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Susana Boronat Guerero

Institutions of which they are part

Senior researcher
Genetics Medicine
Vall Hebron Institut de Recerca

Susana Boronat Guerero

Institutions of which they are part

Senior researcher
Genetics Medicine
Vall Hebron Institut de Recerca

Projects

Neurologia Pediàtrica (GRC)

IP: Alfons Macaya Ruíz
Collaborators: Susana Boronat Guerero, Francina Munell Casadesus, Maria Jose Pérez García, Anna Marcé Grau, Miquel Raspall Chaure, Mireia del Toro Riera, Marta Vila Pueyo
Funding agency: Agència Gestió Ajuts Universitaris i de Recerca
Funding:
Reference: 2014 SGR 1087
Duration: 01/01/2014 - 31/12/2016

Estudio multidimensional del espectro de los trastornos relacionados con la exposición prenatal al alcohol

IP: -
Collaborators: Núria Gómez Barros, Carlos Jacas Escarcellé, Susana Boronat Guerero, Anna Maria Cueto Gonzalez
Funding agency: Instituto de Salud Carlos III
Funding: 99220
Reference: PI12/02289
Duration: 01/01/2013 - 31/12/2015

Estada al Massachusetts General Hospital, Boston (EEUU)

IP: Susana Boronat Guerero
Collaborators: -
Funding agency: Instituto de Salud Carlos III
Funding: 52000
Reference: BA11/00086
Duration: 07/11/2011 - 06/07/2013

Genes y migraña: clonaje posicional en migraña familiar y expresión en la depresión cortical propagada experimental

IP: Alfons Macaya Ruíz
Collaborators: Patricia Pozo Rosich, Susana Boronat Guerero, Miquel Raspall Chaure, Marta Vila Pueyo
Funding agency: Ministerio de Ciencia e Innovación-MICINN
Funding: 90750.02
Reference: SAF2009-13182-C03-03
Duration: 01/01/2010 - 31/12/2012

Ministerio de Ciencia

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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