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1 n protein (PrP), a host-encoded cell surface sialoglycoprotein.
2 ndicating that the erythrocyte receptor is a sialoglycoprotein.
3 incorporated into cell surface and secreted sialoglycoproteins.
4 complex composed of a mucin subunit ascites sialoglycoprotein-1 and a transmembrane subunit ascites
5 sting of a mucin subunit ASGP-1 (for ascites sialoglycoprotein-1) and a transmembrane subunit ASGP-2,
6 onsisting of a mucin subunit ASGP-1 (ascites sialoglycoprotein-1) and a transmembrane subunit ASGP-2,
8 a glycosyl phosphatidylinositol (GPI)-linked sialoglycoprotein and cancer stem cell marker, is associ
10 of two subunits, the mucin component ascites sialoglycoprotein ASGP-1 and the transmembrane subunit A
11 ein complex composed of a sialomucin ascites sialoglycoprotein (ASGP)-1 and a transmembrane subunit A
12 dentified as 65 (major)- and 130 (minor)-kDa sialoglycoproteins by S fimbria immunoblotting and were
14 t of misfolded, self-replicating states of a sialoglycoprotein called the prion protein or PrP(C) The
16 e functional roles of brain gangliosides and sialoglycoproteins consistent with related human congeni
17 rmational conversion of the prion protein, a sialoglycoprotein containing two N-linked oligosaccharid
18 age as well as the endocytic accumulation of sialoglycoproteins, demonstrating a direct link between
19 ce glycoproteins by ex vivo treatment with O-sialoglycoprotein endopeptidase (OSGE) can reverse many
21 alomucin-like molecules that share similar O-sialoglycoprotein endopeptidase sensitivity with other c
22 ed digestion of wild-type neutrophils with O-sialoglycoprotein endopeptidase was used to reduce the P
23 by pretreatment of the KM12-L4 cells with O-sialoglycoprotein endopeptidase, an enzyme that cleaves
27 rophils was dependent on the presence of the sialoglycoprotein fetuin, a constituent of bovine serum.
29 enabled the enrichment and identification of sialoglycoproteins from cultured cells and model organis
30 We have previously identified two mucin-type sialoglycoproteins from porcine intestinal epithelial ce
31 on that depends primarily on the erythrocyte sialoglycoprotein glycophorin A (GYPA) and erythrocyte-b
33 and 3, and the single transmembrane-spanning sialoglycoprotein, GPA, may serve as a model for interac
34 alin (CD43 or sialophorin) is a cell surface sialoglycoprotein implicated in cell adhesion and prolif
35 urified receptors were intestinal mucin-type sialoglycoproteins (IMTGP) isolated from porcine enteroc
39 in (an abnormal isoform of a native cellular sialoglycoprotein) in the central nervous system is a re
40 hat 65- and 130-kDa proteins represent novel sialoglycoproteins involved in the binding of S-fimbriat
41 CD24, a glycosyl phosphatidylinositol-linked sialoglycoprotein, is associated with poor outcome in ur
42 anAg is a novel glycoform of CD43, a surface sialoglycoprotein normally found only on hematopoietic c
45 osialin/sialophorin), the negatively charged sialoglycoprotein of leukocytes, in the binding of mycob
48 yclonal antiserum against MG-160, a membrane sialoglycoprotein of the organelle, and NFTs and SPs wer
49 found that glycophorin A, the most abundant sialoglycoprotein on erythrocytes, engaged neutrophil Si
50 c mice expressing the rat MG160 medial Golgi sialoglycoprotein only in the GA of astrocytes, and visu
51 or a putative low molecular weight, secreted sialoglycoprotein, potentially useful for the diagnosis
54 roach was validated by the identification of sialoglycoproteins such as CD105, neuropilin-1, and CLEC
55 V and have been hypothesized to degrade host sialoglycoproteins that participate in mucosal immune fu
56 study, we used a method to selectively label sialoglycoproteins to identify new membrane and secreted
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