Lista de obras - Clelia Tiziana Storlazzi

4q12 translocations with GSX2 expression identify a CD7(+) acute myeloid leukaemia subset

article

A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia chromosome translocation

artículo científico publicado en 2002

A complex karyotype including a t(2;11) in a paediatric ependymoma: case report and review of the literature.

artículo científico publicado en 2010

A complex rearrangement involving cryptic deletion of ETV6 and CDKN1B genes in a case of childhood acute lymphoblastic leukemia.

artículo científico publicado en 2009

A fluorescence in situ hybridization study of complex t(9;22) in two chronic myelocytic leukemia cases with a masked Philadelphia chromosome

artículo científico publicado en 2004

A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1.

artículo científico publicado en 2003

A novel fusion 5′AFF3/3′BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphoma

scientific article published on 14 July 2008

A novel fusion gene, SS18L1/SSX1, in synovial sarcoma

artículo científico publicado en 2003

A novel t(2;10)(q31;p12) balanced translocation in acute myeloid leukemia

artículo científico publicado en 2012

A rare but recurrent t(8;13)(q24;q14) translocation in B-cell chronic lymphocytic leukaemia causingMYCup-regulation and concomitant loss ofPVT1,miR-15/16andDLEU7

Acute promyelocytic leukemia with additional chromosome abnormalities in a renal transplant case

artículo científico publicado en 2001

Alternative promoters drive the expression of the gene encoding the mouse axonal glycoprotein F3/contactin.

artículo científico publicado en 2001

Amplification of the G allele at SNP rs6983267 in 8q24 amplicons in myeloid malignancies as cause of the lack of MYC overexpression?

artículo científico publicado en 2011

Analysis of clock gene-miRNA correlation networks reveals candidate drivers in colorectal cancer.

scientific article published on 14 June 2016

Assignment to chromosome 12q24.33, gene organization and splicing of the human KRAB/FPB containing zinc finger gene ZNF84

article

BL1391: an established cell line from a human malignant peripheral nerve sheath tumor with unique genomic features

artículo científico publicado en 2020

Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma

artículo científico

Bone marrow ectopic expression of a non-coding RNA in childhood T-cell acute lymphoblastic leukemia with a novel t(2;11)(q11.2;p15.1) translocation

artículo científico publicado en 2008

Breakpoint characterization of der(9) deletions in chronic myeloid leukemia patients

artículo científico publicado en 2002

CBFA2T2 and C20orf112: two novel fusion partners of RUNX1 in acute myeloid leukemia.

artículo científico publicado en 2010

CDKN2A/B alterations impair prognosis in adult BCR-ABL1-positive acute lymphoblastic leukemia patients.

artículo científico publicado en 2011

Characterization of a hotspot region on chromosome 12 for amplification in ring chromosomes in atypical lipomatous tumors.

artículo científico publicado en 2009

CircRNAs and Fusion-circRNAs in cancer: New players in an old game

artículo científico publicado en 2020

Complex karyotype in a polycythemia vera patient with a novel SETD1B/GTF2H3 fusion gene

artículo científico publicado en 2014

Concomitant tetrasomy 3q and trisomy 18 in CD5−, CD13+ chronic lymphocytic leukemia

artículo científico publicado en 2002

Constitutional ring chromosome 11 mosaicism in a Wilms tumor patient: Cytogenetic, molecular and clinico-pathological studies

artículo científico publicado en 2010

Cytogenetic analysis of 101 giant cell tumors of bone: Nonrandom patterns of telomeric associations and other structural aberrations

scientific article published on 01 July 2009

Deletions on der(9) chromosome in adult Ph-positive acute lymphoblastic leukemia occur with a frequency similar to that observed in chronic myeloid leukemia

artículo científico publicado en 2003

Deregulated expression of cryptochrome genes in human colorectal cancer

artículo científico publicado en 2016

Derivative chromosome 9 deletions in chronic myeloid leukemia are associated with loss of tumor suppressor genes

artículo científico publicado en 2004

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

artículo científico publicado en 2011

ETV6 mutations and loss in AML-M0

artículo científico publicado en 2008

Epigenetically induced ectopic expression of UNCX impairs the proliferation and differentiation of myeloid cells

artículo científico publicado en 2017

Episomal amplification of MYCN in a case of medulloblastoma.

artículo científico publicado en 2008

Establishment and genetic characterization of ANGM-CSS, a novel, immortal cell line derived from a human glioblastoma multiforme

artículo científico publicado en 2013

Evolution of chromosome Y in primates

artículo científico publicado en 1997

Evolution of chromosome Y in primates.

artículo científico publicado en 1998

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

artículo científico publicado en 2011

FOSL1 as a candidate target gene for 11q12 rearrangements in desmoplastic fibroblastoma

artículo científico publicado en 2012

FOXP1 and TP63 involvement in the progression of myelodysplastic syndrome with 5q- and additional cytogenetic abnormalities

artículo científico publicado en 2014

Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma

artículo científico publicado en 2003

Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure

artículo científico publicado en 2010

Gene expression deregulation by KRAS G12D and G12V in a BRAF V600E context.

artículo científico publicado en 2008

Genomic deletions on other chromosomes involved in variant t(9;22) chronic myeloid leukemia cases

artículo científico

Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancer

artículo científico publicado en 2014

Heterogeneous pattern of chromosomal breakpoints involving the MYC locus in multiple myeloma.

artículo científico publicado en 2003

High RAD51 mRNA expression characterize estrogen receptor-positive/progesteron receptor-negative breast cancer and is associated with patient's outcome

artículo científico publicado en 2011

IKAROS deletions dictate a unique gene expression signature in patients with adult B-cell acute lymphoblastic leukemia

artículo científico publicado en 2012

IKZF1 (Ikaros) deletions in BCR-ABL1-positive acute lymphoblastic leukemia are associated with short disease-free survival and high rate of cumulative incidence of relapse: a GIMEMA AL WP report

artículo científico publicado en 2009

Identification and molecular characterization of recurrent genomic deletions on 7p12 in the IKZF1 gene in a large cohort of BCR-ABL1-positive acute lymphoblastic leukemia patients: on behalf of Gruppo Italiano Malattie Ematologiche dell'Adulto Acute

artículo científico publicado en 2009

Identification of RUNX1/AML1 as a classical tumor suppressor gene

article

Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies

artículo científico publicado en 2004

Identification of a novel IGH-MMSET fusion transcript in a human myeloma cell line with the t(4;14)(p16.3;q32) chromosomal translocation

artículo científico publicado en 2004

Identification of a novel amplicon at distal 17q containing the BIRC5/SURVIVIN gene in malignant peripheral nerve sheath tumours

artículo científico publicado en 2006

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

artículo científico publicado en 2013

Isolation and chromosomal localization of GPR31, a human gene encoding a putative G protein-coupled receptor

artículo científico publicado en 1997

Late-appearing pseudocentric fission event during chronic myeloid leukemia progression

artículo científico publicado en 2007

MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene

article

Molecular analysis of the HuD gene in neuroendocrine lung cancers.

artículo científico publicado en 2010

Molecular cloning of TER1, a chemokine receptor-like gene expressed by lymphoid tissues

artículo científico publicado en 1996

Molecular cytogenetic characterization of a complex rearrangement involving chromosomes 9 and 22 in a case of Ph-negative chronic myeloid leukemia

artículo científico publicado en 2002

Molecular cytogenetic characterization of a novel additional chromosomal aberration in blast crisis of a Ph-positive chronic myeloid leukemia

scientific article published on 01 April 2002

Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma

scientific article published on 26 August 2005

Molecular cytogenetic resources specific for chromosome 12

artículo científico publicado en 1999

Molecular cytogenetics characterization of a novel translocation involving chromosomes 17 and 19 in a Ph+ adult acute lymphoblastic leukaemia

artículo científico publicado en 2002

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

artículo científico publicado en 2013

Novel chromosomal translocation (17;22)(q12;q12) in a case of myelodisplastic syndrome characterized with signs of hemolytic anemia at presentation

article

Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney

artículo científico publicado en 2005

RALE051: a novel established cell line of sporadic Burkitt lymphoma

artículo científico publicado en 2017

Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor-specific translocation t(X;6)(q13-14;q22)

artículo científico publicado en 2006

Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma

artículo científico publicado en 2013

Ring chromosomes and low-grade gene amplification in an atypical lipomatous tumor with minimal nuclear atypia.

artículo científico publicado en 2003

Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomas

artículo científico publicado en 2014

Similar mechanisms formed ring markers containing chromosome 12 pericentromeric region in two patients with therapy-related acute myeloid leukemia

artículo científico publicado en 2008

T(15;17) in acute promyelocytic leukemia is not associated with submicroscopic deletions on der(17)

scientific article published on 01 July 2002

The PAX5 gene is frequently rearranged in BCR-ABL1-positive acute lymphoblastic leukemia but is not associated with outcome. A report on behalf of the GIMEMA Acute Leukemia Working Party

artículo científico publicado en 2010

The chemokine receptor CCR8 is preferentially expressed in Th2 but not Th1 cells

scientific journal article

The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma

artículo científico publicado en 2004

Therapeutic implications of intratumor heterogeneity for TP53 mutational status in Burkitt lymphoma.

artículo científico publicado en 2015

Three novel fusion transcripts of the paired box 5 gene in B-cell precursor acute lymphoblastic leukemia

artículo científico publicado en 2014

Thrombocytopenia-absent-radius syndrome in a child showing a larger 1q21.1 deletion than the one in his healthy mother, and a significant downregulation of the commonly deleted genes

artículo científico publicado en 2011

Two alternatively spliced 5′BCR/3′JAK2 fusion transcripts in a myeloproliferative neoplasm with a three-way t(9;18;22)(p23;p11.3;q11.2) translocation

artículo científico publicado en 2011

Upregulation of MEL1 and FLJ42875 genes by position effect resulting from a t(1;2)(p36;p21) occurring during evolution of chronic myelomonocytic leukemia

article

Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma

artículo científico publicado en 2007

t(15;21) translocations leading to the concurrent downregulation of RUNX1 and its transcription factor partner genes SIN3A and TCF12 in myeloid disorders.

artículo científico publicado en 2015

t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene

article

t(5;6;12) associated with resistance to imatinib mesylate in chronic myeloid leukemia

artículo científico publicado en 2009

Lista de obras de Clelia Tiziana Storlazzi

4q12 translocations with GSX2 expression identify a CD7(+) acute myeloid leukaemia subset

A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia chromosome translocation

A complex karyotype including a t(2;11) in a paediatric ependymoma: case report and review of the literature.

A complex rearrangement involving cryptic deletion of ETV6 and CDKN1B genes in a case of childhood acute lymphoblastic leukemia.

A fluorescence in situ hybridization study of complex t(9;22) in two chronic myelocytic leukemia cases with a masked Philadelphia chromosome

A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1.

A novel fusion 5′AFF3/3′BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphoma

A novel fusion gene, SS18L1/SSX1, in synovial sarcoma

A novel t(2;10)(q31;p12) balanced translocation in acute myeloid leukemia

A rare but recurrent t(8;13)(q24;q14) translocation in B-cell chronic lymphocytic leukaemia causingMYCup-regulation and concomitant loss ofPVT1,miR-15/16andDLEU7

Acute promyelocytic leukemia with additional chromosome abnormalities in a renal transplant case

Alternative promoters drive the expression of the gene encoding the mouse axonal glycoprotein F3/contactin.

Amplification of the G allele at SNP rs6983267 in 8q24 amplicons in myeloid malignancies as cause of the lack of MYC overexpression?

Analysis of clock gene-miRNA correlation networks reveals candidate drivers in colorectal cancer.

Assignment to chromosome 12q24.33, gene organization and splicing of the human KRAB/FPB containing zinc finger gene ZNF84

BL1391: an established cell line from a human malignant peripheral nerve sheath tumor with unique genomic features

Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma

Bone marrow ectopic expression of a non-coding RNA in childhood T-cell acute lymphoblastic leukemia with a novel t(2;11)(q11.2;p15.1) translocation

Breakpoint characterization of der(9) deletions in chronic myeloid leukemia patients

CBFA2T2 and C20orf112: two novel fusion partners of RUNX1 in acute myeloid leukemia.

CDKN2A/B alterations impair prognosis in adult BCR-ABL1-positive acute lymphoblastic leukemia patients.

Characterization of a hotspot region on chromosome 12 for amplification in ring chromosomes in atypical lipomatous tumors.

CircRNAs and Fusion-circRNAs in cancer: New players in an old game

Complex karyotype in a polycythemia vera patient with a novel SETD1B/GTF2H3 fusion gene

Concomitant tetrasomy 3q and trisomy 18 in CD5−, CD13+ chronic lymphocytic leukemia

Constitutional ring chromosome 11 mosaicism in a Wilms tumor patient: Cytogenetic, molecular and clinico-pathological studies

Cytogenetic analysis of 101 giant cell tumors of bone: Nonrandom patterns of telomeric associations and other structural aberrations

Deletions on der(9) chromosome in adult Ph-positive acute lymphoblastic leukemia occur with a frequency similar to that observed in chronic myeloid leukemia

Deregulated expression of cryptochrome genes in human colorectal cancer

Derivative chromosome 9 deletions in chronic myeloid leukemia are associated with loss of tumor suppressor genes

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

ETV6 mutations and loss in AML-M0

Epigenetically induced ectopic expression of UNCX impairs the proliferation and differentiation of myeloid cells

Episomal amplification of MYCN in a case of medulloblastoma.

Establishment and genetic characterization of ANGM-CSS, a novel, immortal cell line derived from a human glioblastoma multiforme

Evolution of chromosome Y in primates

Evolution of chromosome Y in primates.

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

FOSL1 as a candidate target gene for 11q12 rearrangements in desmoplastic fibroblastoma

FOXP1 and TP63 involvement in the progression of myelodysplastic syndrome with 5q- and additional cytogenetic abnormalities

Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma

Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure

Gene expression deregulation by KRAS G12D and G12V in a BRAF V600E context.

Genomic deletions on other chromosomes involved in variant t(9;22) chronic myeloid leukemia cases

Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancer

Heterogeneous pattern of chromosomal breakpoints involving the MYC locus in multiple myeloma.

High RAD51 mRNA expression characterize estrogen receptor-positive/progesteron receptor-negative breast cancer and is associated with patient's outcome

IKAROS deletions dictate a unique gene expression signature in patients with adult B-cell acute lymphoblastic leukemia

IKZF1 (Ikaros) deletions in BCR-ABL1-positive acute lymphoblastic leukemia are associated with short disease-free survival and high rate of cumulative incidence of relapse: a GIMEMA AL WP report

Identification and molecular characterization of recurrent genomic deletions on 7p12 in the IKZF1 gene in a large cohort of BCR-ABL1-positive acute lymphoblastic leukemia patients: on behalf of Gruppo Italiano Malattie Ematologiche dell'Adulto Acute

Identification of RUNX1/AML1 as a classical tumor suppressor gene

Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies

Identification of a novel IGH-MMSET fusion transcript in a human myeloma cell line with the t(4;14)(p16.3;q32) chromosomal translocation

Identification of a novel amplicon at distal 17q containing the BIRC5/SURVIVIN gene in malignant peripheral nerve sheath tumours

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

Isolation and chromosomal localization of GPR31, a human gene encoding a putative G protein-coupled receptor

Late-appearing pseudocentric fission event during chronic myeloid leukemia progression

MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene

Molecular analysis of the HuD gene in neuroendocrine lung cancers.

Molecular cloning of TER1, a chemokine receptor-like gene expressed by lymphoid tissues

Molecular cytogenetic characterization of a complex rearrangement involving chromosomes 9 and 22 in a case of Ph-negative chronic myeloid leukemia

Molecular cytogenetic characterization of a novel additional chromosomal aberration in blast crisis of a Ph-positive chronic myeloid leukemia

Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma

Molecular cytogenetic resources specific for chromosome 12

Molecular cytogenetics characterization of a novel translocation involving chromosomes 17 and 19 in a Ph+ adult acute lymphoblastic leukaemia

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

Novel chromosomal translocation (17;22)(q12;q12) in a case of myelodisplastic syndrome characterized with signs of hemolytic anemia at presentation

Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney

RALE051: a novel established cell line of sporadic Burkitt lymphoma

Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor-specific translocation t(X;6)(q13-14;q22)

Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma

Ring chromosomes and low-grade gene amplification in an atypical lipomatous tumor with minimal nuclear atypia.

Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomas

Similar mechanisms formed ring markers containing chromosome 12 pericentromeric region in two patients with therapy-related acute myeloid leukemia

T(15;17) in acute promyelocytic leukemia is not associated with submicroscopic deletions on der(17)

The PAX5 gene is frequently rearranged in BCR-ABL1-positive acute lymphoblastic leukemia but is not associated with outcome. A report on behalf of the GIMEMA Acute Leukemia Working Party

The chemokine receptor CCR8 is preferentially expressed in Th2 but not Th1 cells

The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma

Therapeutic implications of intratumor heterogeneity for TP53 mutational status in Burkitt lymphoma.