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1 ouronium salt of 2,3,4,6-tetra-O-acetyl-beta-D-galactose.
2 orylation of the C-1 hydroxyl group of alpha-D-galactose.
3 aris developed in mice treated with low-dose D-galactose.
4 samine and N-acetylgalactosamine relative to d-galactose.
5 nterconversion of beta-D-galactose and alpha-D-galactose.
6 oside (MNPG) rather than five copies of beta-D-galactose.
7 ve for its natural substrates, d-glucose and d-galactose.
8 d is insensitive to sugars like d-glucose or d-galactose.
9 diastereomers such as L-Man, D-glucose, and D-galactose.
10 h the galactosylated E461G enzyme gives only D-galactose.
11 rowth on galactitol and in reduced growth on D-galactose.
12 e AGE breaker phenacylphiazolium bromide and D-galactose.
13 turn over dTDP-3-acetamido-3,6-dideoxy-alpha-d-galactose.
14 pressed by the repressor GalR and induced by D-galactose.
15 utarotase, be achievable by either anomer of D-galactose.
16 the operon in the absence of the gal inducer D-galactose.
17 syl aldehydes from D-glucose, D-mannose, and D-galactose.
18 AATGal is 2-acetamido-4-amino-2,4,6-trideoxy-D-galactose.
19 ize the same binding sites in the absence of d-galactose.
20 o the anthrose saccharide was developed from D-galactose.
21 alR and GalS is inhibited in the presence of d-galactose.
22 ers is lifted in the presence of the inducer D-galactose.
23 motif and harbors the binding site for beta-D-galactose.
24 altering the maximum quench with saturating D-galactose.
25 oform and complexed with its substrate, beta-d-galactose.
26 ture of Polyandrocarpa lectin complexed with D -galactose.
27 alpha- and beta-pyranosides of d-glucose and d-galactose 1-4 were prepared containing single sites of
28 usly reported structures of the Mg(2+)-alpha-d-galactose-1-phosphate-beta-PGM, Mg(2+)-phospho-beta-PG
29 The galactose analog 2-(18)F-fluoro-2-deoxy-d-galactose ((18)F-FDGal) is a suitable PET tracer for m
30 lus cells (CCs), were exposed for 4 hours to D-galactose (2 muM), galactitol (11 muM) and galactose 1
31 3-O-(beta-D-gluco-4-enepyranosyluronic acid)-D-galactose, (2) 2-acetamido-2-deoxy-3-O-(beta-D-gluco-4
32 on aldohexose anomerization were measured in D-galactose 3 and D-talose 8 selectively (13)C- and (2)H
33 s of D-aldohexoses (D-allose 1, D-altrose 2, D-galactose 3, D-glucose 4, D-gulose 5, D-idose 6, D-man
34 with D-fucose, L-arabinose, 6-deoxy-6-fluoro-D-galactose, 6-O-methyl-D-galactose, or D-galacturonic a
35 nteraction of L-fucose with the beta-face of D-galactose), a nonconventional C-H...O hydrogen bond be
36 almost as well as D-galactose, while 2-deoxy-D-galactose affords no substrate protection, indicating
37 cose (QuiNAc), 2-deoxy-2-N-acetylamino-alpha-D-galactose (alpha-D-GalNAc), 2-deoxy-2-N-acetylamino-al
38 he critical step of a metabolic pathway--the D-galactose amphibolic pathway--changes the dynamics of
40 ntrasted, and it was observed that with both d-galactose and 2-deoxy-d-galactose as starting material
41 sport activities of radiolabelled D-glucose, D-galactose and 2-deoxy-D-glucose were restored, consist
42 r chemical structure consists of alternating D-galactose and 3,6-anhydro-L-galactose residues, the la
44 r, specificity of hSGLT3 binding is greater (D-galactose and 4-deoxy-4-fluoro-D-galactose are not hSG
47 in vitro experiments showing that both alpha-D-galactose and beta-D-galactose are capable of inducing
48 lactose differing at the C-1 position, alpha-D-galactose and beta-D-galactose, are widespread in natu
49 to integrate the two small molecule signals, d-galactose and cAMP, that modulate the isoregulators an
52 We report the thermodynamics of binding of d-galactose and deoxy derivatives thereof to the arabino
59 ray structure of Gal1p in complex with alpha-d-galactose and Mg-adenosine 5'-(beta,gamma-imido)tripho
61 de units composed of alternating residues of d-galactose and N-acetyl-d-glucosamine linked beta-(1-4)
62 imers with the monosaccharides D-mannose and D-galactose and the disaccharide D-lactose in their hydr
64 ucrose, trehalose, L-glucose, D-glucose, and D-galactose), and in each case larger amplitude motions
65 D-gluco-4-enepyranosyluronic acid)-4-O-sulfo-D-galactose, and (3) 2-acetamido-2-deoxy-3-O-(beta-D-glu
67 poxanthine, and 75 to 100% utilized citrate, D-galactose, and D-trehalose as sole carbon sources.
68 urrent method has been applied to d-glucose, d-galactose, and d-xylose donors with a nondirecting gro
69 se, d-glucose, l-allose, d-allose, d-gulose, d-galactose, and l-mannose are delineated, and for all e
70 onding beta-galactopyranosyl derivatives and D-galactose, and the formation of the latter represents
71 showing that both alpha-D-galactose and beta-D-galactose are capable of inducing transcription of the
72 anhydro-heptitols derived from D-mannose and D-galactose are enantiomeric and are useful linkers for
73 he peptide and the alpha- or beta-anomers of d-galactose are nearly identical structurally; however,
74 is greater (D-galactose and 4-deoxy-4-fluoro-D-galactose are not hSGLT3 substrates, but have hSGLT1 K
77 erved that with both d-galactose and 2-deoxy-d-galactose as starting materials, the transformations i
78 rated substrates, including 1-O-methyl-alpha-D-galactose as well as unsubstituted benzyl alcohol and
80 strategy to quantify beta-D-glucose and beta-D-galactose at low micromolar to millimolar levels, with
82 78D formed pentamers that bound to GM(1) and D-galactose but failed to assemble with CTA to form holo
84 androcarpa misakiensis specifically binds to D-galactose by coordination of the sugar to a bound calc
85 arrival assay based on labeling with [6-3H]-D-galactose combined with biochemical modification at th
86 BB) receptor is a glycoprotein with an alpha-d-galactose containing trisaccharide in the toxin-bindin
88 s, 5-mo-old C57BL/6 mice were given low-dose D-galactose (D-gal) for 8 wk and evaluated by AGE fluore
92 showed the presence of l-fucose, d-mannose, d-galactose, d-glucose, d-glucuronic acid, N-acetyl-d-ga
93 y relevant underivatized hexoses, d-glucose, d-galactose, d-mannose, and d-fructose, using only mass
94 Gal, GalNAc, and R represent, respectively, D-galactose, D-N-acetyl galactosamine, and reducing end)
96 s exhibit 60-fold lower apparent K(d)'s than D-galactose, demonstrating that binding affinity is sign
98 version at O-2 and O-3 in an easily prepared D-galactose derivative, which proceeds regio- and stereo
100 eficient for lipoprotein lipase treated with D-galactose did not retain lipoproteins to any measureab
103 se prevention group (LDP), respectively; 50% D-galactose for 4 or 8 months and then intervention by a
104 tervention group (8IN), respectively; or 50% D-galactose for 4 or 8 months and then intervention by w
105 ly 14 mg/kg per day) (prevention [PRV]), 50% D-galactose for 6 months followed by intervention with t
106 h the inhibitor (intervention [INT]), or 50% D-galactose for 6 months followed by replacement with th
111 (#5001) plus 50% starch (control [CON]), 50% D-galactose (galactose [GAL]), 50% D-galactose with AL-3
112 ow plus 50% starch, control group (CON); 50% D-galactose, galactose-fed group (GAL); 50% D-galactose
114 of Na+: 1) selective (alphaMDG > D-glucose > D-galactose >> L-glucose approximately D-mannose), 2) in
115 in orthogonally protected D-idopyranose from D-galactose has been developed, which is the first metho
116 haracter, it can metabolize D-glucose and/or D-galactose in both oxidative and fermentative pathways
117 blished Leloir pathway for the catabolism of d-galactose in fungi, the oxidoreductive pathway has bee
119 the conversion of beta-D-galactose to alpha-D-galactose in the Leloir pathway for galactose metaboli
121 ,6-O-ethylidene derivatives of d-glucose and d-galactose in which values of omega and theta; were con
123 hibit wild-type growth, even at up to 100 mM D-galactose, indicating that active transport by AtSTP1
124 peptide Ac-(Gly-Pro-Thr)(10)-NH(2) with beta-d-galactose induces the formation of a collagen triple h
125 the high-affinity substrates, D-glucose and D-galactose, inhibited uptake of radioactive sugar trace
128 lue of k(cat)/K(m) for the reaction of alpha-D-galactose is 10 times that for alpha-D-glucose, and th
132 Ac, where Fuc4NAc is 4-acetamido-4,6-dideoxy-D-galactose, ManNAcA is N-acetyl-D-mannosaminuronic acid
133 Ac, where Fuc4NAc is 4-acetamido-4,6-dideoxy-D-galactose, ManNAcA is N-acetyl-D-mannosaminuronic acid
137 mposed of L-rhamnose and 2-acetamido-2-deoxy-D-galactose (molar ratio, 2:1) with the structure -->2)-
138 urs, including uniform responses (d-lactose, d-galactose, N-acetylglucosamine, N-acetylneuraminic aci
141 Culture in medium containing either 10 mM D-galactose or 30 mM D-glucose resulted in the accumulat
143 of alkene-terminated C-linked glycosides of D-galactose or D-glucose to L-cysteine using thiol-ene "
144 e-deficient mice were injected with low-dose D-galactose or PBS subcutaneously for 8 weeks to induce
145 se, 6-deoxy-6-fluoro-D-galactose, 6-O-methyl-D-galactose, or D-galacturonic acid, suggesting that the
146 with UDP-mannose, UDP-4-deoxy-4-fluoro-alpha-D-galactose, or UDP-4-deoxy-4-fluoro-alpha-D-glucose hav
147 4-dihydropyrimidin-4-one dihydrochloride and D-galactose phenylhydrazone to give the pyranopterin (5a
149 lactofuranose (Gal(f)), the furanoic form of d-galactose produced by UDP-galactopyranose mutases (UGM
150 of peritoneal implants by targeting the beta-d-galactose receptors highly expressed on the cell surfa
155 dlings grow effectively on concentrations of D-galactose that inhibit wild-type growth, even at up to
157 lso indicated that upon binding of Na(+) and d-galactose, the alpha-helical content increased to 53%.
158 cell can make only one of the two anomers of D-galactose, the cell must also convert one anomer to th
159 mutarotase catalyzes the conversion of beta-d-galactose to alpha-d-galactose during normal galactose
160 mutarotase catalyzes the conversion of beta-D-galactose to alpha-D-galactose in the Leloir pathway f
167 an either PBS- or phenacylphiazolium bromide/D-galactose-treated mice at 24 and 72 hours after inject
173 inose-binding protein (ABP) with its ligand, d-galactose, using NMR relaxation and molecular dynamics
174 study, binding of 31 structural analogues of D-galactose was examined by site-directed N-[(14)C]ethyl
176 galactose, D-glucose and 2-acetamido-2-deoxy-D-galactose was obtained after mild acid hydrolysis of t
177 nd k(cat)/K(m) for the mutarotation of alpha-D-galactose were found to be 1.84 x 10(4) s(-1) and 4.6
180 pimer alpha-D-talose binds almost as well as D-galactose, while 2-deoxy-D-galactose affords no substr
181 of a ternary complex of OEDNA with GalR and D-galactose with a different conformation than the GalR-
182 ON]), 50% D-galactose (galactose [GAL]), 50% D-galactose with AL-3152 (approximately 14 mg/kg per day
184 D-galactose, galactose-fed group (GAL); 50% D-galactose with ARI-509 at 25 mg/kg or 10 mg/kg body wt
185 to 10 mM decreased the apparent affinity for d-galactose without altering the maximum quench with sat
187 he xylosides by galactosyltransferase I (UDP-D-galactose:xylose beta1-4-galactosyltransferase) in vit
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