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1 f nonpolar packing interactions of the fifth sugar.
2 id metabolism along with the availability of sugars.
3 stability and high selectivity for reducing sugars.
4 HH mAb-Ds had non-human sugars.
5 nvert lignocellulosic biomass to fermentable sugars.
6 with an overall yield of 0.329 g/g available sugars.
7 ffset the obesogenic effects of some dietary sugars.
8 voring caries to a greater degree than other sugars.
10 bond to the pyranoside ring in higher carbon sugars, a model is advanced that relates the relative co
12 rry shrivel (BS) is characterized by reduced sugar accumulation, low anthocyanin contents, and high a
13 lant exposure to carbon monoxide) can reduce sugar accumulation, thus disrupting or delaying the reco
14 hey contain extraterrestrial amino acids and sugar acids (aldonic acids) with large enantiomeric exce
19 lity, density and viscosity of sorbitol as a sugar alcohol in the ([mmim](MeO)(2)PO(2)) ionic liquid
20 he reduction of GalA to the oxidation of the sugar alcohol sorbitol that has a higher reduction state
22 o-levy tier with removal of some but not all sugar, alongside changes in consumer attitudes and belie
23 etabolism to build and break down ketoacids, sugars, amino acids, and ribonucleotides in much the sam
25 industry because the accumulation of invert sugar and byproducts severely affect sucrose manufacturi
26 yveri showed greater changes in the reducing sugar and free amino acids in fermented cocoa beans.
27 id (Neu5Ac), and the ability to produce this sugar and its subsequent incorporation into cell-surface
29 m together or by building both the conjoined sugar and nucleobase, part-by-part-toward the ultimate g
30 ditives, were assessed to characterise their sugar and phenolic profiles, flavonoid content, as well
33 es of genomic variation to determine whether sugar and starch storage, energy reserves for trees unde
35 lfur compounds, organic acids, water soluble sugars and amino acids in three onion varieties ('Shallo
36 to sink tissues, and to convert the incoming sugars and amino acids into storage compounds in the sin
37 bon and nitrogen, to transport the resultant sugars and amino acids to sink tissues, and to convert t
39 hate-linked and dolichylpyrophosphate-linked sugars and enzymatic glycan extension to generate donor
40 based on the reduction of Cu(II) to Cu(I) by sugars and followed by the formation of a colored Cu(I)-
41 ce fermentation, as indicated by analysis of sugars and organic acids, and ethanol production was mai
43 t neurons are insensitive to nectar-specific sugars and respond to glucose only in the presence of ad
44 ncluding microbial necromass biomarker amino sugars and SOC, from two long-term agricultural field st
45 was a significant decrease in the amount of sugars and sodium in several groups of packaged foods an
49 he contributions of Hoogsten hydrogen bonds, sugar, and phosphate moieties to the specific G-vacancy
50 vertising of food and beverages high in fat, sugar, and salt (HFSS) from 05.30 hours to 21.00 hours (
53 anada, rich in proanthocyanidins (PAs)] or a sugar- and energy-matched apple control beverage (CB) fo
54 the O type in the presence of an additional sugar antigen (GalNAc and Gal, respectively) on the core
55 ernative toluene alters which C-O bonds in a sugar are cleaved by the tris(pentafluorophenyl)borane/H
57 ine pathway intermediates and phosphorylated sugars are abundant when cellular expressions of DHTKD1
58 vity and interaction features of fluorinated sugars are described, as well as their applications as p
59 ble, while nicotinate and non-phosphorylated sugars are when DHTKD1 expression is order(s) of magnitu
62 d starch degradation and increase in soluble sugars, ascorbate, and TPC, together leading to higher g
63 ht loss, pH and titratable acidity, reducing sugars, ascorbic acid, total phenolics, DPPH and ABTS as
64 a, the presence of a contrasting penultimate sugar assembled by a different glycosyltransferase enabl
66 is work highlights that differential dietary sugar availability influences the relationship between t
68 ecological role, and the design of efficient sugar-baited traps will all benefit from understanding t
69 We do so by running transects of salt and sugar baits and inferring the magnitude of environmental
70 iber, carbohydrate-to-fiber ratio, and added sugar based on reported frequencies for individual foods
78 vide insight into transcriptional changes in sugar beet roots during storage resulting in the charact
79 e comparative transcriptomic approach on six sugar beet varieties showing different amount of sucrose
81 oring of dextran synthesis, affinity assays, sugar binding pocket deletions, site-directed mutagenesi
82 mediator between the catalytic site and the sugar-binding pockets of domain V and contributing to a
84 he side chain populations observed for these sugars both in free solution and bound to nonhydrolytic
85 These neurons are stimulated in response to sugar but not artificial sweeteners, and are activated b
86 n the presence of simpler substrates such as sugars but differs significantly among bacterial isolate
87 diabetic patients try to control their blood sugar, but the molecular mechanism of this 'metabolic me
89 l-1 identification of the seven carbon (7-C) sugar C-methyl-scyllo-inositol (mytilitol) in mussels an
90 ons, diets high in processed foods, fat, and sugar can contribute to chronic inflammatory conditions,
93 Western-style diet, which is high in fat and sugar, can cause significant dyslipidemia and nonalcohol
95 ) using metabolomics profiling and cell wall sugar characterization at different developmental stages
96 lent addition of the sugar moiety from a UDP-sugar cofactor to relatively low-molecular weight lipoph
99 led changes in lignin, cellulose, and matrix sugar composition indicating an overall increase in seco
103 haring common risk factors, including excess sugar consumption and tobacco use, as well as underlying
108 ClVST1(97) knockout lines show decreased sugar content and total biomass, whereas overexpression
111 e the observed volume as well as calorie and sugar content of postregulation beverage purchases to a
113 ot been quantified, in particular, tiered or sugar content taxes that provide industry incentives for
115 inferior flavors and aromas, had a reducing sugar content three times higher than the aged cachacas,
117 tion of 6 types based on colour and residual sugar content, 13 wine grape varieties and 4 locations b
120 eric excesses (ee) of chiral amino acids and sugars could be a powerful indicator for extant or extin
123 umor-ECM interactions is the glycocalyx, the sugar-decorated proteins and lipids that act as a buffer
124 melanoidins formed from Glc/Ala contain more sugar degradation products with lower absorption due to
131 double-blind, placebo-controlled trial (the SUGAR-DM-HF trial [Studies of Empagliflozin and Its Card
132 tructural analysis indicates that nucleotide sugar donors for GT-A fold glycosyltransferases bind in
134 rocytosis provides not only amino acids, but sugars, fatty acids and nucleotides for biosynthesis, co
135 as a general increase in the accumulation of sugars, fatty acids, amino acids, and phytosterols in th
136 essed through proximate composition, soluble sugars, fatty acids, color, texture and microbial load,
139 s was shown to modulate the contents of free sugars, free amino acids and polyphenolic compounds such
143 a decline in primary metabolites content as sugars fructose and glucose, and short-chain organic aci
144 he isocaloric effect of substituting dietary sugars (fructose, glucose, sucrose) with other sugars or
145 ogen Toxoplasma gondii transfers a different sugar, fucose, to proteins involved in transcription, mR
146 secondary metabolites, metabolism of simple sugars, fungal cell wall deconstruction, biofilm formati
147 and selectivity for fuel precursors such as sugars, furanics, and lignin-derived monomers pose signi
148 upward trend in volume (ml) of and amount of sugar (g) in purchases of lower-levy-tier drinks was see
149 , the three main stressors present in honey: sugars, gluconic acid, and hydrogen peroxide (H(2)O(2)),
150 Hence, we investigated the influence of sugars (glucose, sucrose and lactose), at log phase (5 h
151 se studies: growth enrichment on alternative sugars, glycerol and galactose, and chemical overproduct
155 electrophysiology, how chronic high-fat high-sugar (HFHS) diet changes the physiology of the VP and w
156 seawater in hydrolysis of seaweed increased sugar hydrolysis yield and subsequent bioethanol product
159 ronutrients fat, protein, carbohydrates, and sugar in over 235,000 individuals of European ancestries
160 was no evidence that volume of or amount of sugar in purchases of all drinks combined was different
161 - 0.30%, 69.19 +/- 0.11% and 63.03 +/- 0.04% sugar in seawater compared with 52.82 +/- 0.16%, 45.93 +
164 incorporated into nucleic diphosphate (NDP) sugars in 4 h, and (13)C labelled peaks were identified
167 ed potent antihyperglycemic activity against sugar-induced postprandial hyperglycemia in rats plausib
168 ss during storage is a major concern for the sugar industry because the accumulation of invert sugar
172 st competitive conversion of biomass-derived sugars into biofuel will require high yields, high volum
174 ed" or l-amino acids and "right-handed" or d-sugars, is a unique property of life that is crucial for
176 ycosylation, extracellular matrix structure, sugars, Krebs cycle intermediates, microbe-derived metab
177 nclude targets involved in metabolism (e.g., sugar, lipid, and cholesterol metabolism), inflammation,
179 assimilate methanol differs from the typical sugar metabolism by only three enzymes, turning a non-me
182 aled a S. parasanguinis-driven alteration in sugar metabolism that restricts biofilm development by S
184 labelling and traced the (13)C flux through sugar metabolites with isotope-ratio mass spectrometry (
185 sponse to Metformin and Glipizide in Humans (SUGAR-MGH), we constructed weighted polygenic scores usi
186 ino-pS moieties and therapeutically relevant sugar modifications in tandem to create novel oligonucle
187 ically catalyze the covalent addition of the sugar moiety from a UDP-sugar cofactor to relatively low
188 ctions at position 8 and deprotection of the sugar moiety gave eight derivatives of pyrazolo-fused de
192 s) are activated by slight cooling, although sugar neurons are insensitive to the same mild stimulus.
193 entrations of arabinoxylan fibre and soluble sugars (notably sucrose, maltose and fructose) increasin
194 influenced the measured T(gs) (P < 0.05) and sugaring of fructose-glucose-water model solutions.
196 effects of 2 wt% emulsifier and crystalline sugar on the isothermal solidification and polymorphic b
201 s were not observed for perceptions of added sugar or positive sugary drink attitudes (p's > 0.10).
202 gars (fructose, glucose, sucrose) with other sugars or starch on cardiometabolic risk markers, includ
204 fruits and juices, nine primary metabolites (sugars, organic acids and vitamin C) were determined in
206 during storage root bulking and analyzed for sugars, organic acids, amino acids, phosphorylated inter
209 d 0.24 per litre, drinks with >=5 to <8 g of sugar per 100 ml (lower levy tier) are taxed at pound 0.
212 d as key to fruit quality aspects, including sugars; phenolic compounds like phenylpropanoids and fla
213 d inhibited complexes while binding multiple sugar phosphates, including its substrate ribulose 1,5-b
215 ntify molecular determinants involved in the sugar polymerization mechanism and that confer its abili
216 d atactic poly(4-methyl-1-pentene) (CB-aPMP) sugar-polyolefin conjugate can be used to exert external
218 nd scalable quantities of a diverse range of sugar-polyolefin FK A15 phases with unique intrinsic phy
219 se by ants all point to factors constraining sugar production: net above-ground productivity, how far
220 f detecting undeclared addition of exogenous sugar products in foods and beverages susceptible to eco
221 ductions were in the proportion of "high in" sugars products (in beverages, milks and milk-based drin
223 thocyanins, saponins, carotenoids, terpenes, sugars, proteins, capsaicinoids, fatty acids, alkaloids
224 nd does not alter the 'clover leaf' bend and sugar puckers that are critical for anchoring the 5'-pho
226 was associated with reductions in volume and sugar purchased in lower-levy-tier drinks before impleme
227 led to a 6.1 g (95% CI 3.9-8.2) increase in sugar purchased in these drinks per household per week.
228 nd -6.4 g (95% CI -9.8 to -3.1) reduction in sugar purchased in these drinks per household per week.
231 vides an in-depth insight into the impact of sugar reduction reformulation on the sensory perception
236 e grains, fruits and vegetables, and high in sugar, salt, saturated fat and ultra-processed foods) ar
237 es of energy and nutrients of concern (total sugars, saturated fats, and sodium, per 100 g/100 mL) an
238 ligosaccharides (HMO) are a diverse range of sugars secreted in breast milk that have direct and indi
239 for the hepatic vagus nerve in transforming sugar sensing by the gut into behavioral reinforcement v
240 of all foods and beverages containing added sugars, sodium, or saturated fats that exceed set nutrie
241 d high levels of nutrients of concern (i.e., sugars, sodium, saturated fat, or energy) according to C
246 dulatory compounds are modified with complex sugar structures (or glycans), which play an important r
248 f HA is dependent on the availability of its sugar substrates, thus linking glycocalyx biology direct
252 he cross-sectional association of cumulative sugar-sweetened beverage (SSB) consumption with concentr
253 st milk is increased in response to maternal sugar-sweetened beverage (SSB) intake in lactation.
256 ition Examination Survey, policy effects and sugar-sweetened beverage-related diseases from meta-anal
257 etary patterns emerged: Home foods (HF(dp)), Sugar-sweetened beverages (SSB(dp)), and Eating out nood
263 alth importance of drinking water in lieu of sugar-sweetened beverages, have raised interest in water
266 c index of diet; lower intakes of trans fat, sugar-sweetened beverages/fruit juices, and red/processe
267 tatistically significant association between sugar-sweetened carbonated beverages and a moderately in
268 her, we evaluated whether maternal intake of sugar-sweetened drinks increased the risk of offspring c
270 ut they also highlight binding to additional sugar targets that have not previously been recognized.
271 the current debate on the implementation of sugar taxation, marketing regulation, and other sugar-re
272 y plants occurs predominantly at night, with sugars that accumulate during the day assisting in mesop
273 a diverse family of 9-carbon alpha-keto acid sugars that are involved in a wide range of functions ac
274 n of intervention drinks over the lower levy sugar threshold had fallen by 33.8 percentage points (95
275 a common practice among producers is to add sugar to adjust sensory deficits in the final product.
280 od glucose lowering properties by inhibiting sugar transporters in the small intestine and improving
281 ata demonstrate that the naturally occurring sugar trehalose at doses safely achieved in humans inhib
282 ody mass index, transaminases, fasting blood sugar, triglyceride, low density lipoprotein level, and
283 he three drivers that best predict exogenous sugar use by ants all point to factors constraining suga
285 atalytic acetylations of partially protected sugars using light as external stimulus and oligopeptide
288 n GL, carbohydrate-to-fiber ratio, and added sugar were associated with modestly reduced fecundabilit
290 de (AA), asparagine and low molecular weight sugars were evaluated during an industrial coffee roasti
293 a unique composition of proteins, salts, and sugars, which can affect the infectivity potential of th
296 m-catalyzed conversion of unprotected aldose sugars with acetylacetone to polyhydroxyalkyl furans or
298 alpis saliva mostly consists of oligomannose sugars, with Man(5)GlcNAc(2) being the most abundant, an