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1 f the predicted beta-propeller domain of the integrin alpha subunit.
2 existence of limiting factors that bind the integrin alpha subunit.
3 genomic clone encoding ITGAD, a novel beta 2-integrin alpha subunit.
4 d binding by the neighboring I domain in the integrin alpha-subunit.
5 es cellular functions differently from other integrin alpha subunits.
6 nct from that of the A-domains found in some integrin alpha subunits.
7 unusual structural motif is prototypical for integrin alpha subunits.
9 ressions of various components of FA such as integrin alpha subunits (alpha(v) , alpha(2) , alpha(11)
11 ng inherited mutations on the ability of the integrin alpha-subunit, also termed glycoprotein IIb (GP
12 the extracellular or transmembrane domain of integrin alpha subunit and suggest that this process is
13 e recently proposed beta-propeller model for integrin alpha subunits and is adjacent to a loop contai
14 phaIIbD224 is not well conserved among other integrin alpha subunits and is located in a region of si
15 hat similar I domains exist in several other integrin alpha subunits and non-integrin proteins, and p
16 reviously demonstrated contrasting roles for integrin alpha subunits and their cytoplasmic domains in
17 that surface expression levels of particular integrin alpha subunits are important determinants of NC
21 f a coordinate increase in expression of the integrin alpha subunit CD11b, the CD14 lipopolysaccharid
27 ata to identify PDZ recognition sequences in integrin alpha subunit cytoplasmic domains and found tha
28 Finally, we have also observed that certain integrin alpha subunit cytoplasmic splice variants diffe
30 lity of ECM binding motifs by their specific integrin alpha subunits determining the biophysical mech
33 chanisms by which the cytoplasmic domains of integrin alpha subunits enhance migration and inhibit ce
39 on is associated with upregulation of select integrin alpha subunits in a proteoglycan-specific manne
40 ation was addressed by ectopic expression of integrin alpha subunits in primary quail skeletal muscle
41 servations demonstrate (1) a specificity for integrin alpha subunits in regulating myoblast prolifera
42 in vitro We identified one of four planarian integrin-alpha subunits inhibition of which phenocopied
44 ID), a ligand binding domain shared by seven integrin alpha-subunits, is a critical region for integr
45 we stained muscles with antibodies to the 10 integrin alpha subunits known to form dimers with beta1,
47 orhabditis elegans homologs of the mammalian integrin alpha subunit plays an essential role in the cl
48 addressed the mechanisms by which changes in integrin alpha subunit ratios regulate this decision.
49 993 to be fully conserved among all 18 human integrin alpha subunits, suggesting that their unusual s
51 nucleotides (aONs) against various mammalian integrin alpha subunits to functionally "knock out" inte
53 vel mechanisms involved in the processing of integrin alpha subunits underscore the significance and
54 f is also present in the I domain of certain integrin alpha subunits, where it constitutes a portion