Çağdaş SON
(Orta Doğu Teknik Üniversitesi, Fen Edebiyat Fakültesi, Moleküler Biyoloji ve Genetik Bölümü, Ankara, Türkiye)
Merve KASAP
(Orta Doğu Teknik Üniversitesi, Fen Edebiyat Fakültesi, Moleküler Biyoloji ve Genetik Bölümü, Ankara, Türkiye)
Proje Grubu: TÜBİTAK TBAG ProjeSayfa Sayısı: 52Proje No: 110T717Proje Bitiş Tarihi: 15.01.2014Türkçe

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Kokain ve amfeetamin ile regüle edilen transcript (CART) peptidini tanıyan G protein kenetli reseptör adaylarının tayini
  • Alexander-Thomas, H., Chemical probes: Sharpen your epigenetic tools, Nat Chem Biol, 7, 499-500, (2011).
  • Atwood, B., Lopez, J., Wager-Miller, J., Mackie, K., & Straiker, A., Expression of G protein-coupled receptors and related proteins in HEK293, AtT20, BV2, and N18 cell lines as revealed by microarray analysis, BMC Genomics, 1-14, (2011).
  • Bouvier, M., Unraveling the structural basis of GPCR activation and inactivation, Nature Structure Moleculer Biology, 539-41, (2013)
  • Brazma, A., Hingamp, P., Quackenbush, J., Sherlock, G., Spellman, P., Stoeckert, C., ve arkadaşları, Minimum information about a microarray experiment (MIAME)—toward standards for microarray data, Nature Genetics, 29, 365 - 371, (2001).
  • Bruno, A., Costantino, G., Fabritiis, G., Pastor, M., & Selent, J., Membrane-Sensitive Conformational States of Helix 8 in the Metabotropic Glu2 Receptor, a Class C GPCR, PloS One, 7(8), 1-9, (2012).
  • Chang, G. W., Proteolytic cleavage of the EMR2 receptor requires both the extracellular stalk and the GPS motif, FEBS Lett., 547, 145–150, (2003).
  • Dominguez, G., Lakatos, A., & Kuhar, M., Characterization of the cocaine- and amphetamine-regulated transcript (CART) peptide gene promoter and its activation by a cyclic AMP-dependent signaling pathway in GH3 cells, Journal of Neurochemistry, 80, 885-893, (2002).
  • Driessler, F., & Baldock, P. A., Hypothalamic Regulation of Bone, Journal of Molecular Endocrinology, 45, 175-181, (2010).
  • Elefteriou, F., Ahn JD, J., Takeda, S., Starbuck, M., Yang, X., Liu, X., ve arkadaşları, Leptin regulation of bone resorption by the sympathetic nervous system and CART, Nature, 434, 514–520, (2005).
  • Filipek, S. S., G protein-coupled receptor rhodopsin: a prospectus, Annual Reviews Physiology, 65, 851– 879, (2003).
  • Filmore, D., It's a GPCR world, American Chemical Society Modern Drug Discovery, 24-28, (2004).
  • Foord, S. M., Jupe, S., & Holbrook, J., Bioinformatics and type II G-protein-coupled receptors, Biochemical Society Transactions, 30 (4), 473-479, (2002).
  • Gether, U., Uncovering molecular mechanisms involved in activation of G protein-coupled receptors, Endocrinology Revision, 2, 90-113, (2000).
  • International HapMap Project. (n.d.). Bead Arrays. Retrieved August 16, 2013, from NCBI: http://www.ncbi.nlm.nih.gov/projects/genome/probe/doc/TechBeadArray.shtml
  • Jones, D., Lakatos, A., & Vicentic, A., The CART receptors: Background and recent advances. Peptides, 27, 1934-1937, (2006).
  • Kim, J. H., Glutamate residues in the second extracellular loop of the human A2a adenosine receptor are required for ligand recognition, Molecular Pharmacology, 49, 683– 691, (1996).
  • Kobe, B., The leucine-rich repeat as a protein recognition motif, Current Opinion in Structural Biology, 725–732, (2001, Aralık).
  • Kolakowski, J. L., GCRDb: a G protein-coupled receptor database. Recept Channel, 2, 1–7, (1994).
  • Koylu, E., Balkan, B., Kuhar, M., & Pogun, S., Cocaine and amphetamine regulated transcript (CART) and the stress response. Peptides, 27, 1956-1969, (2006).
  • Kristiansen, K., Molecular mechanisms of ligand binding, signaling, and regulation within the superfamily of G-protein-coupled receptors: molecular modeling and mutagenesis approaches to receptor structure and function, Science Direct - Pharmacology & Therapeutics,103, 21– 80, (2004).
  • Kroeze, W. K., Molecular biology of serotonin receptors structure and function at the molecular level, Top Med Chem, 2, 507– 528, (2002).
  • Kuemmerle, J. F., Coupling of the insulin-like growth factor-I receptor tyrosine kinase to Gi2 in human intestinal smooth muscle: Gbetagamma-dependent mitogen-activated protein kinase activation and growth, J Biol Chem, 276, 7187–7194, (2001).
  • Kuhar, M., Adams, G., Dominguez, J., Jaworski, J., & Balkan, B., CART peptides, Neuropeptides, 36, 1-8, (2002).
  • Kuhar, M., Lakatos, A., Prinster, S., Vicentic, A., & Hall, R., Cocaine- and amphetamine-regulated transcript (CART) peptide activates the extracellular signal-regulated kinase (ERK) pathway in AtT20 cells via putative G-protein coupled receptors, Neuroscience Letters, 384, 198–202, (2005).
  • Lane, J., & Canals, M., Sequential conformational rearrangements dictate the dynamics of class C GPCR activation, Science Signalling, (2012, Kasım).
  • Langer, I. V., Lysine 195 and aspartate 196 in the first extracellular loop of the PAC1 receptor are essential for high affinity binding of agonists but not of antagonists, Neuropharmacology, 44, 125–131, (2003).
  • Livak, K. J., & Schmittgen, T. D., Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 22DDCT Method, Methods, 25, 402–408, (2001).
  • Macfarlane, S. R., Proteinase-activated receptors, Pharmacology Review, 53, 245–282, (2001).
  • Oikawa, M. S., Effects of protease-activated receptors (PARs) on intracellular calcium dynamics of acinar cells in rat lacrimal glands, Histochemistry and Cell Biology, DOI 10.1007/s00418-013-1082-0, (2013).
  • Okada, T. F., Functional role of internal water molecules in rhodopsin revealed by X-ray crystallography.
  • Proc Natl Acad Sci USA, 99, 5982– 5987, (2002).
  • Pantages, E., & Dulac, C., A novel family of candidate pheromone receptors in mammals, Neuron, 28(3), 835–845, (2000).
  • Pfaffl, M., A new mathematical model for relative quantification in real-time RT–PCR, Oxford Journals Nucleic Acids Research, 29(9), 45, (2001).
  • Pierce, K. L., Seven-transmembrane Receptors, Nat Rev Mol Cell Biol, 3, 639–650, (2002).
  • Roth, C., & Yarmush, M., Nucleic acid biotechnology, Annual Review of Biomedical Engineering, 1, 265-297, (1999).
  • Sakmar, P. T., Clicking class B GPCR ligands, Nature Chemical Biology, 7, 500-502, (2011).
  • Tang, X. W., Orphan G protein-coupled receptors (GPCRs): biological functions and potential drug targets, Acta Pharmacologica Sinica, 33, 363–371, (2012).
  • Thim, L., Kristiensen, P., Wulff, B., & Clausen, J., Tissue Specific Processing of Cocaine and Amphetamine Regulated Transcript Peptides in Rat, Proc Natl Acad Sci USA, 2722-2727, (1999).
  • Vischer, H. F., Ligand selectivity of gonadotropin receptors, Role. Biol Chem, 278, 15505– 15513, (2003).
  • Zhang, M., Han, L., & Xu, Y., Roles of cocaine- and amphetamine-regulated transcript in the central nervous system, Clinical and Experimental Pharmacology Physiology, 39(6), 586-592, (2012).

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