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Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients.
Minelli A, Nacci L, Valli R, Pietrocola G, Ramenghi U, Locatelli F, Brescia L, Nicolis E, Cipolli M, Danesino C. Minelli A, et al. Among authors: cipolli m. Blood Cells Mol Dis. 2016 Sep;60:33-5. doi: 10.1016/j.bcmd.2016.06.007. Epub 2016 Jun 22. Blood Cells Mol Dis. 2016. PMID: 27519942 Free article. No abstract available.
Parental origin of the deletion del(20q) in Shwachman-Diamond patients and loss of the paternally derived allele of the imprinted L3MBTL1 gene.
Nacci L, Valli R, Maria Pinto R, Zecca M, Cipolli M, Morini J, Cesaro S, Boveri E, Rosti V, Corti P, Ambroni M, Pasquali F, Danesino C, Maserati E, Minelli A. Nacci L, et al. Among authors: cipolli m. Genes Chromosomes Cancer. 2017 Jan;56(1):51-58. doi: 10.1002/gcc.22401. Epub 2016 Sep 21. Genes Chromosomes Cancer. 2017. PMID: 27553422
Mesenchymal stromal cells from Shwachman-Diamond syndrome patients fail to recreate a bone marrow niche in vivo and exhibit impaired angiogenesis.
Bardelli D, Dander E, Bugarin C, Cappuzzello C, Pievani A, Fazio G, Pierani P, Corti P, Farruggia P, Dufour C, Cesaro S, Cipolli M, Biondi A, D'Amico G. Bardelli D, et al. Among authors: cipolli m. Br J Haematol. 2018 Jul;182(1):114-124. doi: 10.1111/bjh.15388. Epub 2018 May 16. Br J Haematol. 2018. PMID: 29767474 Free article.
99 results