C. Matteucci

发表

Rescue of genomic information in adult acute lymphoblastic leukaemia (ALL) with normal/failed cytogenetics: a GIMEMA centralized biological study

R. Foà, A. Vitale, M. Vignetti, 2010, British journal of haematology.

Chromosome Abnormalities in HCV-Related Lymphoproliferation

C. Mecucci, C. Matteucci, G. Barba, 2012 .

Different genomic imbalances in low- and high-grade HCV-related lymphomas

C. Mecucci, M. Martelli, R. L. Starza, 2008, Leukemia.

Rearrangement between the MYH11 gene at 16p13 and D12S158 at 12p13 in a case of acute myeloid leukemia M1 (AML‐M1)

P. Marynen, C. Mecucci, M. Martelli, 1998, Genes, chromosomes & cancer.

NPM1 Deletion Is Associated with Gross Chromosomal Rearrangements in Leukemia

A. Aventín, B. Falini, Valeria Nofrini, 2010, PloS one.

High PIM1 expression is a biomarker of T-cell acute lymphoblastic leukemia with JAK/STAT activation or t(6;7)(p21;q34)/TRB@-PIM1 rearrangement

R. Foà, S. Chiaretti, A. Vitale, 2018, Leukemia.

DDX3X-MLLT10 fusion in adults with NOTCH1 positive T-cell acute lymphoblastic leukemia

S. Chiaretti, A. Vitale, D. D. Giacomo, 2014, Haematologica.

DDX3X-MLLT10 fusion in adults with NOTCH1 positive T-cell acute lymphoblastic leukemia

S. Chiaretti, A. Vitale, C. Mecucci, 2014, Haematologica.

The GNAS1 gene in myelodysplastic syndromes (MDS).

C. Mecucci, C. Matteucci, N. Testoni, 2014, Leukemia research.

A NUP98-positive acute myeloid leukemia with a t(11;12)(p15;q13) without HOXC cluster gene involvement.

Valeria Nofrini, C. Mecucci, M. Martelli, 2009, Cancer genetics and cytogenetics.

Cryptic chromosome 9q34 deletion generates TAF-Ialpha/CAN and TAF-Ibeta/CAN fusion transcripts in acute myeloid leukemia.

C. Mecucci, M. Martelli, F. Aversa, 2007 .

14q32 rearrangements deregulating BCL11B mark a distinct subgroup of T and myeloid immature acute leukemia.

S. Aerts, C. Mecucci, Zeynep Kalender Atak, 2021, Blood.

Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults

C. Mecucci, P. Gorello, C. Matteucci, 2022, Leukemia.

Interstitial insertion of AF10 into the ALL1 gene in a case of infant acute lymphoblastic leukemia.

C. Mecucci, G. Cimino, C. Matteucci, 1998, Cancer genetics and cytogenetics.

Cytogenetic/mutation profile of chronic lymphocytic leukemia/malignant melanoma collision tumors of the skin

S. Ascani, C. Mecucci, P. Covarelli, 2018, Molecular Cytogenetics.

MN1-ETV6 fusion gene arising from MDS with 5q-.

Valeria Nofrini, C. Mecucci, P. Gorello, 2011, Leukemia research.

Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study.

M. Mancini, C. Mecucci, A. Cuneo, 1998, Haematologica.

FISH analysis reveals frequent co-occurrence of 4q24/TET2 and 5q and/or 7q deletions.

Valeria Nofrini, C. Mecucci, S. Paolini, 2012, Leukemia research.

New dead/H-box helicase gene (ddx41) mutation in an Italian family with recurrent leukemia

R. Latagliata, C. Mecucci, C. Matteucci, 2021, Leukemia & lymphoma.

Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndrome

Valeria Nofrini, C. Mecucci, M. Martelli, 2009, British journal of haematology.

Cytogenetic characterization of acute myeloid leukemia in Shwachman's syndrome. A case report.

C. Mecucci, M. Martelli, C. Matteucci, 2000, Haematologica.

Comparative genomic hybridization identifies 17q11.2 approximately q12 duplication as an early event in cutaneous T-cell lymphomas.

C. Mecucci, M. Martelli, G. Girolomoni, 2008, Cancer genetics and cytogenetics.

Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment

C. Mecucci, C. Matteucci, P. Di Bartolomeo, 2017, European Journal of Dermatology.

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

C. Mecucci, C. Matteucci, A. Rambaldi, 2014, Blood Cancer Journal.

Multiple EWSR1-WT1 and WT1-EWSR1 copies in two cases of desmoplastic round cell tumor.

P. D. Dal Cin, Valeria Nofrini, C. Mecucci, 2013, Cancer genetics.

Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults

C. Mecucci, P. Gorello, C. Matteucci, 2022, Leukemia.

Interphase FISH for Y chromosome, VNTR polymorphisms, and RT-PCR for BCR-ABL in the monitoring of HLA-matched and mismatched transplants.

C. Mecucci, M. Martelli, F. Aversa, 2000, Cancer genetics and cytogenetics.

Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia.

Valeria Nofrini, C. Mecucci, P. Gorello, 2013, Cancer genetics.

Identification of multiple copies of a 20q-chromosome in a case of myelodysplastic syndrome: a FISH study.

T. L. Hood, P. Marynen, J. Vermeesch, 1999, Leukemia research.

Submicroscopic deletions in 5 q-associated malignancies

P. Marynen, C. Mecucci, M. Martelli, 2004 .

Activating somatic and germline TERT promoter variants in myeloid malignancies

S. Colla, Valeria Nofrini, C. Mecucci, 2020, Leukemia.

Cytogenetic and FISH investigations on tetrasomy 8 in ANLL.

C. Mecucci, M. Martelli, C. Matteucci, 1995, Cancer genetics and cytogenetics.

Genetic profile of T-cell acute lymphoblastic leukemias with MYC translocations.

S. Chiaretti, C. Mecucci, G. Basso, 2014, Blood.

A common 93-kb duplicated DNA sequence at 1q21.2 in acute lymphoblastic leukemia and Burkitt lymphoma.

C. Mecucci, M. Martelli, P. Gorello, 2007, Cancer genetics and cytogenetics.

Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study

Valeria Nofrini, C. Mecucci, P. Gorello, 2020, PloS one.

Microdissection and FISH investigations in acute myeloid leukemia: a step forward to full identification of complex karyotypic changes.

P. Marynen, J. Vermeesch, C. Mecucci, 2000, Cancer genetics and cytogenetics.

Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia

P. Marynen, A. Aventín, C. Mecucci, 2006, Leukemia.

NUP98/11p15 translocations affect CD34+ cells in myeloid and T lymphoid leukemias.

A. Vitale, B. Beverloo, Valeria Nofrini, 2015, Leukemia research.

Combined interphase fluorescence in situ hybridization elucidates the genetic heterogeneity of T-cell acute lymphoblastic leukemia in adults

R. Foà, S. Chiaretti, A. Vitale, 2010, Haematologica.

Characterization of ABL1 expression in adult T-cell acute lymphoblastic leukemia by oligonucleotide array analysis.

E. Ghia, R. Foà, S. Chiaretti, 2007, Haematologica.

Typical genomic imbalances in primary MALT lymphoma of the orbit

P. Galieni, C. Mecucci, M. Martelli, 2003, The Journal of pathology.

Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myelocytic leukemia.

C. Mecucci, M. Martelli, C. Matteucci, 2003, Cancer genetics and cytogenetics.

Interpretation of the complex karyotype and identification of a new 6p amplicon by integrated comparative genomic hybridization and fluorescence in situ hybridization on the U937-I cell line.

P. Marynen, C. Mecucci, A. Orlacchio, 2002, Cancer Genetics and Cytogenetics.

Regression of lymphoproliferative disorder after treatment for hepatitis C virus infection in a patient with partial trisomy 3, Bcl-2 overexpression, and type II cryoglobulinemia.

C. Mecucci, J. Kay, C. Matteucci, 2002, Blood.

Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemia.

A. Vitale, Valeria Nofrini, C. Mecucci, 2011, Cancer genetics.

Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia

R. Foà, S. Chiaretti, C. Mecucci, 2016, Haematologica.

Submicroscopic deletions in 5q- associated malignancies.

P. Marynen, C. Mecucci, M. Martelli, 2004, Haematologica.

Genomic and clinical findings in myeloid neoplasms with PDGFRB rearrangement

C. Mecucci, A. Cuneo, M. Luppi, 2021, Annals of Hematology.

Molecular cytogenetic findings in a four-way t(1;12;5;12)(p36;p13;q33;q24) underlying the ETV6-PDGFRB fusion gene in chronic myelomonocytic leukemia.

P. Marynen, C. Mecucci, M. Martelli, 2007, Cancer genetics and cytogenetics.

TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia

C. Mecucci, M. Martelli, P. Gorello, 2006, Leukemia.

Comparison between Sickle Cell Disease Patients and Healthy Donors: Untargeted Lipidomic Study of Erythrocytes

C. Mecucci, R. Pellegrino, P. Gorello, 2023, International journal of molecular sciences.

A novel mutation of indoleamine 2,3-dioxygenase 1 causes a rapid proteasomal degradation and compromises protein function.

C. Mecucci, L. Ruggeri, U. Grohmann, 2020, Journal of autoimmunity.

Trisomy 6 is the hallmark of a dysplastic clone in bone marrow aplasia.

C. Mecucci, M. Martelli, H. van den Berghe, 1998, Cancer genetics and cytogenetics.

Human homeobox gene HOXC13 is the partner of NUP98 in adult acute myeloid leukemia with t(11;12)(p15;q13)

Massimo Negrini, Pier Giuseppe Pelicci, M. Negrini, 2003, Genes, chromosomes & cancer.

Distinct genomic events in the myeloid and lymphoid lineages in simultaneous presentation of chronic myeloid leukemia and B-chronic lymphocytic leukemia

S. Sacchi, C. Mecucci, M. Martelli, 2002, Leukemia.

Germline GATA2 variant disrupting endothelial eNOS function and angiogenesis can be restored by c-Jun/AP-1 upregulation

C. Mecucci, P. Gresele, C. Matteucci, 2021, Haematologica.

A Novel t(5;7)(q31;q21)/CDK6::IL3 in Immature T-cell Acute Lymphoblastic Leukemia With IL3 Expression and Eosinophilia

E. Sabattini, C. Mecucci, L. Ruggeri, 2022, HemaSphere.

The EMT transcription factor Zeb2 controls adult murine hematopoietic differentiation by regulating cytokine signaling.

H. Fröhlich, D. Huylebroeck, C. Mecucci, 2017, Blood.

Chronic lymphocytic leukaemia Is terminal del(14)(q24) a new marker for prognostic stratification?

C. Mecucci, M. Martelli, C. Matteucci, 2006, Leukemia research.

Design of a comprehensive fluorescence in situ hybridization assay for genetic classification of T-cell acute lymphoblastic leukemia.

R. Foà, S. Chiaretti, A. Vitale, 2020, The Journal of molecular diagnostics : JMD.

AML1/MTG16 fusion gene from a t(16;21)(q24;q22) translocation in treatment-induced leukemia after breast cancer.

C. Mecucci, M. Martelli, C. Matteucci, 2001, Haematologica.

Identification of chromosome changes in acute myeloid leukemia (AML-M2) by molecular cytogenetics.

A. Hagemeijer, C. Mecucci, M. Martelli, 1997, Cancer genetics and cytogenetics.

Role of BCL2L10 methylation and TET2 mutations in higher risk myelodysplastic syndromes treated with 5-Azacytidine

M. Vignetti, M. Voso, S. Hohaus, 2011, Leukemia.

Genomic instability and recurrent breakpoints are main cytogenetic findings in Hodgkin's disease.

B. Falini, C. Mecucci, M. Martelli, 1999, Haematologica.

MN1-ETV6 fusion gene arising from MDS with 5q-.

Valeria Nofrini, C. Mecucci, P. Gorello, 2011, Leukemia research.

Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study.

M. Roberti, N. Piva, R. Bigoni, 1998, Haematologica.