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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

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