Maria Teresa Bassi
- Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis
2013/12/12 by Andrea Citterio, Alessia Arnoldi, Elena Panzeri +11 · 3 citations
Neuroscience · Biochemistry, Genetics and Molecular Biology · #Hereditary Neurological Disorders #Neurological diseases and metabolism #Endoplasmic Reticulum Stress and Disease
- Identification and characterisation of human xCT that co-expresses, with 4F2 heavy chain, the amino acid transport activity system x c -
2001/05/18 by Maria Bassi, Maria Teresa Bassi, Emma Gasol +10 · 2 citations
Biochemistry, Genetics and Molecular Biology · Neuroscience · #Amino Acid Enzymes and Metabolism #Epigenetics and DNA Methylation #Neuroscience and Neuropharmacology Research