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Cited by in F6Publishing
For: Ellwood RA, Piasecki M, Szewczyk NJ. Caenorhabditis elegans as a Model System for Duchenne Muscular Dystrophy. Int J Mol Sci 2021;22:4891. [PMID: 34063069 DOI: 10.3390/ijms22094891] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Ellwood RA, Slade L, Lewis J, Torregrossa R, Sudevan S, Piasecki M, Whiteman M, Etheridge T, Szewczyk NJ. Sulfur amino acid supplementation displays therapeutic potential in a C. elegans model of Duchenne muscular dystrophy. Commun Biol 2022;5:1255. [DOI: 10.1038/s42003-022-04212-z] [Reference Citation Analysis]
2 Wu X, Nagasawa S, Muto K, Ueda M, Suzuki C, Abe T, Higashitani A. Mitochonic Acid 5 Improves Duchenne Muscular Dystrophy and Parkinson’s Disease Model of Caenorhabditis elegans. IJMS 2022;23:9572. [DOI: 10.3390/ijms23179572] [Reference Citation Analysis]
3 Schorr AL, Mejia AF, Miranda MY, Mangone M. An updated C. elegans body muscle transcriptome for studies in muscle formation and function.. [DOI: 10.1101/2022.04.12.488068] [Reference Citation Analysis]
4 Wang L, Qiu Z, Lee M. Mutations in the cell-binding motif of lam-3/laminin α reveal hypercontraction behavior and defective sensitivity to levamisole in Caenorhabditis elegans. MicroPubl Biol 2021;2021. [PMID: 34723150 DOI: 10.17912/micropub.biology.000485] [Reference Citation Analysis]