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RUNX1 gene alterations characterized by allelic preference in adult acute myeloid leukemia.
Cumbo C, Tota G, De Grassi A, Anelli L, Zagaria A, Coccaro N, Tarantini F, Minervini CF, Parciante E, Impera L, Conserva MR, Redavid I, Mestice A, Attolico I, Pierri CL, Musto P, Albano F. Cumbo C, et al. Among authors: pierri cl. Leuk Lymphoma. 2023 Mar;64(3):717-721. doi: 10.1080/10428194.2021.1929960. Epub 2021 May 24. Leuk Lymphoma. 2023. PMID: 34027815 No abstract available.
AGC1/2, the mitochondrial aspartate-glutamate carriers.
Amoedo ND, Punzi G, Obre E, Lacombe D, De Grassi A, Pierri CL, Rossignol R. Amoedo ND, et al. Among authors: pierri cl. Biochim Biophys Acta. 2016 Oct;1863(10):2394-412. doi: 10.1016/j.bbamcr.2016.04.011. Epub 2016 Apr 28. Biochim Biophys Acta. 2016. PMID: 27132995 Free article. Review.
Heterozygous RNF13 Gain-of-Function Variants Are Associated with Congenital Microcephaly, Epileptic Encephalopathy, Blindness, and Failure to Thrive.
Edvardson S, Nicolae CM, Noh GJ, Burton JE, Punzi G, Shaag A, Bischetsrieder J, De Grassi A, Pierri CL, Elpeleg O, Moldovan GL. Edvardson S, et al. Among authors: pierri cl. Am J Hum Genet. 2019 Jan 3;104(1):179-185. doi: 10.1016/j.ajhg.2018.11.018. Epub 2018 Dec 27. Am J Hum Genet. 2019. PMID: 30595371 Free PMC article.
83 results