Ursula Giussani
Bergamo, 24127, Italy
Last Updated: 09/26/2026
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Found 10 publications
Immature Immunoglobulin Gene Rearrangements Are Recurrent in B Precursor Adult Acute Lymphoblastic Leukemia Carrying TP53 Molecular Alterations.
Journal: Genes
Published: July 22, 2020
Double homozygosity in CEP57 and DYNC2H1 genes detected by WES: Composite or expanded phenotype?
Journal: Molecular genetics & genomic medicine
Published: July 12, 2019
Insertional translocation involving an additional nonchromothriptic chromosome in constitutional chromothripsis: Rule or exception?
Journal: Molecular genetics & genomic medicine
Published: July 24, 2018
Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia.
Journal: Oncoscience
Published: July 06, 2014
Frequent occurrence of non-malignant genetic alterations in clinical grade mesenchymal stromal cells expanded for cell therapy protocols.
Journal: Haematologica
Published: April 01, 2014
Highly aggressive T-cell acute lymphoblastic leukemia with t(8;14)(q24;q11): extensive genetic characterization and achievement of early molecular remission and long-term survival in an adult patient.
Journal: Blood cancer journal
Published: January 21, 2014
Mutations in MAP3K1 tilt the balance from SOX9/FGF9 to WNT/β-catenin signaling.
Journal: Human molecular genetics
Published: October 19, 2013
The Polo-Like Kinase 1 (PLK1) inhibitor NMS-P937 is effective in a new model of disseminated primary CD56+ acute monoblastic leukaemia.
Journal: PloS one
Published: October 19, 2012
A novel, highly sensitive and rapid allele-specific loop-mediated amplification assay for the detection of the JAK2V617F mutation in chronic myeloproliferative neoplasms.
Journal: Haematologica
Published: February 09, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026