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1 ghtly, and selectively to echistatin, an RGD disintegrin.
2  the conformational design of antimetastatic disintegrins.
3      Increased expression of metalloprotease-disintegrin ADAM12 is a hallmark of several pathological
4                              Metalloprotease-disintegrin ADAM12 is overexpressed and frequently mutat
5 R2 is shed from cells by the metalloprotease disintegrin ADAM17, whereas NRP-1 is released by ADAM10.
6 a causes upregulation of the metalloprotease-disintegrin ADAM8 (A8) in affected brain regions, spinal
7 sess the contribution of the metalloprotease-disintegrin ADAM9 to ocular neovascularization in mice.
8                     Ectodomain cleavage by A-disintegrin and -metalloproteases (ADAMs) releases many
9     This identified ADAM6, a member of the A disintegrin and A metalloprotease (ADAM) family; members
10 talloproteinase with thrombospondin motif, a disintegrin and a metalloprotease, interleukin (IL)-1bet
11        This study investigates the role of a disintegrin and a metalloproteinase (ADAM) 10 and ADAM17
12                                            A disintegrin and a metalloproteinase domain (ADAM) 9 is k
13 B)-EGF neutralizing antibody or abrogating a disintegrin and matrix metalloproteinase-17 (ADAM-17) ex
14 actor receptor (EGFR) and ADAM17 (a membrane disintegrin and metallopeptidase 17) in lung epithelial
15                  We found that recombinant a disintegrin and metalloprotease (ADAM) 17 cleaved the ec
16                        alpha(5)beta1 binds a disintegrin and metalloprotease (ADAM) 17, a metalloenzy
17 dding of HEPCAM at two alpha-sites through a disintegrin and metalloprotease (ADAM) and at one beta-s
18        Catalytically active members of the A Disintegrin And Metalloprotease (ADAM) family of membran
19  metalloproteases, especially those of the A disintegrin and metalloprotease (ADAM) family, can media
20 embrane-bound precursors by one of several a disintegrin and metalloprotease (ADAM) metalloproteases,
21                                            A disintegrin and metalloprotease (ADAM) proteases are imp
22                         The discovery of the disintegrin and metalloprotease (ADAM) proteins, which h
23                                      Using a disintegrin and metalloprotease (ADAM)-17 radiation chim
24 ion of matrix metalloproteinase (MMP)- and a disintegrin and metalloprotease (ADAM)-family zinc metal
25 e evidence that human Tim-3 is a target of A disintegrin and metalloprotease (ADAM)-mediated ectodoma
26                  The cytoplasmic domain of a disintegrin and metalloprotease (ADAM)10, a transmembran
27  with a TLR3 or TLR4 ligand, we identified a disintegrin and metalloprotease (ADAM)15 as a novel TRIF
28  cycle progression, and siRNA knockdown of a disintegrin and metalloprotease (ADAM)17 had a similar i
29                                         As a disintegrin and metalloprotease (ADAM)s have been implic
30 endogenous AXL was dependent on the sheddase disintegrin and metalloprotease 10 (ADAM10) and the gamm
31                   It is reported here that a disintegrin and metalloprotease 10 (ADAM10) interacts wi
32                                            A disintegrin and metalloprotease 10 (ADAM10) is a ubiquit
33                                            A disintegrin and metalloprotease 10 (ADAM10) is a ubiquit
34    The membrane-anchored metalloproteinase a disintegrin and metalloprotease 10 (ADAM10) is required
35 he alpha-hemolysin binding to its receptor A-disintegrin and metalloprotease 10 (ADAM10) upregulates
36  by an initial shedding event catalyzed by A Disintegrin and Metalloprotease 10 (ADAM10).
37 n of the cellular receptor of alpha-toxin, a disintegrin and metalloprotease 10 (ADAM10).
38 esis or inhibition of mCD23 cleavage by an a disintegrin and metalloprotease 10 inhibitor, GI254023X,
39  (m)CD23 by the endogenous metalloprotease a disintegrin and metalloprotease 10.
40 cytoskeleton morphology and recruitment of a disintegrin and metalloprotease 10.
41  on its shedding and binding activities, the disintegrin and metalloprotease 12 (ADAM12) has been imp
42  was significantly correlated with ADAM12 (A Disintegrin And Metalloprotease 12) expression in these
43 ng enzyme type 2 (ACE2) and an increase in a disintegrin and metalloprotease 17 (ADAM17) activity in
44            Amino acid polymorphisms within a disintegrin and metalloprotease 17 (Adam17) can account,
45                                            A disintegrin and metalloprotease 17 (ADAM17) is a major s
46                We have directly shown that A disintegrin and metalloprotease 17 (ADAM17) is a primary
47    The TNF-alpha converting enzyme (TACE), a disintegrin and metalloprotease 17 (ADAM17), has emerged
48 HER2 trans-activation by IL-1beta required a disintegrin and metalloprotease 17 (ADAM17)-dependent sh
49                                    Lastly, a disintegrin and metalloprotease 17 (ADAM17; also known a
50              The metalloproteinase ADAM17 (a disintegrin and metalloprotease 17) controls EGF recepto
51                                    ADAM17 (a disintegrin and metalloprotease 17) controls pro- and an
52                                    ADAM17 (a disintegrin and metalloprotease 17) is believed to be a
53     Protein ectodomain shedding by ADAM17 (a disintegrin and metalloprotease 17), a principal regulat
54 sis factor alpha-converting enzyme ADAM17 (a disintegrin and metalloprotease 17), which demonstrates
55  vascular epithelial growth factor (VEGF), a disintegrin and metalloprotease 33 (ADAM33), and periost
56 dding is largely attributed to a family of a disintegrin and metalloprotease domain (ADAM) metallopro
57 n of collagen I, CD45, and CD34 or EGFR or a disintegrin and metalloprotease domain 17 and placed in
58 with glutamate and GABA neurotransmission: a disintegrin and metalloprotease domain 22 (Adam22) and h
59                                            A disintegrin and metalloprotease domain-containing protei
60 nuclear factor of activated T-cells; ADAM, a disintegrin and metalloprotease domain; OTM, orthodontic
61 superfamily characterized by the presence of disintegrin and metalloprotease domains.
62                        ADAM10, a member of a disintegrin and metalloprotease family, is an alpha-secr
63 , a member of the matrix metalloproteinase/a disintegrin and metalloprotease family.
64 ed from the cell surface by proteinases of a disintegrin and metalloprotease family; however, the mec
65 ecent studies suggest that serum levels of a disintegrin and metalloprotease protein-12 (ADAM-12) can
66 he length of VWF is regulated by ADAMTS13 (a disintegrin and metalloprotease with a thrombospondin ty
67                                            A disintegrin and metalloprotease with a thrombospondin ty
68                                   ADAMTSs (a disintegrin and metalloprotease with thrombospondin doma
69                                            A disintegrin and metalloprotease with thrombospondin moti
70 tablished in a pilot approach, identifying a disintegrin and metalloprotease with thrombospondin moti
71  pericytes rapidly activated expression of a disintegrin and metalloprotease with thrombospondin moti
72 t out to investigate the role of ADAMTS-5 (a disintegrin and metalloprotease with thrombospondin moti
73 -21 encodes ADT-2, a member of the ADAMTS (a disintegrin and metalloprotease with thrombospondin moti
74                                            A disintegrin and metalloprotease with thrombospondin moti
75 rly active 29/31-kDa form of VEGF-C by the A disintegrin and metalloprotease with thrombospondin moti
76                     These results identify A disintegrin and metalloprotease with thrombospondin moti
77       These proteins belong to the ADAMTS (a disintegrin and metalloprotease with thrombospondin repe
78 dothelial cell (HUVEC)-released ADAMTS-13 (a disintegrin and metalloprotease with thrombospondin repe
79 elated to a severe deficiency in ADAMTS13 (a disintegrin and metalloprotease with thrombospondin type
80  in protein C, protein S, antithrombin and A Disintegrin and Metalloprotease with Thrombospondin type
81 a (TTP) by identifying naturally processed A Disintegrin And Metalloprotease with ThromboSpondin type
82 patients with diabetes, impaired ADAMTS13 (a disintegrin and metalloprotease with thrombospondin type
83 unoglobulin G (IgG) autoantibodies against A Disintegrin And Metalloprotease with ThromboSpondin type
84                     The protease ADAMTS13 (a disintegrin and metalloprotease with thrombospondin type
85 ulman syndrome [USS]) severe deficiency of a disintegrin and metalloprotease with thrombospondin type
86 cleavage of von Willebrand factor (VWF) by A disintegrin and metalloprotease with thrombospondin type
87  from the endothelial surface by ADAMTS13 (a disintegrin and metalloprotease with thrombospondin type
88  (2) serum creatinine >2.25 mg/dL, and (3) a disintegrin and metalloprotease with thrombospondin type
89  encodes a metalloprotease similar to the "a disintegrin and metalloprotease with thrombospondin" (AD
90 ents, we determined whether transmembrane "a disintegrin and metalloprotease" (ADAM) proteins are exp
91    Proteolytically active ADAM (named for "a disintegrin and metalloprotease") family molecules have
92 induced shedding was abrogated by an ADAM (A disintegrin and metalloprotease) 10 and 17 selective inh
93 scular smooth muscles, KK stimulates ADAM (a disintegrin and metalloprotease) 17 activity via a PAR1/
94 latory region (NRR) that protects an ADAM (a disintegrin and metalloprotease) cleavage site.
95 zyme (TACE; ADAM17), a member of the ADAM (a disintegrin and metalloprotease) family of metalloprotea
96 disintegrin-like domain found in the ADAM (a disintegrin and metalloprotease) family of proteins.
97 eddase activity is attributed to the ADAM (a disintegrin and metalloprotease) family of proteins.
98 re we show that receptor cleavage by ADAM (A Disintegrin And Metalloprotease) metalloproteases promot
99 brane metalloproteases of the ADAM family (a disintegrin and metalloprotease), and the initiation com
100   ADAMDEC1 (Decysin-1) is a putative ADAM (a disintegrin and metalloprotease)-like metalloprotease wi
101                                            A disintegrin and metalloprotease-17 (ADAM17) is a major s
102                                            A disintegrin and metalloprotease-17 (ADAM17) is shown to
103 tream matrix metalloproteinases (MMPs) and a disintegrin and metalloproteases (ADAMs) and stimulate p
104 ng mediated by the cell surface proteases "a disintegrin and metalloproteases" (ADAM)-10 and ADAM-17,
105 todomain shedding, which was not mediated by disintegrin and metalloproteases.
106 le of TSPAN33, a tetraspanin implicated in a disintegrin and metalloproteinase (ADAM) 10 maturation,
107 in-22alpha promotor-driven deficiency of the disintegrin and metalloproteinase (ADAM) 17 (SM22-Adam17
108                                            A Disintegrin And Metalloproteinase (ADAM) 17 is one of th
109                          Peptidases of the a-disintegrin and metalloproteinase (ADAM) family are impl
110                              Prodomains of A disintegrin and metalloproteinase (ADAM) metallopeptidas
111              Serial processing of Cad6B by a disintegrin and metalloproteinase (ADAM) proteins and ga
112                                   Specific a disintegrin and metalloproteinase (ADAM) proteins inhibi
113 gulate ectodomain shedding mediated by the A Disintegrin And Metalloproteinase (ADAM) subfamily of pr
114                        We demonstrate that a disintegrin and metalloproteinase (ADAM)10 is the primar
115  downregulation of metalloproteases mainly a disintegrin and metalloproteinase (ADAM)10, ADAM17, ADAM
116 primed B cell increased gene expression of a disintegrin and metalloproteinase (ADAM)10, which is the
117 wo major transmembrane metalloproteinases, a disintegrin and metalloproteinase (ADAM)17 and ADAM10, a
118 ch as matrix metalloproteinases (MMPs) and a disintegrin and metalloproteinase (ADAMs), are critical
119                Membrane CD23 is cleaved by a disintegrin and metalloproteinase 10 (ADAM10) and this c
120                                            A disintegrin and metalloproteinase 10 (ADAM10) is a ubiqu
121                                            A disintegrin and metalloproteinase 10 (ADAM10) is a zinc-
122                                     B cell A disintegrin and metalloproteinase 10 (ADAM10) is require
123 ected from skin and lung fibrosis and that a disintegrin and metalloproteinase 10 (ADAM10) is the maj
124                The proteolytic activity of a disintegrin and metalloproteinase 10 (ADAM10) regulates
125                                            A disintegrin and metalloproteinase 10 (ADAM10), a disinte
126 viously described mice lacking endothelial a disintegrin and metalloproteinase 10 (ADAM10), a key reg
127 es expression of the alpha toxin receptor, a disintegrin and metalloproteinase 10 (ADAM10).
128 how that TACI is sequentially processed by a disintegrin and metalloproteinase 10 and gamma-secretase
129                 In addition, we found that a disintegrin and metalloproteinase 10 expression is upreg
130 estingly, the drug-induced upregulation of a disintegrin and metalloproteinase 10 on MM cells is asso
131      TACI proteolysis involved shedding by a disintegrin and metalloproteinase 10 releasing sTACI fro
132  by the alpha- and beta-secretases ADAM10 (a disintegrin and metalloproteinase 10) and BACE1 (beta-si
133                                    ADAM10 (a disintegrin and metalloproteinase 10) is the principal a
134 sintegrin and metalloproteinase 17 but not a disintegrin and metalloproteinase 10, respectively, whic
135 d high levels of the FcepsilonRII sheddase a disintegrin and metalloproteinase 10, which implies that
136 phiregulin, independent of metalloprotease a disintegrin and metalloproteinase 17 (ADAM17) activity.
137                                            A disintegrin and metalloproteinase 17 (ADAM17) is a membr
138 els of senescence that the metalloprotease A disintegrin and metalloproteinase 17 (ADAM17) is activat
139 evious studies showed that inactivation of A disintegrin and metalloproteinase 17 (ADAM17), a membran
140 viously shown that epidermal deficiency of a disintegrin and metalloproteinase 17 (ADAM17), the princ
141 onse to TSST-1 that includes the sheddase, a disintegrin and metalloproteinase 17 (ADAM17).
142                   Dysregulated activity of A Disintegrin And Metalloproteinase 17 (ADAM17)/TNFalpha C
143 nverting enzyme (TACE; also referred to as a disintegrin and metalloproteinase 17 [ADAM17]), with sma
144  Indeed, inhibition of gamma-secretase and a disintegrin and metalloproteinase 17 but not a disintegr
145 embrane-anchored metalloproteinase ADAM17 (a disintegrin and metalloproteinase 17) in endothelial cel
146                                    ADAM17 (a disintegrin and metalloproteinase 17) is ubiquitously ex
147 n kinase C-dependent activation of ADAM17 (a disintegrin and metalloproteinase 17).
148                                    ADAM17 (a disintegrin and metalloproteinase 17, also referred to a
149                              We found that a disintegrin and metalloproteinase 22 (ADAM22) is a compo
150                                            A disintegrin and metalloproteinase 8 (ADAM8) has been ide
151                                            A disintegrin and metalloproteinase 8 (ADAM8) is involved
152                   The transmembrane ADAM8 (A Disintegrin And Metalloproteinase 8) protein is abundant
153 ng of HB-EGF by TNFalpha-converting enzyme/a disintegrin and metalloproteinase 9 (ADAM9) and ADAM17.
154 PS/TLR4-mediated generation of sMER required disintegrin and metalloproteinase ADAM17 and was indepen
155 proteinases (MMPs) and proteins containing a disintegrin and metalloproteinase domain (ADAM) are impo
156                                            A disintegrin and metalloproteinase domain 10 (ADAM10) is
157                                            A disintegrin and metalloproteinase domain 10 (Adam10), a
158 heir plasma membrane expression of ADAM17 (a disintegrin and metalloproteinase domain 17), an enzyme
159 ot only matrix metalloproteinases but also a disintegrin and metalloproteinase domain family members
160 proteinases matrix metalloproteinase-9 and a disintegrin and metalloproteinase domain-8.
161                           p40 up-regulates a disintegrin and metalloproteinase domain-containing prot
162 eucine-rich, glioma-inactivated 1 (LGI1) and disintegrin and metalloproteinase domain-containing prot
163                                            A disintegrin and metalloproteinase domain-containing prot
164 iotensin-converting enzyme-sheddase ADAM9 (a disintegrin and metalloproteinase domain-containing prot
165 Palpha during inflammation is regulated by a disintegrin and metalloproteinase domain-containing prot
166 eases responsible for ectodomain shedding is disintegrin and metalloproteinase domain-containing prot
167                                            A disintegrin and metalloproteinase domain-containing prot
168 p-regulation of ADAM10, suggesting that this disintegrin and metalloproteinase mediates the chemokine
169      Genetic truncation of the transmembrane disintegrin and metalloproteinase protein ADAM11 resulte
170 tudies have elucidated the significance of a disintegrin and metalloproteinase proteins (ADAMs) in PN
171 ntegrin and metalloproteinase 10 (ADAM10), a disintegrin and metalloproteinase that resides in the po
172 ly in patients with nondeficient ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin
173 hrough continuous proteolysis by ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin
174  adults and mice have implicated ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin
175 lecular-weight rVWF multimers by ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin
176                              Deficiency of a disintegrin and metalloproteinase with a thrombospondin
177  the action of the VWF protease ADAMTS-13 (a disintegrin and metalloproteinase with a thrombospondin
178                                            A disintegrin and metalloproteinase with a thrombospondin
179 opment of autoantibodies against ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin
180                                  ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin
181                                            A disintegrin and metalloproteinase with thrombospondin mo
182 ggrecan, matrix metalloproteinases (MMPs), a disintegrin and metalloproteinase with thrombospondin mo
183 a-inducible factor-2alpha, syndecan-4, and a disintegrin and metalloproteinase with thrombospondin mo
184                                  ADAMTS13 (a disintegrin and metalloproteinase with thrombospondin mo
185                                  ADAMTS16 (a disintegrin and metalloproteinase with thrombospondin mo
186 oproteinase family that cleaves lecticans, a disintegrin and metalloproteinase with thrombospondin mo
187 f1), an endosulfatase gene, and CG4096, an A Disintegrin And Metalloproteinase with ThromboSpondin mo
188 y microenvironment release factors such as a disintegrin and metalloproteinase with thrombospondin mo
189                                            A disintegrin and metalloproteinase with thrombospondin mo
190 ecent studies have implicated the protease a disintegrin and metalloproteinase with thrombospondin mo
191 osteoarthritis include metalloproteinases, a disintegrin and metalloproteinase with thrombospondin mo
192 m whereby two distinct metalloproteinases, a disintegrin and metalloproteinase with thrombospondin mo
193                             Aggrecanase-2 (a disintegrin and metalloproteinase with thrombospondin mo
194            The metalloproteinase ADAMTS-5 (A disintegrin and metalloproteinase with thrombospondin mo
195                Aggrecanases of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin mo
196                                            A disintegrin and metalloproteinase with thrombospondin mo
197  family of extracellular proteases (called a disintegrin and metalloproteinase with thrombospondin mo
198                                The ADAMTS (A Disintegrin and Metalloproteinase with Thrombospondin mo
199  in the development of osteoarthritis, and a disintegrin and metalloproteinase with thrombospondin mo
200 e Yeast Two-Hybrid approach, we identified a disintegrin and metalloproteinase with thrombospondin re
201 MAs often associated with severe ADAMTS13 (a disintegrin and metalloproteinase with thrombospondin ty
202                  One group is the ADAMTSs (a disintegrin and metalloproteinase with thrombospondin ty
203 helial activation and dysfunction, whereas a disintegrin and metalloproteinase with thrombospondin ty
204 g for 9 months and correlating with higher a disintegrin and metalloproteinase with thrombospondin-13
205  thrombospondin-13 activity and lower anti-a disintegrin and metalloproteinase with thrombospondin-13
206           Conversely, the alpha-secretase "a disintegrin and metalloproteinase" 10 (ADAM10) cleaves A
207           ADAM17, a prominent member of the 'Disintegrin and Metalloproteinase' (ADAM) family, contro
208 racterized the catalytic activity of ADAM (a disintegrin and metalloproteinase) 10 toward human CD23.
209 age of membrane-anchored proteins by ADAM (a disintegrin and metalloproteinase) endopeptidases plays
210 idate the role of key members of the ADAM (a disintegrin and metalloproteinase) enzyme family, as wel
211            Like other members of the ADAM (a disintegrin and metalloproteinase) family, the integrin-
212                                     ADAMs (a disintegrin and metalloproteinase) have important roles
213                        Wild-type and Adam (A Disintegrin And Metalloproteinase) knockout mice were ex
214             RECK release disinhibits ADAM (a disintegrin and metalloproteinase) protease-dependent sh
215                                    ADAM15, a disintegrin and metalloproteinase, is capable of counter
216 nd factor (VWF) cleaving enzyme, ADAMTS13 (a disintegrin and metalloproteinase, with a thrombospondin
217 of metalloproteinase inhibitors and blocks A disintegrin and metalloproteinase-10 (ADAM-10) and ADAM-
218 s of matrix metalloproteinase-7 (MMP7) and a disintegrin and metalloproteinase-12 (ADAM12) in alpha(1
219 present study we present new evidence that a disintegrin and metalloproteinase-17 (ADAM17) is respons
220 ates the TNF-alpha convertase enzyme (TACE/a disintegrin and metalloproteinase-17), leading to activa
221 receptor (EGFR) ligand shedding by ADAM17 (a disintegrin and metalloproteinase-17).
222                       To determine whether a disintegrin and metalloproteinase-8 (Adam8) regulates al
223 matrix-specific manner and is required for a disintegrin and metalloproteinase-mediated shedding of t
224                              Expression of a disintegrin and metalloproteinases (ADAMs) 10 and 17, wh
225 t proteases with Cad6B in vitro shows that a disintegrin and metalloproteinases (ADAMs) ADAM10 and AD
226                                            A disintegrin and metalloproteinases (ADAMs) are a family
227                                            A Disintegrin and Metalloproteinases (ADAMs) are the princ
228 -dependent disintegrin metalloproteinases (a disintegrin and metalloproteinases (ADAMs) have been imp
229 omain cleavage of cell-surface proteins by A disintegrin and metalloproteinases (ADAMs) is highly reg
230 m the cell surface was mediated in part by a disintegrin and metalloproteinases 10 and 17.
231              Matrix metalloproteinases and a disintegrin and metalloproteinases are members of the zi
232 atrix metalloproteinases) and the related "a disintegrin and metalloproteinases" (ADAMs) promote tumo
233                                     ADAMs (a disintegrin and metalloproteinases) are a family of mult
234 fect on matrix metalloproteinase (MMP)-13, a disintegrin and MMP with thrombospondin motifs (ADAMTS)-
235            ADAMTS-5 truncates comprising the disintegrin and/or catalytic domains were able to compet
236 his investigation addressed the paradox that disintegrins and small RGD-ligands readily bind to the r
237                One of the proteases is the a-disintegrin-and-metalloprotease 10 (ADAM10) which acts a
238          Endothelial-specific reduction of a disintegrin-and-metalloprotease-domain-10 (Adam10) and i
239 ife-essential molecules from precursors by a-disintegrin-and-metalloproteases (ADAMs) is regulated wi
240            We also found that MMP8 cleaved a-disintegrin-and-metalloproteinase-domain-10 and that MMP
241   Knockdown of MMP8 or incubation with the a-disintegrin-and-metalloproteinase-domain-10 inhibitor GI
242 10 and that MMP8 deficiency reduced mature a-disintegrin-and-metalloproteinase-domain-10 on SPCs.
243 xpression levels of ADAM8, a metalloprotease disintegrin, are correlated with poor clinical outcome.
244  a non-protease member of the ADAM family of disintegrins, as a direct estrogen receptor (ER)-indepen
245 concave face of a rigid module formed by the disintegrin, cysteine-rich, and epidermal growth factor-
246  analysis of ADAM17 revealed that within its disintegrin/cysteine-rich region are two highly conserve
247 f migration by ADAM9-L requires a functional disintegrin domain and integrin binding.
248 matrix metalloproteinase (MT1-MMP), ADAMs (a disintegrin domain and metalloproteinases), and gamma-se
249 -like domain being regulatory and two in the disintegrin domain being structural.
250 egrins alpha6 and beta1 bind to TACE via the disintegrin domain but also that mechanical strain enhan
251  of the RGD integrin-binding sequence in the disintegrin domain of ADAM-15 (MDC-15; metargidin) highl
252 DAM) proteins inhibit reprogramming, and the disintegrin domain of ADAM29 is necessary and sufficient
253 mpetitive inhibitor of human ADAM9 catalytic/disintegrin domain with an overall inhibition constant o
254 nsists of a prodomain, a catalytic domain, a disintegrin domain, and a membrane-proximal domain as we
255 361, designed by structural modelling of the disintegrin domain, prevents ADAM8 multimerization.
256 itional O-fucosylation site was found in the disintegrin domain.
257  membrane-proximal stalk, cysteine-rich, and disintegrin domains of ADAM10 mediated its co-immunoprec
258 endent manner to both VCAM-1 and select ADAM disintegrin domains.
259 quirements for the stalk, cysteine-rich, and disintegrin domains.
260 similar to (resting) integrin binding to the disintegrin echistatin.
261  also decreased the inhibitory effect of the disintegrins, echistatin and eristostatin, and the alpha
262                                        Using disintegrins, echistatin, and VLO4, peptide inhibitors t
263 on of a member of the ADAM metalloproteinase disintegrins family, resulting in concomitant release of
264 n by monoclonal antibody and the met-leu-asp-disintegrin inhibited dermal human microvascular endothe
265 logy, we have recently shown that the ADAM15 disintegrin is significantly overexpressed during the me
266 ow that ADAM11, a transmembrane noncatalytic disintegrin, is the first reported Kv1-interacting prote
267            The proximal metalloprotease (M), disintegrin-like (D), thrombospondin-1 (T), Cys-rich (C)
268 domain containing 5 (Zswim5); and Adamts5 [a disintegrin-like and metallopeptidase (reprolysin type)
269 lthough UL-VWF is proteolysed by ADAMTS13 (a disintegrin-like and metalloprotease domain with thrombo
270 etermined that mice deficient in ADAMTS5, (A Disintegrin-like And Metalloprotease domain with Thrombo
271 cluding matrix metalloproteases (MMPs) and a disintegrin-like and metalloprotease with thrombospondin
272 -1beta and a resultant increase in ADAMTS (a disintegrin-like and metalloprotease with thrombospondin
273 tly, we reported a gene network of ADAMTS (A Disintegrin-like and Metalloprotease with Thrombospondin
274  activity of VWF is modulated by ADAMTS13 (a disintegrin-like and metalloprotease with thrombospondin
275 brand factor (VWF) levels are elevated and a disintegrin-like and metalloprotease with thrombospondin
276 ealed that a significant number of ADAMTS (a disintegrin-like and metalloproteinase (reprolysin type)
277                                The ADAMTS (a disintegrin-like and metalloproteinase domain with throm
278  beta domain of the versican-V1 variant by a disintegrin-like and metalloproteinase domain with throm
279                                  ADAMTS-4 (a disintegrin-like and metalloproteinase with thrombospond
280 CM enzyme ADAMTS5, a member of the ADAMTS (A Disintegrin-like and Metalloproteinase with Thrombospond
281                 ADAMTS5 is a member of the A Disintegrin-like And Metalloproteinase with ThromboSpond
282   LOC306664 is predicted to translate into A Disintegrin-like and Metalloproteinase with Thrombospond
283 tivity and protein expression of ADAMTS13 (a disintegrin-like and metalloproteinase with thrombospond
284                           The discovery of a disintegrin-like and metalloproteinase with thrombospond
285 ated a recombinant soluble version of the gB disintegrin-like domain (gB-DLD).
286                   Mimicry of the ADAM family disintegrin-like domain by HCMV gB represents a novel me
287  sequence similarity to the integrin-binding disintegrin-like domain found in the ADAM (a disintegrin
288 fy the surface provided by the catalytic and disintegrin-like domains of ADAMTS-5 as a legitimate tar
289  interact, and showed that the catalytic and disintegrin-like domains support these intermolecular in
290      Here, we report that melittin activates disintegrin-like metalloproteases (ADAMs) and that downs
291                                            A disintegrin-like metalloproteinase with thrombospondin m
292 loy some combination of ancillary C-terminal disintegrin-like, thrombospondin-1, cysteine-rich, and s
293  and cellular prion (PrP(c)) undergo similar disintegrin-mediated alpha-secretase cleavage yielding N
294                                              Disintegrin metalloproteases (Adam) can manipulate the s
295 etalloproteinase inhibitors or antibodies to disintegrin metalloproteinase 8 (ADAM8), a major eosinop
296 inal 385-amino acid fragment of ADAMTS-18 (a disintegrin metalloproteinase with thrombospondin motifs
297 n of the disulfide-isomerase ERp5 and of the disintegrin-metalloproteinase ADAM10, able to shed the l
298                           The zinc-dependent disintegrin metalloproteinases (a disintegrin and metall
299 nases, the matrix metalloproteinases and the disintegrin metalloproteinases, have consequences well b
300 tion across the four most abundant proteins (disintegrins, phospholipase A(2)'s, serine proteinases,

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