EURO-NEUROSTRESS

Dissecting the Central Stress Response: Bridging the Genotype-Phenotype Gap

 Coordinatore WEIZMANN INSTITUTE OF SCIENCE 

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 Nazionalità Coordinatore Israel [IL]
 Totale costo 1˙500˙000 €
 EC contributo 1˙500˙000 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2010-StG_20091118
 Funding Scheme ERC-SG
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-04-01   -   2016-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    WEIZMANN INSTITUTE OF SCIENCE

 Organization address address: HERZL STREET 234
city: REHOVOT
postcode: 7610001

contact info
Titolo: Dr.
Nome: Alon
Cognome: Chen
Email: send email
Telefono: +972 8 9344490
Fax: +972 8 9344131

IL (REHOVOT) hostInstitution 1˙500˙000.00
2    WEIZMANN INSTITUTE OF SCIENCE

 Organization address address: HERZL STREET 234
city: REHOVOT
postcode: 7610001

contact info
Titolo: Ms.
Nome: Gabi
Cognome: Bernstein
Email: send email
Telefono: 97289346728
Fax: 97289344165

IL (REHOVOT) hostInstitution 1˙500˙000.00

Mappa


 Word cloud

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linked    psychological    mechanisms    homeostasis    neuroendocrine    disorders    pathways    gene    stressful    brain    maintenance    central    molecular    models    responses    circuits    biological    perceived    physiological    stress   

 Obiettivo del progetto (Objective)

'The biological response to stress is concerned with the maintenance of homeostasis in the presence of real or perceived challenges. This process requires numerous adaptive responses involving changes in the central nervous and neuroendocrine systems. When a situation is perceived as stressful, the brain activates many neuronal circuits linking centers involved in sensory, motor, autonomic, neuroendocrine, cognitive, and emotional functions in order to adapt to the demand. However, the details of the pathways by which the brain translates stressful stimuli into the final, integrated biological response are presently incompletely understood. Nevertheless, it is clear that dysregulation of these physiological responses to stress can have severe psychological and physiological consequences, and there is much evidence to suggest that inappropriate regulation, disproportional intensity, or chronic and/or irreversible activation of the stress response is linked to the etiology and pathophysiology of anxiety disorders and depression. Understanding the neurobiology of stress by focusing on the brain circuits and genes, which are associated with, or altered by, the stress response will provide important insights into the brain mechanisms by which stress affects psychological and physiological disorders. This is an integrated multidisciplinary project from gene to behavior using state-of-the-art moue genetics and animal models. We will employ integrated molecular, biochemical, physiological and behavioral methods, focusing on the generation of mice genetic models as an in vivo tool, in order to study the central pathways and molecular mechanisms mediating the stress response. Defining the contributions of known and novel gene products to the maintenance of stress-linked homeostasis may improve our ability to design therapeutic interventions for, and thus manage, stress-related disorders.'

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INVFEST (2010)

Evolutionary and functional analysis of polymorphic inversions in the human genome

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PROTEINSEQ (2012)

"Sensitive, specific high-throughput plasma proteome analysis via ProteinSeq"

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EVOIMMUNOPOP (2012)

Human Evolutionary Immunogenomics: population genetic variation in immune responses

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