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1 enediamine, 1,2-pn; isobutylenediamine, ibn; trans-(+/-)-1,2-diaminocyclohexane, dach; 1,3-propylened
2 A healthy man was given an oral dose of all-trans [10,10',11,11'-(14)C]-beta-carotene (1.01 nmol; 10
3 Following photoaffinity labeling with all-trans-[11,12-(3)H]retinoic acid, the most abundant label
5 anar, bond-equalized radical anion of 1,7-di-trans-[12]annulene (4a(*-)) is lowest in energy; several
6 l anion, [16]annulene radical anion, and tri-trans-[12]annulene radical anion indicate that electron
8 the formation of the anion radical of 1,5-di-trans-[12]annulene, which loses hydrogen and undergoes r
9 o yield two isomers of [12]annulyne (3,11-di-trans-[12]annulyne and 5,9-di-trans-[12]annulyne), both
11 ulyne (3,11-di-trans-[12]annulyne and 5,9-di-trans-[12]annulyne), both of which exhibit a weak paratr
12 -(+)-MR200], cis-(-)-1a [cis-(-)-MR201], and trans-(+/-)-1a [trans-(+/-)-MR204], have been identified
13 hese data clearly demonstrated that compound trans-(+)-1d, due to its sigma1 agonist activity and fav
16 evidenced that trans-(+)-1d, in contrast to trans-(-)-1d, cis-(+)-1d, or cis-(-)-1d, which behave as
18 DPE (100 nmol), but not by the kappa agonist trans-(1S,2S)-3,4-dichloro-N-mathyl-N-[2-(1-pyrrolidinyl
19 propanation biocatalysts complements that of trans-(1S,2S)-selective variants developed here and prev
22 opropane-1-carboxylic acid], and trans-DCCA [trans-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane-1-car
23 .68%), d-allose (3.67%) and 5-Caranol, trans,trans-(+)- (2.14%) were identified from Halodule pinifol
24 MAPA are mostly close to statistical (gauche/trans = 2/1) in other protic solvents, e.g., alcohols.
25 ioavailability of cis (24.5% +/- 6%) and all-trans (23.2% +/- 8%) isomers did not differ, endogenous
27 inima: two doubly trans (26, 27), one triply trans (28), one singly trans (29), one quintuply trans (
28 (26, 27), one triply trans (28), one singly trans (29), one quintuply trans (trannulene-type, 33), a
29 synthesis of a C-activated N-Fmoc-protected trans-(2S,3S)-3-aminotetrahydrofuran-2-carboxylic acid a
30 it 2, resulting in identification of racemic-trans-(3-((4-(aminomethyl)-6-(trifluoromethyl)pyridin-2-
32 (DAMGO), [D-Ala2,D-Leu5]-enkephalin (DADLE), trans-(+/-)-3,4-dichloro-N-methyl-N-(2-[1-pyrrolidinyl]c
33 H-3-benzaze pine hydrochloride) and U50488H (trans-(+/-)-3,4-dichloro-N-methyl-N-[2-(pyrrolidinyl)cyc
37 ectric field showed a significant release of trans-(4.01+/-0.48) and cis-(5.04+/-0.26mug/g) lycopene,
38 enriched not naturally occurring isomers of trans-(-)-(4R,5S)-4b or cis-(+)-(4R,5R)-4a were formed p
39 idiella resinae KCH50 afforded a mixtures of trans-(+)-(4S,5R)-4b with enantiomeric excess ee=99% and
43 esion exists as a mixture of cis-(5R,6S) and trans-(5R,6R) epimers; these modulate base excision repa
45 hat over three-quarters of these eQTL act in trans (78%) and that 86% of these differentially regulat
46 3.1.0(2,7)]dodecane moiety having either the trans (8a-e) or cis (9a-e) relative configuration of the
47 w specificity: many aldehydes, including all-trans-, 9-cis-, 11-cis-, and 13-cis-retinals and even be
48 ,O = kappa2-O,O-acetylacetonate, -Ir- is the trans-(acac-O,O)2Ir(III) motif, R = CH3, C2H5, Ph, PhCH2
49 f libraries to provide a prediction of which trans -acting factors binding sites are disrupted/create
51 ffinity of r(K57D)K3 for the lysine analogue trans-(aminomethyl)cyclohexanecarboxylic acid (AMCHA) wa
52 B-DNA complex formation was similar with (+)-trans- and (+)-cis-BPDE-adducted substrates, suggesting
53 study, we have measured the effects of all -trans- and 11- cis-retinals and -retinols on the opsin's
56 ocols for the high-yielding synthesis of 2,3-trans- and 2,3-cis-6-methoxy-3-substituted morpholine-2-
59 weak acid to give the 1,2-difurylethylenes, trans- and cis-1,2 di(2-(5-phenylfuryl))ethene (trans-1
60 uction" protocol was successfully applied to trans- and cis-2-methyl-N-(pyridin-2-yl)-6-undecylpiperi
61 573 K, and the relative epoxidation rates of trans- and cis-alkenes showed that calixarene ligands di
62 owever, we have successfully docked both the trans- and cis-amide isomers of the benzoquinone ansamyc
63 oxidoreductase 1 (NQO1) in the metabolism of trans- and cis-amide isomers of the benzoquinone ansamyc
64 results of these studies indicate that both trans- and cis-amide isomers of the hydroquinone ansamyc
66 arietal difference in carotenoids as well as trans- and cis-beta-carotenes were noted in both the raw
67 ports the analysis of total carotenoids, and trans- and cis-beta-carotenes, in different varieties of
68 product distributions from the reactions of trans- and cis-beta-methylstyrene reveal that the reacti
69 d for alpha, beta, and gamma isomers of HCH, trans- and cis-chlordane, oxychlordane, or SigmaCHB.
70 pounds determined in both air and water were trans- and cis-chlordanes (TC, CC), trans- and cis-nonac
73 difference between the responses of Notch to trans- and cis-Delta: whereas the response to trans-Delt
74 romatography analysis, which can resolve the trans- and cis-diastereoisomers of alpha-(N(2)-deoxyguan
76 emonstrated here would be useful to evaluate trans- and cis-elements that affect rate of the translat
78 type 1 (HIV-1) to CD4(+) T cells through the trans- and cis-infection pathways; however, little is kn
79 n elaborately designed process in which both trans- and cis-interactions are fine-tuned collectively
80 uces intercellular adhesion clusters through trans- and cis-intercadherin bonds, and the intracellula
82 the aqueous ozonolysis reaction products as trans- and cis-lactols [4-(5-hydroxy-2,2-dimethyltetrahy
83 ter were trans- and cis-chlordanes (TC, CC), trans- and cis-nonachlors (TN, CN), heptachlor exo-epoxi
86 RH transcription factors, but vary widely in trans- and cis-requirements for these inputs and their b
87 ulfide cross-links provide clear readouts on trans- and cis-SNARE arrangements during this fusion eve
89 ficant differences in total UCA content, and trans- and cis-UCA contents between the two samples.
90 s study, the amino acid, biogenic amine, and trans- and cis-urocanic acid (UCA) contents of fifteen c
93 barrier dysfunction that includes increased trans- and para-cellular leakage caused by impaired ente
94 in the transition structures determines high trans- and syn-diastereoselectivities for aldol reaction
96 etone catalyst for asymmetric epoxidation of trans- and trisubstituted olefins was efficiently prepar
97 died catalysts, is an effective catalyst for trans- and trisubstituted olefins, and up to 97% ee has
98 nantioselectivity for hydroboration of cis-, trans-, and gem-disubstituted alkenes in excellent agree
100 in the highest quartile of trans-zeaxanthin, trans -anhydro-lutein, and trans-, cis-, and total beta-
101 [ a]pyrene-derived N (2)-dG adduct, 10 S(+)- trans- anti-[BP]- N (2)-dG ([BP]G*), reveal that an inco
102 he RPTPmu ectodomain that forms a homophilic trans (antiparallel) dimer with an extended and rigid ar
103 YP26A1, which catalyzes the oxidation of all-trans (at)-retinoic acid (RA), is induced moderately by
104 induced receptor dimerization and consequent trans- auto-phosphorylation are among the earliest event
105 ably efficient translesion bypass of the (+)-trans-[BP]-N(2)-dG adducts is observed in all sequences
108 n cell signaling revealed that expression of trans- but not cis-null JAM-A mutants decreased Rap2 act
109 cular docking simulations indicated that the trans- but not the cis-amide isomers of the benzoquinone
112 C. polonica revealed that the levels of 2,3-trans-(+)-catechin and PAs that are produced in the tree
113 orescence anisotropy analysis, for which the trans (cis) isomer in DOPC (DPPC) presents a fast decay
114 e variety of substituted styrenes, including trans-, cis-, and beta,beta-disubstituted styrenes, to y
115 ction was further studied by the reaction of trans-, cis-, and gem-ethylene-d2 upon activation of Cr(
116 trans-zeaxanthin, trans -anhydro-lutein, and trans-, cis-, and total beta-carotene had significant 43
118 nd Ac-NDP-gamma-MSH-NH(2) replaced by Pro or trans-/cis-4-guanidinyl-Pro derivatives were designed an
119 OH)](+)), and Os(IV)-methoxyhydrazido (e.g., trans-/cis-[Os(IV)-N(H)N(H)(OMe)](+), and trans-/cis-[Os
121 2))][PF(6)](2), 2[PF(6)](2), a derivative of trans-[Cl(dppe)(2)Ru(C triple bond C)(6)Ru(dppe)(2)Cl] f
122 MCl2; cagelike adducts of the in,in isomer, trans- Cl2(P((CH2)14)3 P) (M = 2/Pt, 3/Pd, 4/Ni), then f
124 cts of both long-range intra-chromosomal and trans (cross-chromosomal) regulation, we observe modular
125 ost stable in vacuo, while the cis-trans-cis-trans (ctct) or trans-cis-trans-cis (tctc) amide conform
126 ts have been achieved using compounds with a trans-[CuX(4)Y(2)] coordination sphere, which seems to a
127 species could be attributed to both cis- and trans- DNA sequence changes during evolution, but it is
129 rotary motors that harness photoinduced cis-trans (E-Z) isomerization are promising tools for the co
130 atory evolution in both cis (e.g., Creb) and trans (e.g., fork head) for nearly 2000 genes, many of w
131 As we expected, both significant cis- and trans- effects are responsible for the expression diverg
132 expression markers, by integrating cis- and trans- effects from many genomic loci, may overcome limi
136 , CH2Cl2, reflux) give the cage-like trienes trans- Fe(CO)3(P((CH2)mCH horizontal lineCH(CH2)m)3 P) (
137 , 60-80 degrees C) yield the title compounds trans- Fe(CO)3(P((CH2)n)3 P) (4a-c,e, 74-86%; n = 2m + 2
138 )2)4) afford the metal hydride complexes mer,trans-[ Fe(CO)3(H)(P((CH2)n)3 P)](+)BArf(-) (6a-c,e(+)BA
139 n alcohol, new iron dicarbonyl complexes mer-trans-[Fe(Br)(CO)2(P-CH horizontal lineN-P')][BF4] (wher
140 atmosphere to produce the complexes cis- and trans-[Fe(Br)2(CO)(P-CH horizontal lineN-P')]; (2) the r
141 active system generated from the precatalyst trans-[Fe(CO)(Br)(Ph(2)PCH(2)CH horizontal lineN-((S,S)-
142 he mechanism of transfer hydrogenation using trans-[Fe(NCMe)CO(PPh(2)C(6)H(4)CH horizontal lineNCHR-)
143 s, leading to the formation of catechin [2,3-trans-(+)-flavan-3-ol] and epicatechin [2,3-cis-(-)-flav
144 e with their role in the biosynthesis of 2,3-trans-(+)-flavan-3-ols, transcript abundance of Norway s
145 t enzyme involved in the biosynthesis of 2,3-trans-(+)-flavan-3-ols, were identified and functionally
146 -handed all-cis (Form I) and left-handed all-trans (Form II), were determined in the crystalline stat
148 Importantly, expression of gB and gH/gL in trans (gB-expressing cells mixed with other gH/gL-expres
149 NMR dynamics studies show monomers with all trans (Gly-Pro-Hyp)(4) are less flexible than monomers c
152 ups ortho to the azo group, exhibits minimal trans-->cis photoisomerization and extremely rapid cis--
155 xhibit a high photochemical conversion rate (trans --> cis > 98%) and no measurable fatigue over a la
159 all isomeric states of an azobenzene moiety (trans --> cis-(M) --> cis-(P)) are passed step by step.
160 2 elimination the chlorostannylidene complex trans-[H(dmpe)2Mn horizontal lineSn(Cl)(C6H3-2,6-Mes2)]
161 tatively into the stannylidyne complex salts trans-[H(dmpe)2Mn identical withSn(C6H3-2,6-Mes2)]A [A =
165 eplication, some of which can be provided in trans (i.e., via expression from a separate RNA molecule
166 mechanistic study of the reaction of O2 with trans-(IMes) 2Pd(H)(OBz), 1 (IMes = 1,3-dimesitylimidazo
168 plicable for large-scale mapping of cis- and trans- interaction networks of genomic elements and for
171 onditions in CH3CN/TEOA, a common reactive C-trans-[Ir(tpy)(ppy)](0) species, irrespective of the sta
174 d with the more electron-rich model reactant trans-[IrMe(PMe3)2(PMe2Et)] and the higher barriers foun
175 s were modeled using HCCR as weak acids, and trans-{kappaC,N-(3,4,5-(F)3-C6H2)CH2N horizontal lineCH(
180 2)(PhCN)(2)] afforded the Group 10 complexes trans-[MCl(2)(1)(2)] (3a-c, M = Ni, Pd, and Pt, respecti
181 crystal structures of a family of compounds trans-[MCl(2)(NC(5)H(4)X-3)(2)] (M = Pd(II), Pt(II); X =
183 = N,N,N',N'-tetramethylethylenediamine) with trans-[MCl(2)(Pn-Bu(3))(2)] [M = Ni (trans-6a) and Pd (t
184 samples of the cyclic phosphazenes, cis- or trans-[Me(Ph)PN](3), yielded mixtures of the cis and tra
186 of its components, suggest that for G:C W:W Trans , Mg(2+) binding can fine tune the basepair geomet
187 lfide/peroxide bonds, relative to the end-on trans- micro -1,2 structure, which forms two bonds to th
188 -(-)-1a [cis-(-)-MR201], and trans-(+/-)-1a [trans-(+/-)-MR204], have been identified as new potent s
189 l effects on CHGA expression, and that a cis:trans (mRNA:miR) interaction regulates the association o
190 e activates the kinase domain of Stt7 on the trans (negative) side, leading to phosphorylation and re
191 ion of O2 into the palladium-hydride bond of trans-(NHC)2Pd(H)OAc (NHC = N-heterocyclic carbene).
193 omplexes featuring a single fluoride ligand (trans-[Ni(F)(2-C5NF4)(PR3)2], R = Et 1a, Cy 1b, trans-[P
196 ession in cis (in the sensory neurons) or in trans (on neighboring visceral mesoderm) transforms abdo
199 ls and cell membrane were incubated with all-trans- or 11-cis-retinol to study retinyl ester synthesi
202 The stereoselective synthesis of either trans- or cis-3,5-disubstituted pyrazolidines is accompl
203 lyze the hydrolytic dehalogenation of either trans- or cis-3-haloacrylates to yield malonate semialde
206 (2)]), Os(II)-nitrosyl [Os(II)-NO](+) (e.g., trans- or cis-[Os(II)-NO](+)), Os(IV)-hydroxyhydrazido (
210 c dihydroxylation is converted into either a trans- or cis-epoxide, and these are subsequently conver
211 onditions for maintenance of and invasion by trans- or cis-plus-trans-controlled hotspots are broader
212 Amino acid-dependent selectivity for either trans- or cis-substituted piperazinone products has been
213 at it represents an intermediate step in the trans- or dedifferentiation of neurons into astrocytes.
214 SR events occur between chromosome homologs (trans- or interallele CSR), suggesting that the homologo
215 chromosome kissing" between two DNA sites in trans (or in cis) is known to facilitate three-dimension
216 e)]PF(6) = [2]PF(6)), and phosphoraniminato (trans-[Os(IV)(Tp)(Cl)(2)(NP(H)(Et)(2))] = [3], Tp(-) = t
217 ydroquinone (H(2)Q) by the Os(IV) hydrazido (trans-[Os(IV)(tpy)(Cl)(2)(N(H)N(CH(2))(4)O)]-PF(6) = [1]
218 tpy = 2,2':6',2"-terpyridine), sulfilimido (trans-[Os(IV)-(tpy)(Cl)(2)(NS(H)-4-C(6)H(4)Me)]PF(6) = [
219 ions between the Os(VI)-nitrido salts (e.g., trans-[Os(VI)(tpy)(Cl)(2)(N)]PF(6) (tpy = 2,2':6',2"-ter
220 ization of the air-stable nickel(II) complex trans-(PCy(2)Ph)(2)Ni(o-tolyl)Cl is described in conjunc
221 ns-[Ni(F)(2-C5NF4)(PR3)2], R = Et 1a, Cy 1b, trans-[Pd(F)(4-C5NF4)(PCy3)2] 2, trans-[Pt(F){2-C5NF2H(C
222 on that kinetic factors inhibit formation of trans-[Pd(IMes)2(eta(1)-O2)2] at the low temperatures at
223 tion diagram is constructed for formation of trans-[Pd(IPr)2(eta(1)-O2)2] and leads to the conclusion
227 o detect the predicted T-shaped intermediate trans-[Pd(NHC)2(eta(1)-O2)] for either NHC = IMes or IPr
228 ic potential distributions for the compounds trans-[PdCl(2)(NC(5)H(4)X-3)(2)] (X = F, Cl, Br, I) demo
229 nsmetalation from 2 to [NiCl(2)(PPh(3))(2)], trans-[PdCl(2)(PhCN)(2)], or trans-[PtCl(2)(PhCN)(2)] af
230 cinchona alkaloid derivatives; surprisingly, trans-(Ph(3)P)(2)PdCl(2) was found to afford the most dr
231 3)Rh(F)] reacts with CF(3)SiMe(3) to produce trans-[(Ph(3)P)(2)Rh(CF(2))(F)] (1; X-ray), which is equ
232 conditions (3 h at 80 degrees C) to produce trans-[(Ph(3)P)(2)Rh(Ph(2)PF)(Cl)] (2) and ArPh as a res
233 degrees C), 1 decomposes to a 1:1 mixture of trans-[(Ph(3)P)(2)Rh(Ph(2)PF)(F)] (3) and the cyclometal
234 the thermodynamics of addition of methane to trans-(PH3)2IrX are generally strongly disfavored by inc
236 ons were performed on an extensive series of trans-(PH3)2IrXL complexes (L = NH3 and CO; X = various
237 form the palladium cyclopentylmethyl complex trans-[(phen)Pd[CH2CHCH2C(CO2Me)2CH2CHCH2SiEt3](NCAr)]+
238 Thus cis-(PMe(3))Cr(CO)(4)(H(2)) (3) and trans-(PMe(3))Cr(CO)(4)(H(2)) (4) were prepared and char
239 C(5)H(4)N)(2)-p-C(2)B(10)H(10) (1) and 1,12-(trans-(Pt(PEt(3))(2)I)CC)(2)-p-C(2)B(10)H(10) (2), are r
240 pped intermediates to the native molecule by trans-[Pt(en)(2)Cl(2)](2+) may be helpful in facilitatin
241 1a, Cy 1b, trans-[Pd(F)(4-C5NF4)(PCy3)2] 2, trans-[Pt(F){2-C5NF2H(CF3)}(PCy3)2] 3 and of group 4 dif
242 The octahedral Pt(IV) complex trans,trans,trans-[Pt(N(3))(2)(OH)(2)(py)(2)] (1) is potently cytoto
243 anticancer platinum(IV) complex trans,trans,trans-[Pt(N3 )2 (OH)2 (MA)(Py)] (MA=methylamine, Py=pyri
244 d, consequently, the cytotoxicity of cis,cis,trans-[Pt(NH3)2Cl2(O2CCH2CH2COOH)(OCONHR)], 4, where R i
245 ands (and carboxylate ligands in general) in trans-[Pt(OAc)(2)(L)(L')] results in significantly enhan
249 2)(PPh(3))(2)], trans-[PdCl(2)(PhCN)(2)], or trans-[PtCl(2)(PhCN)(2)] afforded the Group 10 complexes
250 ]Cl(2), cis-[PtCl(2)(a(5)-PhobPCH(2)OH)(2)], trans-[PtCl(2)(s-PhobPBu)(2)], and trans-[PtCl(2)(a(7)-P
251 S spectroscopy, trans-[Pt(OAc)2(ox)(en)] and trans-[PtCl2(OAc)2(en)] were observed to be reduced at a
252 oduced instead, along with novel difluorides trans-[(Py)(2)Pd(F)(2)] (3) and trans-[(t-BuPy)(2)Pd(F)(
254 Direct and selective mono-N-pyridylation of trans-(R,R)-cyclohexane-1,2-diamine is described here.
256 -), cis-[Re(4)Os(2)Se(8)(CN)(6)](2-/3-), and trans-[Re(4)Os(2)Se(8)(CN)(6)](2-/3-) couples at E(1/2)
257 An S = 3/2, high-anisotropy building unit, trans-[ReCl(4)(CN)(2)](2-), representing the first param
258 urces of information, we identified putative trans- regulators for a variety of metabolic pathways.
259 ated carbon powder with one of the complexes trans-[ReO(2)(py-X)(4)](+) (py-X = 4-substituted pyridin
260 ) (1)J(PSe) for PhobP(Se)Bu; (ii) nu(CO) for trans-[RhCl(CO)(PhobPBu)(2)], (iii) (1)J(PtP) for the PE
261 mers (PAOs) with the general structure trans,trans-[(RO)3Ph-C[triple bond]C-Pt(PMe3)2-C[triple bond]C
263 fac-[Ru(II)Cl(2)(DMSO)(3)(CTZ)] (1), cis,cis,trans-[Ru(II)Cl(2)(DMSO)(2)(CTZ)(2)] (2), Na[Ru(III)Cl(4
264 I analogs of a general structure [4-R-pyH](+)trans-[Ru(III)Cl4(DMSO)(4-R-py)](-), where 4-R-py stands
266 ammatory activity of ruthenium(II) complexes trans-[Ru(NO(+))(NH3)4(L)](BF4)3 and [Ru(NH3)5(L)](BF4)3
267 ld (Phi(S)(-->)(O) = 0.25), isomerization of trans-[Ru(tpy)(pic)(dmso)](+) occurs with a time constan
269 xes [Ru(tpy)(bpy)(dmso)](OSO(2)CF(3))(2) and trans-[Ru(tpy)(pic)(dmso)](PF(6)) (tpy is 2,2':6',2' '-t
270 nation of acetophenone by the chiral complex trans-[RuCl2{(S)-binap}{(S,S)-dpen}] and KO-t-C4H9 in pr
271 CHPh)2NH2}] and the 18e(-) Ru alkoxo complex trans-[RuH{OCH(CH3)(R)}{(S)-binap}{(S,S)-dpen}] (R = CH3
272 of the Noyori ketone hydrogenation catalyst trans-[RuH2((R)-BINAP)((R,R)-dpen)] (1a) yields trans-M[
274 formation of the potassium amidato complexes trans-[RuH2{(S)-binap}{(S,S)-N(K)H(CHPh)2NH2}] or trans-
276 e example is the 1:1 charge-transfer complex trans--stilbene-2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoqu
277 on reaction and the ratio of trans,cis/trans,trans (t,c/t,t)-conjugated diene oxidation products form
279 ns-[(Py)(2)Pd(Ph)(F)] (1; Py = pyridine) and trans-[(t-BuPy)(2)Pd(Ph)(F)] (2; t-BuPy = 4-tert-butylpy
280 ticancer agents, especially NKP-1339 (sodium trans-[tetrachloridobis(1H-indazole)ruthenate(III)]), wh
282 te(III)] (1, KP1019) and its analogue sodium trans-[tetrachlorobis(1H-indazole)ruthenate(III)] (2, KP
283 especially the clinically studied indazolium trans-[tetrachlorobis(1H-indazole)ruthenate(III)] (KP101
284 enate(III)] (KP1019) and its analogue sodium trans-[tetrachlorobis(1H-indazole)ruthenate(III)] (NKP-1
290 mains of both the cis (GS(m)-bound ring) and trans (the opposite substrate-free ring) show counterclo
292 th the low thermal activation barrier of the trans- to cis-isomerization typical for imine derivative
293 -12)) and one variant regulating 53 genes in trans (top trans interaction: ZNF423, rs3851570, p = 8.2
295 s and presents IL-15 to neighboring cells in trans (trans-presentation of IL-15) through cell-cell co
296 This study revealed the preferential all-trans (TTT) conformation of the three ethylenedioxy link
297 ry that two aspects of lectin functionality (trans- versus cis-activity) respond non-uniformly to a s
299 s N1 cyclization) and the stereoselectivity (trans- vs cis-fused ring system) of the cyclization proc
300 he form H(2)[pz(A(4-n);C(n))], n = 1, and 2 (trans-), where "A" represents peripheral heteroatom (S-
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