ライフサイエンスコーパス: methyl group

1 lectronic effects of the fluorination at the methyl group.

2 acids that differ only by the position of a methyl group.

3 between the tryptophan and the hydroxamate's methyl group.

4 flexibility of the side chain imposed by the methyl group.

5 own the fatty acid chain toward the terminal methyl group.

6 2) an axial 4alpha-OMe group, and (3) a C-18 methyl group.

7 n arginine and a glutamate interact with the methyl group.

8 l core, and (d) the presence of a terminal N-methyl group.

9 together but when they are separated by one methyl group.

10 st likely be attributed to the exchange of a methyl group.

11 tional ZF interacts with a conserved thymine methyl group.

12 s, in which one of the substituents is not a methyl group.

13 hobic interactions with the methylcytosine 5-methyl group.

14 vital interactions through its beta-branched methyl group.

15 e trifluoromethyl group in comparison to the methyl group.

16 a 4-fluorophenyl moiety substitutes for the methyl group.

17 substrates in which the olefin bears a beta-methyl group.

18 ety that include either a trifluoromethyl or methyl group.

19 ffect favoring hydrogen abstraction from the methyl groups.

20 l toluene with all three H isotopes in their methyl groups.

21 sion of key genes to minimize loss of labile methyl groups.

22 ibly converted to betaine, a major source of methyl groups.

23 thyl group to mRNA while demethylases remove methyl groups.

24 stallation of radioactive and stable labeled methyl groups.

25 those of the alpha-methylene, beta- or gamma-methyl groups.

26 easuring of crucial distances between and to methyl groups.

27 " between the hypercoordinate carbon and its methyl groups.

28 ly measure the significance of the beta-face methyl groups.

29 Ms, including phospho, acetyl, ubiquityl and methyl groups.

30 near-depending on the stereochemistry of the methyl groups.

31 ain ten contiguous, stereochemically defined methyl groups.

32 lecule: the BCO, the C19 methoxy and the C18 methyl groups.

33 2-amino/hydroxy nitrobenzenes and activated methyl groups.

34 onds by main-group reagents occur at aryl or methyl groups.

35 tert-butyl substituents on the ligands with methyl groups.

36 m of transferring moieties other than simple methyl groups.

37 the C(sp(3))-H bonds of one of the prochiral methyl groups.

38 , resulting in the four spatially equivalent methyl groups.

39 ne interactions between the alpha- and gamma-methyl groups.

40 tution with a 2-fluoro-4-chloro-phenyl- or a methyl- group.

41 a,b), 3-methyl (6a,b), and both the 3- and 4-methyl group (7a,b) and compared their opioid receptor p

42 studies showed the two subtypes with an N-1 methyl group (9 and 10) inhibited RNase H in low micromo

43 mber and position of hydroxyl, glycosyl, and methyl groups about their aromatic core structure produc

44 Methyl group abstraction is one of the suggested pathway

45 including carboxyl, N-acetyl, fluorine, and methyl groups affect stacking interactions with aromatic

46 preclude Watson-Crick base pairing, the N(6)-methyl group alters the stability of RNA secondary struc

47 is the result of a steric clash between the methyl group and a highly ordered water network in the a

48 Subsequent introduction of the methyl group and functional group transformation complet

49 ify the amount of information stored by each methyl group and show that receptors consume energy in t

50 /Abcb4), resulting in reduced consumption of methyl groups and biliary PC secretion.

51 lex regulatory feedback network between free methyl groups and genomic imprinting at birth.-Tserga, A

52 choline-deficient (MCD) diet, which depletes methyl groups and results in a deleterious decrease in t

53 arent kinetic isotope effects related to the methyl group are more pronounced than for the methylene

54 ecules that lack an easily substituted (11)C-methyl group are often considered to have non-obvious st

55 These methyl groups are in van der Waals contact with a conser

56 (CH3)(Cl)Si(ONO(Q)), in which the phenyl and methyl groups are mutually trans, indicating that the ob

57 he major groove side, and thus their pendant methyl groups are on the minor groove side.

58 Methyl groups are powerful probes for the analysis of st

59 Methyl groups are predominantly installed into biomolecu

60 emical shift assignments for over 95% of the methyl groups are reported.

61 e metabolites [produced when choline-derived methyl groups are used by phosphatidylethanolamine N-met

62 substituted amido group while retaining an N-methyl group as a site for labeling with carbon-11.

63 hodology could expand the application of the methyl group as a useful protecting group.

64 ks on the Cu(110) surface by utilizing the 4-methyl groups as unique connection points.

65 ith heterocyclic aromatic rings and attached methyl groups (as on thymine) are particularly favorable

66 y analysis indicate that introduction of the methyl group at C-7 results in a significant deviation f

67 ween the methyl group at C3 in IPP and the Z-methyl group at C3 in DMAPP (3-OPP) and GPP (4-OPP), res

68 lic diphosphates with a C-C bond between the methyl group at C3 in IPP and the Z-methyl group at C3 i

69 cence and excellent photostability, (b) an N-methyl group at each end of the squaraine core that ensu

70 An N-methyl group at position 33 blocks uncontrolled aggregat

71 ed that the placement of a single side chain methyl group at specific positions in a traptamer determ

72 hat results from the enzymatic addition of a methyl group at the fifth carbon of the cytosine base.

73 Conversely, the introduction of a methyl group at the methylene hinge connecting the 6-ami

74 t C1 and C1' or lack the naturally occurring methyl group at those positions were synthesized and eva

75 The methyl groups at C-7 and C-9 of the pterin ring distingu

76 e, which displays C8-C6' coupling and four O-methyl groups at C6, C7, C3', and C4' as numbered on the

77 n of the pyrimidine, so each of them has two methyl groups at nucleotide positions 1 and 5 from the 5

78 dimethylallyl derivatives bearing deuterated methyl groups at the distal (C3) carbon atom in the doub

79 polysaccharide type 5 equipped with capping methyl groups at the points of propagation of the polysa

80 tect linear peptides by attaching prenyl and methyl groups at their free N- and C-termini.

81 Methyl groups attached to the Sn atom are not transferre

82 bstitution patterns of organic compounds the methyl group attracts one of the phenyl sides to establi

83 hen compared to the analogous dye containing methyl group away from donor.

84 nated and has to move out of the cavity as a methyl group before the hydrides can be formed.

85 AM and the abstraction of hydrogen from this methyl group by 5'-deoxyadenosyl radical that initiates

86 cytosine methylation, iterative oxidation of methyl group by TET dioxygenases, and restoration of unm

87 onbridging phosphate oxygens at A2662 with a methyl group by the introduction of a methylphosphonate

88 TMD interactions, demonstrate that a single methyl group can dictate specificity, and define the min

89 However, methyl groups can only be found in 6 of 19 side-chain be

90 The methyl group (CH3), which was observed in the infrared s

91 serve surface adsorbates, hydrogen atoms and methyl groups, chemisorbed to the nanowire sidewall and

92 Balance of labile methyl groups (choline, methionine, betaine, and folate)

93 The conjugation with methyl groups decreased or did not alter the antiprolife

94 analysis the extraterrestrial origin of the methyl group (delta(2)H +800 to +1100 per thousand, delt

95 , reactions with CdMe2 produce surface bound methyl groups (delta = 0.4 ppm, 0.04-0.22 nm(-2)) that p

96 her yields than those attributable to the C5-methyl group deprotonation in NMe-1.

97 The appended methyl group derives from SAM; however, the enzyme also

98 The methyl group did not determine an excessive destabilizat

99 hat use S-adenosylmethionine (AdoMet) as the methyl group donor.

100 lation, using methylenetetrahydrofolate as a methyl group donor.

101 diated by (1)H-(13)C cross-relaxation within methyl groups due to reorientation dynamics, and results

102 CUG repeats modified with Psi or 2'-O-methyl groups exhibited enhanced structural stability an

103 Oxidative C-H hydroxylation of methyl groups, followed by their removal from DNA, RNA o

104 ine for polyamine biosynthesis and donates a methyl group for histone methylation.

105 this pathway cleaves acetyl-CoA to donate a methyl group for production of methyl-tetrahydrofolate (

106 d 1-carbon transfer are the major sources of methyl groups for 1-carbon metabolism.

107 g homocysteine into methionine and providing methyl groups for DNA methylation.

108 nent of 1-carbon metabolism, which generates methyl groups for DNA methylation.

109 regnant women also used more choline-derived methyl groups for PC synthesis via phosphatidylethanolam

110 (SAM), which is the major cellular donor of methyl groups for protein modification.

111 thymidylate synthesis, and the provision of methyl groups for synthetic, regulatory, and epigenetic

112 synthetic efficiency, deletion of one ortho-methyl group from o,o',o'',o'''-tetramethylbiaryl junctu

113 rase (HNMT) inactivates HA by transferring a methyl group from S-adenosyl-l-methionine to HA, and is

114 s aquaticus that catalyzes the transfer of a methyl group from S-adenosyl-L-methionine to the N6 posi

115 the KMT family catalyze the transfer of the methyl group from S-adenosylmethionine (SAM) to lysine r

116 Ma) and NifB(Mt) can catalyze the removal of methyl group from SAM and the abstraction of hydrogen fr

117 ow that PaMTH1 catalyzes the transfer of the methyl group from SAM to one hydroxyl group of the myric

118 ome substrates to catalyze the transfer of a methyl group from SAM to the epsilon-amino group of hist

119 rase 1 (NTMT1) catalyzes the transfer of the methyl group from the S-adenosyl-l-methionine to the pro

120 The NirE enzyme catalyses the transfer of a methyl group from the SAM to uroporphyrinogen III and se

121 Oxidation of the methyl groups from choline requires formyltetrahydrofola

122 stone deacetylase 3 (HDAC3) gene by removing methyl groups from dimethylated H3K36 at the HDAC3 promo

123 These enzymes catalyze the transfer of donor methyl groups from the cofactor S-adenosylmethionine to

124 -ketoglutarate-dependent demethylases remove methyl groups from tri- and dimethylated lysine 4 of his

125 Polycomb-mediated gene silencing by removing methyl groups from trimethylated histone H3 lysine 27 (H

126 f-function (GOF)], apparently by placing its methyl group further inward and receiving stronger water

127 The nitroxides are designed to have the methyl groups further away from the N-O spin site to dec

128 tain a benzene ring and multiple side methyl methyl groups (galaxolide, 4-MBC) required high energy i

129 s of buprenorphine in which the standard C20-methyl group has been moved to the C7beta position, resu

130 In particular, moving the methyl group has resulted in far more robust kappa opioi

131 yme(s) responsible for the addition of these methyl groups has yet to be identified.

132 ii) a similar cyclization with a loss of the methyl group; (iii) a tandem process of cyclization into

133 iguously to an electronic effect by the para-methyl group in 1b, which increases the contribution of

134 Several naphthalene compounds containing a methyl group in a 1,8-relationship to a metal-complexed

135 ands enables the sequential diarylation of a methyl group in an alanine derivative with two different

136 e that highlights the importance of a single methyl group in biasing the conformation in the acyclic

137 For the substrates with a methyl group in cis- or trans-position of the terminal a

138 CH...O) hydrogen bonds coordinate the AdoMet methyl group in different methyltransferases irrespectiv

139 d benzylsulfanopyridinium amidates bearing a methyl group in position 6 with 2 equiv of diphenylketen

140 onal barrier of the phenyl ring nearby the N-methyl group in rac-2A was estimated to be >> 18.1 kcal/

141 enyl ring is slightly closer to the naphthyl methyl group in the complexes than in their metal-free c

142 w that a minor change, the introduction of a methyl group in the delta position, results in a signifi

143 e created new amino acids that incorporate a methyl group in the gamma-position of the stapling amino

144 er-energy anti conformation, positioning the methyl group in the major groove.

145 labeling studies confirmed the origin of the methyl group in the methanol product is the iridium-meth

146 rom the beta-position of the thiazole to the methyl group in the product.

147 hat 5-methylcytosine and thymine both have a methyl group in the same position, 5-carbon of the pyrim

148 ular hydrogen atom abstraction from benzylic methyl groups in 3, followed by intermolecular hydrogen

149 e that is involved in the removal of two C-4 methyl groups in one of the later steps of cholesterol b

150 The incorporation of methyl groups in the central phenyl unit has been found

151 E isomers depended on number and position of methyl groups in the chroman ring.

152 We show that two methyl groups in the PB side chain, as well as a feature

153 ric protection of the radicals by additional methyl groups in the pendant group.

154 Isotopic labeling indicated that the O-methyl groups in the Stackebrandtia phosphonoglycan aris

155 possesses four mPEG-3 groups replacing four methyl groups in the tert-butyl groups at the 3- and 6-p

156 The shielding effect of a methyl group incorporated in the coumarin derivative nea

157 ethyl group at the 6-position with butyl or methyl groups increased IC50 more than 10-fold.

158 isotope effect), whereas deuteration of the methyl group induces a normal secondary isotope effect.

159 rogen hydrogen-bonded to the protein and the methyl group inserted into a hydrophobic pocket.

160 voring the desired atropisomer in which this methyl group interacts with the S2 pocket of FVIIa.

161 enzo[g]indoles with [1,3] migration of the N-methyl group into the newly formed pyrrole ring; (ii) a

162 ormational constraint does indeed direct the methyl group into the S2 pocket as designed.

163 s an epigenetic modification of DNA, where a methyl group is added at the fifth carbon of the cytosin

164 ereomer is observed when the chiral benzylic methyl group is introduced.

165 urther experiments demonstrated that the C-7 methyl group is not derived from methionine and that met

166 The steric effect exerted by the methyl group is responsible for the nonplanar arrangemen

167 f substituents on the signal of the naphthyl methyl group is small but discernible in the uncomplexed

168 al theory calculations indicate that the SAM methyl group is sterically constrained in complex with N

169 Here we demonstrate that the methyl group is transferred to a precursor-associated su

170 Reductive deiodination to methyl groups is achieved by hydrogenation or catalytic

171 he distance between the nitroxide moiety and methyl groups is effective in lengthening Tm at T > 70 K

172 Quantitatively, a significant use of labile methyl groups is in the production of phosphatidylcholin

173 L) by two distinct mechanisms as revealed by methyl-group labeling.

174 ding suggesting that hydrophobicity of the T-methyl group likely plays a minor role in protein bindin

175 ored by observing the (1)H NMR signal of the methyl group located in the shielding zone of the ring.

176 yldialkylamines show a strong preference for methyl group loss by displacement, as predicted by compu

177 A small N(6)-methyl group maintained binding affinity, with human > m

178 anding of the contribution that the 3- and 4-methyl groups make to the pure antagonist properties of

179 eplacing the transferring hydrogen atom by a methyl group makes the substrate inactive and hence conf

180 ly improved choline and other markers in its methyl group metabolism pathway.

181 alladium(II) carbaporphyrin via an oxidation-methyl group migration process.

182 Solvation of the fibrils does not affect methyl group motions within the hydrophobic core of indi

183 isms by which these unactivated atoms obtain methyl groups nor the actual methyl donors are conserved

184 acking motif with the electron-poor ammonium methyl groups occupying the electron-rich cavity of the

185 howed that inversion of configuration at the methyl group occurs when the chiral toluenes react with

186 Docking studies showed that the methyl group of (R)-11 points toward the cleft created b

187 are ascribable to deprotonation from the C5-methyl group of 1 are observed.

188 Met6p catalyzes transfer of the methyl group of 5-methyl-tetrahydrofolate-glutamate3 to

189 side chain of Glu446 is known to contact the methyl group of 5-methylcytosine (5mC) or thymine (5-met

190 The methyl group of 6-methylazulene was then used as a synth

191 iD is a radical SAM enzyme that converts the methyl group of BChlide c or d into the formyl group of

192 pic composition (delta(13)C) embedded in the methyl group of CH3Hg remains unexplored.

193 The methyl group of dTMP apparently clashes with a highly co

194 and 2 equiv from C-H bond activation of one methyl group of each of the isopropyl groups at the 2- a

195 A methyltransferase responsible for the N(6)-methyl group of m(6)t(6)A in tRNA(Thr) specific for ACY

196 When the methyl group of N-methylaniline is replaced by an isopro

197 nteraction between the phenylalanine and the methyl group of pyruvate.

198 ynaphthalen-2-yl)butanoic acid (in which the methyl group of R-naproxen was replaced by an ethyl grou

199 Mutagenesis of three residues near the methyl group of SAM and the nitrogen atom of the alkaloi

200 e of SAM1 and the other two hydrogens of the methyl group of SAM2 appear in the methylated product.

201 show that a hydrogen is transferred from the methyl group of SAM2 to the 5'-deoxyadenosine of SAM1 an

202 and by making direct contact with the donor methyl group of the cofactor, S-adenosylmethionine.

203 horizontal lineNTol species deprotonates the methyl group of the NacNac ligand.

204 addition to Sc horizontal lineNimide) with a methyl group of the NacNac(NMe2) ligand forming {MeC(NC6

205 oline's aliphatic cyclic structure and the 5-methyl group of the pyrimidine (5mC or T).

206 for radical-mediated C-C bond formation; the methyl group of toluene is positioned between fumarate a

207 toluene metabolism by adding fumarate to the methyl group of toluene to yield (R)-benzylsuccinate.

208 tention or inversion of configuration at the methyl group of toluene, we synthesized both enantiomers

209 We show that all methyl groups of Abeta40 populate direct-contact bound s

210 ith selective isotope labeling of the delta1 methyl groups of isoleucine side chains demonstrates tha

211 ally protonated amino acid moieties, such as methyl groups of isoleucines, valines, or leucines.

212 to probe the reorientation of the isopropyl methyl groups of l-leucine at the air-water interface.

213 en peroxide and ascorbic acid as reagents, S-methyl groups of organosulphur compounds are efficiently

214 is enforced by the steric clash between the methyl groups of the arene ligand and the phenyl rings o

215 i-nor-cholesterol), in which the C18 and C19 methyl groups of the beta-face were eliminated.

216 MR relaxation dispersion measurements of the methyl groups of the Ile, Leu, and Val residues at two s

217 Methyl groups of thymine acts as a steric block, relocat

218 Specifically, we investigated the methyl groups of two leucine residues that belong to the

219 The methyl group on (C5Me5)3ThMe can be removed with [Et3NH]

220 ffering only by the presence or absence of a methyl group on the alpha-carbon, (S)-2-amino-7-[(18)F]f

221 pulsive force and presence of the additional methyl group on the backbone.

222 A dye containing methyl group on the donor side exhibited blue shift in a

223 but also is influenced by the position of a methyl group on the monoterpene ring.

224 ate as the sole carbon source, the resulting methyl group on the pterin was predominantly labeled wit

225 y to overcome this obstacle is to remove the methyl group on these modified bases prior to cDNA synth

226 traints show that the interaction energy for methyl groups on homochiral molecules differs significan

227 ether length, and the presence of isoprenoid methyl groups on one or both lipid tails.

228 The propargyl alcohol and the two terminal methyl groups on the olefinic unit shape the cyclization

229 Incorporation of a methyl group onto a macrocyclic FVIIa inhibitor improves

230 s for tetrahydrofolate-linked oxidation of a methyl group originating from a methylated corrinoid pro

231 l cofactor that during catalysis transfers a methyl group originating from S-adenosyl-l-methionine.

232 The reaction favors the C-H bonds of methyl groups over the methylene C-H bonds and tolerates

233 n favors predominantly the C-H bonds of beta-methyl groups over the unactivated methylene C-H bonds.

234 lectivity by favoring the C-H bonds of alpha-methyl groups over those of the alpha-methylene, beta- o

235 ous in the MRC and reveal the role of Fhs in methyl group oxidation in R. pomeroyi.

236 ed set of genes encoding the upper branch of methyl group oxidation to CO2 as well as membrane-bound

237 d between a Trp and Tyr residue and with the methyl group pointed toward another Trp residue.

238 adopts a rotated conformation in which the 5-methyl group points into the minor groove, rather than t

239 he rigid compounds also suggested that the 3-methyl group present in compound 1 type antagonists may

240 substitution at a bridgehead position with a methyl group produced a quadricyclane that thermally rev

241 A conformationally restricted P2' methyl group provided inhibitors with excellent cell pot

242 by incorporation of P1' alkyl sulfone and P2 methyl groups provided a macrocycle with TF/FVIIa Ki = 1

243 Hydrophobic interactions of the methyl group rather than pi-pi stacking interactions of

244 According to IR and solid-state NMR, the methyl group remains intact, and does not evolve spontan

245 spectively), proceeds via oxidation of the N-methyl group, resulting in the release of formaldehyde.

246 In addition, while free rotation of the beta-methyl group results in a single, averaged gamma-H atom

247 (KDM4A-KDM4D), which selectively remove the methyl group(s) from tri/dimethylated lysine 9/36 of H3,

248 The positions of methyl group(s) on the phenylene bridge allow for an exp

249 n of PAAs was related to the position of the methyl group, showing the same isomer specific preferenc

250 depend, as predicted by calculation, on its methyl group substitution pattern, making 3 by some way

251 phoethanolamine methyltransferases add three methyl groups successively to their substrate to produce

252 er, these results indicate that removal of a methyl group switches PK11195 from a potent antagonist o

253 ns 1 and 5 from the 5 end, resulting in four methyl groups symmetrically positioned in duplex DNA.

254 jos-Parrish ketone isomers with a transposed methyl group (termed "iso-Hajos-Parrish ketones") would

255 tion is predicted to be more in favor of the methyl group than the methylene of the pentyl chain, in

256 precursor and hydrogen abstraction from this methyl group that initiates the radical-based precursor

257 e leads to the selective transformation of a methyl group that is adjacent to an unprotected secondar

258 ing-tunneling microscopy showed well-ordered methyl groups that covered nearly all of the surface.

259 rexinoid, which induced hyperlipidemia, had methyl groups that interacted with helix 7 residues of t

260 Due to the benefit of methyl group, the dyes restrained the formation of aggre

261 rsible synthesis of acetyl-CoA from CO and a methyl group through a series of nickel-based organometa

262 at is involved in subsequent transfer of its methyl group to 5 or 8, H2O, and other nucleophilic comp

263 al SAM enzyme catalyzing the conversion of a methyl group to a t-butyl group.

264 Covalent addition of a methyl group to adenosine N(6) (m(6)A) is an evolutionar

265 B12/rSAM enzyme, catalyses the transfer of a methyl group to an electrophilic carbon atom of tryptoph

266 nsecutive hydroxylation reactions of the C-7 methyl group to form a geminal diol intermediate, which

267 only catalyzes sequential methylations of a methyl group to form ethyl and isopropyl groups but rema

268 cterized protein that oxidizes the pyocyanin methyl group to formaldehyde and reduces the pyrazine ri

269 and 5'-deoxyadenosine and the transfer of a methyl group to l-valine residue.

270 Methyltransferases add a methyl group to mRNA while demethylases remove methyl gr

271 Subsequent steps entail conversion of the 1-methyl group to the 1-(dimethoxymethyl) unit and acid-ca

272 common mRNA modification, the addition of a methyl group to the N(6) position of adenosine (m(6)A),

273 mediates to drive hydrogen transfer from the methyl group to the terminal oxygen, followed by dissoci

274 lglucosamine moiety and CD0243 transfers the methyl group to the threonine.

275 novo DNA methyltransferases DNMT3a/3b adding methyl groups to CG dinucleotides in the hypomethylated

276 DNMT3a/3b can add methyl groups to daughter strands after each cycle of DN

277 methionine ratio, decreasing the transfer of methyl groups to DNA and RNA.

278 Post-translational addition of methyl groups to the amino terminal tails of histone pro

279 The importance of several methyl groups to the potency of the inhibitors is highli

280 ) kinetic isotope effects at the transferred methyl group, together with (1)H3/(3)H3 binding isotope

281 in the E1 form and rotates to contribute its methyl group toward K(+) in the E2 form.

282 to form a methyl Pt(IV)-OOH species with the methyl group trans to the pyridine nitrogen, which then

283 reaction as compared to its isomer with the methyl group trans to the pyridine nitrogen.

284 isomeric methyl Pt(IV)-OOH species with the methyl group trans to the sulfonate.

285 asis of these studies, a mechanism involving methyl group transmetalation between Pd(II) and Pd(IV) i

286 ivities by functionalization of enantiotopic methyl groups under mild conditions.

287 redominant preference for sp(3) C-H bonds of methyl groups via a five-membered ring intermediate over

288 rence for activating sp(3) C-H bonds of beta-methyl groups, via a five-membered ring intermediate, ov

289 rine substitution, while the effect of the 4-methyl group was negligible.

290 A derivative of HMPA in which one of the methyl groups was substituted by a CH2CH2OH unit was syn

291 eriments performed on selectively deuterated methyl groups, we probed the 3-fold symmetric and 2-fold

292 laxation performed on selectively deuterated methyl groups, we probed the dynamics in the threefold s

293 A total of 96 patients in the bardoxolone methyl group were hospitalized for heart failure or died

294 d baseline circulating glycoprotein N-acetyl methyl groups were associated with longitudinal risk of

295 The angular methyl groups were attached by electrophilic cyclopropan

296 e of the incident light, indicating that the methyl groups were bonded directly atop surface Ge atoms

297 Analogues in which the C(6)- and C(12)-methyl groups were replaced by 4-azidobutyl groups were

298 ed to 1, possibly due to the presence of the methyl group, which allows favorable hydrophobic and van

299 m (1)H/(13)C NMR probes at isoleucine delta1 methyl groups, which facilitated (1)H/(13)C methyl TROSY

300 e, we study how AP-1 and Zta recognize these methyl groups within their cognate response elements.