Soledad Alcántara

Molecular characterization of Spanish patients with MECP2 duplication syndrome

M. Roselló, C. Orellana, M. Tejada, 2020, Clinical genetics.

p38 a function in osteoblasts in fl uences adipose tissue homeostasis

Beatriz Gámez, F. Ventura, R. Bartrons, 2020 .

Unraveling Molecular Pathways Altered in MeCP2-Related Syndromes, in the Search for New Potential Avenues for Therapy

J. Armstrong, Soledad Alcántara, E. Cortès-Saladelafont, 2021, Biomedicines.

Discovery of Biomarker Panels for Neural Dysfunction in Inborn Errors of Amino Acid Metabolism

J. Armstrong, A. Ormazabal, R. Artuch, 2019, Scientific Reports.

The HERC2 ubiquitin ligase is essential for embryonic development and regulates motor coordination

J. Guénet, M. Cubillos-Rojas, J. L. Rosa, 2016, Oncotarget.

Comprehensive Analysis of GABAA-A1R Developmental Alterations in Rett Syndrome: Setting the Focus for Therapeutic Targets in the Time Frame of the Disease

J. Armstrong, M. Pineda, Cristina Grau, 2020, International journal of molecular sciences.

Enquiring beneath the surface: can a gene expression assay shed light into the heterogeneity among newborns with neonatal encephalopathy?

C. Tebé, A. García-Alix, Soledad Alcántara, 2020, Pediatric Research.

Discovery of Biomarker Panels for Neural Dysfunction in Inborn Errors of Amino Acid Metabolism

J. Armstrong, A. Ormazabal, R. Artuch, 2019, Scientific Reports.