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1 d cDNA from Brassica napus encoding a hybrid-proline-rich protein.
2 The Glis1 gene encodes an 84.3-kDa proline-rich protein.
3 kout cell envelope, in addition to the small proline rich proteins.
4 microorganisms and with host acidic salivary proline-rich proteins.
5 omponents and processes such as histones and proline-rich proteins.
6 /or fragments of alpha-amylase, albumin, and proline-rich proteins.
7 act with secreted cell surface and cell wall proline-rich proteins.
8 with strong similarity to a family of basic proline-rich proteins.
9 astase-mediated digestion of salivary acidic proline-rich proteins.
12 transcription of neuropeptide y (npy), small proline-rich protein 1a (sprr1a), and vasoactive intesti
13 imilar type of analysis indicates that small proline-rich proteins 1A and 1B (SPR1A and SPR1B) become
15 quamous cell-specific proteins such as small proline-rich protein 1B (SPRR1B) that result in patholog
19 sion of sialyltransferase 4C (SIAT4C), small proline-rich protein 2A (SPRR2A), and resistin-like mole
21 owth factor precursor (DTR; 4.2-fold), small proline-rich protein 2B (SPRR2B; 3.6-fold), metallothion
22 o-predicted targets, keratin 5 (KRT5), small proline-rich protein 2C (SPRR2C), and S100 calcium-bindi
24 onfirm this prediction and show that a small proline-rich protein 3 (SPRR3) variant confers susceptib
26 n of a novel component of mTORC2 named PRR5 (PRoline-Rich protein 5), a protein encoded by a gene loc
27 nal stretch in SbGPRP1 (Sorghum glycine-rich proline-rich protein) acts as an antimicrobial peptide i
28 of stimulated secretion of newly synthesized proline-rich protein, amylase, and endogenous hormones i
29 ain, and a cysteine-rich C-terminal PAC (for proline-rich protein and AGP, containing cysteine) domai
30 ver, in contrast to the endogenous hormones, proline-rich protein and amylase are progressively remov
31 o = 0.72, p = 0.02) and changes in levels of proline-rich protein and mucin 7 following capsaicin (rh
33 ing the upregulation of genes encoding small proline-rich proteins and S100 calcium-binding proteins,
34 ipts, including those encoding various small proline-rich proteins and S100 calcium-binding proteins,
35 and SPRRP2H, members of the family of "small proline rich proteins", and repetin, a member of the "fu
36 envelopes have elevated levels of the small proline-rich proteins, and cell envelopes of both kinds
37 ety of secretory proteins-including amylase, proline-rich proteins, and parotid secretory protein (PS
38 that the ability to bind actin monomers and proline-rich proteins, and the presence of a functional
39 the interaction between a family of salivary proline-rich proteins (aPRPs) and representative pyranoa
40 ies have suggested that salivary amylase and proline-rich protein are sorted differently when express
42 R14 and the mutants, our work uncovered this proline-rich protein as a novel activator of the PI3K pa
44 ochemical analysis revealed that PRR14, as a proline-rich protein, binds to the Src homology 3 (SH3)
45 tions between basic, glycosylated and acidic proline-rich proteins (bPRPS, gPRPs, aPRPs) and P-B pept
46 luded that some salivary proteins, including proline-rich protein, can mediate increased staining of
48 ily old salivary proteins such as mucins and proline-rich proteins contain large regions of tandem re
49 N-WASP is present in a tight complex with a proline-rich protein, CR16, which shares approximately 2
51 have identified these proteins as primarily proline-rich proteins, cystatins, statherin, and histati
52 GP1 protein is a member of a family of basic proline-rich proteins defined by the C-terminal PAC doma
54 differences were found in the phenotypes of proline-rich proteins expressed by these groups of carie
56 mal differentiation markers, including small proline-rich proteins, filaggrins and several keratins,
57 in (GRP), and one displayed high homology to proline-rich proteins from Arabidopsis thaliana (AtPRP2,
59 olecular organization and expression of four proline-rich protein genes from Arabidopsis (AtPRPs).
60 ine, one or more bitter receptor or salivary proline-rich protein genes on chromosome 12 have alleles
62 e proteolytic cleavage products of the basic proline-rich proteins IB-4, IB-5, IB-7, IB-8b, and P-B.
63 the arabinogalactan proteins, extensins, and proline-rich proteins, in reality, a continuum of struct
64 nteracts with phosphoinositides and multiple proline-rich proteins, including the WAS protein (WASp)/
67 describe a novel rat cDNA named keratinocyte proline-rich protein (KPRP) isolated by RNA differential
73 other transglutaminase substrates, the small proline-rich proteins of cornified envelopes found in st
75 ination network, particularly the serine and proline-rich protein Pir1, to control gene expression th
76 y be related to the ability of the glutamine/proline-rich protein PQE-1 to protect C. elegans against
77 rotid proteins, parotid acidic protein (Pa), proline-rich protein (Pr), double-banded protein (Db), g
79 e have used coexpression of a salivary basic proline-rich protein (PRP) along with a proline-rich pro
80 that they encode proteins corresponding to a proline-rich protein (PRP) and a glycine-rich protein (G
82 ucted by adsorbing salivary alpha-amylase or proline-rich protein (PRP) onto amined gold screen-print
85 abundance proteins such as amylases, mucins, proline-rich proteins (PRPs), and secretory IgA complex.
87 lundii and S. gordonii, which bound purified proline-rich proteins (PRPs), recognized several other c
88 ing occurs between MG1 and salivary amylase, proline-rich proteins (PRPs), statherins, and histatins
89 nteraction of Actinomyces oris with salivary proline-rich proteins (PRPs), which serve as fimbrial re
92 ation of mRNAs encoding a putative cell wall proline-rich protein (PvPRP1), cell wall glycine-rich pr
95 unctional characterization of a glycine-rich proline-rich protein (SbGPRP1) from Sorghum which was pr
96 t encodes a new member of the cornifin/small proline-rich protein (spr) family, which we have named c
98 alpha2 type VI (Ca2T6) gene and three small proline-rich protein (SPRR) genes were reproducibly indu
100 ified envelope protein (involucrin and small proline-rich protein [SPRR]-2) expression by the corneal
105 ly forms heterotypic complexes with amylase, proline-rich proteins, statherin, and histatins in saliv
108 glutamine residues in acidic large and small proline-rich proteins, statherin, and the major histatin
109 primary pellicle precursor proteins, acidic proline-rich proteins, statherin, and the major histatin
110 e II, sIgA, IgG, IgM, lactoferrin, lysozyme, proline-rich proteins, statherin, histatin 1, and mucous
111 gy in the TonB C terminus to E. coli YcfS, a proline-rich protein that contains the lysin (LysM) pept
113 ant Nck precipitates endogenous WIP, a novel proline-rich protein that interacts with the Wiskott-Ald
114 n (SMCP) is a rapidly evolving cysteine- and proline-rich protein that is localized in the mitochondr
115 These mutants did not bind, in vitro, to proline-rich proteins that serve as the receptors for Ac
117 ch as phosphoinositide 4,5-bisphosphate, the proline-rich protein VASP and a complex of four to six p
119 , Hwp1, with similarities to mammalian small proline-rich proteins was shown to serve as a substrate
121 red cells, involucrin, envoplakin, and small proline-rich proteins were physically located at desmoso
122 s and the expression of involucrin and small proline-rich proteins, which covalently bind ceramides.
124 ading frame encodes a 308-amino-acid, highly proline-rich protein with homology to the amino terminus