To encourage new collaborative projects, the MarMaRa Institute is launching a call for "incentive action" projects. The aim of this call is to support new innovative projects of excellence between the institute's laboratories (minimum two laboratories) OR between a MarMaRa team and an external team (at national, European or international level).
The research project must be innovative and not a continuation of an ongoing collaborative project. Preliminary data are not mandatory. Priority will be given to projects that draw on interdisciplinary skills and collaborative researchers.
Each project is eligible for a grant of up to €30,000 for a maximum duration of 12 months.
The call description and application forms can be downloaded and completed (see "Documents to download" on the right).
|
Project |
LAST name - First name |
Laboratories - teams |
|---|---|---|
| Investigation of gastrointestinal abnormalities, inflammation and peripheral catecholaminergic deficits in a mouse model of Rett Syndrome | ROUX Jean-Christophe | MMG - INP |
| Generation of a novel human in vitro system to monitor the real-time cell fate commitment of contractile and conductive CMs | D'AMATO Gaetano | MMG - IBDM |
| Identification of stage-specific cell surface markers to study disordered erythropoiesis in rare anaemias | DE GRANDIS Maria | ADES - CRCM |
|
Project |
LAST name - First name |
Laboratories - teams |
|---|---|---|
| "MarMaR' ITA" - Improve Technological Analysis Use of HCR-RNA flow technology to study gene regulatory process in the context of rare diseases | ARGIRO Laurent | MMG - TAGC |
| Identifying the cause of Atrial Septation anomalies in Holt-Oram Syndrome using the mouse model | DE BONO Christopher | MMG - IBDM |
| Epigenetic modifications of the 14q32 miRNA cluster in two types of laminopathies: lipodystrophies and progeroid syndromes | FRANKEL Diane / DESGROUAS Camille | MMG - TAGC |
| Development of a novel gene therapy targeting adipose leptin production to treat Rett syndrome | GAIARSA Jean-Luc | INMED - MMG |
|
Project title |
LAST name - First name |
Laboratories - Teams |
|---|---|---|
| Deciphering the origin of ventricular arrhythmias associated with the Holt-Oram-Syndrome | MIQUEROL Lucile | IBDM - C2VN |
| RNA-sequencing analysis of human neurons in Kcnq2 developmental and epileptic encephaloaphy | VILLARD Laurent | MMG - TAGC |
|
Project title |
LAST name - First name |
Laboratories - teams |
|---|---|---|
| Blocking fibro-adipogenic differentiation in muscle pathologies | HELMBACHER Françoise | IBDM - MMG |
| Probing telomeres and genomic instability in UFM1-defective encephalopathy | LACHAUD Christophe | CRCM - MMG |
|
Project title |
LAST name - First name |
Laboratories - teams |
|---|---|---|
| Extensive phenotypic characterization of mouse models of rare neurodevelopmental disorders | CAUBIT Xavier | IBDM - INMED |
| Creation of iPSC from fibroblasts of patients with monogenic KCC2-related autosomal recessive neurodevelopmental disorders | MEDYNA Igor | INMED - MMG |
| Electrical stimulation to enhance maturation of hiPSC-derived cardiomyocytes in an in vitro model of rare immuno-induced myocarditis | LALEVEE Nathalie | C2VN - MMG |
| Study of valve endothelial-interstitial interactions during microenvironmental changes | ZAFFRAN Stéphane | MMG - IRPHE |
Documents
With funding from the Institute, we have set up a strategy to generate cell models to assess whether genetic and telomere instabilities are present in patients with rare encephalopathies caused by UFMylation deficiency. Depending on future results, we may consider applying for national funding.
