M. Di Segni

发表

Human cardiac and bone marrow stromal cells exhibit distinctive properties related to their origin.

Qingbo Xu, M. Mayr, M. Capogrossi, 2011, Cardiovascular research.

Seizure and EEG Patterns in Angelman's Syndrome

G. Lanzi, F. Lalatta, A. Selicorni, 1995, Journal of child neurology.

Generation of an induced pluripotent stem cell line (EURACi014-A) from a Parkinson's disease patient with an A53T mutation in the SNCA gene by an integration-free reprogramming method.

P. Pramstaller, I. Pichler, Andrew A. Hicks, 2022, Stem cell research.

Human chorionic villus mesenchymal stromal cells reveal strong endothelial conversion properties.

M. Capogrossi, C. Gaetano, V. Meraviglia, 2012, Differentiation; research in biological diversity.

Generation and characterization of three human induced pluripotent stem cell lines (EURACi007-A, EURACi008-A, EURACi009-A) from three different individuals of the same family with arrhythmogenic cardiomyopathy (ACM) carrying the plakophillin2 p.N346Lfs*12 mutation.

P. Pramstaller, V. Meraviglia, B. Motta, 2021, Stem cell research.

Derivation of human induced pluripotent stem cell line EURACi004-A from skin fibroblasts of a patient with Arrhythmogenic Cardiomyopathy carrying the heterozygous PKP2 mutation c.2569_3018del50

P. Pramstaller, V. Meraviglia, A. Rossini, 2018, Stem cell research.

Generation of the Becker muscular dystrophy patient derived induced pluripotent stem cell line carrying the DMD splicing mutation c.1705-8 T>C.

A. Gowran, M. Belicchi, Y. Torrente, 2020, Stem cell research.

Generation of induced pluripotent stem cells from a Becker muscular dystrophy patient carrying a deletion of exons 45-55 of the dystrophin gene (CCMi002BMD-A-9 ∆45-55).

A. Gowran, Pietro Spinelli, P. Nigro, 2018, Stem cell research.

Establishment of a Duchenne muscular dystrophy patient-derived induced pluripotent stem cell line carrying a deletion of exons 51-53 of the dystrophin gene (CCMi003-A).

M. Di Segni, C. Gervasini, Stefania Paganini, 2019, Stem cell research.

Derivation of the Duchenne muscular dystrophy patient-derived induced pluripotent stem cell line lacking DMD exons 49 and 50 (CCMi001DMD-A-3, ∆49, ∆50).

A. Gowran, Pietro Spinelli, P. Nigro, 2017, Stem cell research.

Role of Water in Chromosome Spreading and Swelling Induced by Acetic Acid Treatment: A Ftir Spectroscopy Study

S. Doglia, Diletta Ami, M. Di Segni, 2014, European journal of histochemistry : EJH.

Generation of Induced Pluripotent Stem Cells from Frozen Buffy Coats using Non-integrating Episomal Plasmids.

A. Hicks, P. Pramstaller, A. Lavdas, 2015, Journal of visualized experiments : JoVE.

Increased RISK for 47,XXY on cell‐free DNA screen: Not always Klinefelter syndrome

P. Vizziello, F. Lalatta, M. Bedeschi, 2020, Prenatal diagnosis.

Generation and characterization of induced pluripotent stem cell (iPSC) lines of two asymptomatic individuals carrying a heterozygous exon 7 deletion in Parkin (PRKN) and two non-carriers from the same family.

P. Pramstaller, I. Pichler, Andrew A. Hicks, 2022, Stem cell research.

Early manifestations in a cohort of children prenatally diagnosed with 47,XYY. Role of multidisciplinary counseling for parental guidance and prevention of aggressive behavior

P. Vizziello, F. Lalatta, B. Gentilin, 2012, Italian Journal of Pediatrics.

Generation of human induced pluripotent stem cells (EURACi001-A, EURACi002-A, EURACi003-A) from peripheral blood mononuclear cells of three patients carrying mutations in the CAV3 gene.

P. Pramstaller, V. Meraviglia, B. Motta, 2018, Stem cell research.

Generation of human induced pluripotent stem cell line EURACi015-A from a patient affected by dilated cardiomyopathy carrying the Lamin A/C p.Glu161Lys mutation.

P. Pramstaller, A. Rossini, S. Zacchigna, 2023, Stem cell research.