C
Crocifissa Lo Cunsolo
Publications - 7
Citations - 234
Crocifissa Lo Cunsolo is an academic researcher. The author has contributed to research in topics: Chromosomal translocation & Gene. The author has an hindex of 5, co-authored 6 publications receiving 226 citations.
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Journal ArticleDOI
Transformation of normal human cells in the absence of telomerase activation
Yvette R. Seger,Yvette R. Seger,Marta García-Cao,Sara Piccinin,Crocifissa Lo Cunsolo,Claudio Doglioni,Maria A. Blasco,Gregory J. Hannon,Roberta Maestro +8 more
TL;DR: It is reported that the combined expression of adenovirus E1A, Ha-RasV12, and MDM2 is sufficient to convert a normal human cell into a cancer cell and provides evidence that activation of telomere maintenance strategies is not an obligate characteristic of tumorigenic human cells.
Journal ArticleDOI
Characterization of t(6;11)(p21;q12) in a renal-cell carcinoma of an adult patient.
Lorenza Pecciarini,M. Giulia Cangi,Crocifissa Lo Cunsolo,Ettore Macrì,Elena Dal Cin,Guido Martignoni,Claudio Doglioni +6 more
TL;DR: The first complete cytogenetic and molecular characterization of a t(6;11)‐positive RCC of an adult patient, a 54‐year‐old woman, is reported, contributing to define better this rare RCC type, which is typical not only of childhood but can also be found in adulthood.
Journal ArticleDOI
t(15;21) translocations leading to the concurrent downregulation of RUNX1 and its transcription factor partner genes SIN3A and TCF12 in myeloid disorders
Alberto L'Abbate,Doron Tolomeo,Francesca De Astis,Angelo Lonoce,Crocifissa Lo Cunsolo,D. Mühlematter,Jacqueline Schoumans,Peter Vandenberghe,Achilles Van Hoof,Orazio Palumbo,Massimo Carella,Tommaso Mazza,Clelia Tiziana Storlazzi +12 more
TL;DR: Through a combined approach integrating RNA-Seq, SNP-array, FISH and PCR techniques, two novel t(15;21) translocations leading to the inactivation of RUNX1 and its partners SIN3A and TCF12 are identified.
Journal ArticleDOI
FOXP1 and TP63 involvement in the progression of myelodysplastic syndrome with 5q- and additional cytogenetic abnormalities.
Alberto L'Abbate,Crocifissa Lo Cunsolo,Ettore Macrì,P. Iuzzolino,Cristina Mecucci,Claudio Doglioni,Michelina Coco,Lucia Anna Muscarella,Simona Salati,Enrico Tagliafico,Carla Minoia,Giacoma De Tullio,Attilio Guarini,Nicoletta Testoni,Claudio Agostinelli,Clelia Tiziana Storlazzi +15 more
TL;DR: An apparent role of FOXP1 and TP63, up to now poorly documented, in the progression of MDS is document in a 79-year woman who is lacking mutations in the TP53 tumor suppressor gene normally associated with poor outcome in myelodysplastic syndrome with 5q-.
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A rare but recurrent t(8;13)(q24;q14) translocation in B-cell chronic lymphocytic leukaemia causing MYC up-regulation and concomitant loss of PVT1, miR-15/16 and DLEU7.
Gemma Macchia,Angelo Lonoce,Santina Venuto,Ettore Macrì,Orazio Palumbo,Massimo Carella,Crocifissa Lo Cunsolo,P. Iuzzolino,María Hernández-Sánchez,Jesús M. Hernández-Rivas,Clelia Tiziana Storlazzi +10 more
TL;DR: Single nucleotide polymorphism (SNP) array analysis of the patient’s PB DNA, accomplished on a CytoScan HD Array according to manufacturer protocols using the ChAS Software, confirmed a deletion that included MIR15A/MIR16-1 and DLEU7 on the der(13) and disclosed a deletion on the derivative chromosome 8.