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1 the cell adhesion molecules, E-cadherin and desmocollin.
2 of the desmosomal cadherins, desmogleins and desmocollins.
3 n molecules and comprise the desmogleins and desmocollins.
4 smosomal cadherins, known as desmogleins and desmocollins.
5 , which includes three desmogleins and three desmocollins.
6 ometric relationship between desmogleins and desmocollins.
7 fic differences exhibited by desmogleins and desmocollins.
9 ted proteins, including desmoglein 1 (Dsg1), desmocollin 1 (Dsc1), and keratins 1 and 10 (K1/K10), in
11 se mutations with deleterious predictions in desmocollin 1 and serpin family B member 7, genes encodi
16 downregulated genes (keratin 2A [KRT2A] and desmocollin-1 [DSC-1]) were randomly selected for furthe
17 ifferentiation-specific desmocollin isoforms desmocollin-1 and desmocollin-3 are functionally equival
18 icantly increased abundance of desmoglein-1, desmocollin-1 and plakoglobin in the BPD group with low
19 ample, the desmosome proteins: desmoglein-1, desmocollin-1 and plakoglobin were significantly decreas
22 This raises the question of whether basal desmocollin-1 could alter desmosomal functions and compr
31 ontrast, the interaction of plakoglobin with desmocollin-1a is sensitive to deletion of either end of
33 ed a genome-wide CRISPR screen and uncovered desmocollin 2 (DSC2) as an EBV epithelial receptor and D
35 sembly properties of desmoglein 2 (Dsg2) and desmocollin 2 (Dsc2), which are widely expressed, with D
36 ccumulated levels of desmoglein 2 (Dsg2) and desmocollin 2 increased 1.7-2.0-fold, and both desmosoma
40 of 5' untranslated region till exon 1, 1 the desmocollin-2 (DSC2) duplication of exons 7 to 9, and 1
41 intestinal epithelial desmosomal cadherins, desmocollin-2 (Dsc2) loss promotes colonic epithelial ca
42 mal cadherins termed desmoglein-2 (Dsg2) and desmocollin-2 (Dsc2) that affiliate with the underlying
43 s the desmosomal cadherins, Desmoglein-2 and Desmocollin-2 (Dsc2) that contribute to mucosal homeosta
44 truncation mutation, c.1660C>T (p.Q554X) in desmocollin-2 (DSC2), in affected individuals and determ
45 ns to mediate adhesion, desmoglein-1 (Dsg1), desmocollin-2 (Dsc2a) and plakoglobin were expressed in
46 2 (n=38; 34%), desmoglein-2 (n=30; 26%), and desmocollin-2 (n=1; 1%), whereas 21 patients (16%) had a
47 ll as novel molecules, among them fibulin-2, desmocollin-2, the glycosaminoglycans syndecan-3, and ve
49 the antimetastatic, tumor suppressor genes, desmocollin 3 (DSC3) and MASPIN, which are frequently si
50 nfected with wt p53 revealed both MASPIN and desmocollin 3 (DSC3) to be p53-target genes, even though
55 erved in pemphigus vulgaris, suggesting that desmocollin 3 might be a target of autoantibodies in som
57 ar adhesion, and adsorption with recombinant desmocollin 3 specifically prevents this pathogenic effe
59 redistribution of desmoplakin, desmoglein 3, desmocollin 3, and E-cadherin to the plasma membrane.
60 sera cause loss of keratinocyte cell surface desmocollin 3, but not desmoglein 3 by immunofluorescenc
62 Mice with an epidermal-specific deletion of desmocollin 3, the other major desmosomal cadherin isofo
63 cific desmocollin isoforms desmocollin-1 and desmocollin-3 are functionally equivalent in basal epide
64 hat the desmosomal proteins desmoglein-2 and desmocollin-3, the focal adhesion protein integrin-alpha
65 distinct cellular pathogenic effects in anti-desmocollin and anti-desmoglein pemphigus, despite their
66 between desmosomal cadherins (desmoglein and desmocollin) and plakoglobin, we have sought to identify
68 t, the transmembrane proteins desmoglein and desmocollin are efficiently transported to the cell surf
70 of the desmosomal cadherins, desmoglein and desmocollin, are required for epidermal cell adhesion.
71 al cadherins, comprising the desmogleins and desmocollins, are calcium-dependent transmembrane adhesi
72 onents of the desmosome, the desmogleins and desmocollins, are members of the cadherin family of cell
73 ne desmosomal glycoproteins, desmogleins and desmocollins, are widely considered to function as adhes
74 s a decrease of Dsg3 and desmoplakin but not desmocollin (Dsc) 3 in the Triton-insoluble fraction of
75 ow that heterophilic binding between Dsg and desmocollin (Dsc) is the fundamental adhesive unit of de
78 cell culture samples were immunostained for desmocollin (DSC)2, occludin (OCLN), desmoglein (DSG)1,
80 chments are formed by desmogleins (Dsgs) and desmocollins (Dscs), but the nature of trans-cellular in
81 desmosomal cadherins, desmogleins (Dsgs) and desmocollins (Dscs), comprise the adhesive core of inter
82 he goal of this study was to investigate how desmocollins (DSCs), transmembrane components of desmoso
83 e carboxy-termini of classical cadherins and desmocollins have been shown to play an important role i
84 We propose that the differentiation-specific desmocollin isoforms desmocollin-1 and desmocollin-3 are
85 esmosomal cadherins - called desmogleins and desmocollins - link intermediate filaments (IFs) rather
86 Desmosomal cadherins, desmogleins (Dsgs) and desmocollins, make up the adhesive core of intercellular
88 smosomal components that may be required for desmocollin-mediated adhesion, we constructed a chimeric
89 f the broad cadherin family (desmogleins and desmocollins) that are linked to the intermediate filame
90 n two classes of cadherins, desmogleins, and desmocollins, that bind to the cytoplasmic protein plako
91 ficking of the desmoplakins, desmoglein, and desmocollin to the cell surface; these proteins show a d
92 Three desmoglein isoforms collaborate with desmocollins to build the adhesive core of desmosomes.