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Journal Articles

NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern

Iris H. I. M. Hollink, Marry M. van den Heuvel-Eibrink, Susan T. C. J. M. Arentsen-Peters, Marta Pratcorona, Saman Abbas, Jenny E. Kuipers, Janneke F. van Galen, H. Berna Beverloo, Edwin Sonneveld, Gert-Jan J. L. Kaspers, Jan Trka, Andre Baruchel, Martin Zimmermann, Ursula Creutzig, Dirk Reinhardt, Rob Pieters, Peter J. M. Valk, C. Michel Zwaan

Blood (2011) 118 (13): 3645–3656.

https://doi.org/10.1182/blood-2011-04-346643

Published: 2011

Includes: Supplemental data

Journal Articles

Identification of Novel Recurrent Copy Number Variations and Regions of Copy-Neutral Loss of Heterozygosity by High Resolution Genomic Array in Pre-Treatment and Relapsed B-CLL.

Samantha JL Knight, Elham Sadighi Akha, Adele Timbs, Tariq Enver, Andrew R Pettitt, Jenny Taylor, Chris S Hatton, Anna Schuh

Blood (2009) 114 (22): 1098.

https://doi.org/10.1182/blood.V114.22.1098.1098

Published: 2009

Journal Articles

Epigenetic Signaling Is Required for HoxA9-Based Leukemic Transformation.

Aditya Chaubey, Ph.D., Chinavenmeni S. Velu, PhD, Shane Horman, PhD, Anil Jegga, Monica L. Guzman, PhD, Laurie Risner, Nancy J. Zeleznik-Le, PhD, Craig T. Jordan, PhD, Martin Carroll, MD, Brian Gebelein, Ph.D., H. Leighton Grimes, PhD

Blood (2009) 114 (22): 3966.

https://doi.org/10.1182/blood.V114.22.3966.3966

Published: 2009

Journal Articles

Array CGH Analysis of Nodal T-Cell Lymphomas: Identification of Genomic Alterations Specific to Angioimmunoblastic and Unspecified Subtypes, and Correlation with Transcriptomic Data.

Laurence de Leval, MD, David Rickman, PhD, Emilie Thomas, PhD, Louis Huang, MD, Aurélien de Reynies, PhD, Françoise Berger, MD, Thierry Molina, MD, Josette Brière, MD, Luc Xerri, MD, Christian Gisselbrecht, MD, Philippe Gaulard, MD

Blood (2007) 110 (11): 3567.

https://doi.org/10.1182/blood.V110.11.3567.3567

Published: 2007

Journal Articles

Fluorescence In Situ Hybridization (FISH) Reveals Unexpected Cryptic Chromosome 11 Defects in MDS/AML Patients.

Paolo Bernasconi, MD, Irene Dambruoso, MD, Marina Boni, MD, Paola Maria Cavigliano, MD, Ilaria Giardini, MD, Rita Zappatore, MD, Silvia Calatroni, MD, Barbara Rocca, MD, Marilena Caresana, MD, Mario Lazzarino, MD

Blood (2006) 108 (11): 4413.

https://doi.org/10.1182/blood.V108.11.4413.4413

Published: 2006

Journal Articles

Whole Genome 250K SNP Array Allows for Detection of Previously Unidentified Lesions in Chromosome 5 in Patients with MDS.

Lukasz P. Gondek, MD, Abdo Haddad, MD, Mikkael A. Sekeres, MD,MS, Yasuhito Nannya, Seishi Ogawa, MD, Alan F. List, MD, Jaroslaw P. Maciejewski, MD,PhD

Blood (2006) 108 (11): 2350.

https://doi.org/10.1182/blood.V108.11.2350.2350

Published: 2006

Journal Articles

Loss of Heterozygosity (LOH) of the NUP98 Gene Is an Adverse Prognostic Factor in Acute Myeloid Leukemia (AML).

Magdalena Plasilova, MD, PhD, Hans B. Ommen, MD, Jaroslav Jelinek, MD, PhD, Jean-Pierre Issa, MD, Elyn R. Riedel, Phd, Susan Mathew, PhD, Amy Chadburn, MD, Pengbo Zhou, PhD, Peter Hokland, MD, Malcolm A.S. Moore, PhD

Blood (2006) 108 (11): 2356.

https://doi.org/10.1182/blood.V108.11.2356.2356

Published: 2006

Journal Articles

High Density Oligonucleotide Array CGH Analysis of CLL Reveals Areas of Recurrent Genomic Gain or Loss.

Roelandt F.J. Schop, MD, Catherine Mancini, BS, Wee-Joo Chng, MD, Renee C. Tschumper, BS, Diane F. Jelinek, PhD, Neil E. Kay, MD, Peter Leif Bergsagel, MD, John D. Carpten, PhD, Rafael Fonseca, MD

Blood (2006) 108 (11): 2093.

https://doi.org/10.1182/blood.V108.11.2093.2093

Published: 2006

Journal Articles

Bacterial Artificial Chromosome (BAC) Array CGH Study of B-CLL Patients with 17p13 Deletion.

Vasantha Brito-Babapulle, PhD, Hannah Rudenko, MSc, Claire Dearden, MD, Kerry Fenwick, BSc, Alan Mckay, BSc, Alan Ashworth, PhD, Estella Matutes, MD, Daniel Catovsky, MD, Gareth Morgan, MD

Blood (2005) 106 (11): 2110.

https://doi.org/10.1182/blood.V106.11.2110.2110

Published: 2005

Journal Articles

Loss of Heterozygosity (LOH) for HumACTBP2 (SE33) Is Detected in Philadelphia (Ph)-Positive and Ph-Negative Hematopoietic Cells of Some Patients with Ph-Positive CML.

Haifa K. Al-Ali, MD, Jeanett Edelmann, MD, Sabine Leiblein, PhD, Christel Mueller, Evelin Hennig, Martina Bless, Christina Franke, Dietger W. Niederwieser, MD

Blood (2005) 106 (11): 3286.

https://doi.org/10.1182/blood.V106.11.3286.3286

Published: 2005

Journal Articles

Depletion of NUP98: A Common Leukemogenetic Mechanism in AML?

Magdalena Plasilova, PhD, MD, Ky Chung, MD, Jae Hung Shieh, PhD, Rachel J. Fields, Giovanni Morrone, MD, Amy Chadburn, MD, Daniel M. Knowles, MD, Pengbo Zhou, PhD, Malcolm A.S. Moore, PhD

Blood (2005) 106 (11): 667.

https://doi.org/10.1182/blood.V106.11.667.667

Published: 2005

Journal Articles

Genome Wide SNP Analysis Reveals Frequent Uniparental Disomy (UPD) Due to Somatic Recombination in Acute Myeloid Leukemias.

Manoj Raghavan, MBBS, BA, Debra Lillington, BSc, Spyros Skoulakis, PhD, Silvana Debernardi, BSc, Tracy Chaplin, BSc, Nicola J. Foot, BSc, T. Andrew Lister, MD, Bryan D. Young, PhD.

Blood (2004) 104 (11): 139.

https://doi.org/10.1182/blood.V104.11.139.139

Published: 2004

Journal Articles

A Novel Fusion, KIAA0379 (Ankyrin Repeat Domain 28) to NUP98 in an Adult MDS/AML with a t(3;5;11)(p25;q35;p15).

Maho Ishikawa, Fumiharu Yagasaki, Daisuke Okamura, Tomoya Maeda, Yuichi Sugahara, Motohiro Misumi, Katsuhiko Yoshida, Yuichi Nakamura, Nobutaka Kawai, Akira Matsuda, Itsuro Jinnai, Masami Bessho

Blood (2004) 104 (11): 4278.

https://doi.org/10.1182/blood.V104.11.4278.4278

Published: 2004

Journal Articles

A novel gene, NSD1 , is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia

Rina J. Jaju, Carrie Fidler, Oskar A. Haas, Amanda J. Strickson, Fiona Watkins, Kevin Clark, Nicholas C. P. Cross, Jan-Fang Cheng, Peter D. Aplan, Lyndal Kearney, Jacqueline Boultwood, James S. Wainscoat

Blood (2001) 98 (4): 1264–1267.

https://doi.org/10.1182/blood.V98.4.1264

Published: 2001

Journal Articles

A New Recurrent Translocation, t(5;11)(q35;p15.5), Associated With del(5q) in Childhood Acute Myeloid Leukemia

Rina J. Jaju, Oskar A. Haas, Michael Neat, Jochen Harbott, Vaskar Saha, Jacqueline Boultwood, Jill M. Brown, Hendrati Pirc-Danoewinata, Bernd W. Krings, Ulrich Müller, Stephan W. Morris, James S. Wainscoat, Lyndal Kearney

Blood (1999) 94 (2): 773–780.

https://doi.org/10.1182/blood.V94.2.773

Published: 1999

NARROW

NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern

Identification of Novel Recurrent Copy Number Variations and Regions of Copy-Neutral Loss of Heterozygosity by High Resolution Genomic Array in Pre-Treatment and Relapsed B-CLL.

Epigenetic Signaling Is Required for HoxA9-Based Leukemic Transformation.

Array CGH Analysis of Nodal T-Cell Lymphomas: Identification of Genomic Alterations Specific to Angioimmunoblastic and Unspecified Subtypes, and Correlation with Transcriptomic Data.

Fluorescence In Situ Hybridization (FISH) Reveals Unexpected Cryptic Chromosome 11 Defects in MDS/AML Patients.

Whole Genome 250K SNP Array Allows for Detection of Previously Unidentified Lesions in Chromosome 5 in Patients with MDS.

Loss of Heterozygosity (LOH) of the NUP98 Gene Is an Adverse Prognostic Factor in Acute Myeloid Leukemia (AML).

High Density Oligonucleotide Array CGH Analysis of CLL Reveals Areas of Recurrent Genomic Gain or Loss.

Bacterial Artificial Chromosome (BAC) Array CGH Study of B-CLL Patients with 17p13 Deletion.

Loss of Heterozygosity (LOH) for HumACTBP2 (SE33) Is Detected in Philadelphia (Ph)-Positive and Ph-Negative Hematopoietic Cells of Some Patients with Ph-Positive CML.

Depletion of NUP98: A Common Leukemogenetic Mechanism in AML?

Genome Wide SNP Analysis Reveals Frequent Uniparental Disomy (UPD) Due to Somatic Recombination in Acute Myeloid Leukemias.

A Novel Fusion, KIAA0379 (Ankyrin Repeat Domain 28) to NUP98 in an Adult MDS/AML with a t(3;5;11)(p25;q35;p15).

A novel gene, NSD1 , is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia

A New Recurrent Translocation, t(5;11)(q35;p15.5), Associated With del(5q) in Childhood Acute Myeloid Leukemia

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American Society of Hematology

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ASH Publications

American Society of Hematology

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