Search Results
Chromatin Dynamics and Higher Order Organization (C4)
25-Feb-2009 -
02-Mar-2009
Coeur d'Alene
Idaho
USA
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"Research in the past decade has revealed the intimate link of chromatin structure at the levels of histone modifications and nucleosome remodeling to nuclear functions, especially gene regulation. Yet the molecular mechanisms of higher orders of chromatin organization beyond the nucleosomal array remain largely obscure. Evidence is emerging that chromatin folding and large-scale chromatin interactions, including trans-interactions between chromosomes, play an important role in gene regulation, recombination, and other nuclear processes. Chromatin looping may be a key component of regulatory mechanisms. New roles of non-coding RNAs in regulating chromatin function are also uprising. Furthermore, functional compartments, such as transcription factories, replication factories, and polycomb bodies have been suggested to organize the nucleus. This meeting will focus on recent breakthroughs in our understanding of the mechanisms that govern dynamics of higher-order chromatin architecture in order to gain important insights into gene regulation and disregulation, DNA repair, normal development, stem cell function, epigenetic inheritance and diseases such as cancer. "
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Registration Deadline: 27-Oct-2008
http://www.keystonesymposia.org/Meetings/ViewMeetings.cfm?Meetin
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Polyamines
21-Jun-2009 -
26-Jun-2009
Waterville Valley
NH
USA
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Note: A Gordon-Kenan Graduate Research Seminar (GRS) will be held in conjunction with the Polyamines GRC and will start the Saturday preceding the main GRC. Those interested in attending must submit a separate application for the GRS, in addition to an application for the main GRC. Please see the GRS web page for more information.
The Polyamine Gordon conference will be held at the Waterville Valley Resort in Waterville Valley, New Hampshire from June 21-26, 2009. Since 1975, the Polyamine GRC has been a multidisciplinary conference focused on the polyamine metabolic pathway, the role of polyamines in cellular homeostasis and the development of small molecules that modulate polyamine metabolism as potential therapeutic agents. This meeting is widely regarded as the pre-eminent venue for the presentation and discussion of polyamine research. Polyamines are small organic polycations found in virtually all prokaryotic and eukaryotic cells. Despite their importance and ubiquitous occurrence, the cellular functions of polyamines are not fully understood. Polyamines are closely linked to cell growth, and inhibitors of polyamine biosynthesis are promoted as anti-proliferative agents. Polyamines are highly regulated at the levels of transcription, translation and protein turnover. Thus the field brings together researchers interested in the physiological role of polyamines in a wide array of organisms, and researchers interested in therapeutic applications such as cancer and parasitic or bacterial infection. The 2009 Polyamine GRC will feature presentations from scientists at the forefront of polyamine research in the areas of anticancer and antiparasitic drug development. The meeting will also include presentations outlining the role of polyamine metabolism in cellular homeostasis, with an emphasis on basic mechanisms of genetic, epigenetic and physiological control. It will also include short talks by students or postdocs whose work has been chosen from the poster presentations by the organizing committee. To further encourage the participation of student and postdoctoral scientists in the meeting, the Polyamine GRC will be held in conjunction with the second Gordon-Kenan Graduate Research Seminar (GKGRS) on Polyamines. The GKGRS will be held from June 20-21, and students and postdocs participating in the GKGRS will be expected to also attend the regular GRC meeting, which immediately follows.
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Registration Deadline: 31-May-2009
http://www.grc.org/programs.aspx?year=2009&program=polyamines
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Nucleic Acids
31-May-2009 -
05-Jun-2009
Biddeford
ME
USA
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The Gordon Research Conference on Nucleic Acids was first established more than 50 years ago. Since that time the field of nucleic acids has exploded with tremendous discoveries regarding the chemistry, functional potential and biologic significance of nucleic acids. Through all of these advances the Nucleic Acids GRC has provided a critical forum for discussion of new ideas and interaction between investigators specializing in all the diverse areas of nucleic acids research. In particular, the past decade has brought renewed recognition and excitement regarding the breadth of nucleic acid functions in cells (i.e. all classes of ncRNAs) and the extent to which various steps in nucleic acids biosynthesis and processing are mechanistically intertwined. The involvement of RNAi in chromatin silencing and remodeling is a prime example for the usefulness of bringing seemingly diverse areas of nucleic acid researchers together. The 2009 meeting of the Nucleic Acids GRC will highlight recent advances in these areas of DNA and RNA biology, biochemistry and biophysics with a view toward identifying emerging concepts and technologies in these fields. Specific topics of discussion will include: DNA recombination and repair, DNA replication, Transcription and chromatin dynamics, pre-mRNA processing, small non-coding RNAs, Ribosome assembly and function, Regulation of translation and Catalytic RNA. Young scientists, or those newly engaged in nucleic acids research, will be particularly encouraged to attend and present; with time built into the schedule for short talks selected from submitted abstracts.
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Registration Deadline: 10-May-2009
http://www.grc.org/programs.aspx?year=2009&program=nucacids
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Chronobiology
19-Jul-2009 -
24-Jul-2009
Newport
RI
USA
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The 2009 Gordon Conference on Chronobiology will present cutting-edge research on the molecular, cellular and systems aspects of circadian biology. The Conference will feature a wide range of topics, such as the dynamics of transcription and cell cycles, molecular mechanisms of clocks, genetics of human clocks, metabolism and clocks, novel functions for clock genes, model organism clocks, entrainment mechanisms, and the neurobiology of the suprachiasmatic nucleus. Invited speakers represent a variety of scientific disciplines, including biochemistry, molecular genetics, genetics, genomics, structural biology, cell biology, imaging, modeling, sleep medicine, neuroscience, behavior and human biology. The Conference will bring together a collection of investigators who are at the forefront of their field, and will provide opportunities for junior scientists and graduate students to present their work in poster format and exchange ideas with leaders in the field. Some poster presenters will be selected for short talks. The collegial atmosphere of this Conference, with programmed discussion sessions as well as opportunities for informal gatherings in the afternoons and evenings, provides an avenue for scientists from different disciplines to brainstorm and promotes cross-disciplinary collaborations in the various research areas represented.
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Registration Deadline: 28-Jun-2009
http://www.grc.org/programs.aspx?year=2009&program=chrono
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Archaea: Ecology, Metabolism & Molecular Biology
26-Jul-2009 -
31-Jul-2009
Waterville Valley
NH
USA
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Archaea, one of three major evolutionary lineages of life, are a fascinating and diverse group of microbes with deep roots overlapping those of eukaryotes. The focus of the "Archaea: Ecology Metabolism & Molecular Biology" GRC conference expands on a number of emerging topics highlighting new paradigms in archaeal metabolism, genome function and systems biology; information processing; evolution and the tree of life; the ecology and diversity of archaea and their viruses; and industrial applications. The strength of this conference lies in its ability to couple a field with a rich history in high quality research with new scientific findings in an atmosphere of stimulating exchange. This conference remains an excellent opportunity for younger scientists to interact with world experts in this field.
The Archaeal Gordon Research Conference brings more than 35 internationally renowned speakers who will review the current state of progress and knowledge in the field of the metabolism, molecular biology and ecology of archaea. Leading scientists will present recent unpublished developments in fundamental aspects as well as key advances in industrial applications of archaea. Topics of archaea to be addressed will include:
- systems biology and genome function
- ecology and diversity of archaea and their viruses
- enzyme structure and function
- transcription and gene regulation
- translation and post-transcriptional modification
- physiology and regulation of metabolism
- extremophiles and biotechnology applications
- replication, repair and recombination
- evolution and the tree of life
The GRC on Archaea also invites presentations in the form of posters, from which 3-4 student oral talks will be selected.
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Registration Deadline: 05-Jul-2009
http://www.grc.org/programs.aspx?year=2009&program=archaea
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MECHANISMS OF EUKARYOTIC TRANSCRIPTION
25-Aug-2009 -
29-Aug-2009
Cold Spring Harbor
NY
USA
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The eleventh meeting on transcriptional regulation in eukaryotes will be held at Cold Spring Harbor Laboratory from Tuesday evening, August 25 to Saturday afternoon, August 29, 2009. The program will consist of both oral and poster presentations. The oral presentations will be by a combination of invited speakers and speakers selected from amongst submitted abstracts.
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Registration Deadline: 05-Jun-2009
http://meetings.cshl.edu/meetings/ccell09.shtml
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bHLH transcription factors
07-May-2009 -
08-May-2009
London
UK
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RUNX transcription factors in development and disease
16-Aug-2009 -
19-Aug-2009
Oxford
UK
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Thiol-Based Redox Regulation & Signaling
09-May-2010 -
14-May-2010
Lucca (Barga)
Italy
Italy
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The Gordon Research Conference on Thiol-based Redox Regulation and Signaling will be held May 9-14, 2010 at Il Ciocco in Italy. Redox biology is key to the life sciences as an increasing number of cellular functions and impairments are found linked to redox processes. Many crucial signaling pathways utilize the reversible oxidation and reduction of cysteine thiols as a molecular switch. Transient oxidation of numerous phosphatases, kinases and transcription factors links thiol-based redox chemistry to phosphorylation-based signaling, apoptosis, gene regulation, cell cycle control and other physio-pathological processes. Redox dysregulation has hence major implications for the onset and progression of many complex diseases and is a significant component of the process of aging. This conference is in its third cycle after a two very successful meetings in the U.S. and Italy in 2006 and 2008. The chair and vice-chair are a physician scientist and a basic researcher, respectively, and are representative of the biologists, chemists and clinicians working on varied aspects of the field. This conference provides a venue for the free exchange of ideas and methodologies (the latter often limit progress in this particular field). The topics covered include: redox signaling, regulation and disease; disulfide bond formation and isomerization; redox based inter-organellar and inter-cellular communication; peroxide generation, sensing and clearance; bioinformatics and redoxomics; sulfur metabolism; emerging technologies. While the thematic area is broad-based, its relevance to cancer, cardiovascular diseases and aging is well represented programmatically. By bringing together investigators with varied expertise in biophysical methods, bioinformatics and animal model systems, with physicians focused on disease processes, the meeting is expected to further stimulate collaborations and catalyze scientific progress as has been exemplified by the successes of the previous meetings.
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Registration Deadline: 18-Apr-2010
http://www.grc.org/programs.aspx?year=2010&program=thiol
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Molecular Basis for Chromatin Structure and Regulation
17-Jan-2010 -
22-Jan-2010
Taos
New Mexico
USA
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Chromatin structure and dynamics underlie every aspect of genome function. The past several years have seen an exponential growth in our knowledge of facts, ranging from catalogs of histone protein posttranslational modifications to complete genome sequences of many organisms to atomic resolution structures of many key molecular players. But our mechanistic understanding lags far behind. New reagents, methodologies and concepts are needed. This meeting will bring together leading experts in diverse areas of chromatin biology who are developing and applying new approaches to develop a concrete mechanistic link between chromatin structure and chromatin function. The topics covered include: fundamental in vivo physical chemical studies of transcription factor binding; real-time single molecule in vivo imaging; state-of-the-art methods for discovery, characterization, and manipulation of histone- and nucleosome-modifying enzymes and for the synthesis and characterization of their specifically-modified histone and nucleosome substrates; single molecule biophysics studies of molecular mechanisms; atomic resolution structural studies; and locus- and chromosome-wide phenomena such as heterochromatin formation and dosage compensation.
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Registration Deadline: 17-Jan-2010
http://www.keystonesymposia.org/Meetings/ViewMeetings.cfm?MeetingID=1055&subTab=summary
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Dynamics of Eukaryotic Transcription during Development
07-Apr-2010 -
12-Apr-2010
Big Sky
Montana
USA
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Gene expression in eukaryotes is regulated primarily at the level of transcription. Although much is known about the basic building blocks required to recruit RNA polymerase II to a gene promoter and establish a pre-initiation complex, recent data reveals that a great deal of regulation occurs during transcription elongation, and involves dynamic interactions between the transcription machinery and chromatin structure. This meeting is intended to explore these recently appreciated mechanisms for gene regulation and to showcase the novel techniques that have permitted these advances. Of particular interest are the use of comprehensive, genomic approaches, and their use towards understanding the different patterns of gene expression in different model systems, including stem cells and developing tissues, as well as the application of novel molecular probing and cell imaging techniques to investigate the global nuclear architecture and its impact on gene expression.
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Registration Deadline: 07-Apr-2010
http://www.keystonesymposia.org/Meetings/ViewMeetings.cfm?MeetingID=1058&subTab=summary
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New Directions in Small Molecule Drug Discovery
20-Apr-2010 -
25-Apr-2010
Whistler
British Columbia
Canada
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The purpose of this meeting is to highlight exciting new opportunities in the discovery of small molecule drug candidates, including the following: ユ Novel targets for small molecules, including disruption of protein-protein interactions, allosteric modulation of receptors and enzymes, and direct interactions with transcription factors. ユ Enabling technologies for the discovery of new small molecule leads, including diversity-oriented screening, fragment screening, and affinity screening. ユ The most successful structure-based design approaches to the optimization of leads. A focus of the conference will be successful applications structure-based design in the discovery of therapeutics for the treatment of HCV infection (protease inhibitors) and cancer (protein kinase inhibitors). A session comprising first-time disclosures of Phase 2 clinical candidates will illustrate successful applications of structure-based design in drug discovery.
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Registration Deadline: 20-Apr-2010
http://www.keystonesymposia.org/Meetings/ViewMeetings.cfm?MeetingID=1031&subTab=summary
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Islet Biology
12-Apr-2010 -
17-Apr-2010
Whistler
British Columbia
Canada
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This symposium will focus on advances in our understanding of normal pancreatic b-cell function and mechanisms of beta-cell failure in type 2 diabetes, which has become a pandemic disease with estimates of affected individuals reaching 350 millions in 2030. Defects in pancreatic b-cell function and reduced beta cell mass are now recognized as the event that triggers the transition from pre-diabetes/metabolic syndrome to overt type 2 diabetes. Major advances have been made in our understanding of fundamental beta-cell biology, signaling pathways regulating islet growth, apoptosis, regeneration in normal and disease states, and development of new strategies for enhancing beta-cell survival and function. Leading contributors of academic and industrial contributors alike will carefully discuss recent advances in knowledge in several disciplines, including development, regeneration, stem cells, transcription factors, novel signaling pathways, cell biology, genetics, gene regulation, drug targeting, as well as emerging technologies in islet research.
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Registration Deadline: 12-Apr-2010
http://www.keystonesymposia.org/Meetings/ViewMeetings.cfm?MeetingID=1065&subTab=summary
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Biomolecular Interaction Networks: Function and Disease
07-Mar-2010 -
12-Mar-2010
Quebec
QC
Canada
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The aim of this symposium is to bring together researchers from different fields of computational and experimental biology, to discuss the use of biomolecular interaction networks to study cell function in both physiological and pathological contexts. These interaction maps, also known as interactomes, model protein-protein, protein-DNA and protein-small molecule interaction networks either within an organism or within specific cellular contexts. The function of proteins, nucleic acids, and other biomolecules can only be defined through their interactions in vivo. Such biochemical interactions � including those involved in signal transduction, transcriptional and translational regulation, as well as in the assembly of large molecular complexes � are astonishing in their magnitude and diversity. For instance, it has been shown that most proteins interact with multiple partners, forming intricate interaction networks. Similarly, individual transcription factor can bind to tens of thousands of genomic sites and regulate the expression of thousands of genes, both in isolation and in combinatorial fashion. Regulatory interactions play a key role in determining cellular differentiation, in maintaining cellular and organism homeostasis, and in triggering abnormal differentiation events leading to human disease including cancer. Not surprisingly, even slight genetic and epigenetic perturbations of these regulatory pathways can trigger macroscopic changes in normal cell physiology and lead to disease. Due to the abundance of experimental data, researchers are starting to uncover some general rules and principles underlying molecular interaction networks: their topological properties, the relationships between their components, evolutionary conservation and divergence, and their role in maintaining specific cellular functions and processes. Despite significant advances, however, knowledge about the distinct functional roles of many proteins is still elusive. Thus, interaction networks have emerged as exceedingly useful tools in predicting context-specific molecular function based on knowledge of upstream regulators, cognate binding partners, and downstream regulated targets. Furthermore, molecular interaction networks are starting to provide a unique integrative context to study additional disease-related genetic and epigenetic data, including single nucleotide mutations and polymorphisms, gene copy number alterations and complex, polygenic diseases.
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Registration Deadline: 07-Mar-2010
http://www.keystonesymposia.org/Meetings/ViewMeetings.cfm?MeetingID=1068&subTab=summary
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Nuclear Receptors: Signaling, Gene Regulation and Cancer
21-Mar-2010 -
26-Mar-2010
Keystone
Colorado
USA
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Nuclear receptors (NRs) comprise a large family of ligand-regulated transcription factors that play critical roles in physiology and disease. Much of the focus has been on the nuclear actions of NRs, including interactions with coregulators, modulation of chromatin structure, and regulation of gene expression. Recent studies, however, have also suggested a role for membrane- or cytoplasmic-initiated actions of NRs and crosstalk with other cellular signaling pathways. Current studies are aimed at understanding how the ligand-dependent molecular actions of NRs, including their subcellular localization, binding across the genome, and interaction with the proteome, connect to their roles in physiological and pathophysiological processes, including hormone-regulated cancers. In addition, NRs are being explored as targets for drug development, with many compounds on the market or in ongoing clinical trials. This meeting will highlight recent breakthroughs in NR research, promote interactions between scientists from industry and academia, and provide opportunities for senior scientists to interact with younger researchers and trainees.
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Registration Deadline: 21-Mar-2010
http://www.keystonesymposia.org/Meetings/ViewMeetings.cfm?MeetingID=1056&subTab=summary
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NF-kappaB in Inflammation and Disease
05-Jan-2010 -
10-Jan-2010
Santa Fe
New Mexico
USA
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In the past 10 years, impressive progress has been made on how the NF- kappaB transcription factor is regulated and how diverse signals frequently use ubiquitin-dependent mechanisms to activate NF- kappaB. Many of the signal transducers and regulatory enzymes have been identified and their essential roles in NF- kappaB regulation revealed through genetic analyses in mice. More recent work highlights the importance of NF- kappaB in innate immune signaling by cell surface Toll-like receptors and cytosolic Nod-like receptors. Although current research clearly implicates NF- kappaB in diabetes, inflammatory diseases and cancer, a challenge for the future will be to reveal the precise molecular and cellular mechanisms of NF- kappaB dysfunction in disease. The realization that NF- kappaB activity is regulated by kinases and ubiquitin modifying enzymes presents multiple opportunities for therapeutic intervention. In addition to highlights from basic research, results from clinical trials using IKK and other NF- kappaB inhibitors are expected to be presented at this meeting.
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Registration Deadline: 05-Jan-2010
http://www.keystonesymposia.org/Meetings/ViewMeetings.cfm?MeetingID=1023&subTab=summary
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Deregulation of Transcription in Cancer: Controlling Cell Fate Decisions
21-Jun-2009 -
26-Jun-2009
Killarney
Co. Kerry
Ireland
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Transcription is an intricate process that is regulated with exquisite specificity at both the genetic and epigenetic levels through such aspects as chromatin and core RNA polymerase machinery. Sophisticated mechanisms have been recently deciphered concerning how specific genes and pathways are deregulated in human cancers. Master cancer regulators are commonly transcription factors. Yet a great disparity exists between the nonspecificity of most cancer therapies and this advanced understanding of aberrant gene expression. This conference will focus on exploiting novel mechanistic information to generate more efficacious targeted therapies . Current insights into the mechanisms by which specific genes are deregulated in cancer, the resulting transcriptome signature for particular cancers, and state-of-the-art therapeutic approaches using small molecules or RNA interference will be presented. The goals of this meeting are to explore how transcription as a regulator for cell fate outcomes can be parlayed into specific cancer therapies.
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Registration Deadline: 21-Jun-2009
http://www.keystonesymposia.org/Meetings/ViewMeetings.cfm?MeetingID=1001&subTab=summary
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Nuclear Receptors: Development, Physiology and Disease
21-Mar-2010 -
26-Mar-2010
Keystone
Colorado
USA
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Nuclear receptors represent a family of ligand-regulated transcription factors that play central roles in development, physiology, and metabolism. Upon binding small lipophilic hormones and metabolites, such as steroids, fatty acids, and bile acids, nuclear receptors switch their regulatory status, reprogramming gene expression in target tissues. Current research is aimed at defining roles for these receptors in normal development and metabolism as well as better understanding how nuclear receptor dysfunction contributes to diabetes, cancer, cardiovascular disease, obesity, and neuronal disorders. Nuclear receptors are also a major target for drug development, with many compounds on the market and several in ongoing human trials. This meeting will highlight recent breakthroughs in nuclear receptor research, promote interactions between scientists from industry and academia, and provide opportunities for senior scientists to interact with younger researchers and trainees.
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Registration Deadline: 21-Mar-2010
http://www.keystonesymposia.org/Meetings/ViewMeetings.cfm?MeetingID=1057&subTab=summary
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Genetic Toxicology
10-Jul-2011 -
15-Jul-2011
Lucca (Barga)
Italy
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Genetic toxicology represents the study of genetic damage, the agents that induce such damage, and the biological mechanisms that respond to the consequences of genetic damage. Genotoxic agents are abundant in the environment and are often linked to human activity. The effects these agents have on humans include many common diseases, such as cancer. The response to genetic damage interfaces closely with many aspects of cellular metabolism, such as DNA repair and recombination, replication, transcription, cell cycle regulation and cell death. The interplay between genetic damage and cellular function will be a central focus of the conference.
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Registration Deadline: 12-Jun-2011
http://www.grc.org/programs.aspx?year=2011&program=gentox
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Nucleic Acids
05-Jun-2011 -
10-Jun-2011
Biddeford
ME
USA
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The Gordon Research Conference on Nucleic Acids was first established more than 50 years ago. Since that time the field of nucleic acids has exploded with tremendous discoveries regarding the chemistry, functional potential and biologic significance of nucleic acids. Through these advances the Nucleic Acids GRC has provided a critical forum for discussion of new ideas by promoting interaction between investigators specializing in all the diverse areas of nucleic acids research. In particular, the past decade has brought renewed recognition and excitement regarding the breadth of nucleic acid functions in cells (i.e. all classes of non-coding RNAs) and the extent to which various steps in nucleic acids biosynthesis and processing are mechanistically intertwined. The involvement of RNAi in chromatin silencing and remodeling is a prime example for the usefulness of bringing seemingly diverse areas of nucleic acid researchers together. The 2011 meeting of the Nucleic Acids GRC will highlight recent advances in these areas of DNA and RNA biology, biochemistry and biophysics with a view toward identifying emerging concepts and technologies in these fields. Specific topics of discussion will include: Nucleic acid structure and catalysis, Transcription and chromatin dynamics, Ribosome function and biogenesis, DNA replication, RNA stability and export, Genomic integrity, Non-coding RNA function and biogenesis, and Co- and Post-transcriptional RNA processing. Young scientists, or those newly engaged in nucleic acids research, will be particularly encouraged to attend and present; with time built into the schedule for short talks selected from submitted abstracts.
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Registration Deadline: 08-May-2011
http://www.grc.org/programs.aspx?year=2011&program=nucleic
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Polyamines
19-Jun-2011 -
24-Jun-2011
Waterville Valley
NH
USA
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The Gordon Research Conference (GRC) on Polyamines is a multidisciplinary conference focused on the polyamine metabolic pathway, the role of polyamines in cellular physiology and the development of small molecules that modulate polyamine metabolism as potential therapeutic agents. Polyamines are small organic polycations found in virtually all prokaryotic and eukaryotic cells. Despite their ubiquitous occurrence, the cellular functions of polyamines are not fully understood. Polyamines are closely linked to the control of cell proliferation, and the enzymes of polyamine biosynthesis and catabolism are highly regulated at the levels of transcription, translation and protein turnover. In recent years it has become increasingly clear that polyamines have unique roles in different organisms, and further that the biosynthetic and catabolic pathways, as well as the associated regulatory mechanisms, vary widely among species. Thus, the field encompasses researchers studying the physiological role of polyamines in a broad array of organisms (mammalian cells, yeast, protozoa and bacteria) and researchers interested in therapeutic applications for cancer and parasitic or bacterial infection. This range of scientific disciplines represented at the Polyamines GRC makes for an intellectually stimulating environment for participants.
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Registration Deadline: 22-May-2011
http://www.grc.org/programs.aspx?year=2011&program=polyamines
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Regulated Proteolysis of Cell Surface Proteins
10-Jul-2011 -
15-Jul-2011
Davidson
NC
USA
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Many membrane-bound receptors, growth factors, and ligands are proteolytically processed in or near the membrane. The release of these proteins from vesicles, organelles or the cell surface is accomplished by the sequential action of membrane-tethered sheddases and membrane-embedded proteases in a process known as regulated intramembrane proteolysis or RIP. Many sheddases are members of the A Disintegrin And Metalloproteinase (ADAM) family, including ADAM17 (TNF-alpha converting enzyme or TACE), the meltrins, and ADAM10 (also known as Kuz). Other sheddases of biological and biomedical importance include the aspartyl proteases beta-secretase (BACE1) and its homolog BACE2. Upon release of ectodomains by sheddases, the membrane-bound remnants are often cleaved by membrane-embedded proteases, which include the presenilin-containing gamma-secretases and the SPP, Rhomboid and S2P families. These proteases contain multiple transmembrane domains, and their active sites reside within the boundaries of the lipid bilayer. Proteolysis within the transmembrane region of the substrate leads to release of the cytoplasmic domain, which in some cases can translocate to the nucleus and regulate transcription. Dysregulation of RIP proteases, either the membrane-tethered sheddases or the membrane-embedded proteases, can lead to diseases such as Alzheimer's, cancer, allergies, obesity, cardiac hypertrophy, and autoimmune diseases, and many of these enzymes are targets for potential therapeutic intervention. This conference will focus on the processes and proteases involved in the regulated proteolysis of cell surface proteins as they relate to biology and medicine.
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Registration Deadline: 12-Jun-2011
http://www.grc.org/programs.aspx?year=2011&program=regprot
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