Francesco Chemello - Search Results

Year	Number of Results
2011	1
2013	1
2014	2
2015	2
2017	2
2018	1
2019	5
2020	5
2021	2
2022	3
2023	7
2024	0

1

Ablation of CaMKIIδ oxidation by CRISPR-Cas9 base editing as a therapy for cardiac disease.

Lebek S, Chemello F, Caravia XM, Tan W, Li H, Chen K, Xu L, Liu N, Bassel-Duby R, Olson EN. Lebek S, et al. Among authors: chemello f. Science. 2023 Jan 13;379(6628):179-185. doi: 10.1126/science.ade1105. Epub 2023 Jan 12. Science. 2023. PMID: 36634166 Free PMC article.

2

Base editing correction of hypertrophic cardiomyopathy in human cardiomyocytes and humanized mice.

Chai AC, Cui M, Chemello F, Li H, Chen K, Tan W, Atmanli A, McAnally JR, Zhang Y, Xu L, Liu N, Bassel-Duby R, Olson EN. Chai AC, et al. Among authors: chemello f. Nat Med. 2023 Feb;29(2):401-411. doi: 10.1038/s41591-022-02176-5. Epub 2023 Feb 16. Nat Med. 2023. PMID: 36797478 Free PMC article.

3

CRISPR-Editing Therapy for Duchenne Muscular Dystrophy.

Chemello F, Olson EN, Bassel-Duby R. Chemello F, et al. Hum Gene Ther. 2023 May;34(9-10):379-387. doi: 10.1089/hum.2023.053. Hum Gene Ther. 2023. PMID: 37060194 Review.

4

Elimination of CaMKIIδ Autophosphorylation by CRISPR-Cas9 Base Editing Improves Survival and Cardiac Function in Heart Failure in Mice.

Lebek S, Caravia XM, Chemello F, Tan W, McAnally JR, Chen K, Xu L, Liu N, Bassel-Duby R, Olson EN. Lebek S, et al. Among authors: chemello f. Circulation. 2023 Nov 7;148(19):1490-1504. doi: 10.1161/CIRCULATIONAHA.123.065117. Epub 2023 Sep 15. Circulation. 2023. PMID: 37712250 Free article.

5

Single-swap editing for the correction of common Duchenne muscular dystrophy mutations.

Chai AC, Chemello F, Li H, Nishiyama T, Chen K, Zhang Y, Sánchez-Ortiz E, Alomar A, Xu L, Liu N, Bassel-Duby R, Olson EN. Chai AC, et al. Among authors: chemello f. Mol Ther Nucleic Acids. 2023 Apr 19;32:522-535. doi: 10.1016/j.omtn.2023.04.009. eCollection 2023 Jun 13. Mol Ther Nucleic Acids. 2023. PMID: 37215149 Free PMC article.

6

Net39 protects muscle nuclei from mechanical stress during the pathogenesis of Emery-Dreifuss muscular dystrophy.

Zhang Y, Ramirez-Martinez A, Chen K, McAnally JR, Cai C, Durbacz MZ, Chemello F, Wang Z, Xu L, Bassel-Duby R, Liu N, Olson EN. Zhang Y, et al. Among authors: chemello f. J Clin Invest. 2023 Jul 3;133(13):e163333. doi: 10.1172/JCI163333. J Clin Invest. 2023. PMID: 37395273 Free PMC article.

7

Dysfunctional mitochondria accumulate in a skeletal muscle knockout model of Smn1, the causal gene of spinal muscular atrophy.

Chemello F, Pozzobon M, Tsansizi LI, Varanita T, Quintana-Cabrera R, Bonesso D, Piccoli M, Lanfranchi G, Giacomello M, Scorrano L, Bean C. Chemello F, et al. Cell Death Dis. 2023 Feb 27;14(2):162. doi: 10.1038/s41419-023-05573-x. Cell Death Dis. 2023. PMID: 36849544 Free PMC article.

8

Editorial: MicroRNAs and Muscle Cell Death in Cancer.

Peterson JM, Chemello F, Calore F. Peterson JM, et al. Among authors: chemello f. Front Genet. 2022 May 13;13:892136. doi: 10.3389/fgene.2022.892136. eCollection 2022. Front Genet. 2022. PMID: 35646081 Free PMC article. No abstract available.

9

Correction of muscular dystrophies by CRISPR gene editing.

Chemello F, Bassel-Duby R, Olson EN. Chemello F, et al. J Clin Invest. 2020 Jun 1;130(6):2766-2776. doi: 10.1172/JCI136873. J Clin Invest. 2020. PMID: 32478678 Free PMC article. Review.

10

A Single Cell but Many Different Transcripts: A Journey into the World of Long Non-Coding RNAs.

Alessio E, Bonadio RS, Buson L, Chemello F, Cagnin S. Alessio E, et al. Among authors: chemello f. Int J Mol Sci. 2020 Jan 1;21(1):302. doi: 10.3390/ijms21010302. Int J Mol Sci. 2020. PMID: 31906285 Free PMC article. Review.

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