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Clinical Genetics Lab
Colorectal Cancer Predisposition Lab
DNA MisMatch Repair Lab
Rare TumorS Lab
Global Projects
Global Projects
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Underpining the effects of defective miRNA biogenesis in the formation of thyroid tumors
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DNA MisMatch Repair Lab
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SpadaHC: Spanish DataBase for Hereditary Cancer
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Clinical Genetics Lab
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Role of immune system inborn errors as determinants of the COVID-19 severity in hospitalized patients
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Hereditary Cancer Research Group - AGAUR
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NF1 nonsense suppression by targeted pseudouridylation
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Clarifying the phenotypic spectrum associated with RAD51 partners and the proteomic interplay of RAD51 paralogs.
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Rare TumorS Lab
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MedPerCan: Personalised Medicine in Cancer - Catalonia: A pilot study on the impact of genomic testing in the decision-making process in Oncology
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INGENIO: Integrative genomic, digital imaging and clinical information towards precision oncology optimization
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IMPaCT Genómica: Implementation of Precision Medicine in the Spanish National Health System.
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CRISPR/Cas9-edited organoids for the functional evaluation of gene variants in colorectal cancer
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ProofREAD4MED: Polymerase proofreading-deficient tumors: genetics and immune biology insights for improved predictive medicine
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Comprehensive research in colorectal cancer and polyposis predisposition: searching for genetic and epigenetic causes of the disease
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MicroRNAs in sporadic and familial colorectal cancer
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SOLVE-RD: Solving the unsolved rare diseases
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Colorectal Cancer Predisposition Lab
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Research Teams
Clinical Genetics Lab
Colorectal Cancer Predisposition Lab
DNA MisMatch Repair Lab
Rare TumorS Lab
Global Projects
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To uncover the genetic causes of Gorlin-like patients without an identified molecular cause.
Nevoid basal cell carcinoma syndrome (NBCCS) is characterized by mutations in the gene PTCH1, a tumor suppressor with a central...
November 8, 2022
Elucidating the molecular mechanisms driven by FGFR1 mutants in Low Grade Gliomas
Dysembryoplastic neuroepithelial tumors (DNETs) are low grade brain tumors due to oncogenic alterations in the FGFR1 gene. We showed that...