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1 tensile force takes when applied through the integrin beta-subunit.
2 xY motif within the cytoplasmic tail of most integrin beta subunits.
3 n(s) may be quite distinct from those of the integrin beta subunits.
4 s that act on the short cytoplasmic tails of integrin beta subunits.
5 s that act on the short cytoplasmic tails of integrin beta subunits.
6 r proteins involved in cell adhesion such as integrin beta subunits (all Metazoa).
7 he study point to the similarity between the integrin beta subunits and the MIDAS motif at two of thr
8 in the association of alpha-actinin with the integrin beta subunit, and that PtdIns (3,4,5)-P(3) coul
9 cysteine-rich repeats in the stalk region of integrin beta subunits appear to convey signals impingin
10                                    Thus, the integrin beta subunits appear to present a MIDAS-like mo
11                                          Two integrin beta subunits are encoded in the Drosophila gen
12 her antigenic residues in beta2 and in other integrin beta subunits are present on the front.
13                 Homologous residues in other integrin beta subunits are similarly critical for ligand
14 mic tail but not with tails from three other integrin beta subunits (beta2, beta3, and beta5) or from
15 el gene product that is highly homologous to integrin beta subunits but lacks associating alpha subun
16 ene and gene product related to those of the integrin beta subunits but whose function(s) may be quit
17 ferent than in beta3 integrins, showing that integrin beta subunits can be specialized to assume diff
18 rupting the C-terminal cytoplasmic domain of integrin beta subunits can have dominant negative effect
19 of the components of CR3 and CR4: the common integrin beta subunit CD18 and the alpha subunits CD11b
20  achieved by targeting the leukocyte beta(2)-integrin beta-subunit CD18 was required to reduce neoint
21               Monoclonal antibodies to beta1 integrins beta-subunit (CD29) also strongly induced tumo
22                                              Integrin beta subunits contain a highly conserved I-like
23                                              Integrin beta subunits contain four cysteine-rich repeat
24                         The A-domains within integrin beta subunits contain three metal sites termed
25            The ligand-binding head region of integrin beta subunits contains a von Willebrand factor
26                 The ligand-binding region of integrin beta subunits contains a von Willebrand factor
27 the extracellular and cytoplasmic domains of integrin beta subunits contribute to these differences.
28             We report an interaction between integrin beta subunit cytoplasmic domain and Rack1, a Tr
29 alin phosphotyrosine-binding (PTB) domain to integrin beta subunit cytoplasmic domains (tails) causes
30  protein, physically associates with certain integrin beta subunit cytoplasmic domains (tails) via it
31                                          The integrin beta subunit cytoplasmic domains are important
32                       Kindlins directly bind integrin beta subunit cytoplasmic domains at a site dist
33 to the sequences in talin that interact with integrin beta subunit cytoplasmic domains.
34 n activation is usually mediated through the integrin beta subunit cytoplasmic tail and can be regula
35 binding of the cytoskeletal protein talin to integrin beta subunit cytoplasmic tails leads to the con
36   The talin FERM F3 subdomain binds both the integrin beta-subunit cytoplasmic domain and PIPK1gamma,
37 ated via the binding of talin and kindlin to integrin beta-subunit cytoplasmic tails.
38 and is dependent on interactions between the integrin beta subunit-cytoplasmic tail and the cytoskele
39 at the SDL is responsible for the defects in integrin beta subunit expression and folding in the abse
40  have determined the genomic structure of an integrin beta-subunit gene from the coral, Acropora mill
41 gnificantly more than have been found in any integrin beta-subunit genes from higher animals.
42 nce of an I domain-like structure within the integrin beta subunit has been proposed based on the sim
43 en shown that a conformational change of the integrin beta-subunit headpiece (i.e. the beta I domain
44 e conformations, it is controversial whether integrin beta subunit I-like domains undergo structurall
45 directional signaling pathways controlled by integrin beta subunits in platelets and describe a high-
46  In this study we identify the domain of the integrin beta subunit involved in determining ligand bin
47            The amino-terminal domain of each integrin beta subunit is hypothesized to contain an ion
48 SCF-derived cells and encodes a novel murine integrin beta subunit-like molecule, dubbed Pactolus-1 (
49  suggest that tyrosine phosphorylation of an integrin beta subunit may be important in initiating out
50               Given the similarity among all integrin beta subunits, our results may help us to under
51 s that potentially reduce interaction of the integrin beta subunit plexin-semaphorin-integrin (PSI) a
52 s on how the inserted (I)-like domain in the integrin beta-subunit regulates ligand binding by the ne
53  of mutants, including swaps among different integrin beta-subunits, show that C1-C2 loop lengths of
54 s small domain is highly divergent among the integrin beta subunits, suggesting that it may play a ro
55 d non-integrin proteins, and possibly in all integrin beta subunits, these two loop segments may repr
56 ntegrin, we fused the cytoplasmic domains of integrin beta subunits to an N-terminal sequence contain
57 e length of this loop may have evolved among integrin beta-subunits to adjust the equilibrium between
58                              A wide array of integrin beta subunits was detected in betaTC3 and NIT-1
59 eras of beta3 and beta5, the most homologous integrin beta subunits, were expressed with alphav on th

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