Bibliografías temáticas / Receptores GPCR

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Literatura académica sobre el tema "Receptores GPCR"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 1 de febrero de 2022

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Artículos de revistas sobre el tema "Receptores GPCR"

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Sánchez-Lemus, Enrique, and José A Arias-Montaño. "Transactivación de receptores con actividad de cinasa de tirosina (RTK’s) por receptores acoplados a proteínas G." REVISTA BIOMÉDICA 15, no. 1 (2004): 33–48. http://dx.doi.org/10.32776/revbiomed.v15i1.371.

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Los efectos de los factores de crecimiento y de ciertas hormonas se deben a la activación de receptores con actividad intrínseca de cinasa de tirosina (o RTK’s, por receptor tyrosine kinases), cuya estimulación inicia cascadas de señalización intracelular que regulan eventos transcripcionales esenciales para la proliferación y la diferenciación celulares. Entre los efectos debidos a la estimulación de los RTK’s, destaca la activación de la familia de cinasas de proteína activadas por mitógeno o MAPK’s (mitogen-activated protein kinases). Existen evidencias que indican que la estimulación de al
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Vidad, Ashley Ryan, Stephen Macaspac, and Ho Leung Ng. "Locating ligand binding sites in G-protein coupled receptors using combined information from docking and sequence conservation." PeerJ 9 (September 24, 2021): e12219. http://dx.doi.org/10.7717/peerj.12219.

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GPCRs (G-protein coupled receptors) are the largest family of drug targets and share a conserved structure. Binding sites are unknown for many important GPCR ligands due to the difficulties of GPCR recombinant expression, biochemistry, and crystallography. We describe our approach, ConDockSite, for predicting ligand binding sites in class A GPCRs using combined information from surface conservation and docking, starting from crystal structures or homology models. We demonstrate the effectiveness of ConDockSite on crystallized class A GPCRs such as the beta2 adrenergic and A2A adenosine recepto
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Luttrell, Louis M., та Robert J. Lefkowitz. "The role of β-arrestins in the termination and transduction of G-protein-coupled receptor signals". Journal of Cell Science 115, № 3 (2002): 455–65. http://dx.doi.org/10.1242/jcs.115.3.455.

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β-arrestins are versatile adapter proteins that form complexes with most G-protein-coupled receptors (GPCRs) following agonist binding and phosphorylation of receptors by G-protein-coupled receptor kinases (GRKs). They play a central role in the interrelated processes of homologous desensitization and GPCR sequestration, which lead to the termination of G protein activation. β-arrestin binding to GPCRs both uncouples receptors from heterotrimeric G proteins and targets them to clathrin-coated pits for endocytosis. Recent data suggest that β-arrestins also function as GPCR signal transducers. T
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Paradis, Justine S., Stevenson Ly, Élodie Blondel-Tepaz та ін. "Receptor sequestration in response to β-arrestin-2 phosphorylation by ERK1/2 governs steady-state levels of GPCR cell-surface expression". Proceedings of the National Academy of Sciences 112, № 37 (2015): E5160—E5168. http://dx.doi.org/10.1073/pnas.1508836112.

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MAPKs are activated in response to G protein-coupled receptor (GPCR) stimulation and play essential roles in regulating cellular processes downstream of these receptors. However, very little is known about the reciprocal effect of MAPK activation on GPCRs. To investigate possible crosstalk between the MAPK and GPCRs, we assessed the effect of ERK1/2 on the activity of several GPCR family members. We found that ERK1/2 activation leads to a reduction in the steady-state cell-surface expression of many GPCRs because of their intracellular sequestration. This subcellular redistribution resulted in
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Chattopadhyay, Amitabha. "GPCRs: Lipid-Dependent Membrane Receptors That Act as Drug Targets." Advances in Biology 2014 (October 2, 2014): 1–12. http://dx.doi.org/10.1155/2014/143023.

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G protein-coupled receptors (GPCRs) are the largest class of molecules involved in signal transduction across cell membranes and represent major targets in the development of novel drug candidates in all clinical areas. Although there have been some recent leads, structural information on GPCRs is relatively rare due to the difficulty associated with crystallization. A specific reason for this is the intrinsic flexibility displayed by GPCRs, which is necessary for their functional diversity. Since GPCRs are integral membrane proteins, interaction of membrane lipids with them constitutes an imp
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Kapolka, N. J., G. J. Taghon, J. B. Rowe, et al. "DCyFIR: a high-throughput CRISPR platform for multiplexed G protein-coupled receptor profiling and ligand discovery." Proceedings of the National Academy of Sciences 117, no. 23 (2020): 13117–26. http://dx.doi.org/10.1073/pnas.2000430117.

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More than 800 G protein-coupled receptors (GPCRs) comprise the largest class of membrane receptors in humans. While there is ample biological understanding and many approved drugs for prototypic GPCRs, most GPCRs still lack well-defined biological ligands and drugs. Here, we report our efforts to tap the potential of understudied GPCRs by developing yeast-based technologies for high-throughput clustered regularly interspaced short palindromic repeats (CRISPR) engineering and GPCR ligand discovery. We refer to these technologies collectively as Dynamic Cyan Induction by Functional Integrated Re
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Lorenzen, Emily, Tea Dodig-Crnković, Ilana B. Kotliar, et al. "Multiplexed analysis of the secretin-like GPCR-RAMP interactome." Science Advances 5, no. 9 (2019): eaaw2778. http://dx.doi.org/10.1126/sciadv.aaw2778.

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Receptor activity–modifying proteins (RAMPs) have been shown to modulate the functions of several G protein–coupled receptors (GPCRs), but potential direct interactions among the three known RAMPs and hundreds of GPCRs have never been investigated. Focusing mainly on the secretin-like family of GPCRs, we engineered epitope-tagged GPCRs and RAMPs, and developed a multiplexed suspension bead array (SBA) immunoassay to detect GPCR-RAMP complexes from detergent-solubilized lysates. Using 64 antibodies raised against the native proteins and 4 antibodies targeting the epitope tags, we mapped the int
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Bhattacharya, M., A. V. Babwah, and S. S. G. Ferguson. "Small GTP-binding protein-coupled receptors." Biochemical Society Transactions 32, no. 6 (2004): 1040–44. http://dx.doi.org/10.1042/bst0321040.

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Heterotrimeric GPCRs (G-protein-coupled receptors) form the largest group of integral membrane receptor proteins and mediate diverse physiological processes. In addition to signalling via heterotrimeric G-proteins, GPCRs can also signal by interacting with various small G-proteins to regulate downstream effector pathways. The small G-protein superfamily is structurally classified into at least five families: the Ras, Rho/Rac/cdc42, Rab, Sar1/Arf and Ran families. They are monomeric G-proteins with molecular masses over the range 20–30 kDa, which function as molecular switches to control many e
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Southern, Craig, Jennifer M. Cook, Zaynab Neetoo-Isseljee та ін. "Screening β-Arrestin Recruitment for the Identification of Natural Ligands for Orphan G-Protein–Coupled Receptors". Journal of Biomolecular Screening 18, № 5 (2013): 599–609. http://dx.doi.org/10.1177/1087057113475480.

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A variety of G-protein–coupled receptor (GPCR) screening technologies have successfully partnered a number of GPCRs with their cognate ligands. GPCR-mediated β-arrestin recruitment is now recognized as a distinct intracellular signaling pathway, and ligand-receptor interactions may show a bias toward β-arrestin over classical GPCR signaling pathways. We hypothesized that the failure to identify native ligands for the remaining orphan GPCRs may be a consequence of biased β-arrestin signaling. To investigate this, we assembled 10 500 candidate ligands and screened 82 GPCRs using PathHunter β-arr
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Sutkeviciute, Ieva, and Jean-Pierre Vilardaga. "Structural insights into emergent signaling modes of G protein–coupled receptors." Journal of Biological Chemistry 295, no. 33 (2020): 11626–42. http://dx.doi.org/10.1074/jbc.rev120.009348.

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G protein–coupled receptors (GPCRs) represent the largest family of cell membrane proteins, with >800 GPCRs in humans alone, and recognize highly diverse ligands, ranging from photons to large protein molecules. Very important to human medicine, GPCRs are targeted by about 35% of prescription drugs. GPCRs are characterized by a seven-transmembrane α-helical structure, transmitting extracellular signals into cells to regulate major physiological processes via heterotrimeric G proteins and β-arrestins. Initially viewed as receptors whose signaling via G proteins is delimited to the plasma mem
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Tesis sobre el tema "Receptores GPCR"

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Prischich, Davia. "Development and applications of photoswitchable small molecules and peptides to control protein-protein interactions and GPCR activity." Doctoral thesis, Universitat de Barcelona, 2021. http://hdl.handle.net/10803/671019.

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Photopharmacology is an emerging field that relies on the development of photosensitive compounds to enable precise spatiotemporal control over endogenous proteins. Photochromic ligands· are designed to respond to specific wavelengths of light with a reversible change of structure that enhances or diminishes their activity or affinity towards the desired target. Applications are expected to lead to safer treatments in medicine and to innovative tools to investigate complex signalling networks in biology. Thus, in this thesis we aimed at further expanding the spec
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Callén, Herrero Lucía. "Expresión, función y heteromerización de receptores de cannabinoides CB(2) en el sistema nervioso central." Doctoral thesis, Universitat de Barcelona, 2012. http://hdl.handle.net/10803/101513.

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Dentro del sistema endocannabinoide, los receptores de cannabinoides, hasta ahora clonados y caracterizados, son principalmente dos: el de tipo 1 (CB1R) y el de tipo 2 (CB2R). A pesar de que el CB1R se ha determinado ampliamente en el sistema nervioso central (CNS) y su acción se ha visto mediante de una gran variedad de procesos cognitivos y neurológicos, al receptor CB2 se le había atribuido, desde su clonación, una presencia exclusivamente periférica y un papel fundamental en el sistema inmunológico. Sin embargo, en los últimos años, no han sido desdeñables el número de publicaciones orien
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Kerr, Daniel Shikanai. "Ric-8B, uma GEF putativa do sistema olfatório, interage com Gαolf, Gβ1 e Gγ13." Universidade de São Paulo, 2008. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-22122008-092032/.

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O sistema olfatório de mamíferos é capaz de detectar milhares de substâncias químicas diferentes, mesmo em baixas concentrações. Um odorante disperso no ar pode se ligar a um receptor olfatório (OR) iniciando o processo de detecção. Os ORs são membros da super família de receptores acoplados a proteína G (GPCRs). Apesar de a via de transdução de sinal de odorantes estar bem descrita, pouco se sabe sobre os seus moduladores. Em 2005, nosso laboratório identificou RIC-8B como um possível fator de troca de nucleotídeos de guanina (GEF) que poderia amplificar a atividade da proteína G olfatória (G
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Moreno, Guillén Estefanía. "Heterómeros de receptores de dopamina. Nuevos mecanismos para la regulación de la transmisión dopaminérgica." Doctoral thesis, Universitat de Barcelona, 2012. http://hdl.handle.net/10803/81924.

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El Objetivo General de esta Tesis ha sido investigar la formación y función de heterómeros entre receptores de dopamina y otros receptores que puedan estar implicados en la regulación de la transmisión dopaminérgica, como receptores de galanina, histamina, adrenérgicos o receptores sigma-1. Basándonos en que tanto la galanina como la dopamina modulan la liberación de acetilcolina en el hipocampo, se ha demostrado que los receptores de dopamina de la familia D1 (receptores D1 y D5) pueden formar heterómeros con los receptores de galanina Gal1 y Gal2 y se ha estudiado la función de estos heteróm
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Casallanovo, Fabio. "Estudos conformacionais de seqüências hidrofóbicas de domínios de receptores acoplados a proteínas G (GPCR) e da proteína G. Um estudo de CD e espectroscopia de fluorescência." Universidade de São Paulo, 2004. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-22092015-154017/.

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O estudo fitoquímico do extrato etanólico de caules adultos de Araucaria angustifólia resultou no isolamento e identificação da vanilina, p-hidroxibenzaldeído, coniferaldeído, dois isoflavonóides (cabreuvina e irisolidona), quatro lignanas (pinoresinol, eudesmina, lariciresinol e 9\'-O-acetato de lariciresinol) e &#946;-sitosterol. Foi desenvolvido um protocolo para a obtenção de calos, a partir de caules de plântulas estioladas, dos quais foram isolados e caracterizados mistura de isômeros E e Z do p-cumarato de octadecila e do ferulato de octadecila.<br>Phytochemical investigations carried o
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Gandía, Sánchez Jorge. "Oligomerización del receptor A2A de adenosina: interpretando el receptorsoma." Doctoral thesis, Universitat de Barcelona, 2013. http://hdl.handle.net/10803/134352.

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Los receptores acoplados a proteína G (GPCR) conforman la familia de receptores de membrana más grande. El numeroso y variado tipo de señales que detectan han otorgado a estos receptores un alto interés farmacológico. Además, las interacciones entre diferentes tipos de GPCR formando complejos oligoméricos dan lugar a complejos con características bioquímicas diferenciadas de los protómeros que los forman. En esta Tesis Doctoral se han estudiado diferentes aspectos derivados este tipo de interacciones, centrando estos experimentos alrededor del receptor A2A de adenosina (A2AR), un importante ne
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Meira, Guilherme Louzada Silva. "Analíse da expressão do receptor olfativo M93 em sistemas heterólogos." Universidade de São Paulo, 2004. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-31082016-115408/.

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O sistema olfatório de mamífero pode discriminar milhares de odores presentes no meio ambiente. Aproximadamente 1000 diferentes receptores olfatórios (ORs) são expressos no epitélio olfatório (OE) do nariz, Os ORs detectam os odores e transmitem os sinais resultantes para o bulbo olfatório (OB) no cérebro. Os ORs pertencem a super família dos receptores acoplados a proteína G (GPCR) e apresentam sete domínios transmembrânicos putativos. Por razões desconhecidas, os ORs são retidos no retículo endoplasmático quando expressos em linhagens de células de mamíferos heterólogas. Provavelmente, prote
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Troupiotis-Tsaïlaki, Anastassia. "Lipid-GPCR interactions: from activation of sphingosine-1-phosphate receptors to modulation of vasopressin V2 receptor function." Doctoral thesis, Universite Libre de Bruxelles, 2015. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/216727.

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GPCRs form the largest family of membrane proteins in human genome and mediate signal transmission in a wide panel of essential physiological processes, and they are thus a major source of pharmaceutical targets. Investigating GPCR interactions with their cognate ligands and their membrane environment is crucial to understand their function at a molecular level. While major breakthroughs in the determination of high resolution structures of GPCRs in inactive and active states have shed a new light on the structural basis of GPCR activation process, complementary approaches are needed to invest
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Bahena, Silvia. "Computational Methods for the structural and dynamical understanding of GPCR-RAMP interactions." Thesis, Uppsala universitet, Institutionen för biologisk grundutbildning, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-416790.

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Protein-protein interaction dominates all major biology processes in living cells. Recent studies suggestthat the surface expression and activity of G protein-coupled receptors (GPCRs), which are the largestfamily of receptors in human cells, can be modulated by receptor activity–modifying proteins (RAMPs). Computational tools are essential to complement experimental approaches for the understanding ofmolecular activity of living cells and molecular dynamics simulations are well suited to providemolecular details of proteins function and structure. The classical atom-level molecular modeling o
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Guerrero, Hernández Martina. "Targeting tumor microenvironment crosstalk through GPCR receptors and PI3K pathway." Doctoral thesis, Universitat de Barcelona, 2019. http://hdl.handle.net/10803/667975.

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The tumor microenvironment (TME) is gaining momentum due to its contribution to cancer progression and therapy resistance. This TME has a direct crosstalk with tumor cells that involves the activation of different pathways. Follicular lymphoma (FL) is the most common indolent non-Hodgkin lymphoma. Although FL is generally characterized by slow progression and high response rates to therapy, it is still considered incurable, because almost virtually all the patients relapse. FL is probably the NHL with the highest dependence on microenvironment. PI3K is a common denominator transducing the sig
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Libros sobre el tema "Receptores GPCR"

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Adhesion-GPCRs structure to function. Springer Science+Business Media, 2010.

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Razvi, Enal S. GPCRs: The targets of today's drugs and tomorrow's blockbusters. D&MD Reports, 2002.

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Rajagopal, Senthilkumar, and Murugavel Ponnusamy. Metabotropic GPCRs: TGR5 and P2Y Receptors in Health and Diseases. Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-13-1571-8.

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Gross, Aaron D., Yoshihisa Ozoe, and Joel R. Coats, eds. Advances in Agrochemicals: Ion Channels and G Protein-Coupled Receptors (GPCRs) as Targets for Pest Control. American Chemical Society, 2017. http://dx.doi.org/10.1021/bk-2017-1264.

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Gross, Aaron D., Yoshihisa Ozoe, and Joel R. Coats, eds. Advances in Agrochemicals: Ion Channels and G Protein-Coupled Receptors (GPCRs) as Targets for Pest Control. American Chemical Society, 2017. http://dx.doi.org/10.1021/bk-2017-1265.

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Mason, Peggy. Receiving the Synaptic Message. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190237493.003.0013.

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Ionotropic and metabotropic receptors differ in their speed of action, the variety of effects produced after ligand-binding, and in the number of types present in the nervous system. The participation of two ionotropic glutamate receptors in synaptic plasticity is thought to be the cellular basis of learning. The actions of acetylcholine on nicotinic acetylcholine receptors present at the neuromuscular junction are described. The pharmacological profile of the GABAA receptor, central to most neural functions, is introduced. The properties of metabotropic receptors that are coupled to G protein
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Gpcr Signalling Complexes Synthesis Assembly Trafficking And Specificity. Springer, 2012.

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Jockers, Ralf, Denis J. Dupré, and Terence E. Hébert. GPCR Signalling Complexes - Synthesis, Assembly, Trafficking and Specificity. Springer, 2012.

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Modelling Of Gpcrs A Practical Handbook. Springer, 2012.

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Rajagopal, Senthilkumar, and Murugavel Ponnusamy. Metabotropic GPCRs: TGR5 and P2Y Receptors in Health and Diseases. Springer, 2018.

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Capítulos de libros sobre el tema "Receptores GPCR"

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Connelly, William M., Adam C. Errington, Josue G. Yagüe, Anna Cavaccini, Vincenzo Crunelli, and Giuseppe Di Giovanni. "GPCR Modulation of Extrasynapitic GABAA Receptors." In Extrasynaptic GABAA Receptors. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1426-5_7.

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Harikumar, Kaleeckal G., Maoqing Dong, and Laurence J. Miller. "Secretin Receptor Dimerization: A Possible Functionally Important Paradigm for Family B G Protein-Coupled Receptors." In GPCR Molecular Pharmacology and Drug Targeting. John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470627327.ch6.

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Knapp, Barbara, and Uwe Wolfrum. "Adhesion GPCR-Related Protein Networks." In Adhesion G Protein-coupled Receptors. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-41523-9_8.

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Strasser, Andrea, and Hans-Joachim Wittmann. "G Protein Coupled Receptors." In Modelling of GPCRs. Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-4596-4_2.

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Grinde, Ellinor, and Katharine Herrick-Davis. "Class A GPCR: Serotonin Receptors." In G-Protein-Coupled Receptor Dimers. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-60174-8_6.

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Hamann, Jörg, and Alexander G. Petrenko. "Introduction: History of the Adhesion GPCR Field." In Adhesion G Protein-coupled Receptors. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-41523-9_1.

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Tesmer, John J. G. "Chapter 15. Activation of G Protein-Coupled Receptor (GPCR) Kinases by GPCRs." In Drug Discovery. Royal Society of Chemistry, 2011. http://dx.doi.org/10.1039/9781849733441-00297.

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Strasser, Andrea, and Hans-Joachim Wittmann. "Thermodynamics of Ligand-Receptor Interaction." In Modelling of GPCRs. Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-4596-4_10.

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Langmead, Christopher. "Screening for Allosteric Modulators of G Protein-Coupled Receptors." In GPCR Molecular Pharmacology and Drug Targeting. John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470627327.ch12.

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Gingell, Joseph J., Christopher S. Walker, and Debbie L. Hay. "Class B GPCR: Receptors and RAMPs." In G-Protein-Coupled Receptor Dimers. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-60174-8_11.

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Actas de conferencias sobre el tema "Receptores GPCR"

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Fang, Ye, Anthony G. Frutos, and Joydeep Lahiri. "G protein-coupled receptor (GPCR) microarrays." In International Symposium on Biomedical Optics, edited by Darryl J. Bornhop, David A. Dunn, Raymond P. Mariella, Jr., et al. SPIE, 2002. http://dx.doi.org/10.1117/12.472073.

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Börsch, Michael, Thomas Heitkamp, and Reinhard Grisshammer. "Towards monitoring conformational changes of the GPCR neurotensin receptor 1 by single-molecule FRET." In Multiphoton Microscopy in the Biomedical Sciences XVIII, edited by Ammasi Periasamy, Peter T. So, Xiaoliang S. Xie, and Karsten König. SPIE, 2018. http://dx.doi.org/10.1117/12.2286787.

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Börsch, Michael, Anika Westphal, Stefanie Reuter, Hendrik Sielaff, Ralf Mrowka, and Thomas Heitkamp. "Ligand-induced oligomerization of the human GPCR neurotensin receptor 1 monitored in living HEK293T cells." In Multiphoton Microscopy in the Biomedical Sciences XIX, edited by Ammasi Periasamy, Peter T. So, and Karsten König. SPIE, 2019. http://dx.doi.org/10.1117/12.2506797.

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Insel, Paul A., Krishna Sriram, Shu Z. Wiley, Thalia McCann, Randall P. French, and Andrew M. Lowy. "Abstract 1139: G protein-coupled receptors (GPCRs): unrecognized potential therapeutic targets in cancer." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-1139.

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Martins, SAM, J. Mateus, V. Chu, DMF Prazeres, and JP Conde. "Thin-film amorphous silicon photodiodes with integrated fluorescent filters for monitoring live-cell G-protein coupled receptors (GPCR)." In 2014 IEEE Sensors. IEEE, 2014. http://dx.doi.org/10.1109/icsens.2014.6985298.

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Tsumoto, Kanta, Koki Kamiya, Sayaka Kitaoka, Shin Ogata, Masahiro Tomita, and Tetsuro Yoshimura. "G protein coupled receptors (GPCRs) reconstituted on recombinant proteoliposomes using baculovirus-liposome membrane fusion." In 2009 International Symposium on Micro-NanoMechatronics and Human Science (MHS). IEEE, 2009. http://dx.doi.org/10.1109/mhs.2009.5351994.

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Voli, Florida, Hangyu Yi, Estrella Gonzales-Aloy, and Jenny Yingzi Wang. "Abstract 3906: Targeting a novel G-protein coupled receptor (GPCR) for elimination of leukemia stem cells (LSC)." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-3906.

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Jala, Venkatakrishna R., Haribabu Bodduluri, Brandie Radde, and Carolyn M. Klinge. "Abstract 4548: The role of GPR30/G-protein coupled estrogen receptor (GPER) in lung cancer development." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-4548.

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Castillo, Maryann, Angelique M. Wimbley, Jacob J. Mayfield, Jenifer C. Lascano, and Kevin D. Houston. "Abstract 1305: Activation of G-protein coupled estrogen receptor (GPER) inhibits ELT-3 uterine leiomyoma cell proliferation." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-1305.

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"HOW MUCH BOVINE RHODOPSIN CRYSTAL STRUCTURE IS USEFUL FOR MODELING HUMAN GPCRS? - β2-Adrenergic Receptor as a Test Case". У International Conference on Bio-inspired Systems and Signal Processing. SciTePress - Science and and Technology Publications, 2009. http://dx.doi.org/10.5220/0001542402910298.

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