F. Mottadelli

发表

IKZF1 status as a prognostic feature in BCR-ABL1-positive childhood ALL.

M. D. Den Boer, R. Pieters, M. Schrappe, 2014, Blood.

High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis

G. Scarano, O. Zuffardi, A. Selicorni, 2010, European Journal of Human Genetics.

Heterogeneity of the bone marrow niche in patients with myeloproliferative neoplasms: ActivinA secretion by mesenchymal stromal cells correlates with the degree of marrow fibrosis

M. Serafini, M. Riminucci, A. Biondi, 2020, Annals of Hematology.

Good Outcome for Very High Risk Adult B-cell Acute Lymphoblastic Leukaemia Carrying Genetic Abnormalities t(4;11)(q21;q23) or t(9;22)(q34;q11), if Promptly Submitted to Allogeneic Transplantation, after Obtaining a Good Molecular Remission

M. Fumagalli, G. Cazzaniga, P. Pioltelli, 2015, Mediterranean journal of hematology and infectious diseases.

ALL positive childhood - BCR-ABL1 status as a prognostic feature in IKZF1

R. Pieters, M. L. Boer, H. Cavé, 2014 .

LYMPHOID NEOPLASIA IKZF 1 status as a prognostic feature in BCR-ABL 1 – positive childhood ALL

R. Pieters, M. L. Boer, M. Schrappe, 2014 .

Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients

G. Neri, A. Bentivegna, A. Selicorni, 2006, BMC Medical Genetics.

Differential cytogenomics and miRNA signature of the Acute Myeloid Leukaemia Kasumi-1 cell line CD34+38- compartment.

M. Ferracin, M. Negrini, P. Pelicci, 2010, Leukemia research.

High frequency of mosaic CREBBP deletions in Rubinstein-Taybi syndrome patients and mapping of somatic and germ-line breakpoints.

R. Tenconi, E. Lucci-Cordisco, G. Neri, 2007, Genomics.

Histone acetylation deficits in lymphoblastoid cell lines from patients with Rubinstein–Taybi syndrome

G. Scarano, A. Barco, A. Selicorni, 2011, Journal of Medical Genetics.