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Eduardo Fidel Tizzano

Institutions of which they are part

Head of group
Genetics Medicine
Vall Hebron Institut de Recerca

Eduardo Fidel Tizzano

Institutions of which they are part

Head of group
Genetics Medicine
Vall Hebron Institut de Recerca

Projects

Estudio de los genes que codifican las proteínas que inhiben la inclusión del exón 7 del SMN2 en pacientes con Atrofia Muscular Espinal.

IP: Eduardo Fidel Tizzano
Collaborators: -
Funding agency: asociación GaliciAME
Funding: 12000
Reference: GALICIAME/TIZZANO/2023
Duration: 22/01/2024 - 22/07/2024

Pendent

IP: Eduardo Fidel Tizzano
Collaborators: Núria Martínez Gil, Miriam Izquierdo Sans, Laia Perez Lasarte
Funding agency: Ministerio de Ciencia e Innovación-MICINN
Funding: 64800
Reference: FJC2021-046715-I
Duration: 01/01/2023 - 31/12/2024

Ministerio de Ciencia

Ayudas Margarita Salas

IP: Eduardo Fidel Tizzano
Collaborators: Núria Martínez Gil, Miriam Izquierdo Sans
Funding agency: Ministerio de Universidades
Funding: 0.01
Reference: MIU/M_SALAS/2021/MARTÍNEZ_UB
Duration: 01/04/2022 - 31/03/2022

SMA beyond motoneuron degeneration: multi-system aspects - SMABEYOND

IP: Eduardo Fidel Tizzano
Collaborators: Georg Lindner
Funding agency: EUROPEAN COMMISSION
Funding: 250904.88
Reference: SMABEYOND_MSCA-ITN_H2020-2019
Duration: 01/10/2020 - 30/09/2024

Related news

The results show that, in some patients with mutations in the X chromosome, the healthy gene is inactivated and the mutated gene manifests itself, which favors the onset of the disease.

On January 24, a session was held to explain what these three-dimensional models are and what advantages they have, as well as to review some of their applications in research.

The research has studied the structure and function of proteins related to this degenerative disease and their interaction with SMN2 messenger RNA (mRNA), which is key to the evolution of patients.

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