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Št. zadetkov: 2
Identifying the steps required to effectively implement next-generation sequencing in oncology at a national level in Europe
Denis Horgan, Denis Horgan, Giuseppe Curigliano, Olaf Rieß, Paul Hofman, Reinhard Büttner, Pierfranco Conte, Tanja Čufer, William Gallagher, Nadia Georges, Keith Kerr
Izvirni znanstveni članek
Oznake: clinical standardization;equitable reimbursement;European Alliance for Personalised Medicine;Europe’s Beating Cancer Plan;evidence generation;governance;molecularly guided treatment options;next-generation sequencing;stakeholder awareness and education;testing infrastructure;
Next-generation sequencing (NGS) may enable more focused and highly personalized cancer treatment, with the National Comprehensive Cancer Network and European Society for Medical Oncology guidelines now recommending NGS for daily clinical practice for several tumor types. However, NGS implementation ...
Leto: 2022 Vir: Medicinska fakulteta (UL MF)
UV-radiation and MC1R germline mutations are risk factors for the development of conventional and spitzoid melanomas in children and adolescents
Alexandra Liebmann, Jakob Admard, Sorin Armeanu-Ebinger, Hannah Wild, Michael Abele, Axel Gschwind, Olga Seibel-Kelemen, Christian Seitz, Irina Bonzheim, Olaf Rieß, Maja Česen
Izvirni znanstveni članek
Oznake: paediatric melanoma;exome sequencing;tumour-normal sequencing;rare paediatric tumours;
Background: Genomic characterisation has led to an improved understanding of adult melanoma. However, the aetiology of melanoma in children is still unclear and identifying the correct diagnosis and therapeutic strategies remains challenging. Methods: Exome sequencing of matched tumour-normal pairs ...
Leto: 2023 Vir: Digitalni repozitorij raziskovalnih organizacij Slovenije
Št. zadetkov: 2
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