Double dose against rare diseases

Reference: Abstract: Recently, two teams from CNRS have reported encouraging results in the fight against two rare diseases: “children of the moon” and Rett syndrome. PROJECT DETAILS  beginning: n.a end: n.a Country of research: France Counry of funding source: France Funding organization: National Center for Scientific Research Financing: NATIONAL FUNDINGS – 0 € hyperlink

Epigenetics, NEURITE AND PSYCHOSIS

Reference: ANRn.a.8-MNPSn.a.007 Abstract: Psychotic disorders (schizophrenia, bipolar disorder, pervasive developmental disorders) are disabling disorders of variable clinical expression ?, ?d resulting interaction between genetic and environmental factors during critical periods of brain development. Some candidate genes have been identified . Among them, neuregulin, RGS4, DISC1, reelin, BDNF and glutamatergic receptors are involved in the formation … Read more

Cell bank AP-HP Hopital Cochin: Biological Resource Center for the study of genetic diseases

Reference: ANRn.a.6-CEBSn.a.006 Abstract: GLOBAL PROJECT SUMMARY CRB – General Presentation of the project The cell bank AP-HP (Assistance Publique – Hopitaux de Paris) of the Cochin hospital located in the Department of Biochemistry and Molecular Genetics (Cassini Hall) was established in 1992 in partnership with AFM (French Association against Myopathies). Bank of AP-HP cells Cochin … Read more

Epigenetic Plasticity of the Genome

Reference: 503433 Abstract: In this ‘post-genomic’ era, advances in epigenetic research represent a new frontier that is predicted to yield novel insights for gene regulation, cell differentiation, stem cell plasticity, organismal development, human diseases, cancer, infertility and aging. A central emerging concept proposes that there is an ‘epigenetic code’, which considerably extends the information potential … Read more

Chromatin diseases: from basic mechanisms to therapy

Reference: 238242 Abstract: The scope of this ITN is to promote research and training in the field of chromatin diseases. Chromatin diseases (CD) are genetic pathologies resulting from mutations in structural components of chromatin or in enzymes that biochemically modify chromatin, altering chromatin status and thereby causing drastic effects on gene expression. CD frequency ranges … Read more

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