ライフサイエンスコーパス: MAG

1 (JAM-C) and myelin-associated glycoprotein (MAG).

2 lin, such as myelin-associated glycoprotein (MAG).

3 n induced by myelin-associated glycoprotein (MAG).

4 3 (NT3) and myelin-associated glycoprotein (MAG).

5 vo assembly of metagenome-assembled genomes (MAGs).

6 mes (SAGs) and metagenome-assembled genomes (MAGs).

7 enhance neurite outgrowth in the presence of MAG.

8 trescine's ability to overcome inhibition by MAG.

9 verexpressing p35 can overcome inhibition by MAG.

10 ilar effects on the growth and maturation of MAG.

11 vation of PKC and Rho in response to soluble MAG.

12 nsistent with C1q-mediated neutralization of MAG.

13 romotes neurite outgrowth in the presence of MAG.

14 Before matching, 20% of procedures employed MAG.

15 ellar incorporation of carotenoids, FFAs and MAGs.

16 with 91% purity and 94% overall recovery of MAGs.

17 mune system evasion were detected across the MAGs.

18 osynthesis and export were identified across MAGs.

19 p 6.5 years) for patients receiving SAGs and MAGs.

20 a conserved substrate binding cleft (SBC) in MAGEs.

21 the diverse functions exerted by individual MAGEs.

22 MAG (0-2.5wt%) had no remarkable impact on the chemical

23 The addition of MAG (0.5wt%) suppressed the effectiveness of alpha-tocop

24 after 100 cycles at a current density of 400 mAg(-1).

25 We recovered 36 MAGs, 29 of medium to high quality, and inferred their p

26 Of 5580 participants who underwent MAG, 586 (11%) were women and the mean (SD) age was 60 (

27 nstrate that myelin-associated glycoprotein (MAG), a well known inhibitor of neurite outgrowth, inhib

28 and Gly(18) has been replaced with alanine (Mag-A).

29 AG and SAG patients at 1 year, but lower for MAG after 7 years.

30 Exposing neurons to MAG and CSPGs decreases acetylation of Miro1 on Lysine 1

31 the concentration of triacylglycerols, DAG, MAG and free fatty acids (FFA) and the concentration of

32 nd flow cytometry, and this occurred in NAG, MAG and IM.

33 .1 (4.5-11.7) years for the groups receiving MAG and LITA+SVG, respectively.

34 in the acyltransferase function but exhibits MAG and LPC hydrolase activities.

35 sted the presence of two separate substrate (MAG and LPC)-binding sites in a single polypeptide.

36 These data show that active FA, 2-MAG and membrane lipid biosynthesis are essential for no

37 viously shown to bind an intronic element of MAG and modulate alternative exon inclusion from a MAG m

38 dbcAMP), can block the inhibitory effects of MAG and myelin.

39 Nogo, MAG and OMgp are three prototypical myelin inhibitors th

40 In contrast, deletion of MAG and OMgp stimulates neither axonal growth nor enhanc

41 role for Nogo-A and synergistic actions for MAG and OMgp, presumably through shared receptors.

42 Both mAg and sAg induce F-actin accumulation and actin polyme

43 is study sought to compare intermediate-term MAG and SAG outcomes with enhanced matching to reduce se

44 was no mortality difference between matched MAG and SAG patients (2.4% vs. 2.2%, adjusted hazard rat

45 d the composite outcome were similar between MAG and SAG patients at 1 year, but lower for MAG after

46 phosphorylation in BCR microclusters without mAg and sAg, but with much slower kinetics than those in

47 tion of BCR signalosomes in response to both mAg and sAg.

48 f the SBC disrupted substrate recognition by MAGEs and blocked MAGE-A11 oncogenic activity.

49 iple labeling immunohistochemistry, confocal maging and analysis to investigate the presence and colo

50 (177)Lu-PSMA-I&T and (99m)Tc-PSMA-I&S (for i maging and s urgery) are currently successfully used for

51 ns (based on Mash distances) between African MAGs and other publicly available genomes from the rumen

52 ify 1200 high-quality African rumen-specific MAGs and provides further insight into the rumen functio

53 aroyl lactylate (SSL) and monoacylglycerols (MAG) and Bacillus stearothermophilus maltogenic alpha-am

54 e substrates myelin-associated glycoprotein (MAG) and chondroitin sulfate proteoglycans (CSPGs).

55 yzes the acylation of both monoacylglycerol (MAG) and diacylglycerol (DAG) to generate DAG and TAG, r

56 ic lesions of multifocal atrophic gastritis (MAG) and intestinal metaplasia (IM) have occurred.

57 s revealed the presence of monoacylglycerol (MAG) and lysophosphatidylcholine (LPC) hydrolytic activi

58 ying the magnetic Gruneisen parameter (Gamma(mag)) and entropy arguments, we report on the pivotal ro

59 ysis, fatty acid (FA), 2-monoacylglycerol (2-MAG), and membrane lipid biosynthesis and transport duri

60 near-complete metagenome-assembled genomes (MAGs), and there is a need for reproducible pipelines th

61 anonical definition of temperature and Gamma(mag); and iii) possibility of performing adiabatic magne

62 proteins present in myelin, including Nogo, MAG, and oligodendrocyte-myelin glycoprotein (OMgp), hav

63 Three proteins in mature myelin (Nogo, MAG, and OMgp) have been purported to be critical in cau

64 Three molecules, Nogo-A, MAG, and OMgp, are produced by oligodendrocytes and shar

65 f myelin-associated inhibitors such as Nogo, MAG, and OMgp.

66 ent in two major myelin inhibitors, Nogo and MAG, and their common receptor NgR1 (or NgR).

67 of triacylglycerides, formation of FFAs and MAGs, and micellar incorporation of carotenoids, FFAs an

68 MAG- and CSPG-dependent deacetylation of Miro1 requires

69 solin, are recruited to BCR clusters in both mAg- and sAg-stimulated B cells but with different kinet

70 and its role in BCR signalosome formation in mAg- and sAg-stimulated B cells.

71 Here we report that Cadm4-, MAG-, and Caspr-mediated adhesion cooperate during myeli

72 selectively neutralizing the pathogenic anti-MAG antibodies with carbohydrate-based ligands mimicking

73 of blood IgM memory B cells that recognized MAG antigen.

74 is mediated by IgM autoantibodies binding to MAG antigen.

75 lled or in assays where the gangliosides and MAG are not presented as part of fluid lipid bilayers.

76 Therefore, MAGEs are implicated in a broad range of diseases includ

77 Whereas some MAGEs are ubiquitously expressed in tissues, others are

78 These MAGs are predicted to use diverse energy conservation pa

79 Monoacylglycerols (MAGs) are active mediators involved in multiple biologic

80 , as well as myelin-associated glycoprotein (MAG), are enriched at the internodes below the compact m

81 glycerol was proven to be an alternative to MAG as acyl-group acceptor.

82 or scalable production of n-3 PUFAs enriched MAGs as potential food emulsifier and ingredient.

83 and show the utility of the SGM approach and MAGS as resources for defining novel glycan recognition

84 emical and biophysical studies indicate that MAGEs assemble with E3 RING ubiquitin ligases to form MA

85 MAGEs assemble with E3 ubiquitin ligases and function as

86 (NF155) and myelin-associated glycoprotein (MAG) at axo-glial junctions.

87 enicity and demyelinating properties of anti-MAG autoantibodies are well established, current treatme

88 s of the ~2000 metagenome-assembled genomes (MAGs) available in the database revealed strong ecologic

89 Significantly, an MAG basal to organisms from the phylum Thaumarchaeota th

90 Thermoplasmata metagenome-assembled genomes (MAGs) basal to the Methanomassiliicoccales, we show that

91 by antiganglioside antibodies that override MAG-based neuron growth inhibition.

92 and obtaining metagenome-assembled genomes (MAGs) becomes more effective.

93 e obtained ten metagenome-assembled genomes (MAGs) belonging to potential methanogenic, anaerobic met

94 At the molecular level, many MAGEs bind to E3 RING ubiquitin ligases and, thus, regul

95 between boronic acid and cis-diol moiety of MAGs blocked the formation of multiple adduct ions and t

96 MAG-bound vesicles are deformed similarly, regardless of

97 n by obtaining metagenome-assembled genomes (MAGs); but gaps, local assembly errors, chimeras, and co

98 g through IIS pathway regulate maturation of MAG by promoting the growth of MAG cells.

99 r evoluted to reveal the amount variation of MAGs by d(0)-NPB and d(4)-NPB separately derivatized in

100 MAG can display clarithromycin resistance through the in

101 embers of the Mycobacterium abscessus group (MAG) cause lung, soft tissue, and disseminated infection

102 maturation of MAG by promoting the growth of MAG cells.

103 es, achieve complete (circularized, no gaps) MAGs (CMAGs).

104 ce extend significantly shorter processes on MAG compared with wild-type DRG neurons, and regeneratio

105 ell envelope is the mycolyl-arabinogalactan (mAG) complex.

106 Elucidating microbe-specific differences in mAG composition could advance biotechnological applicati

107 the brains of double mutants (Phr1(Delta8,9/Mag)), confirming that Pam displays dual regulation of t

108 The remaining five MAGs correspond to lineages that are only distantly rela

109 We here showed that SSL but not MAG delays wheat starch hydrolysis by BStA.

110 ssential source of cAMP for BDNF to overcome MAG-dependent inhibition of neurite outgrowth.

111 uivalently premixed with d(0)-NPB to perform MAG derivatization, which resulted in rapid identificati

112 At 7 years, the subgroups for which MAG did not have a lower mortality rate included patient

113 The data show that (1) neurons in the MPN mag display two distinct phenotypes, those with a single

114 tase (Mcr), in metagenome-assembled genomes (MAGs) divergent to existing archaeal lineages.

115 e fatty acids, FFAs, and monoacylglycerides, MAGs) during in vitro digestion of oil-in-water emulsion

116 urther work is required to determine whether MAG dysregulation is a cause or consequence of audiogeni

117 ant for PirB-myelin-associated glycoprotein (MAG) ectodomain interactions.

118 -mRNA and modulates alternative inclusion of MAG exons.

119 covered that myelin-associated glycoprotein (MAG) expression is dramatically decreased in Frings mice

120 We found that mating and MAG extract lower HC occurrence by 53% compared with all

121 en virgin males and either virgin, mated, or MAG extract-injected females and analyzed these recordin

122 To test the hypothesis that mating and MAG fluids inhibit a female's ability to induce HC in ma

123 e was micro-injected with either furaptra or mag-fluo-4, two low-affinity rapidly responding Ca(2+) i

124 w-twitch fibres that had been AM-loaded with mag-fluo-4: 12.4 +/- 0.8 ms and 17.2 +/- 1.7 ms.

125 smic and ER-Ca(2+) (measured with Fura-2 and Mag-Fluo4) levels are decreased and store-operated Ca(2+

126 Much of the initial research on MAGEs focused on exploiting their antigenicity and restr

127 s and subgroups support the consideration of MAG for a broader spectrum of patients who are undergoin

128 me the inhibitory effects of both myelin and MAG for cortical, hippocampal, and DRG neurons.

129 that SPD is able to concentrate n-3 PUFAs in MAG form by distilling at proper TE e.g. 125 degrees C,

130 Thermoplasmatota genomes/MAGs found no evidence of mcrA homologues outside of the

131 tially increasing the number of high-quality MAGs from freshwater lakes.

132 AGs reveals two high-coverage, low-diversity MAGs from Piccard enriched in unique genes related to th

133 Here, we study the mcr-containing archaeal MAGs from several hot springs, which reveal further expa

134 The release of FFAs and MAGs from TAGs proceeded faster than their incorporation

135 We report 1200 newly discovered MAGs from the rumen of Boran cattle.

136 ssembled draft metagenome-assembled genomes (MAGs) from environmental DNA extracted from two hot spri

137 reconstruct 73 metagenome-assembled genomes (MAGs) from two geochemically distinct vent fields in the

138 Competition with chelators mag-fura-2, nitrilotriacetic acid, EDTA, and EGTA estima

139 Using the fluorescent indicator mag-fura-2, the metal released from DHHC3 was identified

140 ing two different calcium probes, Fura-2 and Mag-Fura-2, we found that inactivation of PS in primary

141 We further demonstrate how MAG-ganglioside interactions can be disrupted by antigan

142 Here, we present an approach to characterize MAG-ganglioside interactions in real time, where MAG, GD

143 ganglioside interactions in real time, where MAG, GD1a, and GT1b contents are controlled and they are

144 Analysis of all mcr-containing archaeal MAGs/genomes suggests a hydrothermal origin for these mi

145 A focal MAG gradient induced polarized endocytosis and concomita

146 mes (SAGs) and metagenome-assembled genomes (MAGs) has led to a surge in genome-based discoveries of

147 explain why many cancers aberrantly express MAGEs Here, we present an updated, comprehensive review

148 Here, we present a comprehensive guide to MAGEs highlighting the molecular mechanisms of MRLs and

149 show that a lead double-stapled StAMP named Mag(i+4)1,15(A9K,B21A,N22K,S23K) can kill multidrug-resi

150 Amino acid exporters were identified in MAGs identified as important for host fitness, and pathw

151 a correlation between the reduction of anti-MAG IgM levels and clinical improvement, an immunologica

152 MAG neuropathy producing high levels of anti-MAG IgM was developed.

153 e, considering the multivalent nature of the MAG-IgM interaction, polylysine polymers of different si

154 ctively, act in concert to promote NF155 and MAG in maintaining the stable axo-glial interactions ess

155 Deletion of Jam-c or Mag in mice recapitulates pathology in HNPP.

156 and transport of FAs, membrane lipids, and 2-MAG in rhizobia-soybean symbioses via the RAML-WRI-FatM-

157 NPS co-crystallised with MAG in the oleogel mixtures and influenced the growth of

158 The physical properties of DAG and MAG in the SSO may be related to the chemical stability

159 inhibitory and repulsive turning effects of MAG in vitro.

160 resulted in rapid identification of modified MAGs in biofluids by displaying doublet peak characteris

161 f boron specialized the presence of modified MAGs in MS and led to distinctive identification.

162 umulation of myelin-associated glycoprotein (MAG) in LAMP1(+)perinuclear vesicles that fail to migrat

163 irectly with myelin associated glycoprotein (MAG) in myelin, resulting in reduced activation of growt

164 and maturation of the male accessory gland (MAG) in the red flour beetle, Tribolium castaneum.

165 soluble Ag (sAg) and membrane-associated Ag (mAg) in the secondary lymphoid tissue, yet how the physi

166 termed metadata-assisted glycan sequencing (MAGS), in which we combine information from analyses of

167 The 12 analysed MAGs include representatives from four orders basal to t

168 ome metabolic pathways were specific to some MAGs, including sulfur oxidation, nitrate reduction, and

169 The size of MAG increased from day 1 to day 5 post-adult emergence (

170 Our set of rumen MAGs increases the rate of mapping of rumen metagenomic

171 hibit HC indirectly via the broader range of MAG-induced female refractory mating behaviors.

172 A subset of MAGEs initially garnered interest as cancer biomarkers a

173 se structural findings and the observed PirB-MAG interactions are compatible with a model for interce

174 Ganglioside-MAG interactions are often studied in cellular or animal

175 AMP and putrescine to overcome inhibition by MAG is abolished in the presence of roscovitine, a Cdk i

176 Compared with LITA+SVG, MAG is associated with reduced mortality, repeated revas

177 The mAG is composed of lipid mycolic acids, and arabinofuran

178 This increase in the size of MAG is contributed by an increase in cell size, but not

179 icated that the number of neurons in the MPN mag is greater in males than females but failed to find

180 Sensitive and unambiguous detection of MAGs is thus essential; however, previous methods are bo

181 which remained in an amorphous form, whereas MAG led to strong scattering, indicating the formation o

182 The majority of MAGs linked to oil-contaminated ecosystems were detectab

183 Pretreatment with the monoacylglycerol (MAG) lipase inhibitor JZL-184 also reduced affective dis

184 r myelin genes, such as proteolipid protein, MAG, MBP, and myelin oligodendrocyte glycoprotein, were

185 Mechanistically, MT-I/II ability to overcome MAG-mediated inhibition is transcription-dependent, and

186 quired for dbcAMP and putrescine to overcome MAG-mediated inhibition.

187 CP-mag-micelles are biocompatible, can be delivered to vari

188 These 'theranostic' CP-mag-micelles are composed of monodisperse hydrophobic su

189 A single injection of CP-mag-micelles carrying reporter plasmids in vivo expresse

190 relaxivity of mag-micelles was similar to CP-mag-micelles confirming that coating with cationic polym

191 The T(2) relaxivity of mag-micelles was similar to CP-mag-micelles confirming t

192 e morphology and size distribution of the CP-mag-micelles were characterized and their potential for

193 leneimine (PEI) coated magnetic micelles (CP-mag-micelles) that can deliver nucleic acid-based therap

194 d modulate alternative exon inclusion from a MAG minigene reporter.

195 The Mag-MIP and Mag-NIP were characterized by FTIR, magnetic

196 The capacity of Mag-MIP for biotin adsorption, its kinetics and selectiv

197 lectivity experiments revealed that prepared Mag-MIP had higher selectivity toward biotin compared to

198 odified with molecularly imprinted polymers (Mag-MIP) through core-shell method for the determination

199 esults demonstrate an important new role for MAG molecules in mediating female post-mating behavior.

200 ficacy of two-photon (2P) excitation for two MAG molecules using nonlinear spectroscopy.

201 higher volume MAG surgeons experienced lower MAG mortality.

202 Anti-MAG (myelin-associated glycoprotein) neuropathy is a dis

203 in (MBP) and myelin-associated glycoprotein (MAG) myelin proteins were markedly increased in the cort

204 These results suggest a novel role for MAG/myelin in poor SC-myelin interaction and identify p7

205 ry isolated coronary artery bypass grafting (MAG, n = 5580; LITA+SVG, n = 14496) in the province of B

206 evidence of a treatment effect for IgM anti-MAG neuropathy and diabetic amyotrophy (radiculoplexus n

207 immunological surrogate mouse model for anti-MAG neuropathy producing high levels of anti-MAG IgM was

208 Patients with anti-MAG neuropathy showed substantial clonal expansions of b

209 toward an antigen-specific therapy for anti-MAG neuropathy.

210 th anti-myelin-associated glycoprotein (anti-MAG) neuropathy, an autoimmune disease of the peripheral

211 ration beyond the injury site in either Nogo/MAG/NgR1 triple mutants or NgR1 single mutants.

212 The Mag-MIP and Mag-NIP were characterized by FTIR, magnetic hysteresis,

213 tors such as myelin-associated glycoprotein (MAG), Nogo-A, and oligodendrocyte-myelin glycoprotein.

214 -1beta) and myelin-associated glycoproteins (MAG, Nogo).

215 However, further investigation revealed that MAGEs not only drive tumorigenesis but also regulate pat

216 The Hb/MHAM@Mag-NPs biocomposite is captured at SPCE by a super magn

217 It shows that the MHAM@Mag-NPs composite could increase the adsorption ability

218 The entrapment of Hb at MHAM@Mag-NPs was confirmed by cyclic voltammetry (CV), electr

219 supported iron oxide magnetic nanoparticles (Mag-NPs), is reported.

220 ion of the mixed hemi/ad-micelles of CTAB at Mag-NPs, zeta-potential measurements were performed.

221 captured at SPCE by a super magnet (Hb/MHAM@Mag-NPs/SPCE).

222 only at monoacylglycerol:native phytosterol (MAG:NPS) ratios of 10:0, 7:3 and 5:5.

223 entially novel metagenome-assembled genomes (MAGs) of core bacteria in Daphnia magna.

224 Metagenome-assembled genomes (MAGs) of these Petromonas sp. were obtained and used to

225 We also examined the influence of DAG and MAG on the physical properties of SSO.

226 Finally, when adding SSL or MAG on top of BStA to starch suspensions, the effect of

227 the axon and myelin-associated glycoprotein (MAG) on myelin.

228 f diacylglycerol (DAG) and monoacylglycerol (MAG) on the oxidative stability of stripped soybean oil

229 Genetic deletion of either Cadm4 and MAG or Cadm4 and Caspr resulted in the formation of mult

230 gamma-secretase activity before exposing to MAG or CNS myelin improves SC migration and survival in

231 At 7 years, MAG patients had lower mortality (12.7% vs. 14.3%, AHR:

232 SAG and MAG patients were propensity matched using 38 baseline c

233 MAG-PEI25 reached a maximum adsorption capacity of 6.11

234 MAG percentage was maximum (7mol%) at lower water activi

235 erebral amyloid angiopathy, neither VEGF nor MAG:PLP1 correlated significantly with the severity of s

236 VEGF but not MAG:PLP1 increased with Alzheimer's disease severity, as

237 In frontal cortex the MAG:PLP1 ratio was significantly reduced in Alzheimer's

238 However, MAG:PLP1 showed a significant negative correlation with

239 The decline in MAG:PLP1 strongly suggests pathological hypoperfusion of

240 Although MAG:PLP1 tended to be lowest in cortex from patients wit

241 iated glycoprotein to proteolipid protein 1 (MAG:PLP1) ratio, which declines in chronically hypoperfu

242 ction in EDN1, and positive correlation with MAG:PLP1, in the hypoperfused white matter in Alzheimer'

243 Finally, we show that hnRNPA1 binds MAG pre-mRNA and modulates alternative inclusion of MAG

244 hly expressed on adhesion molecules, such as MAG, present in myelinated nerve fibers.

245 ) of an acylglycerol mixture (containing 67% MAGs) produced by enzymatic glycerolysis of sardine oil

246 -T (-/-) mice exhibited a major reduction in MAG protein levels in CNS myelin compared with WT and si

247 pathways to regulate myelination by means of MAG protein stability in myelin-forming cells of the aud

248 "MAG" PTLs for ionotropic and metabotropic glutamate rece

249 The MILLIPLEX-MAG Rat cytokine-chemokine magnetic bead array was used

250 ain that results in sn-2 monoacylglycerol (2-MAG) rather than LPA as the major product.

251 However, how MAGEs recognize their targets is unknown and has impeded

252 -enhancing mechanism in which C1q binding to MAG reduces MAG signaling to neurons, complement C1q blo

253 ed to be essential in the metabolic study of MAG-related diseases.

254 Five of these MAGs represent under-sampled (Verstraetearchaeota, Metha

255 lin, such as myelin-associated glycoprotein (MAG), represent major obstacles to axonal regeneration f

256 Collectively, our MAGs represented about half of the total microbial commu

257 Over 95% of the recovered MAGs represented novel taxa underscoring the limited rep

258 Metagenome-assembled genome sequences (MAGs) representing allochthonous populations were detect

259 g obtained 527 metagenome-assembled genomes (MAGs), representing 150 bacterial species.

260 Our set of metagenome-assembled genomes (MAGs) represents >400 yet-unnamed genomospecies, substan

261 (NF155) and myelin-associated glycoprotein (MAG) require membrane microdomains containing either sul

262 Metagenome-assembled genomes (MAGs) revealed that phenanthrene degradation is likely m

263 Comparison of nine Sulfurovum MAGs reveals two high-coverage, low-diversity MAGs from

264 Production of monoacylglycerols (MAGs) rich in omega-3 polyunsaturated fatty acids (n-3 P

265 tween a tetrazine-functionalized pro-sensor, Mag-S-Tz, and a strained bicyclononyne conjugated to a g

266 total, our examination of functions in these MAGs shows a diversity of nutrient acquisition and metab

267 echanism in which C1q binding to MAG reduces MAG signaling to neurons, complement C1q blocked both th

268 MAG significantly decreased the interfacial tension of S

269 iency was thought to underlie the defects of MAG splicing in the qk(v) mutant.

270 ing I (QKI) leads to severe dysregulation of MAG splicing.

271 ics and magnitude of F-actin accumulation in mAg-stimulated B cells are greater than those in sAg-sti

272 tional resistance, as well as slowly growing MAG strains and also strains displaying an inducible res

273 Patients of higher volume MAG surgeons experienced lower MAG mortality.

274 ed in glycolysis and the synthesis of FAs, 2-MAG, TAG, and membrane lipids compared to GmWRI1b-OE hai

275 nomassiliicoccales, including a high-quality MAG that likely represents a new order, Ca. Lunaplasma l

276 We highlight MAGs that were taxonomically assigned to groups previous

277 ive to perceptual matching: (1) a midregion (mAG) that overlapped with the default network because it

278 aired trafficking of plasma membrane-derived MAG through the endolysosomal system in primary cells an

279 MASS1 inhibits the ubiquitylation of MAG, thus enhancing the stability of this protein, and t

280 We compared these MAGs to closely related genomes and show that these subs

281 on emulsion presented a higher conversion of MAGs to FFAs during digestion, which led to a higher con

282 formation of multiple adduct ions and tuned MAGs to negatively charged carrying species.

283 an assign genomes from isolate sequencing or MAGs to species-level genome bins built from >230,000 pu

284 enome-assembled genomes (MAGs), we show that MAG transcript abundance can be tied to differences in m

285 MASS1 RNAi or a specific inhibitor abrogates MAG up-regulation.

286 umen microbial metagenome-assembled genomes (MAGs) using approximately 6.5 terabases of short- and lo

287 tion in the use of multiple arterial grafts (MAGs) versus single arterial grafts (SAGs) for patients

288 compare the safety and long-term outcomes of MAG vs LITA+SVG among overall and selected subgroups of

289 val advantage of multiple arterial grafting (MAG) vs the standard use of left internal thoracic arter

290 Compared with LITA+SVG, MAG was associated with reduced mortality rates (hazard

291 The growth of MAG was impaired after double-stranded RNA (dsRNA)-media

292 pathways in 64 metagenome-assembled genomes (MAGs), we show that MAG transcript abundance can be tied

293 zed with a supported lipid bilayer (SLB) and MAG, we detect vesicular GD1a and GT1b binding and deter

294 Only approximately 8% of these MAGs were abundant in U.S. freshwater ecosystems, reveal

295 These MAGs were used as reference database to investigate the

296 nt with extracts from male accessory glands (MAG), which make seminal fluid molecules, female Ae. aeg

297 of the axo-glial junction proteins NF155 and MAG, which interact to maintain the nodal complex.

298 ral HNK-1 epitope blocked the interaction of MAG with pathogenic IgM antibodies from patient sera but

299 traightforward approach by derivatization of MAGs with 3-nitrophenylboronic acid (3-NPB) for sensitiv

300 diacylglycerols (DAG) and monoacylglycerols (MAG) with a high content of polyunsaturated fatty acids