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Therapy-Related Myelodysplasia and Secondary Acute Myelogenous Leukemia After High-Dose Therapy With Autologous Hematopoietic Progenitor-Cell Support for Lymphoid Malignancies

Journal of clinical oncology, 2000-03, Vol.18 (5), p.947-955

2000

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BCL2 and JUNB abnormalities in primary cutaneous lymphomas

British journal of dermatology (1951), 2004-09, Vol.151 (3), p.546-556

2004

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Molecular cytogenetic analysis of cutaneous T-cell lymphomas: identification of common genetic alterations in Sézary syndrome and mycosis fungoides

British journal of dermatology (1951), 2002-09, Vol.147 (3), p.464-475

2002

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Shigella flexneri Spa15 Crystal Structure Verified in Solution by Double Electron Electron Resonance

Journal of molecular biology, 2011-01, Vol.405 (2), p.427-435

2011

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11q23 balanced chromosome aberrations in treatment-related myelodysplastic syndromes and acute leukemia: Report from an International Workshop

Genes chromosomes & cancer, 2002-04, Vol.33 (4), p.362-378

2002

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Detection of Chromosome Abnormalities Pre–High-Dose Treatment in Patients Developing Therapy-Related Myelodysplasia and Secondary Acute Myelogenous Leukemia After Treatment for Non-Hodgkin’s Lymphoma

Journal of clinical oncology, 2001-05, Vol.19 (9), p.2472-2481

2001

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The t(6;11)(q27;q23) translocation in acute leukemia : a laboratory and clinical study of 30 cases

Leukemia, 1998-05, Vol.12 (5), p.788-791

1998

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The t(10;11)(p12;q23) translocation in acute leukaemia : a cytogenetic and clinical study of 20 patients

Leukemia, 1998-05, Vol.12 (5), p.801-804

1998

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High level amplification of N-MYC is not associated with adverse histology or outcome in primary retinoblastoma tumours

British journal of cancer, 2002-09, Vol.87 (7), p.779-782

2002

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Prevalence and Clinical Correlations of MLL Gene Rearrangements in AML-M4/5

Blood, 1994-12, Vol.84 (11), p.3776-3780

1994

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Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias

Cancer research (Chicago, Ill.), 2005-10, Vol.65 (20), p.9152-9154

2005

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A case of adult T‐cell leukaemia/lymphoma characterized by multiplex‐fluorescence in situ hybridization, comparative genomic hybridization, fluorescence in situ hybridization and cytogenetics

British journal of dermatology (1951), 2001-07, Vol.145 (1), p.117-122

2001

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Breakpoint heterogeneity in t(10;11) translocation in AML-M4/M5 resulting in fusion of AF10 and MLL is resolved by fluorescent in situ hybridization analysis

Cancer research (Chicago, Ill.), 1995-10, Vol.55 (19), p.4220-4224

1995

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1,25-Dihydroxyvitamin D3 protects human leukemic cells from tumor necrosis factor-induced apoptosis via inactivation of cytosolic phospholipase A2

Cancer research (Chicago, Ill.), 1998-02, Vol.58 (4), p.633-640

1998

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Genetic susceptibility to Hodgkin's disease and secondary neoplasias: FISH analysis reveals patients at high risk of developing secondary neoplasia

Annals of oncology, 2002-01, Vol.13 (suppl-1), p.40-43

2002

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Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias

Cancer research (Chicago, Ill.), 2005-01, Vol.65 (2), p.375-378

2005

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Specific cytogenetic abnormalities are associated with a significantly inferior outcome in children and adolescents with mature B-cell non-Hodgkin's lymphoma: results of the FAB LMB 96 international study

Leukemia, 2009-02, Vol.23 (2), p.323-331

2009

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Concurrent activation of MYC and BCL2 in B cell non-Hodgkin lymphoma cell lines by translocation of both oncogenes to the same immunoglobulin heavy chain locus

Leukemia, 1996-07, Vol.10 (7), p.1198-1208

1996

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Myeloablative chemotherapy for chemo-sensitive recurrent follicular lymphoma: potential benefit in second relapse

Haematologica (Roma), 2013-04, Vol.98 (4), p.620-625

2013

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Upregulation of lipocortin 1 inhibits tumour necrosis factor-induced apoptosis in human leukaemic cells : a possible mechanism of resistance to immune surveillance

British journal of haematology, 2000-12, Vol.111 (3), p.807-816

2000

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Autologous transplantation with Philadelphia-negative progenitor cells for patients with chronic myeloid leukaemia (CML) failing to attain a cytogenetic response to alpha interferon

Bone marrow transplantation (Basingstoke), 2000-12, Vol.26 (11), p.1165-1172

2000

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Alagille syndrome and deletion of 20p

Journal of medical genetics, 1990-12, Vol.27 (12), p.729-737

1990

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Three further cases of t(8;14)(q11.2;q32) in acute lymphoblastic leukemia

Leukemia, 2001-08, Vol.15 (8), p.1304-1305

2001

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Cytogenetic and molecular evidence of marrow involvement in extramedullary acute myeloid leukaemia

British journal of haematology, 2000-09, Vol.110 (3), p.547-551

2000

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More About: B-Cell Non-Hodgkin's Lymphoma: Evidence for the t(14;18)Translocation in All Hematopoietic Cell Lineages

JNCI : Journal of the National Cancer Institute, 1999-10, Vol.91 (19), p.1687-1688

1999

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Therapy-Related Myelodysplasia and Secondary Acute Myelogenous Leukemia After High-Dose Therapy With Autologous Hematopoietic Progenitor-Cell Support for Lymphoid Malignancies

BCL2 and JUNB abnormalities in primary cutaneous lymphomas

Molecular cytogenetic analysis of cutaneous T-cell lymphomas: identification of common genetic alterations in Sézary syndrome and mycosis fungoides

Shigella flexneri Spa15 Crystal Structure Verified in Solution by Double Electron Electron Resonance

11q23 balanced chromosome aberrations in treatment-related myelodysplastic syndromes and acute leukemia: Report from an International Workshop

Detection of Chromosome Abnormalities Pre–High-Dose Treatment in Patients Developing Therapy-Related Myelodysplasia and Secondary Acute Myelogenous Leukemia After Treatment for Non-Hodgkin’s Lymphoma

The t(6;11)(q27;q23) translocation in acute leukemia : a laboratory and clinical study of 30 cases

The t(10;11)(p12;q23) translocation in acute leukaemia : a cytogenetic and clinical study of 20 patients

High level amplification of N-MYC is not associated with adverse histology or outcome in primary retinoblastoma tumours

Prevalence and Clinical Correlations of MLL Gene Rearrangements in AML-M4/5

Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias

A case of adult T‐cell leukaemia/lymphoma characterized by multiplex‐fluorescence in situ hybridization, comparative genomic hybridization, fluorescence in situ hybridization and cytogenetics

Breakpoint heterogeneity in t(10;11) translocation in AML-M4/M5 resulting in fusion of AF10 and MLL is resolved by fluorescent in situ hybridization analysis

1,25-Dihydroxyvitamin D3 protects human leukemic cells from tumor necrosis factor-induced apoptosis via inactivation of cytosolic phospholipase A2

Genetic susceptibility to Hodgkin's disease and secondary neoplasias: FISH analysis reveals patients at high risk of developing secondary neoplasia

Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias

Specific cytogenetic abnormalities are associated with a significantly inferior outcome in children and adolescents with mature B-cell non-Hodgkin's lymphoma: results of the FAB LMB 96 international study

Concurrent activation of MYC and BCL2 in B cell non-Hodgkin lymphoma cell lines by translocation of both oncogenes to the same immunoglobulin heavy chain locus

Myeloablative chemotherapy for chemo-sensitive recurrent follicular lymphoma: potential benefit in second relapse

Upregulation of lipocortin 1 inhibits tumour necrosis factor-induced apoptosis in human leukaemic cells : a possible mechanism of resistance to immune surveillance

Autologous transplantation with Philadelphia-negative progenitor cells for patients with chronic myeloid leukaemia (CML) failing to attain a cytogenetic response to alpha interferon

Alagille syndrome and deletion of 20p

Three further cases of t(8;14)(q11.2;q32) in acute lymphoblastic leukemia

Cytogenetic and molecular evidence of marrow involvement in extramedullary acute myeloid leukaemia

More About: B-Cell Non-Hodgkin's Lymphoma: Evidence for the t(14;18)Translocation in All Hematopoietic Cell Lineages

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