Stéphane Fourcade

5PUBLICATIONS
9CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Regenerative medicine (incl. stem cells)Molecular targetsEpigenetics (incl. genome methylation and epigenomics)Medical infection agents (incl. prions)
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Publications (5)

|Nov 27, 2020
A novel hypomorphic splice variant in EIF2B5 gene is associated with mild ovarioleukodystrophy.

Agustí Rodríguez-Palmero, Agatha Schlüter, Edgard Verdura

|Jun 09, 2020
High-dose biotin restores redox balance, energy and lipid homeostasis, and axonal health in a model of adrenoleukodystrophy.

Stéphane Fourcade, Leire Goicoechea, Janani Parameswaran

|Jul 13, 2018
Aberrant regulation of the GSK-3β/NRF2 axis unveils a novel therapy for adrenoleukodystrophy.

Pablo Ranea-Robles, Nathalie Launay, Montserrat Ruiz

|Feb 25, 2018
Epigenomic signature of adrenoleukodystrophy predicts compromised oligodendrocyte differentiation.

Agatha Schlüter, Juan Sandoval, Stéphane Fourcade

|Oct 14, 2017
Oxidative stress and mitochondrial dynamics malfunction are linked in Pelizaeus-Merzbacher disease.

Montserrat Ruiz, Mélina Bégou, Nathalie Launay

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Frequent Collaborators

3 joint publications

Aurora Pujol

2 joint publications

Pablo Ranea-Robles

1 joint publications

Isidre Ferrer

1 joint publications

Agustí Rodríguez-Palmero