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Whole genome sequencing reveals a frameshift mutation and a large deletion in YY1AP1 in a girl with a panvascular artery disease.
Raggio V, Dell'Oca N, Simoes C, Tapié A, Medici C, Costa G, Rodriguez S, Greif G, Garrone E, Rovella ML, Gonzalez V, Halty M, González G, Shin JY, Shin SY, Kim C, Seo JS, Graña M, Naya H, Spangenberg L. Raggio V, et al. Among authors: spangenberg l. Hum Genomics. 2021 May 10;15(1):28. doi: 10.1186/s40246-021-00328-1. Hum Genomics. 2021. PMID: 33971976 Free PMC article.
Latitudinal patterns in rodent metabolic flexibility.
Naya DE, Spangenberg L, Naya H, Bozinovic F. Naya DE, et al. Among authors: spangenberg l. Am Nat. 2012 Jun;179(6):E172-9. doi: 10.1086/665646. Epub 2012 Apr 27. Am Nat. 2012. PMID: 22617269
Polysome profiling shows extensive posttranscriptional regulation during human adipocyte stem cell differentiation into adipocytes.
Spangenberg L, Shigunov P, Abud AP, Cofré AR, Stimamiglio MA, Kuligovski C, Zych J, Schittini AV, Costa AD, Rebelatto CK, Brofman PR, Goldenberg S, Correa A, Naya H, Dallagiovanna B. Spangenberg L, et al. Stem Cell Res. 2013 Sep;11(2):902-12. doi: 10.1016/j.scr.2013.06.002. Epub 2013 Jun 10. Stem Cell Res. 2013. PMID: 23845413 Free article.
3697G>A in MT-ND1 is a causative mutation in mitochondrial disease.
Spangenberg L, Graña M, Greif G, Suarez-Rivero JM, Krysztal K, Tapié A, Boidi M, Fraga V, Lemes A, Gueçaimburú R, Cerisola A, Sánchez-Alcázar JA, Robello C, Raggio V, Naya H. Spangenberg L, et al. Mitochondrion. 2016 May;28:54-9. doi: 10.1016/j.mito.2016.03.006. Epub 2016 Mar 24. Mitochondrion. 2016. PMID: 27017994
104 results