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Journal Articles

Genome-Wide Methylation Analysis Using the Digital Restriction Enzyme Analysis of Methylation for Stratification of Patients with Juvenile Myelomonocytic Leukemia

Hironobu Kitazawa, Hideki Muramatsu, MD PhD, Norihiro Murakami, MD PhD, Yusuke Okuno, MD PhD, Manabu Wakamatsu, MD, Taro Yoshida, MD, Masayuki Imaya, MD, Ayako Yamamori, MD, Shunsuke Miwata, MD, Kotaro Narita, MD, Motoharu Hamada, MD PhD, Daisuke Ichikawa, MD, Rieko Taniguchi, MD, Nozomu Kawashima, MD PhD, Eri Nishikawa, MD PhD, Atsushi Narita, Nobuhiro Nishio, MD PhD, Seiji Kojima, MD PhD, Yoshiyuki Takahashi, MD PhD

Blood (2019) 134 (Supplement_1): 2973.

https://doi.org/10.1182/blood-2019-127792

Published: 2019

Journal Articles

Mice with Myelodysplastic Syndrome Respond to Treatment with Azanucleosides: A Preclinical Model for MDS Therapies

Sheryl M Gough, PhD, Yang Jo Chung, PhD, Maegawa Shinji, PhD, Jaroslav Jelinek, MD, PhD, Jean-Pierre Issa, MD, Peter Aplan, MD

Blood (2012) 120 (21): 3829.

https://doi.org/10.1182/blood.V120.21.3829.3829

Published: 2012

Journal Articles

GATA1 mutations Outside the Blast Cell Population in Transient Leukemia of Down Syndrome

Jian Chen, PhD, Agnieszka Wendorff, PhD, Yue Li, MD, Johann K. Hitzler, MD

Blood (2011) 118 (21): 2562.

https://doi.org/10.1182/blood.V118.21.2562.2562

Published: 2011

Journal Articles

Polymorphisms in Exons 2 and 7 of the Human Organic Cation Transporter (hOCT1) (Solute Carrier Family 22, SLC22A1): Correlation with Imatinib Levels and Clinical Course in Chronic Myeloid Leukemia Patients,

Jacob Vine, medical student, Sara Bar Cohen, PhD, Rosa Ruchlemer, MD, Neta Goldschmidt, MD, Moshe Levin, MD, Diana Libster, MD, Alexander Gural, MD, Moshe E. Gatt, MD, David Lavie, Dina Ben-Yehuda, MD, Deborah Rund, MD

Blood (2011) 118 (21): 3487.

https://doi.org/10.1182/blood.V118.21.3487.3487

Published: 2011

Journal Articles

A Novel Nonsense Mutation of F13A1 Gene Causing Inherited Factor XIII Deficiency in a Chinese Han Family

Dawei Wang, Liang Tang, Wei Shi, Heng Mei, Rui Yang, Yan Yang, Yu Hu, MD, Jun Fang, MD, Tao Guo, MD

Blood (2011) 118 (21): 4661.

https://doi.org/10.1182/blood.V118.21.4661.4661

Published: 2011

Journal Articles

Cancer Drivers Affected by Aberrant DNA Methylation in MDS and AML

Jaroslav Jelinek, MD, PhD, Shoudan Liang, PhD, Frank Neumann, MD, PhD, Rong He, Yue Lu, PhD, Jumpei Yamazaki, DVM, PhD, Rodolphe F Taby, MD, Louis Ramagli, PhD, Marcos R Estecio, PhD, Jean-Pierre Issa, MD

Blood (2011) 118 (21): 1716.

https://doi.org/10.1182/blood.V118.21.1716.1716

Published: 2011

Journal Articles

Digital Restriction Enzyme Analysis of Methylation (DREAM) by Next Generation Sequencing Uncovers Epigenetic Disturbances In Acute Myelogenous Leukemia.

Frank Neumann, MD, PhD, Jean-Pierre Issa, MD, Yue Lu, PhD, Marcos R Estecio, PhD, Rong He, Louis Ramagli, PhD, Shoudan Liang, PhD, Jaroslav Jelinek, MD, PhD

Blood (2010) 116 (21): 3635.

https://doi.org/10.1182/blood.V116.21.3635.3635

Published: 2010

Journal Articles

Digital Restriction Enzyme Analysis of Methylation (DREAM) by Next Generation Sequencing Yields High Resolution Maps of DNA Methylation.

Jaroslav Jelinek, MD, PhD, Shoudan Liang, PhD, Marcos R. H. Estecio, PhD, Rong He, Yue Lu, PhD, Louis S. Ramagli, PhD, Jean-Pierre J. Issa, MD

Blood (2009) 114 (22): 567.

https://doi.org/10.1182/blood.V114.22.567.567

Published: 2009

Journal Articles

Serum Dickkopf-1 Is Increased and Correlates with Bone Mineral Density in Patients with Thalassemia-Induced Osteoporosis. Reduction Post Zoledronic Acid Administration

Ersi Voskaridou, Dimitrios Christoulas, Thodoris Pantelaros, Konstantinos Varvagiannis, Charoula Xirakia, Athanasios Papatheodorou, Kleio Sinopoulou, Aggeliki Mpalasopoulou, Antonios Bilalis, Evangelos Terpos

Blood (2008) 112 (11): 3889.

https://doi.org/10.1182/blood.V112.11.3889.3889

Published: 2008

Journal Articles

Janus Kinase (JAK2) V617F Somatic Mutation in Patients with Deep Vein Thrombosis.

Fernanda A. Orsi, Devanira S.P. Costa, Katia B.B. Pagnano, Joyce M. Annichino-Bizzachi

Blood (2007) 110 (11): 1645.

https://doi.org/10.1182/blood.V110.11.1645.1645

Published: 2007

Journal Articles

Novel Mechanism of β0 Thalassemia: Missense Mutation of the Last Nucleotide of β Globin Exon 1 (G->C) Leads to Undetectable Transcript and Mutant Peptide.

Neeraj Agarwal, MD, Mariluz P. Mojica-Henshaw, MD, PhD, Ferdane Kutlar, MD, Amos Gaikwad, MD, Ching N. Ou, PhD, Abdullah Kutlar, MD, Josef T. Prchal, MD

Blood (2006) 108 (11): 1598.

https://doi.org/10.1182/blood.V108.11.1598.1598

Published: 2006

Journal Articles

A Specific Subtype of Sitosterolemia with Macrothrombocytopenia in a Chinese Family.

Yanghua Su, MD, Zhaoyue Wang, Haiyan Yang, M.D, Fang Liu, M.D, Xia Bai, B.M, Changgeng Ruan

Blood (2006) 108 (11): 1103.

https://doi.org/10.1182/blood.V108.11.1103.1103

Published: 2006

Journal Articles

Cryptic MLL , AF10 , ARMC3 Rearrangement in Secondary AML Creates ARMC3-MLL Fusion That Disrupts Gene Encoding Armadillo Repeats Similar to Major Cancer Genes.

Giuseppe Germano, PhD, Blaine W. Robinson, PhD, Carolyn A. Felix, MD

Blood (2005) 106 (11): 4345.

https://doi.org/10.1182/blood.V106.11.4345.4345

Published: 2005

Journal Articles

Effect of Bax G125A Single Nucleotide Polymorphism (SNP) on Bax Gene Expression in Diffuse Large Cell Lymphoma.

Anurag Saxena, MD, Mark Bosch, Tania Qureshi, Kateryna Nokhrina, PhD, Oksana Moshynska, PhD

Blood (2005) 106 (11): 4379.

https://doi.org/10.1182/blood.V106.11.4379.4379

Published: 2005

Journal Articles

Effect of LCR 5′HS4 and 5′HS1 Deletions on β-Like Globin Gene Expression in β-Yac Transgenic Mice.

Susanna Harju, PhD, Halyna Fedosyuk, MS, Kenneth R. Peterson, PhD

Blood (2004) 104 (11): 1209.

https://doi.org/10.1182/blood.V104.11.1209.1209

Published: 2004

Journal Articles

A Gln747→Pro Substitution in the  IIb Subunit Is Responsible for a Moderate  IIb β 3 Deficiency in Glanzmann Thrombasthenia

Seiji Tadokoro, Yoshiaki Tomiyama, Shigenori Honda, Morio Arai, Naomasa Yamamoto, Masamichi Shiraga, Satoru Kosugi, Yuzuru Kanakura, Yoshiyuki Kurata, Yuji Matsuzawa

Blood (1998) 92 (8): 2750–2758.

https://doi.org/10.1182/blood.V92.8.2750

Published: 1998

Journal Articles

Clinical Relevance of Point Mutations in the Cytoplasmic Domain of the Granulocyte Colony-Stimulating Factor Receptor Gene in Patients With Severe Congenital Neutropenia

N. Tidow, C. Pilz, B. Teichmann, A. Müller-Brechlin, M. Germeshausen, B. Kasper, P. Rauprich, K.-W. Sykora, K. Welte

Blood (1997) 89 (7): 2369–2375.

https://doi.org/10.1182/blood.V89.7.2369

Published: 1997

Journal Articles

Absence of oncogene amplifications and occasional activation of N-ras in lymphoblastic leukemia of childhood

S Rodenhuis, JL Bos, RM Slater, H Behrendt, M van 't Veer, LA Smets

Blood (1986) 67 (6): 1698–1704.

https://doi.org/10.1182/blood.V67.6.1698.1698

Published: 1986

Journal Articles

The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes

AE Felice, MP Cleek, K McKie, V McKie, TH Huisman

Blood (1984) 63 (5): 1253–1257.

https://doi.org/10.1182/blood.V63.5.1253.1253

Published: 1984

NARROW

Genome-Wide Methylation Analysis Using the Digital Restriction Enzyme Analysis of Methylation for Stratification of Patients with Juvenile Myelomonocytic Leukemia

Mice with Myelodysplastic Syndrome Respond to Treatment with Azanucleosides: A Preclinical Model for MDS Therapies

GATA1 mutations Outside the Blast Cell Population in Transient Leukemia of Down Syndrome

Polymorphisms in Exons 2 and 7 of the Human Organic Cation Transporter (hOCT1) (Solute Carrier Family 22, SLC22A1): Correlation with Imatinib Levels and Clinical Course in Chronic Myeloid Leukemia Patients,

A Novel Nonsense Mutation of F13A1 Gene Causing Inherited Factor XIII Deficiency in a Chinese Han Family

Cancer Drivers Affected by Aberrant DNA Methylation in MDS and AML

Digital Restriction Enzyme Analysis of Methylation (DREAM) by Next Generation Sequencing Uncovers Epigenetic Disturbances In Acute Myelogenous Leukemia.

Digital Restriction Enzyme Analysis of Methylation (DREAM) by Next Generation Sequencing Yields High Resolution Maps of DNA Methylation.

Serum Dickkopf-1 Is Increased and Correlates with Bone Mineral Density in Patients with Thalassemia-Induced Osteoporosis. Reduction Post Zoledronic Acid Administration

Janus Kinase (JAK2) V617F Somatic Mutation in Patients with Deep Vein Thrombosis.

Novel Mechanism of β0 Thalassemia: Missense Mutation of the Last Nucleotide of β Globin Exon 1 (G->C) Leads to Undetectable Transcript and Mutant Peptide.

A Specific Subtype of Sitosterolemia with Macrothrombocytopenia in a Chinese Family.

Cryptic MLL , AF10 , ARMC3 Rearrangement in Secondary AML Creates ARMC3-MLL Fusion That Disrupts Gene Encoding Armadillo Repeats Similar to Major Cancer Genes.

Effect of Bax G125A Single Nucleotide Polymorphism (SNP) on Bax Gene Expression in Diffuse Large Cell Lymphoma.

Effect of LCR 5′HS4 and 5′HS1 Deletions on β-Like Globin Gene Expression in β-Yac Transgenic Mice.

A Gln747→Pro Substitution in the  IIb Subunit Is Responsible for a Moderate  IIb β 3 Deficiency in Glanzmann Thrombasthenia

Clinical Relevance of Point Mutations in the Cytoplasmic Domain of the Granulocyte Colony-Stimulating Factor Receptor Gene in Patients With Severe Congenital Neutropenia

Absence of oncogene amplifications and occasional activation of N-ras in lymphoblastic leukemia of childhood

The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes

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American Society of Hematology

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American Society of Hematology

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