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1 n of the overlying epidermis is an effect of epiregulin.
2 clin D2, aromatase, inhibin-alpha, SF-1, and epiregulin.
3 -1 (SF-1), cholesterol side chain (SCC), and epiregulin.
4 D2, inhibin-alpha, aromatase, SCC, SF-1, and epiregulin.
5 t Y1173 phosphorylation, but has no bias for epiregulin.
6 y, we found that the addition of recombinant epiregulin, amphiregulin, CX3CL1, and interleukin-11 sig
7  75% amino acid sequence identity with mouse epiregulin, an epidermal growth factor (EGF)-related gro
8                                              Epiregulin, an epidermal growth factor family member, ac
9 factor receptor (HER) ligands neuregulin and epiregulin and activation of the HER2 and HER3 receptors
10 ors that have high gene expression levels of epiregulin and amphiregulin and patients with wild-type
11 that express high levels of the EGFR ligands epiregulin and amphiregulin are more likely to have dise
12 ate-induced but not constitutive shedding of epiregulin and had no effect on betacellulin (BTC) proce
13 epidermal growth factor (EGF)-family ligands epiregulin and HB-EGF, the chemokine CX3CL1, and the tra
14          ET-1 also activated two other genes epiregulin and HB-EGF.
15 th factor (EGF) family members amphiregulin, epiregulin, and beta-cellulin.
16 F-like growth factor (HB-EGF), betacellulin, epiregulin, and epigen.
17 nd ANGPTL-2), as well as ErbB (amphiregulin, epiregulin, and neuregulins) and TGF-ss, which activate
18 oliferation, expression of the hepatomitogen epiregulin, and prevention of apoptosis.
19 wo additions to the family, betacellulin and epiregulin, are exquisitely restricted to the mouse uter
20 inding EGF-like growth factor, amphiregulin, epiregulin, betacellulin, or heregulin beta1 that bind t
21                                 In addition, epiregulin caused rapid EGF receptor activation in RASM
22 uxtamembrane stalks of either pro-BTC or pro-epiregulin ectodomains in vitro.
23 jury-upregulated, low-affinity EGFR ligands (epiregulin, epigen, TGFalpha), which also require solubl
24                                              Epiregulin (EPR) is a recently described member of the e
25 ied with a variety of EGF-like ligands--EGF, epiregulin (EPR), heparin binding EGF (HB-EGF), and here
26 ith amphiregulin (AR), betacellulin (BTC) or epiregulin (EPR), increased fetal type II cell different
27 sforming growth factor-alpha (TGF-alpha) and epiregulin (EPRG) were expressed as FimH fusion proteins
28               RNA expression of EGFR ligands epiregulin (EREG) and amphiregulin (AREG) may correlate
29 her approaches, we show how the EGFR ligands epiregulin (EREG) and epigen (EPGN) stabilize different
30 idermal growth factor receptor (EGFR) ligand epiregulin (EREG) from the basolateral to the apical cel
31 ling, we observed differential expression of epiregulin (EREG) in mouse models of colitis-associated,
32                                              Epiregulin (EREG) induces much weaker asymmetric dimers
33                              The EGFR ligand epiregulin (EREG) is highly expressed in RAS wild-type (
34         Here we report that a soluble factor epiregulin (EREG) is produced by senescent stromal cells
35                    We previously showed that epiregulin (EREG), a dendritic cell type 3-derived epide
36 GFR) pathway, including amphiregulin (AREG), epiregulin (EREG), and ectodomain cleavage protease MMP1
37 h factor C (VEGFC), betacellulin (BTC), EGF, epiregulin (EREG), and other members of the transforming
38 eptor (EGFR) ligands amphiregulin (AREG) and epiregulin (EREG), and systemic lipopolysaccharide admin
39 ated a role for EGFR and its natural ligand, epiregulin (EREG), in pain processing.
40 eptor (EGFR) ligands amphiregulin (AREG) and epiregulin (EREG).
41 on of the EGFR ligand amphiregulin (AREG) or epiregulin (EREG).
42 luding Tenascin C (Tnc), Jagged1 (Jag1), and Epiregulin (Ereg).
43 re tested by next-generation sequencing; and epiregulin (EREG)/amphiregulin (AREG) by RNAseq.
44 tive genes were also identified (e.g. Egr-1, epiregulin, Fra-1, and ABCA1).
45                       LacZ identification of epiregulin from epiregulin-null mice and immunohistochem
46                                          The epiregulin gene (Ereg) is located on mouse chromosome 5
47 several EGFR family ligands (EGF, HB-EGF and epiregulin), however only increases in HB-EGF were detec
48 evidence that expression of betacellulin and epiregulin in the uterus requires the presence of an act
49  Taken together, these results indicate that epiregulin is a potent VSMC-secreted mitogen, induced in
50                                     Although epiregulin is broadly expressed and regulated both spati
51 released by mesenchymal cells, revealed more epiregulin mRNA in fibroblast-like angiofibroma and peri
52                                 Elevation of epiregulin mRNA was confirmed with real-time PCR, and in
53       LacZ identification of epiregulin from epiregulin-null mice and immunohistochemical staining of
54 al staining of wild type mice confirmed that epiregulin, one of the limbal epithelium-enriched genes,
55  also demonstrate that amphiregulin, but not epiregulin, partially compensates for the loss of HB-EGF
56  and beta) receptor 2, decorin, osteoglycin, epiregulin, proliferins 2 and 3, stromal cell-derived fa
57 lso suppressed cyclin D2, inhibin-alpha, and epiregulin promoter-reporter activities.
58 with real-time PCR, and increased amounts of epiregulin protein were demonstrated with immunoprecipit
59 r progression and metastasis, including EREG/epiregulin, PTGS2/COX2, MMP1, MMP2, and CD44, along with
60  (epidermal growth factor), amphiregulin and epiregulin, resulting in autocrine activation of the EGF
61 ectively, our data indicate that Yap-induced Epiregulin signaling promotes the identity of SMG ductal
62                                              Epiregulin stimulated keratinocyte proliferation and pho
63  the epidermal growth factor receptor ligand epiregulin, the cyclooxygenase COX2, and the matrix meta
64                   We cloned the cDNA for rat epiregulin to determine its pattern of expression in G-p
65 ET-1, or alpha-Thr for 1 h, induction of two epiregulin transcripts was observed, including a 4.8-kb
66 lulin, and ADAM17 as the major convertase of epiregulin, transforming growth factor alpha, amphiregul
67     Mice deficient in either amphiregulin or epiregulin, two EGFR ligands, display delayed or reduced
68         Here we found that the expression of epiregulin, urokinase-type plasminogen activator (uPA),
69                              Recombinant rat epiregulin was strongly mitogenic for RASM cells, stimul
70 regulin, follistatin, and inhibin-beta-A and epiregulin were activated by an autocrine loop involving
71 eptor tyrosine phosphorylation stimulated by epiregulin were less than those induced by EGF or betace
72 oduction of a potent epidermal growth factor epiregulin, which may serve as a paracrine survival and
73  reduced expression of the EGF family member Epiregulin, which we show is required for the expansion