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1 o the fuel precursor 2,5-dimethyl furan (2,5-DMF).
2 st molecules, such as N,N-dimethylformamide (DMF).
3 on of biosensors into digital microfluidics (DMF).
4 tegration of ECL with digital microfluidics (DMF).
5 queous desulfurization system (Fe(III/II)-IL/DMF).
6 conditions examined (up to 140 degrees C in DMF).
7 and embedded sensors: "plug-n-play DMF" (PnP-DMF).
8 r solvothermal treatment at 200 degrees C in DMF.
9 rs of disease activity during treatment with DMF.
10 AP recapitulated the antifibrotic effects of DMF.
11 the hydrolytic cleavage of the amide bond in DMF.
12 s applicable to all biosensors integrated to DMF.
13 teine 38 being essential for the activity of DMF.
14 in the compound (K[222-crypt])4 [Sn14 Ni(CO)]DMF.
15 by iron(tetramesitylporphyrin) (Fe(TMP)) in DMF.
16 re collected at baseline and 12 months after DMF.
17 hione (GSH) abrogated ULBP2/5 upregulated by DMF.
18 ransfer and TU to stabilize metal cations in DMF.
19 at baseline, and 1, 3, 6 and 12 months after DMF.
20 nase IRAK4 as a principal cellular target of DMF.
21 on going from nonpolar toluene to more polar DMF.
22 g were associated with the rate of change in dmfs.
23 t [Ni(II)(2)Dy(III)(2)L(4)(DMF)(6)] 2(OTf) 2(DMF) (1) promotes the domino reaction of furfural and am
24 ated with the integration of biosensors into DMF: (1) complete removal of the droplet containing the
26 2 (L3)(H2 O)2 ]n (NJU-Bai 42), and [Cu2 (L4)(DMF)2 ]n (NJU-Bai 43) were prepared and we observed that
27 rmal crystallisation of a new MOF [Yb2(BDC)3(DMF)2]H2O (BDC=benzene-1,4-dicarboxylate and DMF=N,N-dim
28 diiron(II) complex, [Fe(2)(N-Et-HPTB)(NO)(2)(DMF)(2)](BF(4))(3) (2) with [{FeNO}(7)](2) formulation a
29 acid as modulators: [Bi(2)(cpb)(acetato)(2)(dmf)(2)].2dmf CTH-6 forms a rtl-net; 2(H(2)NMe(2))[Cu(2)
30 H-11, show kgd-nets; [Cu(2)(cpb)(acetato)(2)(dmf)(2)].2dmf, CTH-12, forms a mixed coordination and hy
32 on cooling, it resolidifies as solid NaClO4 (DMF)3 , permitting melt casting of the electrolyte into
33 Pressed pellets of microcrystalline NaClO4 (DMF)3 exhibit a conductivity of 3x10(-4) S cm(-1) at roo
36 yl diiron(II) complex, [Fe(2)(N-Et-HPTB)(NO)(DMF)(3)](BF(4))(3) (1) (N-Et-HPTB is the anion of N,N,N'
38 perlattice of monodisperse [Cd54Se32(SePh)48(dmf)4](4-) nanoclusters; the second is a unique porous C
39 H-7 forms a kgd-net; [Fe(4)(cpb)(acetato)(2)(dmf)(4)] CTH-8 and [Co(4)(cpb)(acetato)(2)(dmf)(4)] CTH-
40 )(dmf)(4)] CTH-8 and [Co(4)(cpb)(acetato)(2)(dmf)(4)] CTH-9 are isostructural and form yav-nets; 2(HN
41 RFS], 29%; distant metastasis-free survival [DMFS], 53%; prostate cancer-specific survival [PCSS], 78
42 bimetallic catalyst [Ni(II)(2)Dy(III)(2)L(4)(DMF)(6)] 2(OTf) 2(DMF) (1) promotes the domino reaction
43 y basal prostate cancers (10-year bRFS, 39%; DMFS, 73%; PCSS, 86%; OS, 80%) and luminal A prostate ca
50 tudies thus identify a proteomic hotspot for DMF action that constitutes a druggable protein-protein
53 be positioned between digital microfluidics (DMF) addressing each droplet individually using 2D array
58 need, we examined whether dimethyl fumarate (DMF), an anti-inflammatory drug already in clinical use
60 he addition of trifluoroethanol (TFE), DMSO, DMF and acetone, uniform fiber-like nanoparticles from P
62 and two transformation products of amitraz (DMF and DMPF), were quantified at higher levels in wax a
63 PY to the chlorin moiety in both toluene and DMF and exhibits intense fluorescence of chlorin upon ex
65 high-throughput screening (HTS) methodology, DMF and NaHCO3 were rapidly identified as the most effec
66 se results reveal a new molecular target for DMF and show that a clinically approved drug inhibits M1
67 high risk of PML, were switched from NTZ to DMF and underwent neurological and 3T MRI monitoring for
69 )benzene (H3BTTri) in N,N-dimethylformamide (DMF) and methanol leads to the formation of Co-BTTri (Co
70 adical (CumO(*)) with N,N-dimethylformamide (DMF) and N,N-dimethylacetamide (DMA) was studied by lase
72 at the combination of N,N-dimethylformamide (DMF) and TU has the remarkable ability to form intermedi
73 ere), mOFC/vmPFC, or dorsomedial prefrontal (DMF), and a comparison group of healthy age- and educati
74 hyl acetate, acetone, alcohol, acetonitrile, DMF, and DMSO, identify complex solvent systems, as well
75 ctivity for Br-capped acrylate chain ends in DMF, and moderate activity toward C-F bonds at room temp
78 ulfurizer, Fe(II) and N,N-dimethylformamide (DMF) are introduced to Fe(III)-IL to construct a new non
80 domonas, and Alcaligenes have evolved to use DMF as a sole carbon and nitrogen source for growth via
81 his study was to assess the effectiveness of DMF as a therapy for PAH using patient-derived cells and
83 of dioxygen catalyzed by iron porphyrins in DMF as an example, decreasing [HA] 10-fold lowers etaeff
87 loromethane (DCM) and N,N-dimethylformamide (DMF) as solvents) and relies on the utilization of the g
89 ylacetamide (DMA) and N,N-dimethylformamide (DMF), as the background electrolyte (BGE) to improve the
90 ploying K2CO3 as a base in refluxing THF and DMF at 80 degrees C, respectively, delivers 2-aroylbenzo
92 using Selectfluor in the presence of CsF in DMF at room temperature for 15-60 min provided beta-keto
93 s with the treatment with sodium ethoxide in DMF at room temperature provided highly substituted trie
95 ght, breastfeeding and maternal smoking with dmfs at baseline and over time (trajectories) were asses
97 thin films processed from dimethylformamide (DMF)-based solutions to which either no additive, dimeth
98 nt-related difference was seen in the 5-year DMFS between the observation and CLND arms (67.6% v 64.9
102 shelf agent, appears to be a redox analog of DMF, but its immunomodulatory properties have not been p
103 nthesized and used a novel chemical probe of DMF by incorporating an alkyne functionality and found t
105 tion of benzyl bromide and sodium hydride in DMF can lead to the formation of an amine side product,
109 s Dy2(INO)4(NO3)22 solvent (solvent=DMF (Dy2-DMF), CH3CN (Dy2-CH3CN)), thereby switching the effectiv
111 ating an alkyne functionality and found that DMF covalently modifies p65, with cysteine 38 being esse
113 ges are (1) delivering biological samples to DMF devices and (2) accurately controlling temperatures
114 fabricated into the ITO-coated top plates of DMF devices, allowing for the generation of light from e
119 n (4-nitrophenol and [DMF.H(+)](CF3SO3(-))) (DMF = dimethyl-formamide) or electron (decamethylferroce
120 nzimidazolyl))-2-hydroxy-1,3-diaminopropane; DMF = dimethylformamide) with [Fe(II){FeNO}(7)] formulat
122 agent, N,N-dimethylformamide dimethylacetal (DMF-DMA) and tetramethylammonium hydroxide (TMAH) as met
126 the phases Dy2(INO)4(NO3)22 solvent (solvent=DMF (Dy2-DMF), CH3CN (Dy2-CH3CN)), thereby switching the
129 f the TU-metal chloride complex formed after DMF evaporation is critical to prevent volatilization of
132 rylmethyl bromides using t-BuOK as a base in DMF, followed by Pd(0)-mediated intramolecular Heck coup
133 methodology, based on digital microfluidics (DMF), for rapid determination of individual alterations
135 rollable synthesis of N,N-dimethylformamide (DMF) from dimethylamine and CO(2)/H(2) via blocking reac
136 n at -75 degrees C followed by reaction with DMF gave 2-formyl-4-chloro-3-fluoropyridine 10 regiosele
140 toward different proton (4-nitrophenol and [DMF.H(+)](CF3SO3(-))) (DMF = dimethyl-formamide) or elec
141 framework Co-BDTriP (Co3[(Co4Cl)3(BDTriP)8]2.DMF; H3BDTriP = 5,5'-(5-(1H-pyrazol-4-yl)-1,3-phenylene)
144 itu amine functionalized TMU-60 [Zn(OBA)(L*).DMF] has the potential of converting to a conductor due
146 (PFS), and distant metastasis-free survival (DMFS) (Hazard Ratios [HRs] = 3.5, 3.1, and 3.8, respecti
148 sented here highlight the versatility of PnP-DMF, illustrating how it may be useful for a wide range
151 ur understanding of the proteins modified by DMF in human immune cells and the functional consequence
152 drug, our findings support a broader use of DMF in treatment of cancers and inflammatory conditions.
153 uggest that the antiinflammatory activity of DMF in treatment of MS patients may occur through altern
156 ction is performed in N,N-dimethylformamide (DMF) in a continuous membrane reactor which retains the
157 o explore the efficacy of dimethyl fumarate (DMF) in preventing disease reactivation after NTZ discon
158 number of decayed, missing, or filled teeth (dmfs) in caries-active children, number of episodes of p
161 ver, 36% of the intervention effect on 24-mo DMFS increment was through a mediation effect on 12-mo o
164 d the clinically approved dimethyl fumarate (DMF) induce a cellular antiviral program that potently i
169 ermeable thiol N-acetyl l-cysteine, reverses DMF inhibition of the NFkappaB pathway, supporting the n
172 the block in K63 and/or M1 chain formation, DMF inhibits NFkappaB and ERK1/2 activation, resulting i
174 have recently shown that dimethyl fumerate (DMF) inhibits NF-kappaB acting as a survival factor in C
176 decayed, missing, and filled tooth surfaces (dmfs) (intercept) and rate of change in dmfs over time (
177 ormamidine (DMPF) and 2,4-dimethylformamide (DMF) into 2,4-dimethylaniline (DMA), directly from QuECh
181 show that DMFase from Paracoccus sp. strain DMF is a halophilic and thermostable enzyme comprising a
182 ent is of particular promise in CTCL because DMF is already in successful clinical use in the treatme
186 se models, prompting us to determine whether DMF is effective as a treatment for SSc dermal fibrosis.
195 and contributes to our understanding of how DMF may act clinically to ameliorate pathological proces
198 perties, both thermotropic and lyotropic (in DMF) mesophases were observed in one of metallacycles, i
199 ced in solvent of high dielectric constants (DMF), most likely by photoinduced electron transfer.
201 enedicarboxylic acid, l-lac = l-lactic acid, dmf = N,N'-dimethylformamide) and observed an increase i
202 from the C-H bonds of N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMA), N-formylpyrrolidine (
203 DMF)2]H2O (BDC=benzene-1,4-dicarboxylate and DMF=N,N-dimethylformamide) under solvothermal conditions
204 s of the various areas that comprise the VLF-DMF network in learning rule-based cognitive selections
205 that the basic function expressed by the VLF-DMF network is to exert cognitive control of orofacial a
206 on experiments using polar solvents, such as DMF, no "mixed" products possessing structurally differe
209 al results demonstrate beneficial effects of DMF on key molecular pathways contributing to PAH, and s
210 examined and compared the effects of EP and DMF on MS-relevant activity/functions of T cells, macrop
211 the protective effects of dimethyl fumarate (DMF) on CsA-induced nephrotoxicity by enhancing the anti
216 solvothermal reactions in dimethylformamide (dmf) or dimethylacetamide (dmac) with acetic acid or for
217 ces (dmfs) (intercept) and rate of change in dmfs over time (slope) was examined in 2-level linear mi
222 imal geometry of the sensing surface and the DMF platform providing successful removal of the target
223 he optimum configuration is implemented on a DMF platform with an interdigitated capacitive biosensor
226 face features that have been integrated on a DMF platform: a reagent delivery system and a thermal co
234 nally, we showed that chronic treatment with DMF reduced the firing of the ON cells (cells responding
235 y provides Class II evidence that first-line DMF reduces NFL in both blood and CSF after 6 months and
239 s is not superior to observation in terms of DMFS, RFS, or OS and support not recommending CLND in pa
240 ondrial gene expression is more dependent on DMF's target Nrf2 than hydroxycarboxylic acid receptor 2
241 -free alkylation with methyl bromoacetate in DMF, saponification, and cyclization with acetic anhydri
244 as synthesized by heating dimethylformamide (DMF) solution of the known Ni-centered and Ni(CO)-capped
251 decayed, missing, and/or filled adult teeth [DMF-T] index); 2) gingival inflammation (papillary bleed
252 ic acid esters, including dimethyl fumarate (DMF, Tecfidera; Biogen, Cambridge, MA), have shown thera
253 Dimethyl succinate, the inactive analog of DMF that lacks the electrophilic double bond of fumarate
254 te based ultramicroporous MOF, 1 [Ni-(4PyC)2.DMF], that has the lowest PE for postcombustion CO2 capt
268 ical and radiological activity preceding the DMF treatment might be used as a prognostic marker of th
269 the antiinflammatory contribution of Nrf2 in DMF treatment of the MS model, experimental autoimmune e
273 number of relapses and MRI parameters before DMF treatment were good predictors of disease activity d
276 pression of ULBP2/5 and were unresponsive to DMF treatment, suggesting that the fumarate-stimulating
281 Finally, we demonstrate the ability of the DMF-TU molecular ink chemistry to lead to high-photovolt
282 is paper provides "proof of concept" for PnP-DMF using commercial biosensors for glucose and beta-ket
283 es a mechanism of the antifibrotic effect of DMF via inhibition of Akt1/GSK3beta/TAZ/YAP signaling an
284 By wave 4, the predicted mean difference in dmfs was 1.86 between children with low and normal birth
286 hylacetamide (DMA) or N,N-dimethylformamide (DMF) was used to improve the separation selectivity.
287 entially binds with NR in dimethylformamide (DMF)/water (1:1) solution over other cations such as Fe(
288 duction of formic acid in dimethylformamide (DMF)/water mixtures (Faradaic efficiency of 90 +/- 10%)
290 first-line oral treatment dimethyl fumarate (DMF), we examined dynamics of neurofilament light (NFL)
293 pulation mechanism in digital microfluidics (DMF), where droplets can be actuated over a (super)hydro
294 fumarate (MMF), the bioactive metabolite of DMF, which can stabilize NRF2 and induce antioxidant gen
295 catalyzes electro-assisted H(2) evolution in DMF with distinct mechanisms depending on the strength o
296 ing the automated sample processing power of DMF with the resolving and analytical capacity of HPLC-M
297 e in-line coupling of digital microfluidics (DMF) with HPLC-MS, using a custom, 3D-printed manifold a
298 ination of CO2(*-) in N,N-dimethylformamide (DMF) with the tip generation/substrate collection (TG/SC
299 emiconductors, [Fe(tpma)(xbim)](X)(TCNQ)(1.5)DMF (X=ClO4(-) or BF4(-); tpma=tris(2-pyridylmethyl)amin
300 ral metal-organic framework [Zn2(bdc)(l-lac)(dmf)] (ZnBLD; bdc = 1,4-benzenedicarboxylic acid, l-lac