Elena Belloni

Ontology type: schema:Person     

Person Info





Publications in SciGraph latest 50 shown

  • 2015-10 Lung Cancer Onset in Wild Type Mice Following Bone Marrow Reconstitution with krasv12 Cells in SCIENTIFIC REPORTS
  • 2014-12 PAT-ChIP coupled with laser microdissection allows the study of chromatin in selected cell populations from paraffin-embedded patient samples in EPIGENETICS & CHROMATIN
  • 2014-03 Gene expression profiling reveals GC and CEACAM1 as new tools in the diagnosis of lung carcinoids in BRITISH JOURNAL OF CANCER
  • 2011-12 In vivo expression of an aberrant MYB-GATA1 fusion induces leukemia in the presence of GATA1 reduced levels in LEUKEMIA
  • 2011-04 In vivo expression of an aberrant MYB-GATA1 fusion induces leukemia in the presence of GATA1 reduced levels in LEUKEMIA
  • 2011-03 Genomic characterization of asymptomatic CT-detected lung cancers in ONCOGENE
  • 2008-01 A PDGFRB-positive acute myeloid malignancy with a new t(5;12)(q33;p13.3) involving the ERC1 gene in LEUKEMIA
  • 2005-05 FISH analysis of hematological neoplasias with 1p36 rearrangements allows the definition of a cluster of 2.5 Mb included in the minimal region deleted in 1p36 deletion syndrome in HUMAN GENETICS
  • 2004-01 Molecular characterization of a t(1;3)(p36;q21) in a patient with MDS. MEL1 is widely expressed in normal tissues, including bone marrow, and it is not overexpressed in the t(1;3) cells in ONCOGENE
  • 1998-12 A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis in NATURE GENETICS
  • 1998-04 Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly in HUMAN GENETICS
  • 1997-07 Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly in HUMAN GENETICS
  • 1996-11 Mutations in the human Sonic Hedgehog gene cause holoprosencephaly in NATURE GENETICS
  • 1996-11 Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly in NATURE GENETICS
  • 1995-09 Search for mutations in pancreatic sufficient cystic fibrosis Italian patients: detection of 90% of molecular defects and identification of three novel mutations in HUMAN GENETICS
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