axis provides a novel approach for the long-term treatme

253 The HBZ/NRF-1/TDP1 axis provides new therapeutic targets against ATL and mi

254 lel bone morphogenetic protein (BMP)/Smad1/5 axis (recently identified as a positive regulator of mus

255 component of hypothalamic-pituitary-adrenal axis regulation that prepares the organism for successiv

256 iring was not different and the reproductive axis remained intact.

257 However, the precise role of BM in this axis remains unknown.

258 n had reduced hypothalamic-pituitary-adrenal axis responses to both acute and chronic stress and were

259 ogenase activity and that inhibition of this axis results in suppression of tumour growth in a transg

260 ely to rotate clockwise around their longest axis (right lateralized).

261 lization regardless of the degree of crystal axis rotation.

262 empty fractions (EFs) were provided by short axis (SAX) and area-length methods.

263 Thus, beyond its role as a recombinosome-axis/SC linker molecule, Mer2 has important functions in

264 te such excellent performance to the dense c-axis self-assembled BaZrO3 nanorods, the elimination of

265 RA of all subjects using short axis and long axis slices by steady-state free precession (SSFP) seque

266 tly increased hypothalamic-pituitary-adrenal axis stress response and impaired sensorimotor gating, p

267 a critical K(+)-Ca(2+)-adrenergic signaling axis that acts to dampen thermogenesis, maintain tissue

268 findings establish a unique gene regulatory axis that cancer cells can exploit to circumvent the imm

269 PI3K-PKB-GSK-3 pathway is a novel regulatory axis that is important for controlling the decision betw

270 is through a PKCiota-Ect2-Rac1-NPM signaling axis that is required for lung tumorigenesis.

271 uncover a novel PKCiota-AMOT-YAP1 signaling axis that promotes OSC tumor growth, and provide a ratio

272 Hence, our studies reveal a novel signaling axis that regulates JAK2 in normal and malignant HSPCs a

273 cholinergic nerve-airway smooth muscle (ASM) axis that underlies prolonged airway hyperreactivity (AH

274 the hypothalamic-pituitary-interrenal (HPI) axis, the fish equivalent of the hypothalamic-pituitary-

275 n of anterior pole formation: a polarized AP axis, the pre-existing midline, and the dorsal-ventral m

276 of the hypothalamic-pituitary-adrenal (HPA) axis, the sympathetic nervous system through the greater

277 sing magnetic fields oriented along the wire axis, the wires exhibit a stepwise increase in conductan

278 f bone morphogenetic protein receptor (BMPR) axis: the anti-proliferative arm of TGF-beta super famil

279 l divisions drive tissue expansion along one axis, their contribution to expansion along the orthogon

280 lation of the hypothalamic-pituitary-adrenal axis, thereby affecting an individual's ability to regul

281 g immunity, and delineate the host signaling axis they activate to protect against respiratory infect

282 voltage relationships that cross the voltage axis three times and the first and third zero-current po

283 a3, which activates a PAK4-YAP/TAZ signaling axis to enhance Glut3 expression.

284 nd metabolites that stimulate the "gut-brain axis" to alter neural circuits, autonomic function, and

285 ive microstructures can enable broadband, on-axis transmissive holograms that can project complex ful

286 Axis-tuned neurons thus provide a powerful mechanism for

287 PGE2 and regulation of the PGE2/IL-17A/IL-22 axis via IL-33 signaling during lung fungal exposure.

288 of neurotoxicants that affect the brain-gut axis via the vagus nerve, and then travel to higher cent

289 nz by selectively impairing the GR signaling axis via this enhancer.

290 by bidimensional imaging on a subcostal long-axis view.

291 The PCSK9-LDLR axis was associated with outcomes in patients with HF.

292 The embryonic axis was found to be particularly enriched in palmitic a

293 ably, this novel defined LSD1/integrin beta3 axis, was also detected in human lung adenocarcinoma spe

294 ia their activation of the Smad2/3 signaling axis, we used local injection of adeno-associated viral

295 g and modulation of cardio-renal sympathetic axis were monitored for 3 weeks after myocardial infarct

296 input is organized across the lateral-medial axis whereas NIf input is organized across the rostral-c

297 solid, and stiff to bending, along the long axis, whereas it has a liquid and viscous behavior in th

298 he cofilin N terminus away from the filament axis, which compromises S3D cofilin's ability to weaken

299 ibres led to a bifurcated anterior-posterior axis with fused heads forming in single anterior blastem

300 berculosis by harnessing the SET8-NQO1/TRXR1 axis with its specific and potent inhibitors could lead

301 propose a novel regulation of the ICOS/ICOSL axis, with ADAM10 playing a direct role in regulating IC

302 in regulating an IL-10/CREB/WISP-1 signaling axis, with broad implications in linking innate immune a