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NRF2 connects Src tyrosine kinase to ferroptosis resistance in glioblastoma.
Cirotti C, Taddei I, Contadini C, Di Girolamo C, Pepe G, De Bardi M, Borsellino G, Helmer-Citterich M, Barilà D. Cirotti C, et al. Among authors: helmer citterich m. Life Sci Alliance. 2023 Oct 25;7(1):e202302205. doi: 10.26508/lsa.202302205. Print 2024 Jan. Life Sci Alliance. 2023. PMID: 37879937 Free PMC article.
WWP1 germline variants are associated with normocephalic autism spectrum disorder.
Novelli G, Novelli A, Borgiani P, Cocciadiferro D, Biancolella M, Agolini E, Pietrosanto M, Casalone R, Helmer-Citterich M, Giardina E, Jain SK, Wei W, Eng C, Pandolfi PP. Novelli G, et al. Cell Death Dis. 2020 Jul 23;11(7):529. doi: 10.1038/s41419-020-2681-z. Cell Death Dis. 2020. PMID: 32699206 Free PMC article. No abstract available.
Variants in MHY7 Gene Cause Arrhythmogenic Cardiomyopathy.
Ferradini V, Parca L, Martino A, Lanzillo C, Silvetti E, Calò L, Caselli S, Novelli G, Helmer-Citterich M, Sangiuolo FC, Mango R. Ferradini V, et al. Genes (Basel). 2021 May 22;12(6):793. doi: 10.3390/genes12060793. Genes (Basel). 2021. PMID: 34067482 Free PMC article.
Next Generation Sequencing and Linkage Analysis for the Molecular Diagnosis of a Novel Overlapping Syndrome Characterized by Hypertrophic Cardiomyopathy and Typical Electrical Instability of Brugada Syndrome.
Mango R, Luchetti A, Sangiuolo R, Ferradini V, Briglia N, Giardina E, Ferrè F, Helmer Citterich M, Romeo F, Novelli G, Sangiuolo F. Mango R, et al. Circ J. 2016;80(4):938-49. doi: 10.1253/circj.CJ-15-0685. Epub 2016 Mar 9. Circ J. 2016. PMID: 26960954 Free article.
Human lncRNAs harbor conserved modules embedded in different sequence contexts.
Ballesio F, Pepe G, Ausiello G, Novelletto A, Helmer-Citterich M, Gherardini PF. Ballesio F, et al. Among authors: helmer citterich m. Noncoding RNA Res. 2024 Jun 22;9(4):1257-1270. doi: 10.1016/j.ncrna.2024.06.013. eCollection 2024 Dec. Noncoding RNA Res. 2024. PMID: 39040814 Free PMC article.
135 results