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Journal Articles

CLL in India May Have a Different Biology from That in the West

Renu Saxena, MD, Ravi Kumar, PhD, Sudha Sazawal, PhD, Manoranjan Mahapatra, MD

Blood (2016) 128 (22): 5574.

https://doi.org/10.1182/blood.V128.22.5574.5574

Published: 2016

Journal Articles

Frequency of a Highly Polymorphic Variant, S36N GFI1 , Is Increased in CML Patients

Jaspal S Kaeda, PhD, Leila Amini, BSc, Concetta Quintarelli, PhD, Iris von Wunsch-Rolshoven, Frauke Ringel, PhD, Michaela Schwarz, MD, Fabrizio Pane, MD, Bernd Dörken, MD, Philipp le Coutre, MD

Blood (2014) 124 (21): 3157.

https://doi.org/10.1182/blood.V124.21.3157.3157

Published: 2014

Journal Articles

Fast Detection Of MYD88 -L265P Mutation By PCR-RFLP In Chronic Lymphoproliferative Disorders

Nikoletta Argentou, George Vassilopoulos, MD, PhD, Maria Ioannou, Anastasios Germenis, Matthaios Speletas

Blood (2013) 122 (21): 5076.

https://doi.org/10.1182/blood.V122.21.5076.5076

Published: 2013

Journal Articles

Can Polymorphisms In Oxidative Stress Related Genes Be a Risk Factor For CML?

Ana Cristina Gonçalves, MSc, PhD, Raquel Alves, MSc, PhD, Paulo Freitas-Tavares, MD, Adriana Teixeira, MD, Luísa Mota-Vieira, PhD, José Manuel Nascimento-Costa, MD, PhD, Ana Bela Sarmento-Ribeiro, MD, PhD

Blood (2013) 122 (21): 5156.

https://doi.org/10.1182/blood.V122.21.5156.5156

Published: 2013

Journal Articles

Association of A 313 g Glutathione S-Transferase P1 ( GSTP1 ) Inborn Polymorphism with Susceptibility to De Novo MDS

Sophia Zachaki, Chryssa Stavropoulou, Aggeliki Daraki, Marina Kalomoiraki, Panagoula Kollia, Vassiliki Aleporou, Gabriel Pantelias, Emmanuel Kanavakis, Constantina Sambani

Blood (2012) 120 (21): 1445.

https://doi.org/10.1182/blood.V120.21.1445.1445

Published: 2012

Journal Articles

Analysis of TP53 Codon72, and p21 Codon31 Polymorphisms in CLL Patients Exposed to Ionizing Radiation Due to the Chernobyl NPP Accident

Nadiia Bilous, Iryna Abramenko, Anatoliy Chumak, Zoya Martina, Iryna Kryachok, Iryna Filonenko

Blood (2012) 120 (21): 4580.

https://doi.org/10.1182/blood.V120.21.4580.4580

Published: 2012

Journal Articles

Evidence for Allelic Exclusion of p53 within Single Sorted Human B Cells

Shabirul Haque, Ph.D., Jennifer Nieto, Hyunjoo Lee, Nicholas Chiorazzi, M.D., Patricia Mongini, Ph.D.

Blood (2011) 118 (21): 1122.

https://doi.org/10.1182/blood.V118.21.1122.1122

Published: 2011

Journal Articles

Incidence of the JAK2 V617F Mutation In Mexican Patients with Myeloproliferative Neoplasms (MPNs)

Gregorio Ignacio, MD, Rosa María Arana-Trejo, MD, Verónica Gónzalez, QFB, Maria Paula Hérnandez, MD, Yolanda Lugo, Dr, Luis Solis, Dr, Jesús Castellanos, Dr, Samuel Celestino, Dr, Carlos Váldez, Dr, Ramón Rivas, Dr

Blood (2011) 118 (21): 5180.

https://doi.org/10.1182/blood.V118.21.5180.5180

Published: 2011

Journal Articles

Correlation of Fc Gamma RIIA Polymorphisms with EBV-Positivity and LMP1 Expression in Patients with Low Grade B-Cell Lymphomas

Panagiotis Theodorou Diamantopoulos, Vassiliki Kalotychou, Athanassios Galanopoulos, Nikolaos Spanakis, Katerina Polonyfi, Georgia Diamantopoulou, Efthymia Bazanis, Marina Siakantaris, M.D., Theodoros Vassilakopoulos, Maria K. Angelopoulou, Eleni Variami, Nikolaos Anagnostopoulos, Ioannis Rombos, Konstantinos Konstantopoulos, Panagoula Kollia, Gerasimos Pangalis, John Meletis, Nora-Athina Viniou

Blood (2011) 118 (21): 1600.

https://doi.org/10.1182/blood.V118.21.1600.1600

Published: 2011

Journal Articles

TH17 CD4+ CELLS Disappear FROM BLOOD at the Onset of aGVHD

Andrzej Lange, MD, Antonina Lach, Wojtowicz Agnieszka, Daria Drabczak-Skrzypek, Dlubek Dorota

Blood (2010) 116 (21): 2307.

https://doi.org/10.1182/blood.V116.21.2307.2307

Published: 2010

Journal Articles

Novel Kel null Allele Detected In a Brazilian Woman with the Kell Null Phenotype.

Edmir Boturão-Neto, MD, PhD, Mihoko Yamamoto, MD, PhD, Akemi Kuroda Chiba, MSc, Elisa Yuriko Sugano Kimura, Maria do Carmo V. C. Oliveira, MSc, José Orlando Bordin, MD, PhD

Blood (2010) 116 (21): 1111.

https://doi.org/10.1182/blood.V116.21.1111.1111

Published: 2010

Journal Articles

Genetic Variations in Heparanase Gene (HPSE) Are Associated with Increased Risk of Graft Vs. Host Disease Following Allogeneic Hematopoietic Stem Cell Transplantation: Effect of Discrepancy Between Recipient and Donor.

Olga Ostrovsky, Avichai Shimoni, Israel Vlodavsky, Arnon Nagler

Blood (2009) 114 (22): 3556.

https://doi.org/10.1182/blood.V114.22.3556.3556

Published: 2009

Journal Articles

Defining the Molecular Mechanisms Responsible for the ABO High Expresser Phenotype.

Diarmaid O Donghaile, MD, Vince P Jenkins, PhD, Rachel McGrath, BSc, Lisa Preston, MSc, Roger JS Preston, PhD, William G Murphy, James S O'Donnell, MD, PhD

Blood (2009) 114 (22): 2119.

https://doi.org/10.1182/blood.V114.22.2119.2119

Published: 2009

Journal Articles

The Importance of Pharmacogenomic Variations in the Treatment of Children with Acute Lymphoblastic Leukemia

Chung-Yi Hu, Sheng-Kai Chang, Yung-Li Yang, Shu-Wha Lin, Rong-Jing Chiu, Kai-Hsin Lin, Shiann-Tarng Jou, Meng- Yao Lu, Hsiu-Hao Chang, Kuo-Sin Lin, Dong-Tsamn Lin

Blood (2008) 112 (11): 4847.

https://doi.org/10.1182/blood.V112.11.4847.4847

Published: 2008

Journal Articles

Molecular Events of T-Cell Lymphoblastic Leukemia in Early Childhood

Marcela Braga Mansur, Msc, Mariana Emerenciano, Msc, Lilian Brewer, Kátia Cristina da Cruz Machado Candian, Maria S. Pombo-de-Oliveira, MD, PhD

Blood (2008) 112 (11): 4874.

https://doi.org/10.1182/blood.V112.11.4874.4874

Published: 2008

Journal Articles

Megakaryocytes and Functional Platelets Obtained from Human Subcutaneous Adipocytes in an In Vitro Differentiation System.

Emi Saito, Yumiko Matsubara, PhD, Hidenori Suzuki, PhD, Yasuo Ikeda, MD, Mitsuru Murata, MD

Blood (2007) 110 (11): 3702.

https://doi.org/10.1182/blood.V110.11.3702.3702

Published: 2007

Journal Articles

Primary Graft Failure (GF) after Unrelated Donor Cord Blood Transplants (UCBT): Risk Factors and Management.

Ka Wah Chan, MD, Michael S. Grimley, M.D., Candace Taylor, C.R.A., Donna A. Wall, M.D.

Blood (2006) 108 (11): 44.

https://doi.org/10.1182/blood.V108.11.44.44

Published: 2006

Journal Articles

Use of CSGE, TspRI- RFLP and Western Blot in Carrier Detection in an Indian Family with Type I Glanzmann Thrombasthenia.

Meganathan Kannan, MSc, Firdos Ahmad, M Sc, Rajive Kumar, M D, Ved P. Choudhry, M D, Renu Saxena, M D

Blood (2006) 108 (11): 3975.

https://doi.org/10.1182/blood.V108.11.3975.3975

Published: 2006

Journal Articles

Different Patterns of Cooperating Mutations between De Novo AML Patients with MLL -Partial Tandem Duplication and MLL Translocations.

Lee-Yung Shih, MD, Der-Cherng Liang, MD, Chein-Fuang Huang, PhD, Ya-Tzu Chang, MS, Yu-Shu Shih, MS, Tung-Huei Lin, MS, Huei-Ying Li, MS, Chang-Liang Lai, BS, Tung-Liang Lin, MD, Ming-Chung Kuo, MD

Blood (2006) 108 (11): 2363.

https://doi.org/10.1182/blood.V108.11.2363.2363

Published: 2006

Journal Articles

Efficacy of Performing a Second Non-Myeloablative Allogenic Stem Cell Transplant.

Brian J. Byrne, MD, Joseph H. Antin, MD, Edwin P. Alyea, MD, Nelson J. Choa, MD, David A. Rizzieri, MD

Blood (2005) 106 (11): 3664.

https://doi.org/10.1182/blood.V106.11.3664.3664

Published: 2005

NARROW

CLL in India May Have a Different Biology from That in the West

Frequency of a Highly Polymorphic Variant, S36N GFI1 , Is Increased in CML Patients

Fast Detection Of MYD88 -L265P Mutation By PCR-RFLP In Chronic Lymphoproliferative Disorders

Can Polymorphisms In Oxidative Stress Related Genes Be a Risk Factor For CML?

Association of A 313 g Glutathione S-Transferase P1 ( GSTP1 ) Inborn Polymorphism with Susceptibility to De Novo MDS

Analysis of TP53 Codon72, and p21 Codon31 Polymorphisms in CLL Patients Exposed to Ionizing Radiation Due to the Chernobyl NPP Accident

Evidence for Allelic Exclusion of p53 within Single Sorted Human B Cells

Incidence of the JAK2 V617F Mutation In Mexican Patients with Myeloproliferative Neoplasms (MPNs)

Correlation of Fc Gamma RIIA Polymorphisms with EBV-Positivity and LMP1 Expression in Patients with Low Grade B-Cell Lymphomas

TH17 CD4+ CELLS Disappear FROM BLOOD at the Onset of aGVHD

Novel Kel null Allele Detected In a Brazilian Woman with the Kell Null Phenotype.

Genetic Variations in Heparanase Gene (HPSE) Are Associated with Increased Risk of Graft Vs. Host Disease Following Allogeneic Hematopoietic Stem Cell Transplantation: Effect of Discrepancy Between Recipient and Donor.

Defining the Molecular Mechanisms Responsible for the ABO High Expresser Phenotype.

The Importance of Pharmacogenomic Variations in the Treatment of Children with Acute Lymphoblastic Leukemia

Molecular Events of T-Cell Lymphoblastic Leukemia in Early Childhood

Megakaryocytes and Functional Platelets Obtained from Human Subcutaneous Adipocytes in an In Vitro Differentiation System.

Primary Graft Failure (GF) after Unrelated Donor Cord Blood Transplants (UCBT): Risk Factors and Management.

Use of CSGE, TspRI- RFLP and Western Blot in Carrier Detection in an Indian Family with Type I Glanzmann Thrombasthenia.

Different Patterns of Cooperating Mutations between De Novo AML Patients with MLL -Partial Tandem Duplication and MLL Translocations.

Efficacy of Performing a Second Non-Myeloablative Allogenic Stem Cell Transplant.

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American Society of Hematology

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American Society of Hematology

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