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1  previously documented for inhibitors of the ADAM family.
2 way that separates them from the rest of the ADAM family.
3 y activation of ADAM9, another member of the ADAM family.
4 a substrate for several other members of the ADAM family.
5 ne-anchored metalloprotease belonging to the ADAM family.
6 es in the A Disintegrin And Metalloprotease (ADAM) family.
7  of the A Desintegrin and Metalloproteinase (ADAM) family.
8  a disintegrin and metalloproteinase domain (ADAM) family.
9 rsistent mucosal increases in members of the ADAMs family.
10 d versican, membrane metalloproteases of the ADAM family (a disintegrin and metalloprotease), and the
11 or alpha converting enzyme), a member of the ADAM family (a disintegrin and metalloprotease-family) o
12 sion of a catalytically active member of the ADAM family, ADAM15, is associated with the progression
13      When compared with other members of the ADAM family, ADAMDEC1 displays some unusual features.
14 s proteolytic activation by proteases of the ADAM family and BACE1.
15                 Although most members of the ADAM family are active zinc metalloproteinases, 8 of 21
16  of the a-disintegrin and metalloproteinase (ADAM) family are implicated in cancer cell proliferation
17  proteases, the matrix metalloproteinase and ADAM families, as potential targets for anticoronavirus
18 se of the A disintegrin and metalloprotease (ADAM) family, can mediate NKG2D ligand cleavage and this
19 in of ADAMDEC1, like in other members of the ADAM family, confers catalytic latency.
20 es of the disintegrin and metalloproteinase (ADAM) family control cell signaling interactions via hyd
21  of the 'Disintegrin and Metalloproteinase' (ADAM) family, controls vital cellular functions through
22                               Mimicry of the ADAM family disintegrin-like domain by HCMV gB represent
23 cloned a cDNA encoding a novel member of the ADAM family from a Xenopus laevis neurula stage library.
24                       Because members of the ADAMs family have been implicated in growth factor proce
25 d ADAM17 are the most studied members of the ADAM family in the gastrointestinal tract.
26 t Fish interacts with several members of the ADAMs family, including ADAMs 12, 15, and 19.
27                    Fertilin, a member of the ADAM family, is found on the plasma membrane of mammalia
28  membrane-associated metalloproteases of the ADAM family, leading to the shedding of their ectodomain
29  and chimeric constructs of TACE and another ADAM family member, ADAM-10, we studied the function of
30 lectively, these data indicate that a second ADAM family member, cyritestin, functions with fertilin
31 rs reported to date are not specific to this ADAM family member.
32 e novel fluorescent substrates for the human ADAM family members ADAM17, ADAM10, ADAM8, and ADAM12 th
33 This review provides a comprehensive look at ADAM family members and their role in pathology and prov
34                                 Because many ADAM family members have a putative proteinase function,
35                                  The role of ADAM family members in Th17 cell differentiation is unkn
36                Characterization of these two ADAM family members showed that they are both processed
37                                        Among ADAM family members, ADAM10 stands out as particularly i
38  whether TIMP-1, an inhibitor of some of the ADAM family members, enhances the tumor necrosis factor-
39 osomal cadherin can be regulated by multiple ADAM family members.
40 H binds to and potentially regulates certain ADAM family members.
41 n the complete domain organization common to ADAM family members.
42         A disintegrin and a metalloprotease (ADAM) family members have been implicated in many biolog
43  active A Disintegrin And Metalloproteinase (ADAM) family members.
44  of the A disintegrin and A metalloprotease (ADAM) family; members of this protein family are associa
45  Slit-Robo repulsion, we have identified the Adam family metalloprotease Kuzbanian (Kuz).
46 hich is shed from cells after cleavage by an ADAM family metalloprotease, ADAM17 (TNFalpha-converting
47                  Pericellular proteolysis by ADAM family metalloproteinases has been widely implicate
48 oteinase domain 10 (Adam10), a member of the ADAM family of cell membrane-anchored proteins, has been
49                                          The ADAM family of disintegrin metalloproteases plays import
50 ntified ADAM22, a non-protease member of the ADAM family of disintegrins, as a direct estrogen recept
51           Loss of Kuzbanian, a member of the ADAM family of metalloproteases, produces neurogenic phe
52 e proteolytically released by members of the ADAM family of metalloproteases.
53  we show that sup-17 encodes a member of the ADAM family of metalloproteases.
54 n if this effect involves also modulation of ADAM family of metalloproteinases, which are responsible
55 This profile suggests the involvement of the ADAM family of proteases in the cleavage of ICAM-1.
56 oteases, the broad spectrum inhibitor of the ADAM family of proteases, tumor necrosis factor-alpha pr
57 AM-12, a novel member of the multifunctional ADAM family of proteins is linked to cancer, arthritis a
58                                          The ADAM family of proteins plays an important role in modul
59                     ADAM 12, a member of the ADAM family of transmembrane metalloprotease-disintegrin
60 rs of the A Disintegrin And Metalloprotease (ADAM) family of membrane-anchored metalloproteases are s
61     The a disintegrin and metalloproteinase (ADAM) family of proteinases alter the extracellular envi
62                                          The ADAMs family of membrane-anchored proteins, containing a
63 metalloproteinase potentially related to the ADAM family or MMP family of proteases previously implic
64 by, or redundancy with, other members of the ADAM family or perhaps even with other molecules will be
65 d shedding of cell-surface N-cadherin by the ADAM family protease ADAM10/Kuzbanian.
66 down of a disintegrin and metalloproteinase (ADAM) family protease ADAM10 decreases this constitutive
67                We also provide evidence that ADAM family proteases are required for both constitutive
68 d certain disintegrin and metalloproteinase (ADAM) family proteases in mammals.
69 e inhibitor as it only weakly inhibits other ADAM family proteinases in the micromolar range and does
70  BP-5, we evaluated if one of the members of ADAM family was the BP-5 protease.
71 MMP)- and a disintegrin and metalloprotease (ADAM)-family zinc metalloproteases markedly decreased bo