Search Results
Search for other papers by Katie Wynne in
Google Scholar
PubMed
Search for other papers by Sarah Stanley in
Google Scholar
PubMed
Search for other papers by Barbara McGowan in
Google Scholar
PubMed
Search for other papers by Steve Bloom in
Google Scholar
PubMed
contribute to the diffculty elucidating the receptor subtype that mediates NPY-induced feeding ( Raposinho et al. 2004 ). NPY is part of the pancreatic polypeptide (PP)-fold family of peptides, including peptide YY (PYY) and pancreatic
Search for other papers by B Anguiano in
Google Scholar
PubMed
Search for other papers by R Rojas-Huidobro in
Google Scholar
PubMed
Search for other papers by G Delgado in
Google Scholar
PubMed
Search for other papers by C Aceves in
Google Scholar
PubMed
of transcription 5 (Stat5), which is a key component of the PRL signaling pathway ( Favre-Young et al. 2000 ). In the case of the SNS, THs are known to regulate sympathetic action by modulating the expression of β-adrenergic receptors ( Mayollan
Search for other papers by J Fahrenkrug in
Google Scholar
PubMed
Search for other papers by B Georg in
Google Scholar
PubMed
Search for other papers by J Hannibal in
Google Scholar
PubMed
Search for other papers by H L Jørgensen in
Google Scholar
PubMed
established ( Rookh et al . 1979 , Jordan et al . 1980 , Ottenweller & Hedge 1982 , Wong et al . 1983 , Kalsbeek et al . 2000 , Guo et al . 2015 ). Nerve fibres originating in the SCN innervating thyroid-releasing hormone (TRH) neurons in the
Search for other papers by Giulia Baldini in
Google Scholar
PubMed
Search for other papers by Kevin D Phelan in
Google Scholar
PubMed
insulin receptors on the surface of pro-opiomelanocortin (POMC) neurons to promote processing of POMC to the mature hormone α-melanocyte-stimulating hormone (α-MSH), which signals to decrease energy intake ( Cone 2006 , Ghamari-Langroudi et al. 2011
Department of Physiology, Department of Biological and Medical Sciences, Development and Neuroscience, University of Cambridge, Physiology Building, Downing Street, Cambridge CB2 3EG, UK
Search for other papers by A J Forhead in
Google Scholar
PubMed
Search for other papers by A L Fowden in
Google Scholar
PubMed
.33–0.35G) 50–55 (0.34–0.38G) 17 (0.81G) Follicular >14 (>0.35G) >55 (>0.38G) 18 days–3 weeks postnatally TRH in hypothalamus 10–12 (0.25–0.30G) <60 (0.40G) 16 (0.76G) TSH in anterior pituitary gland and circulation 10–12 <60 17 (0.81G) TSH receptor in
Search for other papers by Chirine Toufaily in
Google Scholar
PubMed
Search for other papers by Gauthier Schang in
Google Scholar
PubMed
Search for other papers by Xiang Zhou in
Google Scholar
PubMed
Search for other papers by Philipp Wartenberg in
Google Scholar
PubMed
Search for other papers by Ulrich Boehm in
Google Scholar
PubMed
Search for other papers by John P Lydon in
Google Scholar
PubMed
Search for other papers by Ferdinand Roelfsema in
Google Scholar
PubMed
Search for other papers by Daniel J Bernard in
Google Scholar
PubMed
Introduction The progesterone receptor (PR, product of the Pgr gene) plays fundamental and pleiotropic roles in the control of reproduction. This is perhaps most clearly demonstrated in female Pgr -knockout mice, which are infertile because
Search for other papers by Melody L Allensworth-James in
Google Scholar
PubMed
Search for other papers by Angela Odle in
Google Scholar
PubMed
Search for other papers by Anessa Haney in
Google Scholar
PubMed
Search for other papers by Melanie MacNicol in
Google Scholar
PubMed
Search for other papers by Angus MacNicol in
Google Scholar
PubMed
Search for other papers by Gwen Childs in
Google Scholar
PubMed
increased numbers of somatotropes just before birth. In addition, thyrotropin-releasing hormone (TRH) also stimulates GH in neonates ( Fink et al. 2012 ). Thus, as inhibitors of GH and their receptors are expressed differentially throughout development, GH
Centre for Neuroendocrinology and Department of Anatomy, Maurice Wilkins Centre for Molecular Biodiscovery, University of Otago, PO Box 913, Dunedin 9054, New Zealand
Search for other papers by David R Grattan in
Google Scholar
PubMed
the portal blood accounted for changes in prolactin secretion in various physiological conditions ( Ben-Jonathan et al . 1977 , 1980 , Gibbs & Neill 1978 , De Greef & Neill 1979 ). Dopamine receptors were identified on lactotroph cells in the
Search for other papers by Eliane Correa-de-Santana in
Google Scholar
PubMed
Search for other papers by Bianca Fröhlich in
Google Scholar
PubMed
Search for other papers by Marta Labeur in
Google Scholar
PubMed
Search for other papers by Marcelo Páez-Pereda in
Google Scholar
PubMed
Search for other papers by Marily Theodoropoulou in
Google Scholar
PubMed
Search for other papers by Jose Luis Monteserin in
Google Scholar
PubMed
Search for other papers by Ulrich Renner in
Google Scholar
PubMed
Search for other papers by Günter K Stalla in
Google Scholar
PubMed
multiple bacterial cell wall components through a series of pattern recognition molecules expressed on the cell surface such as toll-like receptors (TLRs; Takeda et al . 2003 ). In response to cytokines released by activated immune cells, FS cells produce
Search for other papers by Riccardo Dore in
Google Scholar
PubMed
Search for other papers by Luka Levata in
Google Scholar
PubMed
Search for other papers by Hendrik Lehnert in
Google Scholar
PubMed
Search for other papers by Carla Schulz in
Google Scholar
PubMed
Introduction In quest of novel appetite regulating molecules, in 2006, Oh-I and coworkers re-discovered NEFA/nucleobindin2 ( Nucb2 ), a peroxisome proliferator γ receptor (PPARG)-activated gene in immortalized cell lines ( Oh-I et al. 2006