ライフサイエンスコーパス: axis

1 on of electron reorganization (the "reaction axis").

2 rectional communication along the 'gut-brain axis'.

3 d role in patterning the dorsal-ventral body axis.

4 and functional abnormalities of T(FH)-B cell axis.

5 probe polarization aligns perpendicular to b axis.

6 regulation of the Lrp5-CSF1-CD105 regulatory axis.

7 tion of myosin motors along their apicobasal axis.

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

9 ripotency through an EGFR-ERK-EGR1-dependent axis.

10 the antiphagocytic CD47-SIRPalpha signalling axis.

11 ming and/or through the microbiome-gut-brain axis.

12 activation of the Hsp90 /Smad3 and p53/CTGF axis.

13 olymer samples with a well-defined molecular axis.

14 f schizophrenia via the microbiota-gut-brain axis.

15 ogression by targeting the FAK-YAP signaling axis.

16 er chromatids are connected to a polymerized axis.

17 f to the side of the catalytic Pol3-PCNA-DNA axis.

18 lates that intersect along a 6-fold rotation axis.

19 along and perpendicular to the ICl molecular axis.

20 and how the brain regulates the somatotropic axis.

21 iformly represented along the CA3 transverse axis.

22 of position along the germline developmental axis.

23 MSC migration via the ATX/LPA/LPA1 signaling axis.

24 traditional IOLs to the pseudophakic visual axis.

25 SNS/brown adipose tissue (BAT)/thermogenesis axis.

26 g a lack of a single life history/physiology axis.

27 s through the regulation of the NE/JNK/Bmal1 axis.

28 of VP3 spanning the region around the 3-fold axis.

29 er checkpoints of the tumor-T cell signaling axis.

30 presence of a segmented spine along its main axis.

31 induced fat-to-pancreas interorgan signaling axis.

32 mental patterns along the anterior-posterior axis.

33 s, which in turn further activate the stress axis.

34 IL36RN) but not elements of the IL-17/IL-23 axis.

35 suppression of the HIF-1alpha/LOX/ITGA5/FN1 axis.

36 ably tilted with respect to the retinal long axis.

37 ethionine-dependent signaling and regulatory axis.

38 an ATR/CHK1/CDC25A/CDK2 DNA damage response axis.

39 hich also establishes the second stereogenic axis.

40 ertically transmitted via the entero-mammary axis.

41 ion that change along the posterior-anterior axis.

42 ttributed to an EpAT-cardiomyocyte paracrine axis.

43 oral responses, mostly related to the stress axis.

44 ner wall surface implode towards the central axis.

45 mmation mediated by the IL-23/IL-1beta/IL-17 axis.

46 rom GnRH neurons to control the reproductive axis.

47 le, Long-Evans rats along the CA3 transverse axis.

48 l protection through an arginase 1-polyamine axis.

49 odulate the gut microbiota and the gut-liver axis.

50 indings of neuroeconomic gameplay studies in Axis 1 psychiatric disorders and advocates the use of th

51 (Ang-II)/angiotensin type 1 receptor (AT1R) axis, a deleterious arm of RAS, unleashing its detriment

52 ng the principal sensorimotor-to-association axis across the entire human cortex, and scale with sing

53 a cells exhibit KRAS/RAC1/ROS/NLRP3/IL-1beta axis activity.

54 interaction studies show that the Fat4-Dchs1 axis acts in parallel to the core-Vangl2 PCP axis to con

55 hway ignited by NANOG is a central molecular axis and a potential target for immune-refractory tumor.

56 d immune regulation through the IL18-IL18RAP axis and antigen presentation involving HLA-DRB1, which

57 uctured by dynamic cytodifferentiation, body-axis and cell-proliferation gene sets that were further

58 criptional level via the IRE1alpha/miR-17-5p axis and demonstrate that inhibition of the IRE1alpha ac

59 (BM) traffic to the lungs along a CCL2/CCR2 axis and differentiate into monocyte-derived alveolar ma

60 and the other spanning a unimodal-transmodal axis and dominated by measures of dynamic range.

61 cs, one spanning a ventromedial-dorsolateral axis and dominated by measures of signal autocorrelation

62 Cs and HNSCC tumors through the CXCR3-CXCL11 axis and elucidate the role of the triterpenoid CF(3)DOD

63 the influence of the IL-23/T helper 17 cell axis and is characterized by intense inflammation and pr

64 esenchymal population lines the crypt-villus axis and is the source of the epidermal growth factor (E

65 genes already known to be required for body axis and limb formation, thus validating our approach; p

66 receptors, and the induction of CXCL11-CXCR3 axis and phosphatidylinositol 3-kinase/AKT pathways.

67 s of the upregulation of the ACE2/Ang1-7/Mas axis and previously demonstrated benefits of lung functi

68 l gene expression along the corticomedullary axis and quantitation of osmotically regulated genes, al

69 fiber for the maintenance of a straight body axis and spine morphogenesis in adult zebrafish.

70 ut microbiome affecting the gut-immune-brain axis and the molecular mechanisms involved in this proce

71 ffector T cells via the canonical PD-L1-PD-1 axis and were sufficient to accelerate tumorigenesis, ev

72 e analysis explained 70.5% (horizontal first axis) and 21.6% (vertical second axis) of the constraine

73 The scaffolds were 3.56 +/- 0.43 mm (x-axis) and 4.02 +/- 0.44 mm (y-axis) in diameter and 0.54

74 tered intestinal barrier function (gut-liver axis) and by episodes of sepsis to cause cholestasis and

75 Each vector was defined by structural (x-axis) and functional (y-axis) components.

76 quiring a few millimeters along the ion path axis) and is easier to operate than prior generations of

77 Epidermal Growth Factor Receptor (EGFR)-Akt axis, and finally cell death.

78 VP1 surrounds the 5-fold axis, and our past work indicates that this region likel

79 undergo elongation along an anteroposterior axis, and we use spatial transcriptomics to show that th

80 dentify the Wnt-KDM4C-beta-catenin signaling axis as a critical mechanism for glioma tumorigenesis th

81 Our results identify the Src/YAP axis as a key player in promoting the proliferation and

82 n, and highlight the Sdc1-Itgbeta7 signaling axis as a key regulatory control point for bcCML growth

83 , our study identifies REGgamma-PP2Ac-PRAS40 axis as a new layer in regulating mTORC1 activity and do

84 ting therapeutic targeting of this signaling axis as a viable option for melanoma treatment.

85 l field (VF) index was used for the vertical axis as the functional score.

86 the angiotensin II receptor type 1 (AT(1) R) axis associated with oxidative stress.

87 These findings indicate that the AhR-FoxM1 axis, at least in part, mediates colonic stem/progenitor

88 into BMRMs, with the CX3CR1/CX3CL1 signaling axis being essential for the maintenance and regeneratio

89 at are oriented along the same rostro-caudal axis but not during movement planning.

90 specifying and reorienting the cell division axis, but how general such reorientation events are, and

91 gnaling polarizes cells with respect to this axis, but how these two signaling systems interact durin

92 alternative, and potentially reno-protective axis by enhancing Ang (1-7) production.

93 sults suggest that the microbiome-gut-immune axis can be modified by DEHP and emphasize the value of

94 A dysregulation in the IL-23/IL-17 axis can lead to inflammation of barrier tissues, wherea

95 Surprisingly, CARM1-Pontin-FOXO3a signaling axis can work in the distal regions and activate autopha

96 demonstrates that microbiota-gut-brain (MGB) axis changes are associated with depression onset, but t

97 ned by structural (x-axis) and functional (y-axis) components.

98 HY5/PIF-dependent shoot module, a regulatory axis composed of auxin biosynthesis and auxin perception

99 hesis that an abnormal ECM-integrin receptor axis contributes to BM megakaryocytosis in JAK2V617F+ PM

100 These findings identify an IL-36/ IFN-I axis contributing to extracutaneous inflammation in psor

101 ur findings indicate that the KLHL42-PPP2R5e axis controls profibrotic signaling in SSc lung fibrobla

102 Interestingly, the ADAM17-EGFR signaling axis coordinates neighboring cell migration toward oncog

103 cytes were found all along the dorso-ventral axis, counting however for only 11% of newborn cell popu

104 ngle-carrier and multicarrier mechanisms for axis-dependent conduction polarity and their identifying

105 origins of the two different mechanisms for axis-dependent conduction polarity.

106 thus accounting for a deranged crypt/villus axis development in CD.

107 including heart rate; P, R, and T axis; R-T axis deviation; PR interval, QRS duration, QT, and QTc i

108 Additionally, the MCP-1/CCR2 signaling axis drives the migration of circulating monocytes into

109 ing quiescence of the reproductive endocrine axis during childhood before its reawakening at puberty

110 gocytes and interact with the RhoA-PRK-pyrin axis during infection.

111 Orienting the OEEF off the reaction axis enables control over stereoselectivity, enantiosele

112 ess extended conjugation along one molecular axis, engendering low optical bandgaps and improved osci

113 onstrated that the agonism of the 41BB-41BBL axis enhanced costimulatory signals and effector functio

114 eport a stroma-epithelium ISLR-YAP signaling axis essential for stromal cells to modulate epithelial

115 chanical properties of cells leads to robust axis extension.

116 ity, rendering cells reliant on the ATR/CHK1 axis for survival.

117 ll molecule inhibitor of the p22phox-Rubicon axis for the treatment of ROS-driven diseases such as RA

118 Deciphering the mechanisms of axis formation in amphioxus is a key step to understandi

119 o longevity and resource allocation along an axis from annual to perennial species - provides a frame

120 In LFP recordings along the dorsal CA1-DG axis from sleeping male mice, we detected and classified

121 s, consistent with a life history-physiology axis from slow-growing winter annuals to fast-growing sp

122 illating pattern of the IRF5-IRF4 regulatory axis function was revealed.

123 e find limited support for alteration in HPA axis functioning as a general mechanism for the health c

124 evidence has demonstrated that the gut-brain-axis has a central function in the perpetuation of IBS,

125 The DEPTOR-mTORC1/2 axis has been shown to play an important, but a context

126 influence the root trajectory after the main axis has passed the obstacle.

127 Immunotherapy directed at the PD-L1/PD-1 axis has produced treatment advances in various human ca

128 targeting the programmed cell death 1 (PD-1) axis, has shown promising results for the treatment of c

129 ubstrates it tends to align with the shorter axis; however, the magnitude of the anisotropy stays the

130 s deviations of the actual director from the axis imposed by confinement.

131 45 +/- 10, 90 +/- 10, or 135 +/- 10 degrees axis in 1 or both eyes.

132 Targeting a specific chemokine/receptor axis in atherosclerosis remains challenging.

133 ol of color perception along the blue-yellow axis in blind patients with RP by electrically stimulati

134 rate a protective function for the IL-33-ST2 axis in bronchial epithelial repair, and implicate ST2 i

135 Our data establish an immune-neuroendocrine axis in calibrating rapid 5-HT release for intestinal ho

136 hrough promoting expression of the Maf/IL-10 axis in effector Th cells, Malat1 is a nonredundant regu

137 n of Cdkl5, identify a pathogenic Cdkl5-Sox9 axis in epithelial cell-death, and support CDKL5 antagon

138 a critical role for the RAP1/RAC1 signaling axis in HNSCC cell migration.

139 existence of a functional 5-HT/5-HT(2B)/AhR axis in human macrophages and indicate that 5-HT potenti

140 We identified a Notch3-MMP-3 axis in human prostate cancer bone metastases that contr

141 in maintenance of the autophagy-inflammasome axis in innate murine immune cells.

142 that the LRP5/6-beta-catenin-IL-10 signaling axis in intestinal CD11c(+) APCs protects mice from CAC

143 a pivotal regulatory role for the SphK1/S1P axis in maintaining the balance between immunosurveillan

144 s dissect the role of the miR-211-DUSP6-ERK5 axis in melanoma tumor growth and suggest a mechanism fo

145 on, we investigated the glucocorticoid/CXCR4 axis in mice.

146 s, we conclude that targeting the Sirt1-Nox4 axis in muscles is an effective therapeutic intervention

147 at furin activates the IGF1R/STAT3 signaling axis in ovarian cancer cells.

148 o effectively target endocan-EGFR regulatory axis in patients with TKI-resistant NSCLC.

149 provide insight into the role of the meiotic axis in patterning recombination frequency within plant

150 harmacological blockade of the AXL signaling axis in PIK3R2-amplified ovarian cancer.

151 m and the effect of PEA-OXA on the gut-brain axis in rats subjected to experimental colitis induced b

152 pindles reorient to align with the long cell axis in regions where isotropic tension is elevated, but

153 ine the role of the SP/NK1R/TGF-beta1/miR-31 axis in regulating biliary proliferation and liver fibro

154 reviously unrecognized role for a SIK1/HDAC7 axis in regulating cardiac stress responses and implicat

155 lored the role of the interleukin-10 (IL-10) axis in restoring murine microglia homeostasis following

156 ignaling networks, such as the GNAS/PKA/PP2A axis in SCLC.

157 stal axis of origin in CA1 and distoproximal axis in subiculum are related to a rostrocaudal axis of

158 novel role for mTORC2-Akt(S473)-FoxO1-T-bet axis in suppressing the transcriptional signature of imm

159 ata highlight the importance of the ER-Golgi axis in the control of autoinflammation and inform thera

160 ly has represented a fundamental neuroimmune axis in the development of itch because of the tradition

161 Our results suggest that the cAMP-Fyn axis in the DMS dMSNs is a molecular transducer of mecha

162 and mechanistic insight into targeting this axis in the treatment of inflammatory and neuropsychiatr

163 ng an important role for the HIF/NICI/SLC2A3 axis in this malignancy.

164 is essential for the development of the body axis in zebrafish embryos.

165 +/- 0.43 mm (x-axis) and 4.02 +/- 0.44 mm (y-axis) in diameter and 0.542 +/- 0.035 mm thick (z-axis),

166 This immune-response axis independently aligns with the major plasma composit

167 tive feedback at the level of the GATA3-BMP4 axis induces fast, irreversible commitment to differenti

168 ma co-treatment activated the JAK/STAT1/IRF1 axis, inducing nitric oxide production and driving caspa

169 gly, interfering with the mTORC1/4E-BP/eIF4E axis inhibited the growth potential endowed by accumulat

170 0.98 per mille (SD)) using a laser-based off-axis integrated cavity output spectroscopy (OA-ICOS) tec

171 ining this understanding of the brain-immune axis integrated with numerous related studies by others.

172 We posit that the VEGFR2/AMPK/PEG3 axis integrates the anti-angiogenic and pro-autophagic b

173 se studies provide evidence that a signaling axis involving key UPS components contributes to oligode

174 Our study suggests that the VEGF-C/NRP2/GLI axis is a novel and conserved paracrine means by which E

175 The IL-23/T helper type 17 cell axis is a target for psoriasis.

176 then show that the TOR-LARP1-5'TOP signaling axis is conserved in plants and regulates expression of

177 tal remodeling; and (d) TRPV4-Rac1 signaling axis is critical in fusogenic cytokine-induced FBGC form

178 , we demonstrate that the autocrine FGF/FGFR axis is essential for multiple myeloma cell survival and

179 first direct evidence that the nectin-afadin axis is essential for proper palate shelf elevation and

180 udies establish that the thrombin/fibrinogen axis is fundamental to host antimicrobial defense, offer

181 iton propagation, as their auxiliary optical axis is in the plane.

182 Pathological signaling of the VGLUT3-mGluR5 axis is linked to Parkinson disease, anxiety disorders,

183 e mollusks, suggests that the dorsal-ventral axis is patterned via Activin/Nodal signaling.

184 izes baculoviral DNA and that the cGAS-STING axis is primarily responsible for the attenuation of tra

185 hat a tight balance in the Wnt-Adamts19-Klf2 axis is required for proper valve maturation and mainten

186 ever, the effect of gut inflammation on this axis is unknown despite reports of taste changes in gast

187 cord and brain) that underlies the gut-brain axis, is via spinal afferent neurons, with cell bodies i

188 Mechanistically, we define a signaling axis linking PIM1 to Drp1 and mitochondrial fission in l

189 ons suggest that the CD82-PKCalpha signaling axis may be a potential therapeutic target for attenuati

190 This control axis may further inform the development of therapeutic a

191 Thus, the St3gal2-GT1b-TLR2 axis may offer a novel therapeutic target for the treatm

192 gesting that dysregulation of the AHR/CYP1A1 axis may play a role in inflammatory skin disease.

193 of concept that targeted inhibition of this axis may represent a new therapeutic strategy.

194 The PI3K/AKT-TBL1XR1-ERK1/2-Sox2 axis may represent a target for the treatment of GC.

195 Targeting this axis might provide an effective PDA therapeutic strategy

196 This brain-brown fat-liver axis might provide new insights into brown adipose tissu

197 Here, a 5-axis MiRA6 CNC milling machine, specifically designed fo

198 the rotational plane hypothesis and the dual-axis model.

199 The hypothalamic-pituitary-adrenal axis modulates immunity in response to stress.

200 tes, the Reissner fiber, which controls body axis morphogenesis in the zebrafish embryo.

201 Visual axis obscuration (US-Cat: 28.38%; BS-Cat: 23.81%; BT-Cat

202 Single-cell sequencing analysis revealed an axis of activity-dependent gene expression amongst a sub

203 Together, our findings provide a signaling axis of CARM1-Pontin-FOXO3a and further expand the role

204 nd that miR-671-5p more potently silenced an axis of CDR1as and its antisense transcript, cerebellar

205 e read by the spindle, which then guides the axis of cell division.

206 xed in anisotropic cells and aligns with the axis of cell growth.

207 enation delivers the product with the second axis of chirality established.

208 ones produces a product with one established axis of chirality, and second, a stereoselective arene h

209 ion of a metal-carbene bond which induces an axis of chirality.

210 icroRNA-155 and PU.1 (as upstream regulatory axis of FcepsilonRI) and transcription factors Elf-1 and

211 eadmill' with no bounds for motion along the axis of gravity.

212 indings uncover a novel role for 4.1N in the axis of hypothalamus-pituitary gland-reproductive system

213 The gut-joint axis of inflammation in SpA is further reinforced by sim

214 cation confirming an important enterohepatic axis of metabolite-microbiome interaction resulting in m

215 A proximodistal axis of origin in CA1 and distoproximal axis in subiculu

216 Along the vertical axis of plant shoot apical meristems (SAMs), stem cells

217 Taken together, these findings define an axis of posttranscriptional control, endocytosis, and si

218 a component of the counteracting hypotensive axis of RAS.

219 is RNF26 complex represents a new modulatory axis of STING and innate immune signalling at the ER mem

220 ed inverted cylinders rotate along a central axis of symmetry to form circular hoops.

221 s in subiculum are related to a rostrocaudal axis of termination in the entorhinal cortex.

222 of metabolic enzymes along the portocentral axis of the acinus are a long-known feature of liver met

223 anesthesia, or across the anterior/posterior axis of the brain.

224 utward movement with respect to the symmetry axis of the channel in the presence of the full agonist

225 ectron delocalization along the longitudinal axis of the columnar pai-stacking architectures.

226 isenberg antiferromagnetic chain along the a-axis of the crystal.

227 rphogen gradient patterns the dorsal-ventral axis of the early Drosophila embryo, and we found that a

228 potencies at different levels along the body axis of the embryo.

229 (glycoprotein gp120 of HIV and the fivefold axis of the EV-A71 capsid).

230 degrees relative to the CTD along the major axis of the molecule, an orientation that forms a positi

231 imately influencing the brain-gut-microbiome axis of their host, a bidirectional communication system

232 ontal first axis) and 21.6% (vertical second axis) of the constrained variation in the distribution o

233 Recurrent visual axis opacification (VAO) occurred in 7.5% and was associ

234 Visual axis opacification is common after IOL implantation in e

235 outcome, and the need for surgery for visual axis opacification.

236 egies to target the increased risk of visual axis opacity (VAO) after primary intraocular lens (IOL)

237 Visual axis opacity occurred in 67 eyes (45%), typically within

238 ression lines close to the line of unity and axis origin.

239 relevance of this microbiome-gut-brain (MGB) axis outside the laboratory remains unexplored.

240 lation orients the microrobot's axisymmetric axis perpendicular to the wall and then propels it later

241 dy was to determine the effect of rotational axis position (RAP and thus g-gradient) during short-arm

242 at hindlimb regions drives the vagal-adrenal axis, producing anti-inflammatory effects that depend on

243 ogical inhibition of the MNK-eIF4E signaling axis protected against and reversed spontaneous pain and

244 ndencies that constitute the LGG neuroimmune axis provides insights into the role of neurons and immu

245 variables including heart rate; P, R, and T axis; R-T axis deviation; PR interval, QRS duration, QT,

246 ans and suggest that a NUAK2-Hippo signaling axis regulates cytoskeletal processes that govern cell s

247 Thus, ECM- integrin alpha6-STAT3-TET3 axis regulates hydroxymethylation of genes important for

248 dence that a thermogenic fat-epithelial cell axis regulates intestinal disease tolerance during exper

249 spindles detect and align with the long cell axis remain poorly understood.

250 pattern the mesoderm along the dorsoventral axis, representing a critical facet of cell identity reg

251 Targeting the HDAC6-RAC1 axis represents a promising therapeutic option for impro

252 ogramming of the PVN results in aberrant HPA axis responsiveness when exposed to the hormonal changes

253 n of human PrSPCs by activating the p62-NRF2 axis, resulting in epithelial cell transformation.

254 cally projected" into the 3(rd) dimension (z-axis), separated by size, and photo-captured in the gel

255 ch are arranged along the crystallographic c axis, separated by nonmagnetic K ions.

256 ate that the ROS-ATM-CHK2-Beclin 1-autophagy axis serves as a physiological adaptation pathway that p

257 Therefore, the pVHL-SFMBT1-SPHK1 axis serves as a potential therapeutic avenue for ccRCC.

258 s monolithically grown on CMOS-compatible on-axis Si (001) substrates by using III-V quantum dots.

259 t PC cells suppresses androgen receptor (AR) axis signaling and induces the neural BRN2 transcription

260 lator of mesoderm development and left-right axis specification; components for nervous system develo

261 he angiocrine-metabolic-epigenetic signaling axis specified by the endothelium is essential for repro

262 e originating from this fiber to ensure body axis straightening is not understood.

263 3-independent mechanisms of the netrin-UNC5B axis, such as those involving PP2A, assumes greater clin

264 Thus, the CD47-SIRPA axis suppresses phagocytosis by inhibiting inside-out ac

265 ized LepR neuron Sh2b1/SNS/BAT/thermogenesis axis that combats obesity and metabolic disease.

266 ntify a putative endogenous immune signaling axis that drives neurodegeneration in AD and has strong

267 these findings establish a HMGB2-TOP1cc-cGAS axis that enables cytoplasmic chromatin recognition and

268 ly reveal a novel PRMT1-HSP70-BCL2 signaling axis that is crucial to pancreatic cancer cell survival

269 This study identifies a novel axis that links core transcriptional drivers of cancer c

270 We thus uncovered a DEL-1/alphavbeta3/RUNX1 axis that promotes Treg responses at barrier sites and o

271 entified a TFEB-mediated gut-liver signaling axis that regulates hepatic cholesterol and bile acid ho

272 stant cell lines revealed a TGFBR2 signaling axis that regulates HMGCR, defining an actionable addict

273 M9-bound hotspots and the nascent chromosome axis through its component cohesin pREC8.

274 e regulation of a novel PRMT5/YBX1/NF-kappaB axis through PRMT5-mediated YBX1-R205 methylation.

275 pithelial, and immune checkpoints along this axis to be potentially exploitable in future Crohn disea

276 cies diversity of the ability of ISG15/USP18 axis to control IFN-I signaling and reveal the therapeut

277 axis acts in parallel to the core-Vangl2 PCP axis to control mesenchymal cell clustering.

278 BigTop uses the z-axis to display minor allele frequency of each SNP, allo

279 S100A6 plays a key role in the PPP5C-FKBP51 axis to inhibit I(SOC) and protect the endothelial barri

280 horts in defined numbers and co-organize the axis together with 2 functionally distinct cohesin compl

281 hymal markers (through the ERK-ZEB1-vimentin axis under certain conditions) and in vivo lung metastas

282 nistered PLGA nanoparticles on the gut-liver axis under conditions of caloric excess in C57BL/6 mice.

283 enesis by activating a calcium-mitochondrial axis upstream of PGC-1alpha transcriptional upregulation

284 utrophil extracellular traps (NETs)/thrombin axis, using COVID-19 specimens, cell-based inhibition st

285 Furthermore, the PHB/JAK2 axis was found as a novel mechanism in the maintenance o

286 r medulla, to represent the corticomedullary axis, was performed.

287 enhancer sog_Distal along the dorso-ventral axis, we hypothesized Opa's role is more general.

288 description of a conserved liver-alpha-cell axis where glucagon is a critical regulator of amino aci

289 An OEEF along the "reaction axis", which is the direction whereby electronic reorgan

290 ection through a bile acid-pDC-IFN signaling axis, which affects viremia, dissemination, and potentia

291 formed by precursor fusion along the stretch axis, which computational modeling explained as a conseq

292 our results demonstrate a beta2AR-ROS redox axis, which if disturbed, interferes with proper recepto

293 is and pain are controlled by the endothelin axis, which is a pathway comprised of the endothelin A a

294 monocytes overexpressed a distinct chemokine axis, which may orchestrate inflammatory myeloid cell re

295 network analysis (WGCNA) clusters of the MGB axis, which were consistently enriched in fatty acyl, sp

296 naling is essential for patterning of the AP axis while planar cell polarity (PCP) signaling polarize

297 A better understanding of the gut-CNS axis will shed new light on the mechanisms of disease pa

298 by a current winding around the optical beam axis with a magnitude proportional to its quantized OAM

299 r, repeated elements, and orientation of the axis with respect to the membrane plane.

300 in diameter and 0.542 +/- 0.035 mm thick (z-axis), with a mean pore size of 0.420 +/- 0.028 x 0.328