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1 kin domain, which is a common feature of the plakins.
2 re mediated through different domains on the plakins.
3 unique epitopes in the tail domains of these plakins.
4 This is the first reported mutation of desmo-plakin and also the first inherited skin disorder in whi
6 mmary, proteomic analysis of uEVs identified plakins and complement as disease-associated proteins in
8 l actin binding proteins that are related to plakins and dystrophin and expressed in axons during dev
13 ctin binding domains; regions of homology to plakins at either end of the giant polypeptide; 29 copie
15 -spectrin, suggesting that the SH3 domain of plakins contributes to the stability and rigidity of thi
16 ural and mechanistic insights into an entire plakin domain and provides a basis for understanding the
17 mino-acid N-terminal region of DP contains a plakin domain common to members of the plakin family.
19 ay scattering analysis shows that the entire plakin domain has an "L" shape, with a long arm and a sh
20 specific interactions with plakoglobin, the plakin domain of desmoplakin, plakophilin 1, and the cyt
21 ing (SAXS) to elucidate the structure of the plakin domain of plectin, extending our previous analysi
22 ins include an actin-binding domain (ABD), a plakin domain, a coiled coil (CC) rod domain, two differ
23 elucidate the architecture of desmoplakin's plakin domain, as well as its constituent tandem SRs.
24 een described previously and consists of the plakin domain, the CC rod domain, and the first IFBD.
26 esmosomes are mediated through the so-called plakin domain, which is a common feature of the plakins.
27 roteins, and spans what has been termed the "plakin domain," which includes residues 180-1022 and con
31 rvation, we propose that the architecture of plakin domains is defined by two pairs of spectrin repea
32 ontinuous versus segmented structures of the plakin domains of plectin and desmoplakin give insight i
34 -SR9 region, which is conserved in all other plakin domains, forms a rigid segment stabilized by uniq
39 oteins of the homologous tail region of five plakin family members, including the recently cloned per
43 -like repeats may enable some members of the plakin family of cytolinkers to laterally bind and stabi
44 1-e, also known as BP230) is a member of the plakin family of hemidesmosome cytoskeletal linker prote
45 ology to envoplakin and other members of the plakin family of intermediate filament connector molecul
46 far as autoantigens in PNP all belong to the plakin family of proteins and include desmoplakin, the 2
49 d that the 195-kD protein is a member of the plakin family of proteins, to which envoplakin, desmopla
53 omes belong to the cadherin superfamily, the plakin family, and the armadillo repeat protein family.
55 s in PPL being consistent with that of other plakin genes: 21 small exons, separated by large introns
56 ammalian orthologue of the Drosophila kakapo plakin genetically involved in epidermal-muscle adhesion
58 While ACF7/kakapo is divergent from other plakins in its IF-binding domain, it has at least one ac
59 homologous region in the carboxy-terminus of plakins, including the newly characterized periplakin, s
61 ntains a putative actin-binding domain and a plakin-like domain that are highly homologous to dystoni
62 desmoplakin give insight into how different plakins might respond to tension and transmit mechanical
63 ciency in beta4 integrin or knockdown of the plakin protein Bullous Pemphigoid Antigen 1e (BPAG1e).
65 ypothesis that the beta4 integrin-associated plakin protein, bullous pemphigoid antigen 1e (BPAG1e) f
66 ding SR is also observed in plectin, another plakin protein, but not in alpha-spectrin, suggesting th
68 esmosomal proteins, is found in a variety of plakin proteins, and spans what has been termed the "pla
71 in the shot locus, which encodes a series of plakin repeats similar to the COOH terminus of plakins s
79 we identify the integrin-binding cytolinker plakin (VAB-10A) and integrin (INA-1/PAT-3) as key BM-BM
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