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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Simona Brillante

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EMBO Molecular Medicine|October 4, 2022

miR-181a/b downregulation: a mutation-independent therapeutic approach for inherited retinal diseasesSabrina Carrella, Martina Di Guida, Simona Brillante, et al.

American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 30, 2022

Biallelic variants in CENPF causing a phenotype distinct from Strømme syndromeGerarda Cappuccio, Simona Brillante, Roberta Tammaro, et al.

Cell Reports|November 9, 2022

Targeting the MITF/APAF-1 axis as salvage therapy for MAPK inhibitors in resistant melanomaPietro Carotenuto, Alessia Romano, Anna Barbato, et al.

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Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 13 results.

EMBO Molecular Medicine|October 4, 2022

miR-181a/b downregulation: a mutation-independent therapeutic approach for inherited retinal diseasesSabrina Carrella, Martina Di Guida, Simona Brillante, et al.

American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 30, 2022

Biallelic variants in CENPF causing a phenotype distinct from Strømme syndromeGerarda Cappuccio, Simona Brillante, Roberta Tammaro, et al.

Cell Reports|November 9, 2022

Targeting the MITF/APAF-1 axis as salvage therapy for MAPK inhibitors in resistant melanomaPietro Carotenuto, Alessia Romano, Anna Barbato, et al.

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