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Tram B Doan Westmead Institute for Medical Research, Sydney Medical School – Westmead, University of Sydney, Sydney, New South Wales, Australia

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J Dinny Graham Westmead Institute for Medical Research, Sydney Medical School – Westmead, University of Sydney, Sydney, New South Wales, Australia

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Christine L Clarke Westmead Institute for Medical Research, Sydney Medical School – Westmead, University of Sydney, Sydney, New South Wales, Australia

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Introduction Breast cancer is the most common cancer diagnosed in women worldwide ( Ferlay et al. 2015 ). Over the past decades, substantial progress toward treatment of primary estrogen receptor-positive (ER+) breast cancer has been made

Article Type:
Review Article
DOI:
https://doi.org/10.1530/JME-16-0082
Volume/Issue:
Volume 58: Issue 3
Free access
Pia Kiilerich INRA, CNRS UMR5239, Department of Biology, Inserm, UR1037 Fish Physiology and Genomics, Campus de Beaulieu, 35000 Rennes, France

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Gérard Triqueneaux INRA, CNRS UMR5239, Department of Biology, Inserm, UR1037 Fish Physiology and Genomics, Campus de Beaulieu, 35000 Rennes, France

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Nynne Meyn Christensen INRA, CNRS UMR5239, Department of Biology, Inserm, UR1037 Fish Physiology and Genomics, Campus de Beaulieu, 35000 Rennes, France

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Vincent Trayer INRA, CNRS UMR5239, Department of Biology, Inserm, UR1037 Fish Physiology and Genomics, Campus de Beaulieu, 35000 Rennes, France

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Xavier Terrien INRA, CNRS UMR5239, Department of Biology, Inserm, UR1037 Fish Physiology and Genomics, Campus de Beaulieu, 35000 Rennes, France

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Marc Lombès INRA, CNRS UMR5239, Department of Biology, Inserm, UR1037 Fish Physiology and Genomics, Campus de Beaulieu, 35000 Rennes, France

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Patrick Prunet INRA, CNRS UMR5239, Department of Biology, Inserm, UR1037 Fish Physiology and Genomics, Campus de Beaulieu, 35000 Rennes, France

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Introduction The glucocorticoid and mineralocorticoid receptors (GR and MR) belong to a superfamily of ligand-activated transcription factors, the NR3C steroid receptor subgroup. The cytoplasmic steroid receptors are activated upon ligand binding

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JME-15-0002
Volume/Issue:
Volume 55: Issue 1
Free access
Edith Bonnelye Institut de Génomique Fonctionnelle de Lyon, INSERM U664, Department of Molecular Genetics, Université de Lyon, Université Lyon 1, CNRS, INRA, Ecole Normale Supérieure de Lyon, 69007 Lyon, France
Institut de Génomique Fonctionnelle de Lyon, INSERM U664, Department of Molecular Genetics, Université de Lyon, Université Lyon 1, CNRS, INRA, Ecole Normale Supérieure de Lyon, 69007 Lyon, France

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Frédéric Saltel Institut de Génomique Fonctionnelle de Lyon, INSERM U664, Department of Molecular Genetics, Université de Lyon, Université Lyon 1, CNRS, INRA, Ecole Normale Supérieure de Lyon, 69007 Lyon, France

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Anne Chabadel Institut de Génomique Fonctionnelle de Lyon, INSERM U664, Department of Molecular Genetics, Université de Lyon, Université Lyon 1, CNRS, INRA, Ecole Normale Supérieure de Lyon, 69007 Lyon, France

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Ralph A Zirngibl Institut de Génomique Fonctionnelle de Lyon, INSERM U664, Department of Molecular Genetics, Université de Lyon, Université Lyon 1, CNRS, INRA, Ecole Normale Supérieure de Lyon, 69007 Lyon, France

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Jane E Aubin Institut de Génomique Fonctionnelle de Lyon, INSERM U664, Department of Molecular Genetics, Université de Lyon, Université Lyon 1, CNRS, INRA, Ecole Normale Supérieure de Lyon, 69007 Lyon, France

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Pierre Jurdic Institut de Génomique Fonctionnelle de Lyon, INSERM U664, Department of Molecular Genetics, Université de Lyon, Université Lyon 1, CNRS, INRA, Ecole Normale Supérieure de Lyon, 69007 Lyon, France

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Introduction Osteoclasts (OCs) are large multinucleated cells of hematopoietic origin formed by the differentiation and fusion of mononuclear monocyte–macrophage lineage precursors after stimulation by receptor activator of nuclear factor κB

Article Type:
Research Article
DOI:
https://doi.org/10.1677/JME-10-0024
Volume/Issue:
Volume 45: Issue 6
Open access
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R S Bhaskaran Department of Pharmacology, Carver College of Medicine, 2-319B BSB, 51 Newton Road, University of Iowa, Iowa City, Iowa 52242-1109, USA

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M Ascoli Department of Pharmacology, Carver College of Medicine, 2-319B BSB, 51 Newton Road, University of Iowa, Iowa City, Iowa 52242-1109, USA

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phenomenon include: (a) an impairment in the functional properties of the cell surface LH receptor (LHR) that results in a decrease in adenylyl cyclase activation ( Ekstrom & Hunzicker-Dunn 1989 , Sánchez-Yagüe et al. 1993 , Lamm & Hunzicker-Dunn 1994

Article Type:
Research Article
DOI:
https://doi.org/10.1677/jme.1.01745
Volume/Issue:
Volume 34: Issue 2
Free access
Lorella Bonaccorsi Department of Clinical Physiopathology, Andrology Unit, Center for Transfer, High Education and Technology ‘DeNothe’, University of Florence, Florence, Italy
Department of Human Anatomy, Histology and Forensic Medicine, University of Florence, Florence, Italy

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Daniele Nosi Department of Clinical Physiopathology, Andrology Unit, Center for Transfer, High Education and Technology ‘DeNothe’, University of Florence, Florence, Italy
Department of Human Anatomy, Histology and Forensic Medicine, University of Florence, Florence, Italy

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Monica Muratori Department of Clinical Physiopathology, Andrology Unit, Center for Transfer, High Education and Technology ‘DeNothe’, University of Florence, Florence, Italy
Department of Human Anatomy, Histology and Forensic Medicine, University of Florence, Florence, Italy

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Lucia Formigli Department of Clinical Physiopathology, Andrology Unit, Center for Transfer, High Education and Technology ‘DeNothe’, University of Florence, Florence, Italy
Department of Human Anatomy, Histology and Forensic Medicine, University of Florence, Florence, Italy

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Gianni Forti Department of Clinical Physiopathology, Andrology Unit, Center for Transfer, High Education and Technology ‘DeNothe’, University of Florence, Florence, Italy
Department of Human Anatomy, Histology and Forensic Medicine, University of Florence, Florence, Italy

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Elisabetta Baldi Department of Clinical Physiopathology, Andrology Unit, Center for Transfer, High Education and Technology ‘DeNothe’, University of Florence, Florence, Italy
Department of Human Anatomy, Histology and Forensic Medicine, University of Florence, Florence, Italy

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Introduction Trafficking of growth factor receptors is an important process in the pathogenesis of cancer ( Polo et al. 2004 ). Although until a few years ago, ligand-induced receptor internalization was considered a mechanism

Article Type:
Research Article
DOI:
https://doi.org/10.1677/jme.1.02155
Volume/Issue:
Volume 38: Issue 1
Free access
A M Tarrant
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S R Greytak
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G V Callard
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M E Hahn
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Introduction The estrogen receptor-related receptors (ERRs) are members of the nuclear receptor superfamily of transcription factors ( Giguere et al. 1988 ). Three ERR genes have been identified in mammals, ERRα (NR3B1), ERRβ (NR3B

Article Type:
Research Article
DOI:
https://doi.org/10.1677/jme.1.01976
Volume/Issue:
Volume 37: Issue 1
Free access
Ángel A Rivas-Boyero Department of Biochemistry and Molecular Biology, Institute of Neurosciences of Castilla y León (INCYL), University of Salamanca, 37007 Salamanca, Spain

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M Javier Herrero-Turrión Department of Biochemistry and Molecular Biology, Institute of Neurosciences of Castilla y León (INCYL), University of Salamanca, 37007 Salamanca, Spain

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Veronica Gonzalez-Nunez Department of Biochemistry and Molecular Biology, Institute of Neurosciences of Castilla y León (INCYL), University of Salamanca, 37007 Salamanca, Spain
Department of Biochemistry and Molecular Biology, Institute of Neurosciences of Castilla y León (INCYL), University of Salamanca, 37007 Salamanca, Spain

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Fátima Macho Sánchez-Simón Department of Biochemistry and Molecular Biology, Institute of Neurosciences of Castilla y León (INCYL), University of Salamanca, 37007 Salamanca, Spain
Department of Biochemistry and Molecular Biology, Institute of Neurosciences of Castilla y León (INCYL), University of Salamanca, 37007 Salamanca, Spain

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Katherine Barreto-Valer Department of Biochemistry and Molecular Biology, Institute of Neurosciences of Castilla y León (INCYL), University of Salamanca, 37007 Salamanca, Spain
Department of Biochemistry and Molecular Biology, Institute of Neurosciences of Castilla y León (INCYL), University of Salamanca, 37007 Salamanca, Spain

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Raquel E Rodríguez Department of Biochemistry and Molecular Biology, Institute of Neurosciences of Castilla y León (INCYL), University of Salamanca, 37007 Salamanca, Spain
Department of Biochemistry and Molecular Biology, Institute of Neurosciences of Castilla y León (INCYL), University of Salamanca, 37007 Salamanca, Spain

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Introduction The opioid receptor-like 1 (ORL1) or nociceptin receptor (NOP) is a G-protein-coupled receptor (GPCR) that exhibits a significant degree of sequence identity with the three opioid receptors: μ (MOR), δ (DOR), and κ (KOR; Waldhoer et

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JME-10-0130
Volume/Issue:
Volume 46: Issue 2
Free access
D Liu Gene Regulation Section, Laboratory of Reproductive and Developmental Toxicology, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina 27709, USA

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Z Zhang Gene Regulation Section, Laboratory of Reproductive and Developmental Toxicology, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina 27709, USA

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C T Teng Gene Regulation Section, Laboratory of Reproductive and Developmental Toxicology, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina 27709, USA

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Introduction Nuclear receptors constitute an important group of transcription factors that regulate diverse biological functions through multiple signaling pathways (see reviews by Tsai & O’Malley (1994 ) and Mangelsdorf et al

Article Type:
Research Article
DOI:
https://doi.org/10.1677/jme.1.01586
Volume/Issue:
Volume 34: Issue 2
Free access
Meghan S Perkins Department of Biochemistry, Stellenbosch University, Matieland, South Africa

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Renate Louw-du Toit Department of Biochemistry, Stellenbosch University, Matieland, South Africa

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Donita Africander Department of Biochemistry, Stellenbosch University, Matieland, South Africa

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, 2008 a , Marjoribanks et al. 2017 ). Estrogens predominantly mediate their effects by binding to the estrogen receptor (ER), while progestins are synthetic progestogens (progesterone receptor (PR) ligands) that were designed to mimic the activity

Article Type:
Review Article
DOI:
https://doi.org/10.1530/JME-18-0094
Volume/Issue:
Volume 61: Issue 4
Free access
Roger López-Bellido Department of Biochemistry and Molecular Biology, Institute of Neuroscience of Castilla y León, University of Salamanca, C/Pintor Fernando Gallego No. 1, Lab‐13, 37007 Salamanca, Spain

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Katherine Barreto-Valer Department of Biochemistry and Molecular Biology, Institute of Neuroscience of Castilla y León, University of Salamanca, C/Pintor Fernando Gallego No. 1, Lab‐13, 37007 Salamanca, Spain

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Raquel E Rodríguez Department of Biochemistry and Molecular Biology, Institute of Neuroscience of Castilla y León, University of Salamanca, C/Pintor Fernando Gallego No. 1, Lab‐13, 37007 Salamanca, Spain

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Introduction The biological actions of the tachykinin family – substance P (SP), neurokinin A (NKA) and NKB, hemokinin-1, and endokinins – are mediated by transmembrane G-protein-coupled receptors (GPCRs) and they have been classified within the NK

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JME-12-0199
Volume/Issue:
Volume 50: Issue 2
Free access