Repositorio Dspace

Listar por autor "Vaiani, Elisa"

Listar por autor "Vaiani, Elisa"

Ordenar por:Orden:Resultados:

  • Generation of an iPSC line from congenital hypopituitarism patient with a nonsense heterozygous variant in FOXA2 
    Camilletti, María Andrea; Chirino Felker, Gonzalo Tomás; Castañeda, Sheila; Zabalegui, Federico; Amin, Guadalupe; Belgorosky, Alicia; Ciaccio, Marta; Di Palma, Maria Isabel; Vaiani, Elisa; Waisman, Ariel; Miriuka, Santiago Gabriel; Pérez Millán, María Inés; Moro, Lucia Natalia (Elsevier, 2025-07-15)
    Forkhead box A2 (FOXA2) is a pioneer transcription factor, necessary for human development. Mutations in FOXA2 were recently associated with congenital hypopituitarism (CH); however, the pathogenic mechanism remains unknown. ...