Di Resta C - Search Results

1

Transcriptional role of androgen receptor in the expression of long non-coding RNA Sox2OT in neurogenesis.

Tosetti V, Sassone J, Ferri ALM, Taiana M, Bedini G, Nava S, Brenna G, Di Resta C, Pareyson D, Di Giulio AM, Carelli S, Parati EA, Gorio A. Tosetti V, et al. Among authors: di giulio am, di resta c. PLoS One. 2017 Jul 12;12(7):e0180579. doi: 10.1371/journal.pone.0180579. eCollection 2017. PLoS One. 2017. PMID: 28704421 Free PMC article.

2

SETBP1 accumulation induces P53 inhibition and genotoxic stress in neural progenitors underlying neurodegeneration in Schinzel-Giedion syndrome.

Banfi F, Rubio A, Zaghi M, Massimino L, Fagnocchi G, Bellini E, Luoni M, Cancellieri C, Bagliani A, Di Resta C, Maffezzini C, Ianielli A, Ferrari M, Piazza R, Mologni L, Broccoli V, Sessa A. Banfi F, et al. Among authors: di resta c. Nat Commun. 2021 Jun 30;12(1):4050. doi: 10.1038/s41467-021-24391-3. Nat Commun. 2021. PMID: 34193871 Free PMC article.

3

Next-generation sequencing approach for the diagnosis of human diseases: open challenges and new opportunities.

Di Resta C, Galbiati S, Carrera P, Ferrari M. Di Resta C, et al. EJIFCC. 2018 Apr 30;29(1):4-14. eCollection 2018 Apr. EJIFCC. 2018. PMID: 29765282 Free PMC article.

4

Genetic testing in neurology exploiting next generation sequencing: state of art.

Di Resta C, Ferrari M. Di Resta C, et al. Neural Regen Res. 2020 Feb;15(2):265-266. doi: 10.4103/1673-5374.265554. Neural Regen Res. 2020. PMID: 31552897 Free PMC article. No abstract available.

5

High-throughput genetic characterization of a cohort of Brugada syndrome patients.

Di Resta C, Pietrelli A, Sala S, Della Bella P, De Bellis G, Ferrari M, Bordoni R, Benedetti S. Di Resta C, et al. Hum Mol Genet. 2015 Oct 15;24(20):5828-35. doi: 10.1093/hmg/ddv302. Epub 2015 Jul 28. Hum Mol Genet. 2015. PMID: 26220970

6

Next Generation Sequencing: From Research Area to Clinical Practice.

Di Resta C, Ferrari M. Di Resta C, et al. EJIFCC. 2018 Nov 7;29(3):215-220. eCollection 2018 Nov. EJIFCC. 2018. PMID: 30479607 Free PMC article.

7

New molecular approaches to Alzheimer's disease.

Di Resta C, Ferrari M. Di Resta C, et al. Clin Biochem. 2019 Oct;72:81-86. doi: 10.1016/j.clinbiochem.2019.04.010. Epub 2019 Apr 21. Clin Biochem. 2019. PMID: 31018113 Review.

8

A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia.

Rossi D, Gigli L, Gamberucci A, Bordoni R, Pietrelli A, Lorenzini S, Pierantozzi E, Peretto G, De Bellis G, Della Bella P, Ferrari M, Sorrentino V, Benedetti S, Sala S, Di Resta C. Rossi D, et al. Among authors: di resta c. Heart Rhythm. 2020 Feb;17(2):296-304. doi: 10.1016/j.hrthm.2019.08.018. Epub 2019 Aug 19. Heart Rhythm. 2020. PMID: 31437535

9

Impaired turnover of hyperfused mitochondria in severe axonal neuropathy due to a novel DRP1 mutation.

Longo F, Benedetti S, Zambon AA, Sora MGN, Di Resta C, De Ritis D, Quattrini A, Maltecca F, Ferrari M, Previtali SC. Longo F, et al. Among authors: di resta c. Hum Mol Genet. 2020 Jan 15;29(2):177-188. doi: 10.1093/hmg/ddz211. Hum Mol Genet. 2020. PMID: 31868880

10

Current scenario of the genetic testing for rare neurological disorders exploiting next generation sequencing.

Di Resta C, Pipitone GB, Carrera P, Ferrari M. Di Resta C, et al. Neural Regen Res. 2021 Mar;16(3):475-481. doi: 10.4103/1673-5374.293135. Neural Regen Res. 2021. PMID: 32985468 Free PMC article. Review.

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