Clara Marco-Marin (Clara Marco-Marín)

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 4

Top Topics

Recombinant Human

Tyrosine Kinase

Top Venues

Journal of inherited metabolic disease

International journal of molecular sciences

The FEBS journal

Annals of clinical and translational neurology

This page only lists publications with an associated author ORCID identifier.

Publications

Nadine Gougeard, Enea Sancho-Vaello, María Leonor Fernández-Murga, Borja Martínez-Sinisterra, Badr Loukili-Hassani, Johannes Häberle, Clara Marco-Marin, Vicente Rubio
Use of pure recombinant human enzymes to assess the disease-causing potential of missense mutations in urea cycle disorders, applied to N-acetylglutamate synthase deficiency. Journal of inherited metabolic disease (2024)
Dolores Martínez-Rubio, Isabel Hinarejos, Herminia Argente-Escrig, Clara Marco-Marin, María Ana Lozano, Nerea Gorría-Redondo, Vincenzo Lupo, Itxaso Martí-Carrera, Concepción Miranda, María Vázquez-López, Asunción García-Pérez, Ana Victoria Marco Hernández, Miguel Tomás-Vila, Sergio Aguilera-Albesa, Carmen Espinós
Genetic Heterogeneity Underlying Phenotypes with Early-Onset Cerebellar Atrophy. International journal of molecular sciences 24 (22) (2023)
Vicente Rubio, Clara Marco-Marin, José Luis Llácer
Nitrogen storage regulation by PII protein: lessons learned from taxonomic outliers. The FEBS journal 287 (3) (2020)
Pamela Magini, Clara Marco-Marin, Juan M Escamilla-Honrubia, Diego Martinelli, Carlo Dionisi-Vici, Francesca Faravelli, Francesca Forzano, Marco Seri, Vicente Rubio, Emanuele Panza
P5CS expression study in a new family with ALDH18A1-associated hereditary spastic paraplegia SPG9. Annals of clinical and translational neurology 6 (8) (2019)