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Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder.
Nemirovsky SI, Córdoba M, Zaiat JJ, Completa SP, Vega PA, González-Morón D, Medina NM, Fabbro M, Romero S, Brun B, Revale S, Ogara MF, Pecci A, Marti M, Vazquez M, Turjanski A, Kauffman MA. Nemirovsky SI, et al. PLoS One. 2015 Feb 3;10(2):e0116358. doi: 10.1371/journal.pone.0116358. eCollection 2015. PLoS One. 2015. PMID: 25646853 Free PMC article.
A novel mutation in PSEN1 (p.Arg41Ser) in an Argentinian woman with early onset Parkinsonism.
Gatto EM, Rojas GJ, Nemirovsky SI, Da Prat G, Persi G, Cesarini M, Etcheverry JL, Rojas NG, Parisi V, Cordoba M, Sevlever G, Allegri RF, Turjanski AG. Gatto EM, et al. Among authors: nemirovsky si. Parkinsonism Relat Disord. 2020 Aug;77:21-25. doi: 10.1016/j.parkreldis.2020.06.005. Epub 2020 Jun 17. Parkinsonism Relat Disord. 2020. PMID: 32590294
Heme Oxygenase 1 Impairs Glucocorticoid Receptor Activity in Prostate Cancer.
Leonardi DB, Anselmino N, Brandani JN, Jaworski FM, Páez AV, Mazaira G, Meiss RP, Nuñez M, Nemirovsky SI, Giudice J, Galigniana M, Pecci A, Gueron G, Vazquez E, Cotignola J. Leonardi DB, et al. Among authors: nemirovsky si. Int J Mol Sci. 2019 Feb 26;20(5):1006. doi: 10.3390/ijms20051006. Int J Mol Sci. 2019. PMID: 30813528 Free PMC article.
17 results