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1 alloproteinase-dependent proteolysis of this desmosomal cadherin.
2 f possible synergism between a classical and desmosomal cadherin.
3 ness depends on the organised arrangement of desmosomal cadherins.
4 nents, in which they link desmoplakin to the desmosomal cadherins.
5 nity to desmoglein 3, desmocollin 3, or both desmosomal cadherins.
6 ent (IF)-binding protein desmoplakin (DP) to desmosomal cadherins.
7 attention has been paid to the importance of desmosomal cadherins.
8 ensus sequence not conserved among the other desmosomal cadherins.
9 , including both acetylcholine receptors and desmosomal cadherins.
10 not dependent on the equimolar expression of desmosomal cadherins.
11 report a novel role of Gal3 in stabilizing a desmosomal cadherin and intercellular adhesion in intest
12 smocollin 2 increased 1.7-2.0-fold, and both desmosomal cadherin and plaque components were recruited
14 these diseases, autoantibodies against other desmosomal cadherins and E-cadherin may also be present.
18 rminal desmoplakin polypeptide (DP-NTP), the desmosomal cadherins and plakoglobin were observed in pu
19 histone deacetylase inhibition up-regulates desmosomal cadherins and prevents the loss of adhesion i
20 ll adhesion by compromising the link between desmosomal cadherins and the intermediate filament cytos
21 ing list of human mutations that target both desmosomal cadherins and their associated cytoskeletal a
22 atable connection between both classical and desmosomal cadherins and their respective cytoskeletal l
23 he intermediate filament cytoskeleton to the desmosomal cadherins and thereby confers structural stab
24 ividing epidermal cells, DP and PG anchor to desmosomal cadherins and to each other, forming an order
28 etween adjacent cells, this study implicates desmosomal cadherins as key components of a signaling ax
29 suggest that desmocollin-1 can function as a desmosomal cadherin both in basal and suprabasal cells.
30 igus is caused by IgG autoantibodies against desmosomal cadherins, but the precise mechanisms are in
32 dillo repeat region reduces the affinity for desmosomal cadherins, calorimetric measurements show no
33 g2 processing, supporting the idea that this desmosomal cadherin can be regulated by multiple ADAM fa
35 arm repeats exhibit distinct binding to the desmosomal cadherins comparable in strength to that of t
40 wn that one of the two intestinal epithelial desmosomal cadherins, desmocollin-2 (Dsc2) loss promotes
42 re the structure of the entire ectodomain of desmosomal cadherin desmoglein 2 (Dsg2), using a combina
43 lgaris (PV), autoantibodies (IgG) target the desmosomal cadherin desmoglein 3 (Dsg3) and compromise k
44 mporal dynamics of order and disorder of the desmosomal cadherin desmoglein 3 (Dsg3) in living cells.
45 ted a central role for downregulation of the desmosomal cadherin desmoglein 3 (DSG3) in the pathogene
47 dies against the extracellular domain of the desmosomal cadherin desmoglein 3 cause potentially fatal
49 we have focused on the palmitoylation of the desmosomal cadherin desmoglein-2 (Dsg2) and characterize
50 vulgaris (PV) pathogenic antibodies bind the desmosomal cadherin desmoglein-3 (dsg3), causing epiderm
53 caused by autoantibodies primarily targeting desmosomal cadherins desmoglein 3 (DSG3) and DSG1, leadi
54 understand the reciprocal regulation between desmosomal cadherins (desmoglein and desmocollin) and pl
55 FR inhibition results in accumulation of the desmosomal cadherin, desmoglein 2 (Dsg2), at cell-cell i
59 dy we show that loss of the other intestinal desmosomal cadherin, desmoglein-2 (Dsg2) that pairs with
60 filaments (IFs) by its interaction with the desmosomal cadherins, desmoglein (Dsg), and desmocollin
66 n desmosome assembly, interactions among the desmosomal cadherins, desmoplakin, and the armadillo fam
67 nstrating that the binding of plakoglobin to desmosomal cadherins does not require its soluble state
70 ogether, these data demonstrate that partner desmosomal cadherins Dsg2 and Dsc2 play opposing roles i
71 -Dsc or -Dsg antibodies demonstrate that the desmosomal cadherins, Dsg2 and Dsc1a, are involved in a
72 ring disease in which antibodies against the desmosomal cadherin, DSG3 (desmoglein-3), cause acanthol
73 e potential role of differentiation-specific desmosomal cadherins during apoptosis has not been exami
74 lds but, with the exception of classical and desmosomal cadherin EC1 domains, most of them do not app
75 uggest that the extracellular domains of the desmosomal cadherins exhibit functional properties disti
76 n desmoglein 4 (DSG4), a novel member of the desmosomal cadherin family that is expressed in the hair
77 omes contain multiple representatives of the desmosomal cadherin family, which includes three desmogl
78 This fit suggests an arrangement in which desmosomal cadherins form trans interactions but are too
81 d the cytoplasmic tails of the transmembrane desmosomal cadherins, has been proposed to link IF to th
82 uses a reduction in the levels of endogenous desmosomal cadherins in a dose-dependent manner, leading
84 othesized that the arrangement, or order, of desmosomal cadherins in the intercellular space is criti
85 els of 2 genes as the primary genes: DSG2, a desmosomal cadherin involved in Wnt/beta-catenin signali
86 c deletion of desmocollin 3, the other major desmosomal cadherin isoform expressed in the basal epide
88 , which are characterized by the presence of desmosomal cadherins, known as desmogleins and desmocoll
90 -terminal fragment of desmoglein 2 (Dsg2), a desmosomal cadherin often overexpressed in malignancies.
92 ify a role for desmoplakin in organizing the desmosomal cadherin-plakoglobin complex and provide new
94 and highlight a novel mechanism by which the desmosomal cadherins regulate beta-catenin signaling.
95 punctate structures made up of transmembrane desmosomal cadherins termed desmoglein-2 (Dsg2) and desm
98 ly upon the up-regulation of desmoglein 1, a desmosomal cadherin that maintains the integrity and dif
100 atively normal intercellular distribution of desmosomal cadherins, their cytoplasmic plaques are spar
102 cyte adhesion in linking the transmembranous desmosomal cadherins to the cytoplasmic keratin filament
105 role for endocytic trafficking in regulating desmosomal cadherin turnover and function and raise the
106 Our observations illustrate a new mechanism desmosomal cadherins use to control their surface levels
107 olved in the interaction of plakoglobin with desmosomal cadherins, we have developed direct binding a
109 esmosomes mediate cell-cell adhesion through desmosomal cadherins, which differ from classical cadher
111 somes mediate intercellular adhesion through desmosomal cadherins, which interface with plakoglobin (
112 keleton, but only gamma-catenin binds to the desmosomal cadherins, which links them to intermediate f
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