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progenitors ( Barak et al . 2012 ). Our data indicated that FGF9 may also participate in maintaining the stemness of adipose progenitor cells to balance the maturation process of adipocytes. Notably, we observed a transit repression of several WNT
Thyroid Neoplasia Study Group, Departament de Biologia Cel‐lular, Departments of Endocrinology and Nutrition, General Surgery, Pathology IIB, EDUAB‐HSP, Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine (CIBER‐BBN)
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Thyroid Neoplasia Study Group, Departament de Biologia Cel‐lular, Departments of Endocrinology and Nutrition, General Surgery, Pathology IIB, EDUAB‐HSP, Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine (CIBER‐BBN)
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Thyroid Neoplasia Study Group, Departament de Biologia Cel‐lular, Departments of Endocrinology and Nutrition, General Surgery, Pathology IIB, EDUAB‐HSP, Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine (CIBER‐BBN)
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regulation of Wnt-dependent genes ( Kuphal & Behrens 2006 ). We also analyzed integrin transmembrane receptors, ITGB1 and integrin β1-binding protein 1 ( ICAP1 ), genes involved in the progression of malignancy, chemoresistance, morphogenesis, terminal
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). Calcineurin Aa ( Ppp3ca ) was increased in both GAST and LA muscle from both mAR ΔZF2 lines ( Fig. 6 ). Figure 6 Q-PCR showing expression of putative AR target genes Odc1 , Amd1 , Wnt4 , Fzd4 , p57 , Igf2 , Tceal7 , Itgb1bp3 , Tgfb1 , Tgfb2
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(TFs) such as cbfa-1 and peroxisome proliferators-activated receptor γ ( Hofbauer & Heufelder 2001 ). The osteoblastic protein of the Wnt signalling pathway, β-catenin, also regulates RANKL and OPG expression in mice and is therefore involved in the
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exemplified by the cell adhesion molecule WNT5A (wingless-type MMTV integration site family, member 5A), contributing to invasion and metastasis ( Leandersson et al . 2006 ). In addition to RBPs having opposing functions in regulating mRNA stability
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consequence of elevated Bmp2 levels, wingless-type MMTV integration site (WNT) family member 4 ( Wnt 4 ) is induced in the stroma. Both BMP2 and WNT 4 – along with COUP-TFII and IHH – are essential for PGR-dependent endometrial stromal cell
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nearby PR-negative cells ( Fata et al . 2001 ), including mammary stem or progenitor cells ( Asselin-Labat et al . 2010 , Joshi et al . 2010 ). Specifically, PR-positive cells secrete Wnt4 and RANKL, which act on PR-null mammary stem cells to activate
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-cytokines/lymphocyte enhancers (TCF/LEF) transcriptional activity to activate the Wnt signaling pathway. Further studies are required to determine the molecule mechanism by which VDR interacts with E-cadherin and β-catenin and the relationship between VDR and β-catenin/Wnt
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Weinberg RA 2000 Essential function of Wnt-4 in mammary gland development downstream of progesterone signaling . Genes and Development 14 650 – 654 . Ciarloni L Mallepell S Brisken C 2007 Amphiregulin is an essential mediator of
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change their bone turnover markers, most likely through the PTH and Wnt pathways ( Nuche-Berenguer et al. 2010a ). In aged ovariectomized rats, exendin-4 can prevent osteopenia by promoting bone formation and suppressing bone resorption ( Ma et al