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EUROFANCOLEN.EU

EuroFancolen Project

EuroFancoLen is a project to develop a multicentric gene therapy trial for Fanconi Anemia patients. Fanconi Anemia (FA) is a rare inherited syndrome characterized by the early development of bone marrow failure and increasing predisposition to cancer with age.

http://www.eurofancolen.eu/

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EuroFancolen Project | eurofancolen.eu Reviews
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EuroFancoLen is a project to develop a multicentric gene therapy trial for Fanconi Anemia patients. Fanconi Anemia (FA) is a rare inherited syndrome characterized by the early development of bone marrow failure and increasing predisposition to cancer with age.
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EuroFancolen Project | eurofancolen.eu Reviews

https://eurofancolen.eu

EuroFancoLen is a project to develop a multicentric gene therapy trial for Fanconi Anemia patients. Fanconi Anemia (FA) is a rare inherited syndrome characterized by the early development of bone marrow failure and increasing predisposition to cancer with age.

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Private Area

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EuroFancolen Project

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Elementos disponibles en su pedido. Phase I/II Gene therapy trial of Fanconi anemia patients with a new Orphan Drug consisting of a lentiviral vector carrying the FANCA gene: A Coordinated International Action. Is a rare inherited syndrome characterized by the early development of bone marrow failure and increasing predisposition to cancer with age. Follow us on Twitter.

3

EurFancolen Project Description

http://www.eurofancolen.eu/apps/displayFile/en/eurofancolen/public/pages/eurofancolen-project-description.cms_xhtml

Elementos disponibles en su pedido. The genetic correction of autologous hematopoietic stem cells (HSC) with lentiviral vectors constitutes a recent and safe alternative for the treatment of different genetic diseases affecting mature cells from different tissues and/or committed progenitors of the hematopoietic system. Our innovative approach to develop for the first time an efficient and safe gene therapy of FA is based on two recent innovations:. As the diagnostic studies progress, WP2. Will be initia...

4

News & Events

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Elementos disponibles en su pedido. Presentación de la Terapia Génica para la anemia de FANCONI en el Fred Hutchinson Centre. El Dr Juan Bueren presenta laTerapia Génica para la anemia de FANCONI en el Fred Hutchinson Centre. br/ https:/ twitter.com/SuNAlakira/status/777253614192427009 br/. The EUROFANCOLEN project appear in the newspaper El Mundo of Spain. Anemia de Fanconi: that's it the first Spanisch trial gene therapy. Congress of Gene Therapy. Third anual meeting of Eurofancolen Project.

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EuroFancolen Project Dissemination

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Elementos disponibles en su pedido. Associations and organizations links. Asociación Española de Anemia de Fanconi. UK Fanconi Anemia Clinical Network. Association Française de la Maladie de Fanconi. Fanconi Anemia Research Fund. Sheffield Children's NHS Foundation Trust.

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Elementos disponibles en su pedido. Phase I/II Gene therapy trial of Fanconi anemia patients with a new Orphan Drug consisting of a lentiviral vector carrying the FANCA gene: A Coordinated International Action. Is a rare inherited syndrome characterized by the early development of bone marrow failure and increasing predisposition to cancer with age. Follow us on Twitter.

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