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Yingkai Sun Department of Endocrinology and Metabolism, China National Research Center for Metabolic Diseases, Shanghai, China

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Rui Wang Department of Endocrinology and Metabolism, China National Research Center for Metabolic Diseases, Shanghai, China

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Shaoqian Zhao Department of Endocrinology and Metabolism, China National Research Center for Metabolic Diseases, Shanghai, China

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Wen Li Department of Endocrinology and Metabolism, China National Research Center for Metabolic Diseases, Shanghai, China

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Wen Liu Department of Endocrinology and Metabolism, China National Research Center for Metabolic Diseases, Shanghai, China

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Lingyun Tang State Key Laboratory of Medical Genomics, Research Center for Experimental Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine (SJTUSM), Shanghai, China

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Zhugang Wang State Key Laboratory of Medical Genomics, Research Center for Experimental Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine (SJTUSM), Shanghai, China

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Weiqing Wang Department of Endocrinology and Metabolism, China National Research Center for Metabolic Diseases, Shanghai, China

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Ruixin Liu Department of Endocrinology and Metabolism, China National Research Center for Metabolic Diseases, Shanghai, China

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Guang Ning Department of Endocrinology and Metabolism, China National Research Center for Metabolic Diseases, Shanghai, China

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Jiqiu Wang Department of Endocrinology and Metabolism, China National Research Center for Metabolic Diseases, Shanghai, China

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Jie Hong Department of Endocrinology and Metabolism, China National Research Center for Metabolic Diseases, Shanghai, China

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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

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E Mato 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)
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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C González 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)
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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A Moral 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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J I Pérez 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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O Bell 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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E Lerma 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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A de Leiva 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)
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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Kesha Rana Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia

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Maria W S Chiu Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia

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Patricia K Russell Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia

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Jarrod P Skinner Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia

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Nicole K L Lee Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia

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Barbara C Fam Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia

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Jeffrey D Zajac Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia

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Helen E MacLean Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia

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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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Simona Mencej
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Omar M E Albagha Faculty of Pharmacy, Rheumatology Section, Department of Endocrinology, Chair of Clinical Biochemistry, University of Ljubljana, Askerceva cesta 7, SI-1000 Ljubljana, Slovenia

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Janez Preželj Faculty of Pharmacy, Rheumatology Section, Department of Endocrinology, Chair of Clinical Biochemistry, University of Ljubljana, Askerceva cesta 7, SI-1000 Ljubljana, Slovenia

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Tomaž Kocjan Faculty of Pharmacy, Rheumatology Section, Department of Endocrinology, Chair of Clinical Biochemistry, University of Ljubljana, Askerceva cesta 7, SI-1000 Ljubljana, Slovenia

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Janja Marc
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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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Ayse Elif Erson-Bensan Department of Biological Sciences, Orta Dogu Teknik Universitesi (ODTU) (METU), Universiteler Mahallesi, Cankaya, Ankara, Turkey

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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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Francesco J DeMayo Reproductive and Developmental Biology Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA

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John P Lydon Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, USA

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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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Katherine A Leehy Department of Medicine and Pharmacology University of Minnesota Twin Cities Minneapolis, Minnesota, USA

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Tarah M Regan Anderson Department of Medicine and Pharmacology University of Minnesota Twin Cities Minneapolis, Minnesota, USA

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Andrea R Daniel Department of Medicine and Pharmacology University of Minnesota Twin Cities Minneapolis, Minnesota, USA

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Carol A Lange Department of Medicine and Pharmacology University of Minnesota Twin Cities Minneapolis, Minnesota, USA

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Julie H Ostrander Department of Medicine and Pharmacology University of Minnesota Twin Cities Minneapolis, Minnesota, USA

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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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Yali Ling National Clinical Research Center for Metabolic Diseases, Hunan Provincial Key Laboratory of Metabolic Bone Diseases, and Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China

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Feng Xu National Clinical Research Center for Metabolic Diseases, Hunan Provincial Key Laboratory of Metabolic Bone Diseases, and Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China

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Xuedi Xia National Clinical Research Center for Metabolic Diseases, Hunan Provincial Key Laboratory of Metabolic Bone Diseases, and Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China

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Dexing Dai National Clinical Research Center for Metabolic Diseases, Hunan Provincial Key Laboratory of Metabolic Bone Diseases, and Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China

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Ruoman Sun National Clinical Research Center for Metabolic Diseases, Hunan Provincial Key Laboratory of Metabolic Bone Diseases, and Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China

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Zhongjian Xie National Clinical Research Center for Metabolic Diseases, Hunan Provincial Key Laboratory of Metabolic Bone Diseases, and Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China

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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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Paolo Accornero Department of Veterinary Morphophysiology, University of Torino, Via Leonardo da Vinci 44, 10095 Grugliasco, (TO), Italy

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Silvia Miretti Department of Veterinary Morphophysiology, University of Torino, Via Leonardo da Vinci 44, 10095 Grugliasco, (TO), Italy

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Laura Starvaggi Cucuzza Department of Veterinary Morphophysiology, University of Torino, Via Leonardo da Vinci 44, 10095 Grugliasco, (TO), Italy

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Eugenio Martignani Department of Veterinary Morphophysiology, University of Torino, Via Leonardo da Vinci 44, 10095 Grugliasco, (TO), Italy

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Mario Baratta Department of Veterinary Morphophysiology, University of Torino, Via Leonardo da Vinci 44, 10095 Grugliasco, (TO), Italy

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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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Yingyu Feng Department of Endocrinology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People’s Republic of China

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Lei Su Department of Geriatrics, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People’s Republic of China

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Xing Zhong Department of Endocrinology, Second Affiliated Hospital of Anhui Medical University, Hefei, Anhui, People’s Republic of China

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Wei Guohong Department of Endocrinology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People’s Republic of China

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Haipeng Xiao Department of Endocrinology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People’s Republic of China

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Yanbing Li Department of Endocrinology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People’s Republic of China

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Lingling Xiu Department of Endocrinology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People’s Republic of China

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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

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