Dependence receptors: from basic research to drug development

Autor: Patrick Mehlen, Dale E. Bredesen
Přispěvatelé: Equipe 1, Centre de Recherche en Cancérologie de Lyon ( CRCL ), Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 ( UCBL ), Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Centre National de la Recherche Scientifique ( CNRS ) -Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 ( UCBL ), Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Centre National de la Recherche Scientifique ( CNRS ), Biological and Medical Informatics [San Francisco] ( BMI ), University of California [San Francisco] ( UCSF ), Centre de Recherche en Cancérologie de Lyon (UNICANCER/CRCL), Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM), Biological and Medical Informatics [San Francisco] (BMI), University of California [San Francisco] (UCSF), University of California-University of California
Jazyk: angličtina
Rok vydání: 2011
Předmět:
MESH : Drug Design
Angiogenesis
MESH: Low Back Pain
MESH : Prospective Studies
MESH : Aged
MESH : Receptors
Cell Surface

Apoptosis
MESH : Analysis of Variance
Dependence receptor
MESH: Pain Measurement
MESH : Models
Biological

Pharmacology
MESH: Drug Design
Ligands
medicine.disease_cause
Biochemistry
[ SDV.CAN ] Life Sciences [q-bio]/Cancer
0302 clinical medicine
MESH : Chronic Disease
Basic research
MESH: Ligands
MESH: Double-Blind Method
MESH : Pain Measurement
MESH : Female
Receptor
MESH: Physical Therapy Modalities
MESH: Treatment Outcome
MESH: Receptors
Cell Surface

MESH: Aged
0303 health sciences
MESH : Ligands
MESH: Middle Aged
Neurodegeneration
MESH: Disability Evaluation
MESH : Questionnaires
MESH : Adult
MESH: Patient Compliance
MESH: Interviews as Topic
Drug development
MESH : Motivation
Caspases
030220 oncology & carcinogenesis
MESH: Cell Adhesion Molecules
Netrin Receptors
MESH : Male
MESH: Motivation
Receptors
Cell Surface

[SDV.CAN]Life Sciences [q-bio]/Cancer
MESH : Disability Evaluation
MESH : Treatment Outcome
Biology
Models
Biological

MESH : Patient Compliance
MESH : Cell Adhesion Molecules
03 medical and health sciences
MESH: Analysis of Variance
MESH : Adolescent
medicine
Humans
MESH : Double-Blind Method
MESH : Middle Aged
Molecular Biology
030304 developmental biology
MESH: Adolescent
MESH: Caspases
MESH: Humans
MESH: Questionnaires
MESH: Apoptosis
MESH: Chronic Disease
MESH : Humans
MESH: Models
Biological

MESH: Adult
Cell Biology
medicine.disease
MESH: Male
MESH: Prospective Studies
MESH : Low Back Pain
MESH : Physical Therapy Modalities
Drug Design
MESH : Interviews as Topic
MESH : Caspases
Carcinogenesis
Cell Adhesion Molecules
Neuroscience
MESH: Female
Function (biology)
MESH : Apoptosis
Zdroj: Science Signaling
Science Signaling, American Association for the Advancement of Science, 2011, 4 (157), pp.mr2. 〈10.1126/scisignal.2001521〉
Science Signaling, American Association for the Advancement of Science, 2011, 4 (157), pp.mr2. ⟨10.1126/scisignal.2001521⟩
ISSN: 1937-9145
DOI: 10.1126/scisignal.2001521〉
Popis: International audience; The fourth meeting on dependence receptors featured descriptions of previously unknown dependence receptors. New mechanistic data were presented on the switch between the trophic, antiapoptotic response with the proapoptotic response that occurs with loss of trophic support. The possibility that the loss of trophic support may also involve the binding of an active antitrophin was also discussed. New in vivo data were presented on the roles of dependence receptors in development, angiogenesis, oncogenesis, and neurodegeneration, as well as new therapeutic approaches based on dependence receptor function. The next meeting on dependence receptors is scheduled for 2012.
Databáze: OpenAIRE