87 results on '"Coccaro, Nicoletta"'
Search Results
52. RARA and RARG gene downregulation associated with EZH2 mutation in acute promyelocytic-like morphology leukemia
53. Genomic BCR-ABL1 breakpoint characterization by a multi-strategy approach for “personalized monitoring” of residual disease in chronic myeloid leukemia patients
54. Overexpression of the LSAMP and TUSC7 genes in acute myeloid leukemia following microdeletion/duplication of chromosome 3
55. Erythrocytosis with JAK2GGCC_46/1 haplotype and without JAK2V617F mutation is associated with CALRrs1049481_G allele
56. A novel t(3;9)(q21.2; p24.3) associated with SMARCA2 and ZNF148 genes rearrangement in myelodysplastic syndrome
57. SETBP1 dysregulation in congenital disorders and myeloid neoplasms
58. Systemic Mastocytosis With Associated Chronic Lymphocytic Leukemia: A Matter Of Diseases Or Prognostic Factors
59. Stat3-positive tumor cells contribute to vessels neoformation in primary central nervous system lymphoma
60. Droplet digital PCR analysis of NOTCH1 gene mutations in chronic lymphocytic leukemia
61. TP53 gene mutation analysis in chronic lymphocytic leukemia by nanopore MinION sequencing
62. MYEOV gene overexpression in primary plasma cell leukemia with t(11;14)(q13;q32)
63. A novel t(3;9)(q21.2; p24.3) associated with SMARCA2 and ZNF148 genes rearrangement in myelodysplastic syndrome.
64. Droplet Digital PCR Analysis for Diagnosis and Minimal Residual Disease Monitoring in Adult Ph+ Acute Lymphoblastic Leukemia
65. Absolute quantification of the pretreatmentPML-RARAtranscript defines the relapse risk in acute promyelocytic leukemia
66. Myelodysplastic syndrome with 5q deletion following IgM monoclonal gammopathy, showing gene mutation MYD88 L265P
67. ADAMTS2 gene dysregulation in T/myeloid mixed phenotype acute leukemia
68. 5‘RUNX1-3’USP42 chimeric gene in acute myeloid leukemia can occur through an insertion mechanism rather than translocation and may be mediated by genomic segmental duplications
69. Centromeric fragment of chromosome 7 in atypical chronic myeloid leukemia with the SET binding protein 1 gene mutation
70. Acute myeloid leukemia with t(16;16) (p13;q22) showing a new CBFB-MYH11 fusion transcript associated with an atypical leukemic blasts morphology
71. BCL6 corepressor gene dysregulation due to chromosomal translocation in acute myeloid leukemia: a new mechanism based on long non-coding RNA dislocation?
72. Lymphoid enhancer binding factor-1 (LEF1) expression as a prognostic factor in adult acute promyelocytic leukemia
73. A novel t(4;16)(q25;q23.1) associated with EGF and ELOVL6 deregulation in acute myeloid leukemia
74. Gene expression profiling of chronic myeloid leukemia with variant t(9;22) reveals a different signature from cases with classic translocation
75. Chronic Myeloid Leukemia with Variant t(9;22) Shows Dysregulated Expression of Genes Included in Pivotal Cellular Pathways
76. The Behavior of Cytogenetic/Molecular Markers Associated with JAK2 Mutation Status Before and After Primary Myelofibrosis Progression Supports the Hypothesis of the Leukemic Clone's Independence From the JAK2 Mutation
77. TRIB2 Gene Overexpression Is Associated with Adult Minimally Differentiated Acute Myeloid Leukemia
78. Non random distribution of genomic features in breakpoint regions involved in chronic myeloid leukemia cases with variant t(9;22) or additional chromosomal rearrangements
79. Genomic Segmental Duplications at the Basis of t(9;22) Rearrangement in Chronic Myeloid Leukemia.
80. Lymphoid Enhancer Binding Factor-1 (LEF1) Expression As a Prognostic Factor In Adult Acute Promyelocytic Leukemia
81. Non random distribution of genomic features inbreakpoint regions involved in chronic myeloidleukemia cases with variant t(9;22) or additionalchromosomal rearrangements.
82. Centromeric fragment of chromosome 7 in atypical chronic myeloid leukemia with the SET binding protein 1 gene mutation.
83. JAK2Negative Erythrocytosis Associated with JAK2GGCC_46/1 Haplotype, Calrrs1049481_G, and Normal Erythropoietin Level: Is This a New Entity?
84. Nanopore Targeted Sequencing for Rapid Gene Mutations Detection in Acute Myeloid Leukemia.
85. TRIB2Gene Overexpression Is Associated with Adult Minimally Differentiated Acute Myeloid Leukemia
86. Absolute quantification of the pretreatment PML-RARA transcript defines the relapse risk in acute promyelocytic leukemia.
87. Lymphoid enhancer binding factor-1 (LEF1) expression as a prognostic factor in adult acute promyelocytic leukemia.
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