1 sing the chromogenic substrate o-nitrophenyl-
beta-galactoside.
2 with the artificial substrate o-nitrophenyl-
beta-galactoside.
3 d signaling requires binding to cell surface
beta-galactosides.
4 re exposed to substantial amounts of dietary
beta-galactosides.
5 share a conserved sequence and affinity for
beta-galactosides.
6 lectin family given the lack of affinity for
beta-galactosides.
7 s of FV was also affected in the presence of
beta-galactosides.
8 this modification blocks galectin binding to
beta-galactosides.
9 secondary carbon sources such as alpha- and
beta-galactosides.
10 drate recognition domain that interacts with
beta-galactosides.
11 sing beta-galactosidase gene, high levels of
beta-galactoside activity were observed.
12 usly that n-butyrate can reduce the level of
beta-galactoside alpha 2,6-sialyltransferase expression
13 actions between a tryptophan residue and the
beta-galactoside alpha face are observed.
14 Myeloid-specific deletion of
beta-galactoside alpha(2,6)-sialyltransferase 1, which p
15 Finally, we show that ST3
beta-galactoside alpha-2,3-sialyltransferase (ST3Gal1) e
16 d loss-of-function screen and identified ST3
beta-galactoside alpha-2,3-sialyltransferase 1 (ST3GAL1)
17 ymes, beta-1,3-glucosyltransferase (B3GLCT),
beta-galactoside alpha-2,3-sialyltransferase 5 (ST3GAL5)
18 esent study we identified high expression of
beta-galactoside alpha-2,3-sialyltransferase, ST3GAL6, i
19 Our results suggest that the
beta-galactoside alpha-2,6-sialyltransferase 1 (ST6Gal-I
20 ,4-Galactosyltransferase 1 (B4GALT1) and ST6
beta-galactoside alpha-2,6-sialyltransferase 1 (ST6GAL1)
21 ed whether inactivation of the UDP-galactose:
beta-galactoside-
alpha1-3-galactosyltransferase (alpha1,
22 nteraction is regulated by the activity of a
beta-galactoside alpha2, 6-sialyltransferase that can in
23 Knockdown of
beta-galactoside alpha2,6-sialyltransferase (ST6Gal-1) b
24 t acts to inhibit galectin signaling, namely
beta-galactoside alpha2,6-sialyltransferase (ST6Gal-I).
25 ialylation of the Fc fragment is mediated by
beta-galactoside alpha2,6-sialyltransferase 1 (ST6Gal-1)
26 ting from overexpression of the Golgi enzyme
beta-galactoside:
alpha2-6-sialyltransferase (ST6Gal-I).
27 Here we show that DDAOG, a conjugate of
beta-galactoside and 7-hydroxy-9H-(1,3-dichloro-9,9-dime
28 alectin family defined by their affinity for
beta-galactosides and by their conserved carbohydrate re
29 tinctive preferences for growth on different
beta-galactosides are observed within Bifidobacterium me
30 Galectin-9 is a
beta-galactoside binding lectin capable of modulating im
31 Galectin-3 is a
beta-galactoside binding lectin that is highly expressed
32 Galectin-9, a
beta-galactoside binding lectin, has recently been isola
33 Thomsen-Friedenreich antigen (T antigen) and
beta-galactoside binding lectins (galectins) have been i
34 tudies performed with a model ligand on both
beta-galactoside binding lectins showed additional inter
35 proteins, have been traditionally defined as
beta-galactoside binding lectins.
36 e (TDG) analogues as recognition elements of
beta-galactoside binding lectins.
37 H kinase (PI3K) and Ras is suppressed by the
beta-galactoside binding protein (betaGBP) molecule, a c
38 We report here that
beta-galactoside binding protein (betaGBP), an antiproli
39 Galectin-3 (Gal-3), a member of the
beta-galactoside binding protein family containing the N
40 induced cellular expression of the secreted
beta-galactoside binding protein Galectin 1-like 2 (Drga
41 Alterations in the production of the
beta-galactoside binding protein galectin-3 and of MUC2
42 The
beta-galactoside binding protein galectin-3 modulates th
43 Galectin-3 is a
beta-galactoside binding protein that has also been asso
44 Galectin-3, a
beta-galactoside binding protein, contains a C-terminal
45 upregulates intracellular expression of the
beta-galactoside binding protein, Galectin-3 (Gal-3).
46 Recently, the overexpression of a
beta-galactoside binding protein, galectin-3 (LGALS3), h
47 Galectin-1, a
beta-galactoside binding protein, is produced by thymic
48 Galectin-3, a
beta-galactoside binding protein, plays a significant ro
49 nctionally related to the galectin family of
beta-galactoside binding proteins.
50 is divided into four exons, with the entire
beta-galactoside binding site encoded by exon III.
51 We have isolated CLC
beta-galactoside binding sites from both orangutan (Pong
52 Galectin-3 is a member of the
beta-galactoside-
binding animal lectin family expressed
53 Galectin-3 is a member of a
beta-galactoside-
binding animal lectin family.
54 The
beta-galactoside-
binding animal lectin galectin-3 is pre
55 Galectin-7 is a
beta-galactoside-
binding animal lectin specifically expr
56 Galectin-3 is a member of a large family of
beta-galactoside-
binding animal lectins and is composed
57 Galectin-3 is a member of a family of
beta-galactoside-
binding animal lectins expressed abunda
58 Galectin-3 belongs to a family of
beta-galactoside-
binding animal lectins expressed in sev
59 Galectins are a family of
beta-galactoside-
binding animal lectins with conserved c
60 tin-3 is a member of a newly named family of
beta-galactoside-
binding animal lectins, which has been
61 alectin-3 is a member of a growing family of
beta-galactoside-
binding animal lectins.
62 Galectin-3 is a member (if a large family of
beta-galactoside-
binding animal lectins.
63 ctin-3 is a member of the galectin family of
beta-galactoside-
binding animal lectins.
64 Here, we show that galectin-3 (Gal3), a
beta-galactoside-
binding cytosolic lectin, unifies and c
65 Galectin-4 (Gal-4), a member of the
beta-galactoside-
binding galectin family, plays a role i
66 Here, we show that a
beta-galactoside-
binding lectin [galectin-3 (gal3)] that
67 Galectin (Gal)-3 is a
beta-galactoside-
binding lectin and currently intensely
68 Galectin-3 (gal-3) is a
beta-galactoside-
binding lectin expressed in diverse fib
69 Galectin-3 (Gal-3) is a member of the
beta-galactoside-
binding lectin family and plays an impo
70 Here we show that galectin-12, a member of a
beta-galactoside-
binding lectin family preferentially ex
71 Galectin-1 is a member of the conserved
beta-galactoside-
binding lectin family that binds galact
72 Galectin-12, a member of the
beta-galactoside-
binding lectin family, is preferentiall
73 f carbohydrate binding to the 14 kDa dimeric
beta-galactoside-
binding lectin galectin-1 (Gal-1) from
74 NK immune surveillance by overexpressing the
beta-galactoside-
binding lectin galectin-1.
75 The role played by the
beta-galactoside-
binding lectin galectin-3 (Gal-3) in ai
76 Several lines of evidence implicate the
beta-galactoside-
binding lectin galectin-3 in developmen
77 We hypothesized that human galectin-3, a
beta-galactoside-
binding lectin involved in immune regul
78 Galectin-3 is a
beta-galactoside-
binding lectin previously designated as
79 l lines exhibited increased affinity for the
beta-galactoside-
binding lectin RCA-I in the presence of
80 Galectin-3 is a
beta-galactoside-
binding lectin that is highly expressed
81 Galectin-3 is a
beta-galactoside-
binding lectin that plays an important
82 Galectin-3 is a
beta-galactoside-
binding lectin widely expressed on epit
83 Galectin-3 (GAL3), a
beta-galactoside-
binding lectin, confers chemoresistance
84 Galectin-1 (Gal1), a
beta-galactoside-
binding lectin, has recently emerged as
85 Galectin-3, a
beta-galactoside-
binding lectin, is abnormally increased
86 Galectin-1 (Gal-1), a
beta-galactoside-
binding lectin, is critical for HSC act
87 Galectin-1, a
beta-galactoside-
binding lectin, is involved in many phy
88 Galectin-3, an endogenous
beta-galactoside-
binding lectin, is present on colon can
89 We show that expression of galectin-3, a
beta-galactoside-
binding lectin, is up-regulated in a mo
90 his study, we demonstrate that galectin-8, a
beta-galactoside-
binding lectin, is upregulated in the e
91 Galectin-1 (Gal-1), a
beta-galactoside-
binding lectin, plays a profound role i
92 ectin-1 (Gal-1), an evolutionarily conserved
beta-galactoside-
binding lectin, plays essential roles i
93 Galectin-9, a
beta-galactoside-
binding lectin, promotes immune suppres
94 The expression of galectin-3, a
beta-galactoside-
binding lectin, was studied in atherosc
95 a terminal sugar, the expression profile of
beta-galactoside-
binding lectins (galectins) in MDA-MB-4
96 Galectin-1 is a member of a family of
beta-galactoside-
binding lectins that are soluble adhesi
97 Galectins are
beta-galactoside-
binding lectins that regulate diverse c
98 of the prototype galectin family, which are
beta-galactoside-
binding lectins, exhibit subunit-specif
99 e members of a genetically related family of
beta-galactoside-
binding lectins.
100 Galectin-3 is a member of the
beta-galactoside-
binding protein family shown to be invo
101 Galectin (Gal)-3, a M(r) 31000 member of the
beta-galactoside-
binding protein family, is a multifunct
102 Galectin-3 (Gal-3), a member of the
beta-galactoside-
binding protein family, is implicated i
103 Galectin-3 (Gal-3), a member of a
beta-galactoside-
binding protein family, is involved in
104 Galectin-7, a member of the
beta-galactoside-
binding protein family, is primarily ex
105 We identified the
beta-galactoside-
binding protein galectin-1 as a biomark
106 Mammalian
beta-galactoside-
binding protein Galectin-3 (Gal-3) modu
107 The
beta-galactoside-
binding protein galectin-3 has pleiotro
108 The
beta-galactoside-
binding protein galectin-3 is widely ex
109 The
beta-galactoside-
binding protein galectin-9 is critical
110 Galectin-1, a
beta-galactoside-
binding protein highly expressed in the
111 Galectin-3 is a multifunctional
beta-galactoside-
binding protein implicated in apoptosis
112 Galectin-3 is a
beta-galactoside-
binding protein implicated in diverse b
113 Galectin-3 is a
beta-galactoside-
binding protein implicated in tumor pro
114 Galectin-3 (Gal-3), a
beta-galactoside-
binding protein is expressed in a speci
115 Galectin-1 is a
beta-galactoside-
binding protein secreted by animal cell
116 Galectin-3 (Gal3) is a
beta-galactoside-
binding protein that has been implicate
117 Galectin-3 (Gal-3) is a
beta-galactoside-
binding protein that is involved in can
118 Galectin-3 is a
beta-galactoside-
binding protein that is secreted from m
119 Galectin 3 is a
beta-galactoside-
binding protein whose expression has be
120 Galectin-1 (Gal-1), a
beta-galactoside-
binding protein, can alter fate and eff
121 d Thomsen-Friedenreich glycoantigen with the
beta-galactoside-
binding protein, galectin-3.
122 cally interacting with endothelium-expressed
beta-galactoside-
binding protein, galectin-3.
123 The Lgals3 gene encodes a multifunctional
beta-galactoside-
binding protein, galectin-3.
124 Galectin-3 (Gal-3), a
beta-galactoside-
binding protein, has been implicated in
125 Galectin-3, a
beta-galactoside-
binding protein, has been implicated in
126 Galectin-3, a
beta-galactoside-
binding protein, has been implicated in
127 Galectin-3, a
beta-galactoside-
binding protein, has been shown to be i
128 t human galectin-1 (dGal-1), a small dimeric
beta-galactoside-
binding protein, induces phosphatidylse
129 Galectin-3, a
beta-galactoside-
binding protein, is implicated in cell
130 Galectin-1 (Gal-1) is a
beta-galactoside-
binding protein, the expression of whic
131 Galectin-3 (Gal-3), a pleiotropic
beta-galactoside-
binding protein, was shown to be involv
132 sulfated C4S, which binds less galectin-3, a
beta-galactoside-
binding protein.
133 (Treg), which directly killed NK cells using
beta-galactoside-
binding protein.
134 Galectin-3 (gal-3), a member of the
beta-galactoside-
binding proteins family, was identified
135 -3 is a member of a growing family of animal
beta-galactoside-
binding proteins shown to be involved i
136 Galectins are a family of
beta-galactoside-
binding proteins that are frequently al
137 Galectins are a family of
beta-galactoside-
binding proteins that are widely found
138 Galectins are a family of
beta-galactoside-
binding proteins that contain character
139 Galectins are a family of mammalian
beta-galactoside-
binding proteins that positively and ne
140 Two
beta-galactoside-
binding proteins were found to be promi
141 member of the galectin family consisting of
beta-galactoside-
binding proteins with conserved carbohy
142 Galectins, a family of
beta-galactoside-
binding proteins, control cell membrane
143 Tumor-derived galectin-1 (Gal-1), a
beta-galactoside-
binding S-type lectin, has been shown t
144 ll known inhibitors of galectin-3 target its
beta-galactoside-
binding site in the carbohydrate recogn
145 1 and HUK-921 bind galectin-3 outside of its
beta-galactoside-
binding site.
146 The data further show that
beta-galactosides block the interaction between FV and G
147 chromogenic substrate 4-methyl umbelliferyl-
beta-galactoside confirmed that host-cell lysosomal beta
148 lectins are soluble-type lectins recognizing
beta-galactoside containing glycans.
149 the galectin family that has an affinity for
beta-galactoside containing glycoconjugates.
150 tazoan proteins that show binding to various
beta-galactoside-
containing glycans.
151 rbohydrate-binding protein with affinity for
beta-galactoside-
containing glycoconjugates, is upregula
152 Galectin-8 (Gal8) interacts with
beta-galactoside-
containing glycoproteins and has recent
153 tant of cultured malignant T cells induced a
beta-galactoside-
dependent inhibition of normal T-cell p
154 inhibition of overexpressed Gal-3 by, e.g.,
beta-galactoside-
derived inhibitors is hence promising f
155 is a glycan-binding protein (GBP) that binds
beta-galactoside glycan structures to orchestrate a vari
156 hough the hydrophobic patch displayed by the
beta-galactoside in Le(x) is essential in both cases for
157 Gal3 bound to N-linked
beta-galactosides in Dsg2 extracellular domain and co-se
158 esent evidence that it has high affinity for
beta-galactosides in vitro.
159 ous galectin-3, an animal lectin recognizing
beta-galactosides,
in regulating dendritic cell motility
160 bohydrate-binding proteins with affinity for
beta-galactosides,
is a key modulator of diverse cell fu
161 l-1), a special lectin with high affinity to
beta-galactosides,
is implicated in protection against i
162 e lubricin glycome is enriched with terminal
beta-galactosides,
known binding partners for a family o
163 ed member of the galectin family of secreted
beta-galactoside lectins containing a conserved carbohyd
164 no acids shown to interact directly with the
beta-galactoside ligand.
165 A 36-kDa
beta-galactoside mammalian lectin protein, designated as
166 Thus,
beta-galactoside-
mediated intravascular heterotypic and
167 erimental conditions, benzochlorin without a
beta-galactoside moiety or the related glucose conjugate
168 The protein galectin-3 (Gal-3) binding
beta-galactosides of cellular glycoproteins plays an imp
169 receptor of a known ECA via affinity for the
beta-galactosides present on this receptor.
170 -33% of the LNCX level, and the induction by
beta-galactosides ranged from 6-11-fold to 29-54-fold.
171 he galectin-binding data indicate a possible
beta-galactoside-
recognized protein specificity of the g
172 lls incubated with lactose (known to bind to
beta-galactoside-
recognized proteins) prior to the addit
173 Galectin-8 is a
beta-galactoside-
recognizing protein having an important
174 operons needed for utilization of alpha- and
beta-galactosides,
slowed growth on diverse carbon sourc
175 Galectin-3 is a
beta-galactoside-
specific lectin implicated in diverse p
176 Galectin-3 is a
beta-galactoside-
specific, carbohydrate-recognizing prot
177 Our results suggest that
beta-galactosides,
structural features common to chondro
178 ved in vitro to catalyze the hydrolysis of a
beta-galactoside substrate 500 times more efficiently (k
179 a-galactoside sugar melibiose as well as the
beta-galactoside sugar lactose.
180 e lectins called galectins, it does not bind
beta-galactoside sugars and has atypical sequences at no
181 ned amino acids that are crucial for binding
beta-galactoside sugars.
182 family member, the Drosophila galectin bound
beta-galactoside sugars.
183 er and respond to the information encoded by
beta-galactoside sugars.
184 Galectins are a family of lectins that bind
beta-galactosides through their conserved carbohydrate r
185 nmetabolizable galactose analogue thiomethyl-
beta-galactoside (
TMG) by a permease-catalyzed sugar:H(+
186 in a lacF lacR double mutant (lacF encodes a
beta-galactoside transport protein) grown in medium cont
187 ose could be transported by the overproduced
beta-galactoside transporters and cause the induction of
188 se a model in which lacR mutants overproduce
beta-galactoside transporters, thereby overwhelming the
189 viral expression vectors that are induced by
beta-galactosides upon stable transduction in mammalian
190 ort, an efficient route for the synthesis of
beta-galactosides using a bacterial beta-4-galactosyltra
191 attributed to the constitutive expression of
beta-galactoside utilization genes in lacR mutants.
192 y of the ABC transporter encoded by the same
beta-galactoside utilization locus.
193 alpha-Mannoside or
beta-galactoside was immobilized on a gold disk electrod