Iskalni niz:
išči po
išči po
išči po
išči po
Vrsta gradiva:
Jezik:
Št. zadetkov: 3
Izvirni znanstveni članek
Oznake: CTNNB1 neurodevelopmental syndrome;β-catenin;genotype;phenotype;genotype-phenotype correlations;
CTNNB1 neurodevelopmental syndrome is a rare disorder caused by de novo heterozygous variants in the CTNNB1 gene encoding β-catenin. This study aims to characterize genetic variants in individuals with CTNNB1 neurodevelopmental syndrome, systematically assess the spectrum of clinical phenotypes usin ...
Leto: 2025 Vir: Digitalni repozitorij raziskovalnih organizacij Slovenije
Pregledni znanstveni članek
Oznake: gene therapy;rare genetic diseases;Slovenia;CAR-T cells;cancer;immune gene therapy;
Gene therapy has transitioned from a long-awaited promise to a clinical reality, offering transformative treatments for rare congenital diseases and certain cancers, which have a significant impact on patients’ lives. Current approaches focus on gene replacement therapy, either in vivo or ex vivo, m ...
Leto: 2025 Vir: Kemijski inštitut (KI)
Zbornik strokovnih ali nerecenziranih znanstvenih prispevkov na konferenci
Oznake: radioterapija;
Leto: 2024 Vir: Onkološki inštitut Ljubljana (OI)
Št. zadetkov: 3
Ključne besede:
Leto izdaje:
Avtorji:
Repozitorij:
Tipologija:
Jezik: