MECUCCI, Cristina
 Distribuzione geografica
Continente #
NA - Nord America 6.414
EU - Europa 5.095
AS - Asia 1.930
Continente sconosciuto - Info sul continente non disponibili 12
OC - Oceania 6
SA - Sud America 6
AF - Africa 4
Totale 13.467
Nazione #
US - Stati Uniti d'America 6.398
IE - Irlanda 1.247
UA - Ucraina 1.101
IT - Italia 827
SE - Svezia 797
SG - Singapore 719
HK - Hong Kong 563
FI - Finlandia 309
DE - Germania 277
VN - Vietnam 272
CN - Cina 260
RU - Federazione Russa 229
GB - Regno Unito 91
FR - Francia 41
KR - Corea 41
CZ - Repubblica Ceca 40
BE - Belgio 34
TR - Turchia 32
CH - Svizzera 30
AT - Austria 18
UZ - Uzbekistan 17
NL - Olanda 16
LB - Libano 13
GR - Grecia 12
EU - Europa 11
CA - Canada 10
PL - Polonia 9
IL - Israele 6
ES - Italia 5
MX - Messico 5
IN - India 4
RO - Romania 4
AU - Australia 3
BR - Brasile 3
EG - Egitto 3
NZ - Nuova Zelanda 3
SK - Slovacchia (Repubblica Slovacca) 3
BG - Bulgaria 2
A1 - Anonimo 1
BD - Bangladesh 1
BO - Bolivia 1
DK - Danimarca 1
EC - Ecuador 1
JP - Giappone 1
MA - Marocco 1
NO - Norvegia 1
PA - Panama 1
PH - Filippine 1
PT - Portogallo 1
PY - Paraguay 1
Totale 13.467
Città #
Chandler 1.280
Dublin 1.241
San Mateo 658
Jacksonville 590
Hong Kong 563
Singapore 559
Boardman 418
Santa Clara 326
Perugia 304
Medford 277
Princeton 274
Dong Ket 272
Altamura 236
Ann Arbor 208
Lawrence 202
Wilmington 201
Andover 154
Beijing 111
Redmond 89
Saint Petersburg 81
Helsinki 76
San Paolo di Civitate 61
Dearborn 59
Ashburn 56
Munich 53
Norwalk 53
Woodbridge 48
New York 40
Seoul 40
Los Angeles 39
Des Moines 38
Brno 32
Izmir 32
Brussels 31
Houston 25
Auburn Hills 22
Moscow 19
Dallas 18
Rome 18
San Diego 15
Redwood City 14
Falls Church 13
Shanghai 12
Milan 9
Florence 8
Bologna 7
Chengdu 7
Amsterdam 6
Den Haag 6
Chicago 5
Forlì 5
Fremont 5
Como 4
Edinburgh 4
Frankfurt Am Main 4
Lappeenranta 4
Lausanne 4
Madrid 4
Nanjing 4
Nürnberg 4
Santarcangelo di Romagna 4
Shenzhen 4
Simi Valley 4
Terni 4
Toronto 4
Arezzo 3
Bilqas 3
Boston 3
Cuneo 3
Espoo 3
Fairfield 3
Kiryat Ono 3
Liège 3
Ludwigshafen 3
Naples 3
Padova 3
Palermo 3
Ponte 3
Reggio Nell'emilia 3
San Mango Piemonte 3
Todi 3
Vienna 3
Aprilia 2
Arienzo 2
Auckland 2
Avigliano 2
Bratislava 2
Cambridge 2
Collazzone 2
Deruta 2
Essen 2
Falkenstein 2
Foligno 2
Fort Worth 2
Groningen 2
Gualdo Tadino 2
Guangzhou 2
Hadera 2
Menlo Park 2
New Haven 2
Totale 9.055
Nome #
Both carboxy-terminus NES motif and mutated tryptophan(s) are crucial for aberrant nuclear export of nucleophosmin leukemic mutants in NPMc+ AML. 113
Role of BCL2L10 methylation and TET2 mutations in higher risk myelodysplastic syndromes treated with 5-Azacytidine 107
Mutated nucleophosmin detects clonal multilineage involvement in acute myeloid leukemia: Impact on WHO classification 96
Acute myeloid leukemia carrying cytoplasmic/mutated nucleophosmin (NPMc+ AML): biological and clinical features 95
Design of a Comprehensive Fluorescence in Situ Hybridization Assay for Genetic Classification of T-Cell Acute Lymphoblastic Leukemia 92
14q+ chromosome marker in a T-cell-rich B-cell lymphoma. 90
Regions of juxtaposition in unbalanced 1q rearrangements of malignant hemopathies 89
Pervasive mutations of JAK-STAT pathway genes in classical Hodgkin lymphoma 89
Molecular cytogenetic analysis of the 5Q-chromosome in the HL60 cell-line and in the 5Q-Syndrome 87
Translocations and mutations involving the nucleophosmin (NPM1) gene in lymphomas and leukemias. 86
AML with mutated NPM1 carrying a normal or aberrant karyotype show overlapping biologic, pathologic, immunophenotypic, and prognostic features 86
e6a2 BCR/ABL1 fusion with cryptic der(9)t(9;22) deletions in a patient with chronic myeloid leukemia 86
Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology. 85
Acute myeloid leukemia bearing cytoplasmic nucleophosmin (NPMc+AML) shows a distinct gene expression profile characterized by up-regulation of genes involved in stem-cell maintenance 84
Acute lymphoblastic leukaemia in Noonan syndrome 83
Activating somatic and germline TERT promoter variants in myeloid malignancies 82
Acute myeloid leukemia is propagated by a leukemic stem cell with lymphoid characteristics in a mouse model of CALM/AF10-positive leukemia 78
t(3;11)(q12;p15)/NUP98-LOC348801 fusion transcript in acute myeloid leukemia 77
Myeloid cell differentiation arrest by miR-125b-1 in myelodysplastic syndrome and acute myeloid leukemia with the t(2;11)(p21;q23) translocation 77
NPM1 deletion is associated with gross chromosomal rearrangements in leukemia 77
Detection of the NUP214-ABL rearrangement in T-ALL by high-density oligonucleotide arrays: Evidence of the value of this approach in the identification of gene amplifications 76
Interstitial insertion of AF10 into the ALL1 gene in a case of infant acute lymphoblastic leukemia 76
Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9) 76
FIP1L1-PDGFRA in chronic eosinophilic leukemia and BCR-ABL1 in chronic myeloid leukemia affect different leukemic cells 75
3q aberration and monosomy 7 in ANLL presenting with high platelet count and diabetes insipidus. 75
A common 93-kb duplicated DNA sequence at 1q21.2 in acute lymphoblastic leukemia and Burkitt lymphoma 75
Clinical-Grade Expanded Regulatory T Cells Prevent Graft-versus-Host Disease While Allowing a Powerful T Cell Dependent Graft-versus-Leukemia Effect in Murine Models 74
Alterazioni strutturali del cromosoma 12p dei disordini mieloidi 73
Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia. 73
Genetic profile of acute myeloid leukemia 72
NPM1 mutations and cytoplasmic nucleophosmin are mutually exclusive of recurrent genetic abnormalities: a comparative analysis of 2562 patients with acute myeloid leukemia. 70
Blastic plasmacytoid dendritic cell neoplasm and chronic myelomonocytic leukemia: a shared clonal origin 70
Genetic pathways in low-and high-grade HCV-related lymphomas are different 69
Full haplotype-mismatched hematopoietic stem-cell transplantation: A phase II study in patients with acute leukemia at high risk of relapse 69
RNA sequencing unravels the genetics of refractory/relapsed T-cell acute lymphoblastic leukemia. Prognostic and therapeutic implications 68
Imatinib mesylate can induce molecular complete remission in idiopathic hypereosinophilic syndrome (HES). A phase II multicentric Italian clinical trial 67
Overexpression of sPRDM16 coupled with loss of p53 induces myeloid leukemias in mice 67
t(4;11) translocation involving NUP98 and RAP1GDS1 genes. Characterisation of a new subset of T acute lymphoblastc leukaemia 67
Succeful use of the same slide for consecutive fluorescence in situ hybridization (FISH) experiments. 67
The hypereosinophilic syndrome: fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinases 67
AML1/MTG16 fusion gene from a t(16;21)(q24;q22) translocation in treatment-induced leukemia after breast cancer 67
Exon-12 nucleophosmin (NPM) mutation and aberrant cytoplasmic expression of NPM protein in leukemia cell line OCI-AML3 66
Immunohistochemistry predicts nucleophosmin (NPM) mutations in acute myeloid leukemia 66
5q- in a case of blastic phase of chronic myeloid leukemia. 66
5q- anomaly in a patient with erythroleukemia (M6 FAB classi¬fication) 66
5q- syndrome in a patient with chronic exposure to ionizing radiation. 66
Cytogenetic and FISH investigations on Tetrasomy 8 in ALL. 66
Blast crisis Ph+ chronic myeloid leukemia with NUP98/HOXA13 up-regulating MSI2. 66
Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies 65
A novel mutation of indoleamine 2,3-dioxygenase 1 causes a rapid proteasomal degradation and compromises protein function 65
The ETV6,CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberrations in different hematological malignancies. 64
A NUP98-positive acute myeloid leukemia with a t(11;12)(p15;q13) without HOXC cluster gene involvement 64
Acute leukemia with PICALM-MLLT10 fusion gene: diagnostic and treatment struggle 64
Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study. 64
Prognostic impact of genetic characterization in the GIMEMA LAM99P study for newly diagnosed adult AML. Relevance of combined analysis of conventional karyotyping, FLT3 and NPM mutational status 63
Simultaneous detection of NPM1 and FLT3-ITD mutations by capillary electrophoresis in acute myeloid leukemia 63
Acute myeloblastic leukemia after adjuvant chemo¬therapy with melphalan in breast cancer. Case report with cytogenetic analysis. 63
4q12 translocations with GSX2 expression identify a CD7(+) acute myeloid leukaemia subset 63
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. 63
null 63
Dual-color split signal fluorescence in situ hybridization assays for the detection of CALM/AF10 in t(10;11)(p13;q14-q21)-positive acute leukemia 62
Combined interphase fluorescence in situ hybridization elucidates the genetic heterogeneity of T-cell acute lymphoblastic leukemia in adults 62
MYB rearrangements and over-expression in T-cell acute lymphoblastic leukemia 62
5q- syndrome termi¬nating in acute myeloid leukemia: karyotype evolution and immunological characterization of blast cells. 61
Clustering of genomic breakpoints at the MLL locus in therapy-related acute leukemia with t(4;11)(q21;q23). 61
DHPLC analysis of NPM1 mutations in adult primary AML. 61
Born to be exported: COOH-terminal nuclear export signals of different strength ensure cytoplasmic accumulation of nucleophosmin leukemic mutants 61
New somatic TERT promoter variants enhance the Telomerase activity in Glioblastoma 61
Targeted resequencing analysis of 31 genes commonly mutated in myeloid disorders in serial samples from myelodysplastic syndrome patients showing disease progression 61
Combined translocation with ZNF198-FGFR1 gene fusion and deletion of potential tumor suppressors in a myeloproliferative disorder 60
Rescue of genomic information in adult acute lymphoblastic leukaemia (ALL) with normal/failed cytogenetics: a GIMEMA centralized biological study 60
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 60
MN1-ETV6 fusion gene arising from MDS With 5q- 60
Aberrant subcellular expression of nucleophosmin and NPM-MLF1 fusion protein in acute myeloid leukaemia carrying t(3;5): a comparison with NPMc+ AML. 60
Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia 60
Cryptic insertion producing two NUP98/NSD1 chimeric transcripts in adult refractory anemia with an excess of blasts 59
Mechanism of altered nucleo-cytoplasmic traffic of nucleophosmin in acute myelogenous leukemia carrying exon12 NPM mutations (NPMc plus AML) 59
Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study 59
A simple prognostic scoring system for newly diagnosed cytogenetically normal acute myeloid leukemia: retrospective analysis of 530 patients 58
CALM/AF10-positive leukemias show upregulation of genes involved in chromatin assembly and DNA repair processes and of genes adjacent to the breakpoint at 10p12. 58
DDX3X-MLLT10 fusion in adults with NOTCH1 positive T-cell acute lymphoblastic leukemia. 58
Cytoplasmic nucleophosmin in myeloid sarcoma occurring 20 years after diagnosis of acute myeloid leukaemia 58
Identification of two independent clones underlying the co-existence of myelodysplastic syndrome with excess of blasts type 2 and isolated 5q- and smoldering multiple myeloma 58
Nucleoporin genes in human diseases 58
Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndrome 57
Acute myeloid leukemia 57
A PDGFRB-positive acute myeloid malignancy with a new t(5;12)(q33;p13.3) involving the ERC1 gene 57
Blockade of Oncogenic NOTCH1 With the SERCA Inhibitor CAD204520 in T Cell Acute Lymphoblastic Leukemia 57
Mismatched hematopoietic stem cell transplantation in secondary leukemia 56
Coinvolgimento del cromosoma 1 nella mielofibrosi e nelle mielodisplasie. 56
Trisomy 8 in PDGFRB-negative cells in a patient with imatinib-sensitive chronic myelomonocytic leukemia and t(5;16)(q33;p13), PDGFRB-NDE1 fusion 56
Different genomic imbalances in low- and high-grade HCV-related lymphomas 56
NOTCH1 PEST domain mutation is an adverse prognostic factor in B-CLL. 56
Targeted sequencing identifies associations between IL7R-JAK mutations and epigenetic modulators in T-cell acute lymphoblastic leukemia 56
Cytoplasmic mutated nucleophosmin is stable in primary leukemic cells and in a xenotransplant model of NPMc+ acute myeloid leukemia in SCID mice 56
Submicroscopic deletions in 5q- associated malignancies 56
Non-B, non-T acute lymphoblastic leukaemia terminating in malignant histiocytosis: a new case and a review of the literature. 55
Metachronous cardiac and cerebral sarcomas: case report with focus on molecular findings and review of the literature 55
NUP98/11p15 translocations affect CD34+ cells in myeloid and T lymphoid leukemias 55
MYB deregulation from a EWSR1-MYB fusion at leukemic evolution of a JAK2 V617F positive primary myelofibrosis 55
Totale 6.811
Categoria #
all - tutte 62.881
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 62.881


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020906 0 0 0 0 156 44 158 35 165 143 51 154
2020/20212.357 7 174 82 194 648 135 171 43 262 124 205 312
2021/20222.382 84 467 46 153 87 13 17 726 31 85 335 338
2022/20234.113 293 765 39 353 314 371 7 203 1.596 8 123 41
2023/20241.709 110 165 94 25 23 3 341 30 280 37 288 313
2024/20251.304 89 404 189 132 490 0 0 0 0 0 0 0
Totale 14.138