Gene editing and the patients perspective. The Patients Network for Medical Research and Health EGAN is an alliance of both National Genetic Alliances and European disease specific patient organisations with a special interest in genetics, genomics and biotechnology. Especially, but not only, genetic disorders are represented within EGAN. EGANeu is our corporate website. In addition, we host www.

G2C is an international collaborative program initiated by Professor Seth Grant. And supported by the Wellcome Trust following the discovery that multiprotein complexes formed by intracellular proteins and neurotransmitter receptors were important for neuronal plasticity and behaviour. G2C collaborators include scientists with compleme.

Genetic Engineering and Model Validation. French partners and academic networks. New data in rare disease model. The study showed the epigenetic consequences of EHMT1 haploinsufficiency in Kleefstra syndrome. Published in on 9 March 2018. PHENOMIN augments its Learning and Memory panel with the Active Avoidance test. PHENOMIN now offers a mouse model of hypoxia-induced pulmonary hypertension. Now available at PHENOMIN-ICS! To comp.

Welcome to the Intellectual Disability Cell Bank. Lymphoblast, fibroblast intellectual disability cell bank. The clinical data concerning the patients are collected in a continuously updated cell bank database. The cell bank is supported by experts for clinical information revision. CellBank Design By Roham Tayyebifar.

To generate any kind of chromosomal rearrangement to generate mice and rat trisomy 21. Read the recent publication in Scientific Report.