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Rare Genetic Diseases: Nature's Experiments on Human Development.
Lee CE, Singleton KS, Wallin M, Faundez V. Lee CE, et al. Among authors: singleton ks. iScience. 2020 May 22;23(5):101123. doi: 10.1016/j.isci.2020.101123. Epub 2020 May 1. iScience. 2020. PMID: 32422592 Free PMC article. Review.
Systemic proteome phenotypes reveal defective metabolic flexibility in Mecp2 mutants.
Zlatic SA, Werner E, Surapaneni V, Lee CE, Gokhale A, Singleton K, Duong D, Crocker A, Gentile K, Middleton F, Dalloul JM, Liu WL, Patgiri A, Tarquinio D, Carpenter R, Faundez V. Zlatic SA, et al. Among authors: singleton k. Hum Mol Genet. 2023 Dec 12;33(1):12-32. doi: 10.1093/hmg/ddad154. Hum Mol Genet. 2023. PMID: 37712894
Systemic Proteome Phenotypes Reveal Defective Metabolic Flexibility in Mecp2 Mutants.
Zlatic SA, Werner E, Surapaneni V, Lee CE, Gokhale A, Singleton K, Duong D, Crocker A, Gentile K, Middleton F, Dalloul JM, Liu WL, Patgiri A, Tarquinio D, Carpenter R, Faundez V. Zlatic SA, et al. Among authors: singleton k. bioRxiv [Preprint]. 2023 Sep 1:2023.04.03.535431. doi: 10.1101/2023.04.03.535431. bioRxiv. 2023. PMID: 37066332 Free PMC article. Updated. Preprint.
12 results