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Journal Articles

Epigenetic Control of Foxp3, CAMTA1 and FUT7 Genes in Human Regulatory T Cells

Ekaterina Minskaia, PhD, Barbara C Saraiva, Maria Soares, PhD, Ana I.S. Vieira, MSc, Joao F Lacerda, MD PhD

Blood (2017) 130 (Supplement 1): 1004.

https://doi.org/10.1182/blood.V130.Suppl_1.1004.1004

Published: 2017

Journal Articles

Dose Dependent Role of Gfi1 in Human MDS and AML and Its Suitability As a Novel Target

Judith Maria Hönes, M.Sc., Lacramioara Botezatu, PhD, Lars C. Michel, Christian Thiede, MD, Bert van der Reijden, PhD, Michael Heuser, MD, Hideki Makishima, MD PhD, Jaroslaw P. Maciejewski, MD PhD, Tomas Radiovoyevitch, Gerhard Ehninger, MD, Ulrich Dührsen, Tarik Moroy, PhD, Cyrus Khandanpour, MD

Blood (2014) 124 (21): 777.

https://doi.org/10.1182/blood.V124.21.777.777

Published: 2014

Journal Articles

Importance and Determinants of Comorbidities, Functional Limitations and Multiple Myeloma (MM)-Specific Risk Factors: Further Development of an Improved and Weighted MM-Risk Score (Freiburg Comorbidity Index [FCI])

Anne-Saskia Domm, Stefanie Hieke, Gabriele Ihorst, Milena Pantic, Bernd Koch, Martina Kleber, MD, Johannes Waldschmidt, MD, Martin Schumacher, PhD, Ralph Wäsch, MD, Monika Engelhardt, MD

Blood (2014) 124 (21): 733.

https://doi.org/10.1182/blood.V124.21.733.733

Published: 2014

Journal Articles

Amplification of 1q21 Is Associated with Other High Risk Cytogenetic Abnormalities and Has No Independent Prognostic Significance in Patients Treated with Novel Agents

Efstathios Kastritis, MD, Evangelos Terpos, Maria Gavriatopoulou, Maria Roussou, Evangelos Eleutherakis-Papaiakovou, Marios Bakogeorgos, Despoina Kalapanida, Spyros Orfanopoulos, Vasiliki Bampali, Thaleia Meletiou, Dimitra Gika, Despoina Mparmparoussi, Charis Matsouka, Meletios A. Dimopoulos

Blood (2014) 124 (21): 3464.

https://doi.org/10.1182/blood.V124.21.3464.3464

Published: 2014

Journal Articles

Prognostic Value of Chromosome 1 Abnormalities in Myelodysplastic Syndrome

Blood (2014) 124 (21): 3240.

https://doi.org/10.1182/blood.V124.21.3240.3240

Published: 2014

Journal Articles

Hyperhaploid Multiple Myeloma (MM): A Rare Karyotypic Subgroup Retaining Disomy 18 and 1q12∼23 Amplification

Jeffrey Sawyer, Erming Tian, Christoph Heuck, MD, Qing Zhang, Janet Lukacs, Regina Lichti Binz, Edward Thomas, Gael Sammartino, Charles Swanson, Sarah Waheed, MD, Saad Z Usmani, MD FACP, Frits van Rhee, MD, PhD, Bart Barlogie, MD

Blood (2012) 120 (21): 3983.

https://doi.org/10.1182/blood.V120.21.3983.3983

Published: 2012

Journal Articles

CBL, CBLB, TET2, ASXL1 , and IDH1/2 Mutations as Well as Additional Chromosomal Aberrations Constitute Molecular Events Contributing to Malignant Progression In Advanced Philadelphia Chromosome-Positive Disorders.

Hideki Makishima, MD, PhD, Anna Jankowska, MSC, Michael A McDevitt, MD, PhD, Simon Dujardin, Heather Cazzolli, Bartlomiej Przychodzen, Courtney Prince, John Nicoll, Siddaiah Harish, MD, Mohammed Shaik, MD, Eric Hsi, MD, Anjali Advani, MD, Ronald Paquette, MD, Jaroslaw P Maciejewski, MD, PhD, FACP

Blood (2010) 116 (21): 3396.

https://doi.org/10.1182/blood.V116.21.3396.3396

Published: 2010

Journal Articles

Concomitant Detection of BCR-ABL Translocation and JAK2 V617F Mutation In 6 Myeloproliferative Neoplasm at Diagnosis

M. Rosario Uriarte Escuder, Monica Cappetta, Gonzalo Manrique, Veronica Perez, María Noel Zubillaga, Victoria Elizondo, Susana Boschi, Ines Prosper, Rossana Bonomi, Santiago Pomoli, Lilian Diaz, Lem Martinez

Blood (2010) 116 (21): 4832.

https://doi.org/10.1182/blood.V116.21.4832.4832

Published: 2010

Journal Articles

On Being Duped: Duplication of Chromosome 1 [Dup(1)(q21q32)] as the Sole Cytogenetic Abnormality In a Patient Previously Treated for AML

Douglas F. Beach, MD, Barry Barnoski, PhD, FACMG, Vimal Patel, MD, Roland Schwarting, MD, Roger Strair, MD, PhD, Neil A. Lachant, MD

Blood (2010) 116 (21): 4863.

https://doi.org/10.1182/blood.V116.21.4863.4863

Published: 2010

Journal Articles

Second Clones In Molecularly-Defined Biclonal Multiple Myeloma Are Derived From Unrelated B Cells, Can Be Present at High Frequency and Exhibit Chromosomal Abnormalities

Jitra Kriangkum, PhD, Carina Debes Marun, BSc, Sarah Motz, BSc, Andrew Belch, MD, Linda M. Pilarski, PhD

Blood (2010) 116 (21): 2981.

https://doi.org/10.1182/blood.V116.21.2981.2981

Published: 2010

Journal Articles

Congenic interval of CD45/Ly-5 congenic mice contains multiple genes that may influence hematopoietic stem cell engraftment

Amanda Waterstrat, Ying Liang, Carol F. Swiderski, Brent J. Shelton, Gary Van Zant

Blood (2010) 115 (2): 408–417.

https://doi.org/10.1182/blood-2008-03-143370

Published: 2010

Includes: Supplemental data

Journal Articles

Mosaicism due to myeloid lineage–restricted loss of heterozygosity as cause of spontaneous Rh phenotype splitting

Günther F. Körmöczi, Eva-Maria Dauber, Oskar A. Haas, Tobias J. Legler, Frederik B. Clausen, Gerhard Fritsch, Markus Raderer, Christoph Buchta, Andreas L. Petzer, Diether Schönitzer, Wolfgang R. Mayr, Christoph Gassner

Blood (2007) 110 (6): 2148–2157.

https://doi.org/10.1182/blood-2007-01-068106

Published: 2007

Journal Articles

A Validated Gene Expression Signature of High Risk Multiple Myeloma Is Defined by Deregulated Expression of Genes Mapping to Chromosome 1.

John D. Shaughnessy, Jr., Fenghuang Zhan, Bart Burington, Yongsheng Huang, Ichiro Hanamura, James P. Stewart, Klaus Hollmig, Mauricio Pineda-Roman, Guido Tricot, Frits van Rhee, Maurizio Zangari, John Crowley, Bart Barlogie

Blood (2006) 108 (11): 111.

https://doi.org/10.1182/blood.V108.11.111.111

Published: 2006

Journal Articles

Fine Mapping and Expression Analysis of Chromosome 1 with the Aim of Defining Critically Deregulated Genes Important in the Pathogenesis of Myeloma.

Paola E. Leone, PhD, Matthew W. Jenner, MD, Brian A. Walker, PhD, David C. Johnson, BSc, David Gonzalez, PhD, Fiona M. Ross, PhD, Faith E. Davies, MD, Gareth J. Morgan, MD, PhD

Blood (2006) 108 (11): 112.

https://doi.org/10.1182/blood.V108.11.112.112

Published: 2006

Journal Articles

Rbm15 Affects Notch Signaling and Myelopoiesis.

Matthew J. Renda, PhD, MS, Ee-Chun Cheng, B.S., Lin Wang, M.S., Xian-Young Ma, Ph.D., Diane S. Krause, M.D., Ph.D.

Blood (2006) 108 (11): 2545.

https://doi.org/10.1182/blood.V108.11.2545.2545

Published: 2006

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

Familial Myelodysplastic Syndromes with Centromere Instability of Chromosome 1 Origin.

Klas Raaschou-Jensen, MD, Mette Klarskov Andersen, MD,PhD, Bendt Nielsen, MD,PhD, Eigil Kjeldsen, MD,PhD, Lars Kjeldsen, MD,PhD

Blood (2006) 108 (11): 4855.

https://doi.org/10.1182/blood.V108.11.4855.4855

Published: 2006

Journal Articles

A validated gene expression model of high-risk multiple myeloma is defined by deregulated expression of genes mapping to chromosome 1

Blood (2006) 109 (6): 2276–2284.

https://doi.org/10.1182/blood-2006-07-038430

Published: 2006

Journal Articles

High Hyperdiploidy and t(12; 21) (p13; q22) Translocation Is Not a so Rare Association: A Report of 4 Cases in the Experience of Armand Trousseau Hospital (Paris).

Paola Ballerini, Christine Perot, Francoise Bellmann, Anne Auvrignon, Marie-Dominique Tabone, Stephanie Haouy, Dalila Adjaoud, Jacqueline Van Den Akker, M.F. Portnoi, Luc Douay, Guy Leverger, Judith Landman-Parker

Blood (2006) 108 (11): 2283.

https://doi.org/10.1182/blood.V108.11.2283.2283

Published: 2006

Journal Articles

C/EBP Suppression by Interruption of CUGBP1 Resulting from a Complex Rearrangement of MLL.

William T. Choi, Matthew R. Folsom, Mohammed F. Azim, Claus Meyer, PhD, Eric Kowarz, Rolf Marschalek, PhD, Nicolai A. Timchenko, PhD, Rizwan A. Naeem, MD, Dean A. Lee, MD, PhD

Blood (2006) 108 (11): 2080.

https://doi.org/10.1182/blood.V108.11.2080.2080

Published: 2006

NARROW

Epigenetic Control of Foxp3, CAMTA1 and FUT7 Genes in Human Regulatory T Cells

Dose Dependent Role of Gfi1 in Human MDS and AML and Its Suitability As a Novel Target

Importance and Determinants of Comorbidities, Functional Limitations and Multiple Myeloma (MM)-Specific Risk Factors: Further Development of an Improved and Weighted MM-Risk Score (Freiburg Comorbidity Index [FCI])

Amplification of 1q21 Is Associated with Other High Risk Cytogenetic Abnormalities and Has No Independent Prognostic Significance in Patients Treated with Novel Agents

Prognostic Value of Chromosome 1 Abnormalities in Myelodysplastic Syndrome

Hyperhaploid Multiple Myeloma (MM): A Rare Karyotypic Subgroup Retaining Disomy 18 and 1q12∼23 Amplification

CBL, CBLB, TET2, ASXL1 , and IDH1/2 Mutations as Well as Additional Chromosomal Aberrations Constitute Molecular Events Contributing to Malignant Progression In Advanced Philadelphia Chromosome-Positive Disorders.

Concomitant Detection of BCR-ABL Translocation and JAK2 V617F Mutation In 6 Myeloproliferative Neoplasm at Diagnosis

On Being Duped: Duplication of Chromosome 1 [Dup(1)(q21q32)] as the Sole Cytogenetic Abnormality In a Patient Previously Treated for AML

Second Clones In Molecularly-Defined Biclonal Multiple Myeloma Are Derived From Unrelated B Cells, Can Be Present at High Frequency and Exhibit Chromosomal Abnormalities

Congenic interval of CD45/Ly-5 congenic mice contains multiple genes that may influence hematopoietic stem cell engraftment

Mosaicism due to myeloid lineage–restricted loss of heterozygosity as cause of spontaneous Rh phenotype splitting

A Validated Gene Expression Signature of High Risk Multiple Myeloma Is Defined by Deregulated Expression of Genes Mapping to Chromosome 1.

Fine Mapping and Expression Analysis of Chromosome 1 with the Aim of Defining Critically Deregulated Genes Important in the Pathogenesis of Myeloma.

Rbm15 Affects Notch Signaling and Myelopoiesis.

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

Familial Myelodysplastic Syndromes with Centromere Instability of Chromosome 1 Origin.

A validated gene expression model of high-risk multiple myeloma is defined by deregulated expression of genes mapping to chromosome 1

High Hyperdiploidy and t(12; 21) (p13; q22) Translocation Is Not a so Rare Association: A Report of 4 Cases in the Experience of Armand Trousseau Hospital (Paris).

C/EBP Suppression by Interruption of CUGBP1 Resulting from a Complex Rearrangement of MLL.

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American Society of Hematology

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American Society of Hematology

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