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EPIMAC SIGNED

The next generation epigenetic medicine for inflammation

Total Cost €

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EC-Contrib. €

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Partnership

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 EPIMAC project word cloud

Explore the words cloud of the EPIMAC project. It provides you a very rough idea of what is the project "EPIMAC" about.

chronic    nicodeme    area    healthcare    gene    deregulated    world    epinova    overcome    adjust    named    histone    regulatory    educate    successful    versatile    nature    mechanisms    2010    precise    bowel    genetics    master    worldwide    immuno    pharmacology    train    multidisciplinary    innovative    2012    inhibitors    gsk    inflammation    group    etiology    et    epimac    modifications    validation    pharmaceutical    pipeline    epigenetic    sme    reports    treatment    implementations    units    led    therapeutic    conjunction    hdac    environmental    unclear    gastrointestinal    time    modality    team    aberrant    clinical    compound    severe    academic    suggest    treating    clear    epigenetics    pursue    regulation    strategies    good    diseases    bear    ibd    people    millions    generation    deacetylase    disease    glaxosmithkline    discovery    excellent    tract    companies    performance    cells    specializing    therapeutics    cues    expression    kruidenier    inflammatory    skilled    scientists    preclinical    ambition    doctoral    al    excitement    chroma    disabling    drug   

Project "EPIMAC" data sheet

The following table provides information about the project.

Coordinator
AMC MEDICAL RESEARCH BV 

Organization address
address: MEIBERGDREEF 9
city: AMSTERDAM ZUIDOOST
postcode: 1105AZ
website: n.a.

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Netherlands [NL]
 Project website http://www.epimac.eu/
 Total cost 1˙294˙785 €
 EC max contribution 1˙294˙785 € (100%)
 Programme 1. H2020-EU.1.3.1. (Fostering new skills by means of excellent initial training of researchers)
 Code Call H2020-MSCA-ITN-2014
 Funding Scheme MSCA-ITN-EID
 Starting year 2015
 Duration (year-month-day) from 2015-01-01   to  2019-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    AMC MEDICAL RESEARCH BV NL (AMSTERDAM ZUIDOOST) coordinator 1˙021˙497.00
2    GLAXOSMITHKLINE RESEARCH AND DEVELOPMENT LTD. UK (BRENTFORD) participant 273˙287.00
3    ACADEMISCH MEDISCH CENTRUM BIJ DE UNIVERSITEIT VAN AMSTERDAM NL (AMSTERDAM) participant 0.00
4    Eureka NL (Mechelen) partner 0.00
5    UNIVERSITAIR MEDISCH CENTRUM UTRECHT NL (UTRECHT) partner 0.00

Map

 Project objective

Epigenetic mechanisms allow cells to adjust gene expression in response to environmental cues. Increased understanding of this area has led to excitement about the potential of applying epigenetic regulation to drug discovery. EPIMAC aims to pursue the potential of epigenetics as a novel and innovative therapeutic modality for immuno-inflammatory diseases, in particular Inflammatory Bowel Disease (IBD). IBD is a severe and disabling chronic inflammation of the gastrointestinal tract affecting millions of people worldwide. Current treatment strategies are not successful because the precise etiology unclear. It is increasingly clear that deregulated epigenetic processes are associated with the aberrant inflammatory response seen in IBD. Recent reports suggest that inhibitors of epigenetic modifications developed by GlaxoSmithKline (GSK), such as histone deacetylase (HDAC) inhibitors, bear potential in treating inflammatory states (Nicodeme et al, Nature 2010; Kruidenier et al, Nature 2012). The EPIMAC consortium has the ambition to educate a group of next-generation scientists that master genetics, epigenetics, target discovery, pharmacology, preclinical validation and regulatory issues, and at the same time have a good understanding of clinical implementations of the drug pipeline of our pharmaceutical partner GSK. GSK is one of the world's leading research-based pharmaceutical and healthcare companies that aims to team up with academic partners in EPIMAC through its dedicated discovery performance unit named EpiNova in conjunction with 2 immuno-pharmacology units. An SME specializing in epigenetic compound targeting to inflammatory cells, Chroma Therapeutics, will contribute technology to EPIMAC. EPIMAC will educate and train these scientists by providing them with a versatile and multidisciplinary doctoral program, allowing them to become excellent scientists skilled to overcome the current challenges in IBD.

 Deliverables

List of deliverables.
Management, administration and finance 5d Documents, reports 2020-01-14 14:21:31
Research dissemination Other 2020-01-14 14:21:31
Management, administration and finance 5c Documents, reports 2019-07-10 15:36:56

Take a look to the deliverables list in detail:  detailed list of EPIMAC deliverables.

 Publications

year authors and title journal last update
List of publications.
2018 Andrew Y. F. Li Yim, Jessica R. de Bruyn, Nicolette W. Duijvis, Catriona Sharp, Enrico Ferrero, Wouter J. de Jonge, Manon E. Wildenberg, Marcel M. A. M. Mannens, Christianne J. Buskens, Geert R. D’Haens, Peter Henneman, Anje A. te Velde
A distinct epigenetic profile distinguishes stenotic from non-inflamed fibroblasts in the ileal mucosa of Crohn’s disease patients
published pages: e0209656, ISSN: 1932-6203, DOI: 10.1371/journal.pone.0209656
PLOS ONE 13/12 2019-07-10
2018 Annette E. Neele, Marion J.J. Gijbels, Saskia van der Velden, Marten A. Hoeksema, Marieke C.S. Boshuizen, Koen H.M. Prange, Hung-Jen Chen, Jan Van den Bossche, Cindy P.P.A. van Roomen, Annelie Shami, Johannes H.M. Levels, Jeffrey Kroon, Tina Lucas, Stefanie Dimmeler, Esther Lutgens, Menno P.J. de Winther
Myeloid Kdm6b deficiency results in advanced atherosclerosis
published pages: 156-165, ISSN: 0021-9150, DOI: 10.1016/j.atherosclerosis.2018.05.052
Atherosclerosis 275 2019-07-10
2016 Jan Van den Bossche, Jeroen Baardman, Natasja A. Otto, Saskia van der Velden, Annette E. Neele, Susan M. van den Berg, Rosario Luque-Martin, Hung-Jen Chen, Marieke C.S. Boshuizen, Mohamed Ahmed, Marten A. Hoeksema, Alex F. de Vos, Menno P.J. de Winther
Mitochondrial Dysfunction Prevents Repolarization of Inflammatory Macrophages
published pages: 684-696, ISSN: 2211-1247, DOI: 10.1016/j.celrep.2016.09.008
Cell Reports 17/3 2019-07-10
2016 Andrew Y. F. Li Yim, Nicolette W. Duijvis, Jing Zhao, Wouter J. de Jonge, Geert R. A. M. D’Haens, Marcel M. A. M. Mannens, Adri N. P. M. Mul, Anje A. te Velde, Peter Henneman
Peripheral blood methylation profiling of female Crohn’s disease patients
published pages: , ISSN: 1868-7075, DOI: 10.1186/s13148-016-0230-5
Clinical Epigenetics 8/1 2019-07-10
2017 Vincent A. van der Mark, Mohammed Ghiboub, Casper Marsman, Jing Zhao, Remco van Dijk, Johan K. Hiralall, Kam S. Ho-Mok, Zoë Castricum, Wouter J. de Jonge, Ronald P. J. Oude Elferink, Coen C. Paulusma
Phospholipid flippases attenuate LPS-induced TLR4 signaling by mediating endocytic retrieval of Toll-like receptor 4
published pages: 715-730, ISSN: 1420-682X, DOI: 10.1007/s00018-016-2360-5
Cellular and Molecular Life Sciences 74/4 2019-07-10

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