ライフサイエンスコーパス: SAM

1 SAM binds to the unique iron atom of a site-differentiat

2 SAM develop endothelial dysfunction.

3 SAM domain and HD domain-containing protein 1 (SAMHD1),

4 SAM vaccines are based on engineered self-amplifying mRN

5 SAM-functionalised organic devices give rise to complete

6 SAM-WD showed increased endothelial inflammation (interc

7 At week 24, SAM-WD had developed HFpEF, characterized by diastolic d

8 tion and abrogated by the deletion of SLP-76 SAM domain (DeltaSAM) or mutation of Tyr-113, Tyr-128, a

9 A SAM carboxylate-oxygen is an M(+) ligand, and EPR and ci

10 il with the H3K9 methyltransferase Clr4 in a SAM (S-adenosyl-methionine)-dependent manner, and Clr4 i

11 Thus, SAMTOR is a SAM sensor that links methionine and one-carbon metaboli

12 ometallic center in which the 5' carbon of a SAM-derived deoxyadenosyl moiety forms a bond with the u

13 te architecture of viperin with bound SAH (a SAM analog) or 5'-dAdo and l-Met (SAM cleavage products)

14 Abrupt SAM initiation favors a strong influence of climate in a

15 y, cells that lack PE methylation accumulate SAM, which leads to hypermethylation of histones and the

16 gauges for studying charge tunneling across SAMs.

17 grow a naked pin while maintaining an active SAM.

18 erase bound to a novel S-adenosylmethionine (SAM) analog in which a 4-fluorophenyl moiety substitutes

19 that the methyl donor S-adenosylmethionine (SAM) disrupts the SAMTOR-GATOR1 complex by binding direc

20 belongs to the radical S-adenosylmethionine (SAM) enzyme family.

21 is an unusual radical S-adenosylmethionine (SAM) enzyme involved in the first step of diphthamide bi

22 IFN-inducible radical S-adenosylmethionine (SAM) enzyme that inhibits viral replication.

23 stalled by the radical S-adenosylmethionine (SAM) enzyme, StrB.

24 Radical S-adenosylmethionine (SAM) enzymes are emerging as a major superfamily of biol

25 Radical S-adenosylmethionine (SAM) enzymes exist in organisms from all kingdoms of lif

26 determined two radical S-adenosylmethionine (SAM) enzymes, one each from an SNP gene and a differenti

27 lyzes the formation of S-adenosylmethionine (SAM) from ATP and methionine.

28 ls of the methyl donor S-adenosylmethionine (SAM) is critical for a wide variety of biological proces

29 S-adenosylmethionine (SAM) is the methyl donor for biological methylation modi

30 dicted class C radical S-adenosylmethionine (SAM) methylase, catalyzes both the transfer of a C1 unit

31 amin-dependent radical S-adenosylmethionine (SAM) methyltransferase.

32 at encodes the As(III) S-adenosylmethionine (SAM) methyltransferase.

33 gdom have ArsM As(III) S-adenosylmethionine (SAM) methyltransferases that methylates inorganic As(III

34 as well as with bound S-adenosylmethionine (SAM) or S-adenosylhomocysteine (SAH) in the catalytic si

35 member of the radical S-adenosylmethionine (SAM) superfamily of enzymes, but it does not catalyze th

36 of the growing radical S-adenosylmethionine (SAM) superfamily of enzymes, which use a reduced [4Fe-4S

37 the methyl group from S-adenosylmethionine (SAM) to lysine residues in histone tails and core histon

38 eads to an increase in S-adenosylmethionine (SAM), which is the major cellular donor of methyl groups

39 The S-adenosylmethionine (SAM)-I riboswitch is a noncoding RNA that regulates the

40 acyl conjugation with S-adenosylmethionine (SAM).

41 effect transistor (ISFET) with the afforded SAM resulted in the production of a KI-sensitive sensor.

42 regulated enhancer controls expression of an SAM domain protein that confers survival in anemia.

43 as ultra-sensitive label-free biosensors and SAM/organic transistors that can be used as robust exper

44 ges in readability measures, word count, and SAM score between original and revised handouts.

45 Structural studies with 6-CP and SAM also reveal electron density consistent with the est

46 nd profiling tool for use with BAM, CRAM and SAM sequencing files.

47 rd applications of our approach to FASTQ and SAM archives require a few lines of code, produce soluti

48 t RNA motifs sensitive to magnesium ions and SAM.

49 olecular junctions (both single-molecule and SAM-based) formed by ferrocene-based molecules.

50 domain in complex with an H3K36M peptide and SAM or SAH.

51 At 24 weeks, both SAM on WD (SAM-WD) and SAM on regular diet displayed endothelial dysfunction, a

52 Administration of an anti-PAR2 antibody, SAM-11, after the initial development of airway inflamma

53 We present a method for converting arbitrary SAM states into total angular momentum states characteri

54 s a rapid and user-friendly interface to BAM/SAM/CRAM files, global sequence alignment operations and

55 An interesting positive association between SAM/SAH ratio and high H19 methylation levels was detect

56 general material-mediated connection between SAM and OAM of light and may find applications in produc

57 The cooperation between SAM and magnesium in stabilizing important tertiary inte

58 Using a bifunctional SAM containing PEG moieties and a tethered redox thiol,

59 ion by SAM, explains the requirement of both SAM and magnesium to form the fully collapsed metabolite

60 At 24 weeks, both SAM on WD (SAM-WD) and SAM on regular diet displayed end

61 ostridium thermocellum ATCC 27405, with both SAM and an N-terminal fragment of its peptidyl-substrate

62 ium, in combination with P1 stabilization by SAM, explains the requirement of both SAM and magnesium

63 ervous system (SNS) upregulates NE uptake by SAMs and shifts the SAM profile to a more proinflammator

64 NE uptake by SAMs is prevented by genetic deletion of Slc6a2 or inhib

65 The new role of the versatile cofactor SAM is likely to be found in other examples of enzyme ca

66 uctures like peptide and DNA mixed-component SAMs.

67 methyltransferase fold containing conserved SAM-binding and catalytic motifs, the isolated TlyA carb

68 1408 methyltransferases within its conserved SAM-binding fold but the region linking core beta strand

69 d, as human sympathetic ganglia also contain SAMs expressing the analogous molecular machinery for NE

70 In assays containing SAM, BChlide c or d, and sodium dithionite, BciD catalyz

71 tivity by interactions with the cosubstrate, SAM, which is bound to the catalytic iron-sulfur cluster

72 The total number of current SAM cases (prevalent cases) increases by the number of n

73 have generated a drug-free, all-in-one dCAS9-SAM vector that can activate endogenous gene expression

74 ategy to express the components of the dCas9-SAM system to create an artificial transcriptional compl

75 ase, CDP-Glc 4,6-dehydratase, NADH-dependent SAM:C-methyltransferase, and NADPH-dependent CDP-3-C-met

76 reased H3K4me3 caused by knockdown of either SAM synthetase (Sam-S) or the histone methyltransferase

77 These elements-SAM-to-orbital angular momentum (OAM) converters-are bas

78 ing embryogenesis to establish the embryonic SAM and to specify cotyledon boundaries, and STM control

79 mildly spiral growth, and flat and enlarged SAM, including those related to plant hormones and those

80 horylation levels upon deletion of the EphA2 SAM domain (EphA2DeltaS) in DU145 and PC3 prostate cance

81 on these results, we conclude that the EphA2 SAM domain inhibits kinase activity by reducing receptor

82 l domain exhibits no detectable affinity for SAM.

83 gs thus reveal a novel motif requirement for SAM binding by TlyA and set the stage for future mechani

84 for this unexpectedly low value of beta for SAMs of S(EG)nCH3 rests on the possibility of disorder i

85 .01 A(-1)) indistinguishable from values for SAMs of oligophenyls (beta(Ph)n = 0.28 +/- 0.03 A(-1)),

86 es indicate that greenhouse gases will force SAM into its positive phase even if stratospheric ozone

87 atalyzes both the transfer of a C1 unit from SAM to 3-methylindolic acid linked to Cys8 of a syntheti

88 Furthermore, SAM-4/Myrlysin, a subunit of BORC, promotes the GDP-to-G

89 any fast alignment algorithm that generates SAM files.

90 In this study, we have identified SAM domain-carrying non-receptor tyrosine kinase, activa

91 o imaging shows that after the immunization, SAM Ag expression has an initial gradual increase.

92 Rail-RNA outputs alignments in SAM/BAM format; but it also outputs (i) base-level cover

93 ant understanding of inflammatory changes in SAM, which may lead to improved therapies.

94 Genetic ablation of Slc6a2 in SAMs increases brown adipose tissue (BAT) content, cause

95 on of methionine metabolic genes to increase SAM, which in turn leads to an increase in global H3K4me

96 sh a temporary state that limits the initial SAM-encoded Ag expression.

97 ENDOR measurements establishes its intimate, SAM-mediated interaction with the cluster.

98 investigated different approaches involving SAMs of aromatic thiols, namely p-mercaptobenzoic acid (

99 usly upregulated in vegetative stages of ltm SAMs, among them, the antiflorigen gene SELF PRUNING (SP

100 y sympathetic neuron-associated macrophages (SAMs) as a population of cells that mediate clearance of

101 sed management of severe acute malnutrition (SAM) has been shown to be safe and cost-effective, but p

102 of children with severe acute malnutrition (SAM).

103 esponding value obtained with length-matched SAMs of oligophenyls (HS(Ph)nH) and n-alkanethiols (HS(C

104 Based on this mechanism, SAMs of oligo(ethylene glycol)s are good conductors (by

105 /Cas9-based synergistic activation mediator (SAM) system to identify potential lncRNAs capable of reg

106 at the flanks of the shoot apical meristem (SAM) following auxin maxima signals; however, little is

107 ent and doming of the shoot apical meristem (SAM) is a hallmark of the transition from vegetative gro

108 contained within the shoot apical meristem (SAM) is maintained in Arabidopsis by the homeodomain pro

109 ith model plants, the shoot apical meristem (SAM) of Moso is composed of six layers of cells.

110 e phloem to reach the shoot apical meristem (SAM).

111 nts to maintain their shoot apical meristem (SAM).

112 und SAH (a SAM analog) or 5'-dAdo and l-Met (SAM cleavage products) is consistent with the canonical

113 rmination process in response to metabolite (SAM) binding.

114 aromatic amino acid, S-adenosyl methionine (SAM) and folate biosynthetic pathways.

115 ogenous) methyl donor S-adenosyl methionine (SAM) did not affect CpG methylation and IEG gene express

116 es two equivalents of S-adenosyl methionine (SAM) to insert a carbide atom and fuse two substrate [Fe

117 S-Adenosyl methionine (SAM)-dependent C-methyltransferases are responsible for

118 erase (CCoAOMT) is an S-adenosyl methionine (SAM)-dependent O-methyltransferase responsible for methy

119 ures of RlmH bound to S-adenosyl-methionine (SAM) and the methyltransferase inhibitor sinefungin.

120 ates the methyl donor S-adenosyl-methionine (SAM), which is converted via methylation to S-adenosyl-h

121 AH) and low levels of S-adenosyl-methionine (SAM).

122 (NosL) is a radical S-adenosyl-l-methionine (SAM) enzyme that catalyzes the formation of 3-methyl-2-i

123 FL-AE) is a radical S-adenosyl-l-methionine (SAM) enzyme that installs a catalytically essential glyc

124 Radical S-adenosyl-l-methionine (SAM) enzymes are widely distributed and catalyze diverse

125 )-dependent radical S-adenosyl-l-methionine (SAM) methyltransferases have been identified through seq

126 a putative radical S-adenosyl-l-methionine (SAM) protein, are unable to synthesize BChl e but accumu

127 report a versatile S-adenosyl-l-methionine (SAM)-dependent enzyme, LepI, that can catalyse stereosel

128 perazyl scaffold is S-adenosyl-l-methionine (SAM)-dependent.

129 ethylation cofactor S-adenosyl-l-methionine (SAM).

130 ansferase activity, S-adenosyl-l-methionine (SAM).

131 combined with the standard addition method (SAM), allows for the absolute quantification of uric aci

132 ENDOR studies of the PFL-AE/[(13)C-methyl]-SAM complex show that the target sulfonium positioning v

133 METHODS AND Senescence-accelerated mice (SAM, n=18) and control mice with normal senescence (n=15

134 The Southern Annular Mode (SAM) is the main driver of climate variability at mid to

135 o the family of synaptic adhesion molecules (SAMs) due to its impact on synapse formation and synapti

136 ents that convert the spin angular momentum (SAM) of light into vortex beams have found applications

137 ester (DTSP) as a self-assembled monolayer (SAM) agent.

138 ide mimotope mixed self-assembled monolayer (SAM) biointerface and dilution of the analysis buffer.

139 the first time, a self-assembled monolayer (SAM) derived from calixtubes was formed on a SiO2 surfac

140 biofunctionalized self assembled monolayer (SAM) functionalized on gold nanoparticles (GNPs) in poly

141 ted tip contacts a self-assembled monolayer (SAM) of OPDs on Au.

142 issociation of the self-assembled monolayer (SAM) was detected by the naked eye and analysed using an

143 ific adsorption, a Self-Assembled Monolayer (SAM) was developed.

144 sfer (ET) across a self-assembled monolayer (SAM) was the developed for highly sensitive detection of

145 layer, a molecular self-assembled monolayer (SAM), and a ballistic carrier emitter.

146 Functionalized self-assembled monolayers (SAMs) are the focus of ongoing investigations because th

147 Self-assembled monolayers (SAMs) can be formed on (semi-)conductor and dielectric s

148 Self-assembled monolayers (SAMs) have been found to effectively reduce the impact o

149 ly based on mixed self-assembled monolayers (SAMs) of thiol-modified oligonucleotides and alkanethiol

150 tunneling across self-assembled monolayers (SAMs) of thiol-terminated derivatives of oligo(ethylene

151 transport across self-assembled monolayers (SAMs) of two donor-acceptor systems consisting of a poly

152 are known to form self-assembled monolayers (SAMs) on the surface of liquids.

153 philic terminated self-assembled monolayers (SAMs) sensor surfaces are compared to a hydrophobic term

154 ers such as thiol self-assembled monolayers (SAMs) to physisorbed monolayers as well as for complex s

155 on of homogeneous self-assembled monolayers (SAMs) via Ti-O-P linkages.

156 graphene sheets, self-assembled monolayers (SAMs) with chemical patterns, and mutants of the protein

157 layers (SLBs) and self-assembled monolayers (SAMs).

158 unique in possessing a sterile alpha motif (SAM domain) at their C-terminal ends.

159 (Samd14-Enh) encoding a sterile alpha motif (SAM) domain protein.

160 us of Shank3 contains a sterile alpha motif (SAM) domain that is essential for its postsynaptic local

161 145, "3Y") as well as a sterile alpha motif (SAM) domain whose function is unclear.

162 re based on engineered self-amplifying mRNA (SAM) replicons encoding an Ag, and formulated with a syn

163 otein G was covalently immobilized on 11-MUA SAM via amine coupling and bioaffinity-based oriented im

164 Ph with mutant SAM disrupts clustering of endogenous PcG complexes and

165 osensor with self-assembly gold nanoislands (SAM-AuNIs) can be used to detect and distinguish exosome

166 Together, the new SAM analog and the high-resolution crystal structure are

167 gs including homopolymer pCB brushes and OEG-SAMs.

168 lkanethiolate self-assembled monolayers (OEG-SAMs) are studied using the polarization modulation infr

169 ontrast to free carboxy-group-terminated OEG-SAMs, only a partial deactivation of EDC/NHS-activated z

170 In the absence of SAM, frequent open-to-closed conformational transitions

171 ect reductive cleavage of the 5' C-S bond of SAM to form a 5'-deoxyadenosyl 5'-radical (5'-dA(*)) int

172 he homolytic cleavage of the S-C(5') bond of SAM.

173 that would promote the reductive cleavage of SAM, 6-CP is turned over to 6-deoxyadenosylpterin (6-dAP

174 dylethanolamine (PE), is a major consumer of SAM.

175 dithionite, BciD catalyzed the conversion of SAM into 5'-deoxyadenosine and BChlide c or d into BChli

176 ome methyl sinks to enable the conversion of SAM to SAH.

177 h America (SAS), to quantify the coupling of SAM and regional wildfire variability using recently cre

178 stic simulations, we calculate the effect of SAM and magnesium ions on the folding free energy landsc

179 However, the functions of SAM domains in Eph receptors remain elusive.

180 cently created multicentury proxy indices of SAM for the years 1531-2010 AD.

181 tion through sequestration and inhibition of SAM-bound SET domain methyltransferases.

182 hanistically, Runx2 bound to the promoter of SAM-pointed domain-containing Ets-like factor (SPDEF), a

183 tom relief in such patients via reduction of SAM and mitral regurgitation.

184 Survivors of SAM had functional deficits consisting of weaker hand gr

185 and RUTF use in the outpatient treatment of SAM was maintained over 4 wk of follow-up with a monthly

186 hildren eligible for outpatient treatment of SAM were provided a monthly ration of RUTF.

187 ethylation of PE facilitates the turnover of SAM for the synthesis of cysteine and glutathione throug

188 stablish that APLPs show typical features of SAMs and indicate that increased surface expression, as

189 hether APLP1 and APLP2 also show features of SAMs.

190 pplications emerging from the integration of SAMs in an organic device.

191 ics, discuss the mechanism of interaction of SAMs in a microscopic device, and highlight the applicat

192 We also observed an increased proportion of SAMs in the SNS of two mouse models of obesity.

193 (-1)), and significantly lower than those of SAMs of n-alkanethiolates (beta(CH2)n = 0.94 +/- 0.02 na

194 teins, HemW contains three cysteines and one SAM coordinating an [4Fe-4S] cluster, and we observed on

195 es are required for methylation and that one SAM (SAM1) is converted to 5'-deoxyadenosine and the sec

196 anti-Escherichia coli O157:H7 antibody onto SAM-modified gold electrodes.

197 that the N-terminal sterile alpha motif (or SAM) domain of SMSr drives self-assembly of the protein

198 ation of 5'-deoxyadenosin-5'-yl or any other SAM-derived radical.

199 cocultured neurons, similar to APP and other SAMs.

200 ave shown that ERI significantly outperforms SAM and Localfdr in detecting early responding molecules

201 uce medium chain fatty acids and overproduce SAM, we obtain medium chain FAMEs at titers of 0.56 g/L,

202 We also find that patterned SAMs and protein mutants, having the same number of nonp

203 may be a useful strategy to increase primary SAM expression and the resulting vaccine potency.

204 ivation of a floral antagonist that promotes SAM growth in concert with floral transition protects it

205 imply that viperin does not act as a radical SAM enzyme in regulating FPPS.

206 Aminofutalosine synthase (MqnE) is a radical SAM enzyme involved in the menaquinone biosynthetic path

207 )-OH-BChlide c and d Thus, BciD is a radical SAM enzyme that converts the methyl group of BChlide c o

208 Here, we report that a radical SAM protein, the heme chaperone HemW from bacteria, is r

209 nsertion of the Fe/S cofactor into a radical SAM protein.

210 ovel rRNA methylation mechanism by a radical SAM superfamily enzyme, indicating that two resistance m

211 Of particular interest are radical SAM enzymes, such as heme chaperones, that insert heme i

212 hat differs from other characterized radical SAM methyltransferases.

213 onstitution of a cobalamin-dependent radical SAM enzyme catalyzing the conversion of a methyl group t

214 mechanistic links among SPASM domain radical SAM enzymes and supports the involvement of non-cysteiny

215 the emerging family of SPASM domain radical SAM enzymes, likely contains three [4Fe-4S] clusters.

216 chanisms of how viperin acquires its radical SAM Fe/S cluster to gain antiviral activity are poorly u

217 Recently, a novel radical SAM enzyme catalyzing the formation of a lysine-tryptoph

218 conditions highlights the ability of radical SAM enzymes to carry out both polar and radical transfor

219 arrel fold that is characteristic of radical SAM enzymes, as well as a C-terminal SPASM domain that c

220 ynthesis requires a unique family of radical SAM enzymes, which contain multiple [4Fe-4S] clusters, t

221 Finally, the human HemW orthologue radical SAM domain-containing 1 (RSAD1) stably bound heme.

222 viperin is similar to several other radical SAM enzymes, including the molybdenum cofactor biosynthe

223 As other radical SAM proteins, HemW contains three cysteines and one SAM

224 [4Fe-4S] cluster associated with the radical SAM chemistry for generating the central carbide.

225 -bearing carbon is prevented and the radical SAM machinery sits adjacent rather than opposite to the

226 sion, our findings indicate that the radical SAM protein family HemW/RSAD1 is a heme chaperone cataly

227 ion, concurrent with the preliminary reduced SAM Ag expression.

228 In cells, methionine starvation reduces SAM levels below this dissociation constant and promotes

229 ditional function in vertebrates to regulate SAM homeostasis.

230 e the role of the early type I IFN response, SAM vaccines were evaluated in IFN receptor knockout mic

231 onverted to 5'-deoxyadenosine and the second SAM (SAM2) is converted to S-adenosyl-l-homocysteine (SA

232 the dissociation process of the EphA2-SHIP2 SAM-SAM domain heterodimer complex using unrestrained al

233 ethyl donor in the reaction, in our studies, SAM itself plays this role, giving rise to S-adenosylhom

234 This observation suggests SAMs derived from these or electronically similar molecu

235 StrB, in various forms, including apo SuiB, SAM-bound SuiB, and a complex of SuiB with SAM and its p

236 ces are compared to a hydrophobic terminated SAM coating.

237 duce the hydrophobicity of methyl-terminated SAMs most effectively not when they are clustered togeth

238 , and deposited on an electrode as a ternary SAM configuration, is a suitable platform to develop cli

239 nalysis by methods such as student's t-test, SAM, and Empirical Bayes often searches for statisticall

240 Our results indicate that SAM domain deletion (EphA2DeltaS-GFP) increases oligomer

241 These results suggest that SAM domain deletion induced constitutive activation of E

242 n-alkanethiols (HS(CH2)nH) demonstrates that SAMs of oligo(ethylene glycol) have values of beta (beta

243 The SAM domain deletion mutant, EphA2DeltaS-GFP, also underw

244 The SAM pointed domain containing ETS transcription factor (

245 expression of human MAT2A, which encodes the SAM synthetase expressed in most cells.

246 In addition, we estimated the SAM surface coverage fraction from the surface tension m

247 rests on the possibility of disorder in the SAM and a systematic discrepancy between different estim

248 Substitution of conserved residues in the SAM binding pocket reveals a functional dichotomy in the

249 In the SAM, they form a transcriptional activation complex with

250 mRNA and protein localization domains in the SAM.

251 Positive phases of the SAM are associated primarily with warm conditions in the

252 escence study to investigate the role of the SAM domain in EphA2 function.

253 y is synchronous with positive phases of the SAM over the years 1665-1995.

254 EHF activates expression of the SAM pointed domain-containing ETS transcription factor,

255 The formation of the SAM was confirmed by X-ray photoelectron spectroscopy, s

256 ing signals can result in termination of the SAM, usually by its differentiation into a flower.

257 h conformational changes upon binding of the SAM-analog sinefungin.

258 ion perturb the electronic properties of the SAM-chelated iron-sulfur cluster.

259 llapsed metabolite-bound closed state of the SAM-I riboswitch.

260 on the folding free energy landscape of the SAM-I riboswitch.

261 Pre-organization of the SAM-II riboswitch allows rapid detection of ligand with

262 rtially closed and open conformations of the SAM-II riboswitch in the absence of ligand.

263 ate the folding free energy landscape of the SAM-II riboswitch.

264 6 N-terminal tyrosines (3Y) dependent on the SAM domain.

265 One monomer provides the SAM-binding site, whereas the conserved C-terminal tail

266 The algorithm reads the SAM files generated by the alignment algorithms using mu

267 ne-induced activation of mTORC1 requires the SAM binding capacity of SAMTOR.

268 upregulates NE uptake by SAMs and shifts the SAM profile to a more proinflammatory state.

269 We showed previously that the SAM domain has two binding regions that mediate dimer an

270 he desired biosynthetic end product via the (SAM-dependent) retro-Claisen rearrangement catalysed by

271 he simplified Simmons equation) across these SAMs with the corresponding value obtained with length-m

272 glycol) (HS(CH2CH2O)nCH3; HS(EG)nCH3); these SAMs are positioned between gold bottom electrodes and G

273 ronic and supramolecular structures of these SAMs were well characterized.

274 ifferent estimates of the thickness of these SAMs.

275 This SAM vaccine-induced type I IFN response has the potentia

276 ecular surface coverage, the tip radius, tip-SAM adhesion force (F), and sample elastic modulus (E),

277 le elastic modulus (E), we find that the tip-SAM contact area is approximately 25 nm(2), correspondin

278 (acetyl-CoA, carbamoyl-P), methyl transfers (SAM), prenyl transfers (IPP), glucosyl transfers (UDP-gl

279 In this context, dNTP triphosphohydrolase SAM domain and HD domain-containing protein 1 (SAMHD1) h

280 Product analysis demonstrates that two SAM molecules are required for methylation and that one

281 ood (RUTF) in the treatment of uncomplicated SAM, in terms of clinical response to treatment and hous

282 We propose that, under SAM-limiting conditions, METTL16 occupancy on hp1 increa

283 Upon SAM depletion by methionine starvation, cells induce MAT

284 na users (MAR), smoking-and-marijuana users (SAM), marijuana-and-drinking users (MAD), and users of a

285 ting biosynthetic reaction pathways by using SAM as the cofactor.

286 M functions to suppress SP in the vegetative SAM In agreement, SP-overexpressing wild-type plants exh

287 ring and precocious doming of the vegetative SAM LTM encodes a kelch domain-containing protein, with

288 ts exhibited precocious doming of vegetative SAMs combined with late flowering, as found in ltm plant

289 n in SP restored the structure of vegetative SAMs in ltm sp double mutants, and late flowering was pa

290 nscriptional activation systems, namely VPR, SAM and SunTag, have been developed for animal cells (2-

291 At 24 weeks, both SAM on WD (SAM-WD) and SAM on regular diet displayed endothelial dy

292 associations with mortality in children with SAM.

293 in = 2.0 A) as well as binary complexes with SAM (dmin = 2.3 A) or the reaction product S-adenosylhom

294 CcR was covalently coupled with SAM layers on GNPs by using EDC and NHS.

295 ection-site tissues from mice immunized with SAM-based vaccine revealed an early and robust induction

296 3-ketopentanoyl-ACP (9) were incubated with SAM and BonMT2 from module 2 of the bongkrekic acid poly

297 al interaction between exosomes and MVs with SAM AuNIs.

298 , SAM-bound SuiB, and a complex of SuiB with SAM and its peptide substrate, SuiA.

299 Functionalisation with SAMs is important not only for imparting stability to th

300 performing surface chemistry tailoring with SAMs constitutes a versatile approach towards the tuning