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1 close this connection by contraction of the submaxillary and petrohyoid muscles, drastically reducin
2 pparent molecular weight was found for mouse submaxillary beta-NGF and recombinant human beta-NGF.
3 aracteristics of leukocytes infiltrating the submaxillary gland (SMG) were analyzed in infected BALB/
4 These results demonstrate that the porcine submaxillary gland core 1 beta 3-galactosyltransferase a
7 ently labeled the SP receptor present on rat submaxillary gland membranes with a radioiodinated photo
8 only found on biopharmaceuticals) and bovine submaxillary gland mucin (BSM), here we demonstrate that
9 in vivo glycosylation pattern of the porcine submaxillary gland mucin (PSM) tandem repeat containing
10 odulating the O-glycosylation of the porcine submaxillary gland mucin 81 residue tandem repeat by ppG
12 he 80+ residue tandem repeat from the canine submaxillary gland mucin was obtained and characterized.
13 re analyzed, including bovine fetuin, bovine submaxillary gland mucin, and serum immunoglobulin A (Ig
18 mRNA transcript levels were highest in mouse submaxillary gland, epididymus, ovary, and thymus; with
21 s of rodents the Abpa genes expressed in the submaxillary glands appear to be evolving under a simila
24 tion between the Abpa genes expressed in the submaxillary glands of species of New World and Old Worl
27 ptic tandem repeat glycopeptide from porcine submaxillary mucin (PSM) has been isolated and its glyco
29 ch those determined from the purified bovine submaxillary mucin and also show 68-94% identity to publ
30 y mucin is closely related to that of bovine submaxillary mucin and contains similar tandem repeats i
31 r hand, TleA was capable of degrading bovine submaxillary mucin and leukocyte surface glycoproteins C
33 and in vitro immunoreactivity toward bovine submaxillary mucin and tetrazine reactivity were assesse
34 on product was generated using asialo-bovine submaxillary mucin as an acceptor; treatment with O-glyc
36 , both bovine submaxillary mucin and porcine submaxillary mucin contain similar N-terminal and C-term
37 half-cystine at residues 13244 and 13246 in submaxillary mucin expressed both monomers and dimers of
39 h domain at the carboxyl terminus of porcine submaxillary mucin have been used to determine the possi
40 e that S. pyogenes is able to bind to bovine submaxillary mucin in solid-phase microtiter plate assay
41 his indicates that the core protein of ovine submaxillary mucin is closely related to that of bovine
42 In contrast, the central domain of porcine submaxillary mucin is reported to consist of 81-amino-ac
43 signal peptides of SMGC, human MUC19 and pig submaxillary mucin suggest that rat and mouse Smgc and M
44 y and enzymatically prepared form of porcine submaxillary mucin that possesses a molecular mass of ap
45 ncoding the amino-terminal region of porcine submaxillary mucin were modified by site-specific mutage
46 ulfide-rich domain (240 residues) of porcine submaxillary mucin were shown to form disulfide-bonded d
47 residues from the amino terminus of porcine submaxillary mucin were used to determine whether this r
48 aining glycoproteins (transferrin and bovine submaxillary mucin) was monitored by measuring the imped
49 cific lectin, for a modified form of porcine submaxillary mucin, a linear glycoprotein, with a molecu
50 chromatography on immobilized asialo-bovine submaxillary mucin, and gel filtration chromatography on
51 tuin and the clustered Tn-rich asialo-bovine submaxillary mucin, were subsequently chosen as model gl
52 ve distinct protein domains (I-V) for bovine submaxillary mucin, which is encoded by two genes, BSM1
53 to 70 ng of transferrin and 40 ng of bovine submaxillary mucin, with a limit of detection of 20 ng f
56 n A, neuraminyl lactoses, bovine and porcine submaxillary mucins (BSM and PSM), and hyaluronic acid a
57 rom studies using ovine, bovine, and porcine submaxillary mucins and Chinese hamster ovary cells tran
58 oprotein, fetuin, porcine gastric and bovine submaxillary mucins, and the glycolipid sulfatide, all o
59 surgery, GL transection, and sublingual and submaxillary salivary gland extirpation were found to ha
61 heromaxein A was limited to the prostate and submaxillary salivary glands from both the boar and sow,
63 rrect, and extirpation of the sublingual and submaxillary salivary glands reduced average performance
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