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Terminal deoxynucleotidyl transferase promotes acute myeloid leukemia by priming FLT3-ITD replication slippage

Blood, 2019-12, Vol.134 (25), p.2281-2290

2019

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The histone acetyl transferase activity of monocytic leukemia zinc finger is critical for the proliferation of hematopoietic precursors

Blood, 2009-05, Vol.113 (20), p.4866-4874

2009

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A Murine Model of CML Blast Crisis Induced by Cooperation between BCR/ABL and NUP98/HOXA9

Proceedings of the National Academy of Sciences - PNAS, 2002-05, Vol.99 (11), p.7622-7627

2002

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MLL is Fused to CBP, a Histone Acetyltransferase, in Therapy-Related Acute Myeloid Leukemia with a t(11;16)(q23;p13.3)

Proceedings of the National Academy of Sciences - PNAS, 1997-08, Vol.94 (16), p.8732-8737

1997

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Molecular roulette: nucleophosmin mutations in AML are orchestrated through N-nucleotide addition by TdT

Blood, 2019-12, Vol.134 (25), p.2291-2303

2019

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Chromosome Aberrations and Cancer

Science (American Association for the Advancement of Science), 1991-11, Vol.254 (5035), p.1153-1160

1991

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Molecular Analysis of Acute Promyelocytic Leukemia Breakpoint Cluster Region on Chromosome 17

Science (American Association for the Advancement of Science), 1990-09, Vol.249 (4976), p.1577-1580

1990

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NUP98-NSD1 fusion in association with FLT3-ITD mutation identifies a prognostically relevant subgroup of pediatric acute myeloid leukemia patients suitable for monitoring by real time quantitative PCR

Genes chromosomes & cancer, 2013-11, Vol.52 (11), p.1053-1064

2013

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Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome

Nature, 2004-02, Vol.427 (6975), p.640-645

2004

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The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein

Nature genetics, 1996-09, Vol.14 (1), p.33-41

1996

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Schizophrenia Susceptibility Associated with Interstitial Deletions of Chromosome 22q11

Proceedings of the National Academy of Sciences - PNAS, 1995-08, Vol.92 (17), p.7612-7616

1995

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The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9

Nature genetics, 1996-02, Vol.12 (2), p.159-167

1996

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All patients with the T(11;16)(q23;p13.3) that involves MLL and CBP have treatment-related hematologic disorders

Blood, 1997-07, Vol.90 (2), p.535-541

1997

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Characterization of a Zinc Finger Gene Disrupted by the t(15;17) in Acute Promyelocytic Leukemia

Science (American Association for the Advancement of Science), 1991-11, Vol.254 (5036), p.1371-1374

1991

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Diagnosis of acute promyelocytic leukaemia by RT‐PCR: detection of PML‐RARA and RARA‐PML fusion transcripts

British journal of haematology, 1992-11, Vol.82 (3), p.529-540

1992

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Identification of an angiogenic factor that when mutated causes susceptibility to Klippel–Trenaunay syndrome

Nature (London), 2004-02, Vol.427 (6975), p.640-645

2004

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A somatic cell hybrid map of the long arm of human chromosome 17, containing the familial breast cancer locus (BRCAI)

American journal of human genetics, 1993-04, Vol.52 (4), p.702-710

1993

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Molecular analysis of the t(15;17) translocation in acute promyelocytic leukaemia

Borrow, Julian

1992

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The human ICAM2 gene maps to 17q23–25

Genomics (San Diego, Calif.), 1991-10, Vol.11 (2), p.462-464

1991

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Molecular analysis of simple variant translocations in acute promyelocytic leukemia

Genes chromosomes & cancer, 1994-04, Vol.9 (4), p.234-243

1994

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Molecular Analysis of Acute Promyelocytic Leukemia Breakpoint Cluster on Chromosome 17

Science (American Association for the Advancement of Science), 1990-09, Vol.249 (4976), p.1577-1577

1990

Volltextzugriff (PDF)

The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP96 and class I homeoprotein HOXA9

Nature genetics, 1996-02, Vol.12 (2), p.159-167

1996

Volltextzugriff (PDF)

Construction and regional localization of clones from a NotI linking library from human chromosome 17q

Genomics (San Diego, Calif.), 1991-06, Vol.10 (2), p.477-480

1991

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Molecular analysis of the t(15;17) translocation in acute promyelocytic leukaemia

Baillière's clinical haematology, 1992-10, Vol.5 (4), p.833-856

1992

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Terminal deoxynucleotidyl transferase promotes acute myeloid leukemia by priming FLT3-ITD replication slippage

The histone acetyl transferase activity of monocytic leukemia zinc finger is critical for the proliferation of hematopoietic precursors

A Murine Model of CML Blast Crisis Induced by Cooperation between BCR/ABL and NUP98/HOXA9

MLL is Fused to CBP, a Histone Acetyltransferase, in Therapy-Related Acute Myeloid Leukemia with a t(11;16)(q23;p13.3)

Molecular roulette: nucleophosmin mutations in AML are orchestrated through N-nucleotide addition by TdT

Chromosome Aberrations and Cancer

Molecular Analysis of Acute Promyelocytic Leukemia Breakpoint Cluster Region on Chromosome 17

Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia

NUP98-NSD1 fusion in association with FLT3-ITD mutation identifies a prognostically relevant subgroup of pediatric acute myeloid leukemia patients suitable for monitoring by real time quantitative PCR

Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome

The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein

Schizophrenia Susceptibility Associated with Interstitial Deletions of Chromosome 22q11

The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9

All patients with the T(11;16)(q23;p13.3) that involves MLL and CBP have treatment-related hematologic disorders

Characterization of a Zinc Finger Gene Disrupted by the t(15;17) in Acute Promyelocytic Leukemia

Diagnosis of acute promyelocytic leukaemia by RT‐PCR: detection of PML‐RARA and RARA‐PML fusion transcripts

Identification of an angiogenic factor that when mutated causes susceptibility to Klippel–Trenaunay syndrome

A somatic cell hybrid map of the long arm of human chromosome 17, containing the familial breast cancer locus (BRCAI)

Molecular analysis of the t(15;17) translocation in acute promyelocytic leukaemia

The human ICAM2 gene maps to 17q23–25

Molecular analysis of simple variant translocations in acute promyelocytic leukemia

Molecular Analysis of Acute Promyelocytic Leukemia Breakpoint Cluster on Chromosome 17

The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP96 and class I homeoprotein HOXA9

Construction and regional localization of clones from a NotI linking library from human chromosome 17q

Molecular analysis of the t(15;17) translocation in acute promyelocytic leukaemia

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