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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
5                   The AQP5 cDNA from a human submaxillary gland library contains a 795-base pair open
6 r respiratory lymph nodes (LN), cervical LN, submaxillary gland LN, and spleens.
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
11 1 Ser/Thr residues in the 81-residue porcine submaxillary gland mucin tandem repeat.
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
14 at domains of blood group A-negative porcine submaxillary gland mucin.
15                    With the exception of the submaxillary gland of an African rodent, no other source
16  as well as bladder, breast, lung, prostate, submaxillary gland, and testis carcinomas.
17 heart, thyroid, skeletal muscle, eye, ovary, submaxillary gland, epididymus, and liver.
18 mRNA transcript levels were highest in mouse submaxillary gland, epididymus, ovary, and thymus; with
19                           In the parotid and submaxillary gland, there are very high levels of [125I]
20 mation from persistent MCMV infection of the submaxillary gland.
21 s of rodents the Abpa genes expressed in the submaxillary glands appear to be evolving under a simila
22                                          The submaxillary glands of boars contain a low molecular mas
23  of the secretoglobin family produced in the submaxillary glands of house mice (Mus musculus).
24 tion between the Abpa genes expressed in the submaxillary glands of species of New World and Old Worl
25                             Adult male mouse submaxillary glands served as the preferred starting mat
26  shown to interact and aggregate with bovine submaxillary mucin (BSM) in the distributions of both se
27 ligosaccharide-alditols isolated from bovine submaxillary mucin (BSM).
28 ptic tandem repeat glycopeptide from porcine submaxillary mucin (PSM) has been isolated and its glyco
29          Immobilized GalNAc and asialo-ovine submaxillary mucin (rich in O-linked glycans) were also
30 ower degree of glycosylation (~60%) - bovine submaxillary mucin - a weaker but still demonstrable int
31 ch those determined from the purified bovine submaxillary mucin and also show 68-94% identity to publ
32 y mucin is closely related to that of bovine submaxillary mucin and contains similar tandem repeats i
33 r hand, TleA was capable of degrading bovine submaxillary mucin and leukocyte surface glycoproteins C
34                         However, both bovine submaxillary mucin and porcine submaxillary mucin contai
35  and in vitro immunoreactivity toward bovine submaxillary mucin and tetrazine reactivity were assesse
36 on product was generated using asialo-bovine submaxillary mucin as an acceptor; treatment with O-glyc
37 to human nasal mucin was inhibited by bovine submaxillary mucin but not by fibrinogen.
38 , both bovine submaxillary mucin and porcine submaxillary mucin contain similar N-terminal and C-term
39  half-cystine at residues 13244 and 13246 in submaxillary mucin expressed both monomers and dimers of
40 NA encoding the polypeptide chain of porcine submaxillary mucin has been determined.
41 h domain at the carboxyl terminus of porcine submaxillary mucin have been used to determine the possi
42 e that S. pyogenes is able to bind to bovine submaxillary mucin in solid-phase microtiter plate assay
43 his indicates that the core protein of ovine submaxillary mucin is closely related to that of bovine
44   In contrast, the central domain of porcine submaxillary mucin is reported to consist of 81-amino-ac
45 signal peptides of SMGC, human MUC19 and pig submaxillary mucin suggest that rat and mouse Smgc and M
46 y and enzymatically prepared form of porcine submaxillary mucin that possesses a molecular mass of ap
47 ncoding the amino-terminal region of porcine submaxillary mucin were modified by site-specific mutage
48 ulfide-rich domain (240 residues) of porcine submaxillary mucin were shown to form disulfide-bonded d
49  residues from the amino terminus of porcine submaxillary mucin were used to determine whether this r
50 aining glycoproteins (transferrin and bovine submaxillary mucin) was monitored by measuring the imped
51 cific lectin, for a modified form of porcine submaxillary mucin, a linear glycoprotein, with a molecu
52  chromatography on immobilized asialo-bovine submaxillary mucin, and gel filtration chromatography on
53 tuin and the clustered Tn-rich asialo-bovine submaxillary mucin, were subsequently chosen as model gl
54 ted by the analysis of O-glycans from bovine submaxillary mucin, which identified mono- and di-O-acet
55 ve distinct protein domains (I-V) for bovine submaxillary mucin, which is encoded by two genes, BSM1
56 ucted a bottom-up analysis of isolated ovine submaxillary mucin, which supported our findings that mu
57  to 70 ng of transferrin and 40 ng of bovine submaxillary mucin, with a limit of detection of 20 ng f
58 tity to published peptide sequences of ovine submaxillary mucin.
59 oprotein, fetuin, colominic acid, and bovine submaxillary mucin.
60 n A, neuraminyl lactoses, bovine and porcine submaxillary mucins (BSM and PSM), and hyaluronic acid a
61 rom studies using ovine, bovine, and porcine submaxillary mucins and Chinese hamster ovary cells tran
62 oprotein, fetuin, porcine gastric and bovine submaxillary mucins, and the glycolipid sulfatide, all o
63  surgery, GL transection, and sublingual and submaxillary salivary gland extirpation were found to ha
64            Extirpation of the sublingual and submaxillary salivary glands also attenuated sugar respo
65 heromaxein A was limited to the prostate and submaxillary salivary glands from both the boar and sow,
66 jor 16-androstene-binding protein present in submaxillary salivary glands of the boar.
67 rrect, and extirpation of the sublingual and submaxillary salivary glands reduced average performance