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Gordon Conference on "Phosphorylation and G Protein Signaling Networks"

Gordon Conference on "Phosphorylation and G Protein Signaling Networks"
戈登会议“磷酸化和 G 蛋白信号网络”
批准号:
7385961
负责人:
Henrik G. Dohlman
金额:
$1.27万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-04-01 至 2009-03-31
关键词:
5&apos-AMP-activated protein kinaseAcademiaActinsAddressAffectAgeAgingAgonistApoptoticArabidopsisAreaAsiansAttentionBiochemicalBiochemical ReactionBiochemistryBioinformaticsBiologicalBiological AssayBiologyBloodBrainBreedingCaliforniaCanadaCardiovascular DiseasesCardiovascular PhysiologyCatalytic DomainCategoriesCell CommunicationCell Cycle RegulationCell DeathCell Differentiation processCell PolarityCell Proliferation RegulationCell SizeCell physiologyCellsCellular biologyChemicalsChemistryClassClinicalCollaborationsColoradoCommunicable DiseasesCommunicationComplementComplexComputer SimulationCongenital AbnormalityCountCountryCyclic AMPCyclic NucleotidesCytoskeletonDNA Tumor VirusesDatabasesDependenceDetectionDevelopmentDiabetes MellitusDisabled PersonsDisciplineDiseaseDisease PathwayDisease ResistanceDisruptionDrosophila eyeEndopeptidasesEnzyme Inhibitor DrugsEnzyme InhibitorsEnzymesEquilibriumEukaryotaEukaryotic CellEventFacultyFailureFamilyFeedbackFemaleFilamentFluorescenceFocal AdhesionsFosteringFoundationsFundingG Protein-Coupled Receptor GenesG Protein-Coupled Receptor SignalingG-Protein-Coupled ReceptorsGTP-Binding ProteinsGene ExpressionGene SilencingGene TargetingGenesGeneticGenetic ProgrammingGenetic TranscriptionGenomicsGermanyGoalsGrantGrowthGrowth FactorGrowth and Development functionGuidelinesHealthHeartHispanicsHumanHypertensionImmuneImmune responseImmune systemIndividualInduction of ApoptosisIndustryInflammationInflammatoryInstitutionInsulinInsulin ResistanceInternationalInterventionKnock-outKnowledgeLearningLinkLocationLongevityLungMAPK8 geneMEKsMailsMaineMalignant NeoplasmsMapsMass Spectrum AnalysisMassachusettsMediatingMembraneMesenchymal Stem CellsMetabolicMetabolic DiseasesMetabolismMethodsMichiganMiningMinorityMinority GroupsMinority-Serving InstitutionMitotic Cell CycleModelingModificationMolecularMolecular BiologyMolecular ProfilingMolecular and Cellular BiologyMonitorMorphogenesisMuscleMusculoskeletal DiseasesNamesNeoplasm MetastasisNerve DegenerationNetherlandsNeuronsNew EnglandNobel PrizeNorth CarolinaNucleic AcidsNumbersNursesNutrientObesityOperative Surgical ProceduresOralParticipantPathogenesisPathway interactionsPattern FormationPeptide HydrolasesPhagocytosis InhibitionPharmacologic SubstancePheromonePhosphorylationPhosphotransferasesPhysiologyPlantsPlayPost-Translational Protein ProcessingPostdoctoral FellowPoxviridaePrincipal InvestigatorProcessProductionProtein Binding DomainProtein EngineeringProtein IsoformsProtein KinaseProtein Tyrosine KinaseProtein Tyrosine PhosphataseProteinsProteomicsPublished CommentRNA InterferenceReceptor SignalingRecruitment ActivityRegulationResearchResearch PersonnelResolutionRoleSaccharomyces cerevisiaeSan FranciscoScaffolding ProteinScheduleScientistScotlandScreening procedureSecond Messenger SystemsSenior ScientistShapesSignal PathwaySignal TransductionSignal Transduction PathwaySignaling MoleculeSiteSmall RNASocietiesStagingStressStudentsSystemT-Cell ReceptorTNF Receptor-Associated FactorsTexasTherapeuticTherapeutic InterventionThinkingTimeTitleTrainingTranscriptional ActivationTransforming Growth Factor betaTyrosine Kinase InhibitorUbiquitinUnderrepresented MinorityUnited States National Institutes of HealthUniversitiesVibrio parahaemolyticusVirulence FactorsWeekWheelchairsWomanWorkWorld Health OrganizationYeastsYersiniabasebiological adaptation to stresscareercell growthcell growth regulationcell motilitycell typechemical geneticsconceptcytokinedaydesigndetection of nutrientdevelopmental diseasedirect applicationdisabilitydriving forceexperiencefollow-upforkhead proteinfrontierhandicapping conditionhuman FRAP1 proteinhuman diseaseimmunological synapseinnovationinsightinterestknowledge basemacrophagemedical schoolsmembermetabolomicsmetaplastic cell transformationmicrobialmouse modelmultidisciplinarynew technologynovelnovel strategiesnovel therapeuticspathogenpostersprofessorprogramsprotein protein interactionreceptorresponsescaffoldsecond messengersensorsmall moleculesmall molecule librariessocialsorting nexinssrc-Family Kinasessuccesssymposiumtherapeutic targettraffickingtranscription factoryeast genetics

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DESCRIPTION (provided by applicant): We request partial funding support for operation of the Gordon Research Conference (GRC) on Phosphorylation and G protein Signaling Networks. This conference, formerly known as "Second Messengers and Protein Phosphorylation" has been held annually since 1970, and has been a premier venue for the presentation of new discoveries in signal transduction. Investigators who initiated and attended this meeting from its inception were leaders who established the field of signal transduction, including several who have received Nobel Prizes (e.g., Earl Sutherland, Al Oilman, Stanley Cohen, Edwin Krebs, Edmond Fischer, Paul Nurse). The conference focuses on signal transduction mechanisms that regulate cell growth, differentiation, survival, and metabolism. A full understanding of these signaling mechanisms is scientifically and clinically important because their failure plays a direct role in contemporary health problems that affect millions of people worldwide, such as diabetes, obesity, cancer, aging, infectious disease, cardiovascular disease, neurodegeneration, and developmental disorders. Meeting topics cover networks of intracellular signaling pathways from a mechanistic viewpoint, and continue to highlight cutting edge discoveries by emerging from studies focused on protein covalent modifications, protein-protein and protein-nucleic acid interactions, and control by small molecule effectors. The University of New England became the new site for this meeting in 2005, and provides a rustic and handicapped-accessible venue to promote open interaction among participants. The 2006 meeting will be held from Sunday night June 11 and end on Thursday evening June 16. The speakers are encouraged to integrate biochemical, structural, cell-biological, and genomic approaches that provide a comprehensive understanding of the molecular aspects of signaling mechanisms as they relate to disease. Two plenary speakers were selected to set the stage for the conference and to challenge the participants to think about signal transduction from perspectives of the chemistry-biology interface. The conference will consist of 8 sessions, each with a discussion leader and 3-5 speakers, selected from investigators who have made important recent contributions. At least 45% of the invited speakers are either women or members of minority groups and 23% of invited speakers are new investigators (Asst/Assoc. level). Speakers in each session will develop the important paradigms in signal transduction. The emphasis will be on structural and functional understanding of the defining molecular mechanisms and their implications for disease and potential treatment strategies. The co-chairs will select 135 participants from applicants, including representatives from industry and academia, senior scientists, postdoctoral fellows and graduate students. A special effort will be made to recruit minority participants and participants from industry by a direct emailing program. Participants will be encouraged to present posters on new and interesting results each afternoon. Importantly, the conference provides a forum for young investigators to see the connection between fundamental scientific inquiry and the application of scientific methods to the design of efficacious interventions for human disease. To emphasize this goal, 8 poster presentations that complement the themes of the meeting will be selected for short oral presentations during the main sessions.
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