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Journal Articles

TFDP3 and DDX53 are Highly Re-Expressed after One Cycle of Azacitidine in Myelodysplastic Syndrome Patients Achieving Complete Response: A Cancer Testis Antigen RNA-Seq Screening

Ana M Hurtado López, Tzu Hua Chen-Liang, Joaquín Panadero, Eduardo José Salido, MD, Victor Beltrán, Begoña Muiña, Noelia Navarro-Villamor, Inés Calabria, Ana Isabel Antón, Francisco José Ortuño, Vicente Vicente, MD PhD, Andres Jerez

Blood (2018) 132 (Supplement 1): 4340.

https://doi.org/10.1182/blood-2018-99-117851

Published: 2018

Journal Articles

Dissecting the Role of Individual Bcl-2 Members in Response and Resistance to Ibrutinib or Venetoclax in CLL

Fabio Brocco, Hanneke ter Burg, Stacey Fernandes, Constantine S. Tam, MBBS, MD FRACP, FRCPA, Francesco Forconi, MD DM, PhD FRCPath, Rachel M Guerra, Gregory Bird, Loren D Walensky, Jennifer R. Brown, MD PhD, Arnon P Kater, Eric Eldering

Blood (2017) 130 (Supplement 1): 262.

https://doi.org/10.1182/blood.V130.Suppl_1.262.262

Published: 2017

Journal Articles

Severe Reduction of Free ADAMTS13, Unbound to Von Willebrand Factor, in Plasma Milieu Is a Unique Feature of HELLP Syndrome

Yoko Yoshida, PhD, Ayami Isonishi, Toshiyuki Sado, MD, PhD, Masaki Hayakawa, MD, Hideo Yagi, MD.PhD, Hiroshi Kobayashi, MD, PhD, Yoshihiro Fujimura, MD, PhD, Masanori Matsumoto, MD.PhD

Blood (2016) 128 (22): 134.

https://doi.org/10.1182/blood.V128.22.134.134

Published: 2016

Journal Articles

Differentially Expressed Protein Patterns in Chronic Lymphocytic Leukemia (CLL) after Thymosin beta4 (Tb4) and Lenalidomide (Len) Treatment: Two-Dimensional Gel Electrophoresis (2DE) Analysis

Sabrina Bossio, Laura De Stefano, Mariavaleria Pellicanò, PhD, Angela Palummo, Francesca Storino, Nadia Caruso, Giovanni Iaquinta, Giovanna Cutrona, PhD, Massimo Gentile, MD, Ernesto Vigna, Anna Grazia Recchia, PhD, Fortunato Morabito, MD, Antonino Neri, MD

Blood (2015) 126 (23): 1729.

https://doi.org/10.1182/blood.V126.23.1729.1729

Published: 2015

Journal Articles

Rapid Simultaneous Detection of Multiple Micro-Ribonucleic Acids By Surface Plasmon Resonance Array in Cell Lysates of Myelodysplastic Syndromes Patients

Jan E. Dyr, professor, Jaroslav Cermak, Hana Vaisocherova, Zdenek Krejcik, Hana Sipova, Marketa Bockova, Ivana Visova, Tomas Springer, Marie Laura Ermini, Leona Chrastinova, Ondrej Pastva, Kristyna Pimkova, Roman Kotlin, Jaromir Novak, Jiri Homola

Blood (2014) 124 (21): 5605.

https://doi.org/10.1182/blood.V124.21.5605.5605

Published: 2014

Journal Articles

Development of 99mTcHYNIC-Tocilizumab as Imaging Agent In Multiple Myeloma

Eloísa Riva, MD, Victoria Calzada, BSc, Eugenia Gutiérrez, Marcelo Fernández, BSc, Natalia Oddone, BSc, María Moreno, PhD, Juan Benech, PhD, José A. Chabalgoity, PhD, Atanasio Pandiella, Sr., MD, PhD, Pablo Cabral, MSc

Blood (2010) 116 (21): 4081.

https://doi.org/10.1182/blood.V116.21.4081.4081

Published: 2010

Journal Articles

AML in Israel: Younger Age at Diagnosis Does Not Improve Prognosis.

Neta Goldschmidt, MD, Sarah Cohen, PhD, Deborah Rund, MD

Blood (2009) 114 (22): 4130.

https://doi.org/10.1182/blood.V114.22.4130.4130

Published: 2009

Journal Articles

MDR1 gene Polymorphisms Are Related to Efflux-Independent P-Glycoprotein Overexpression in Brazilian AML Patients

Marcos Antonio Mauricio Scheiner, Sr., MSc, Pharmacist, Flavia da Cunha Vasconcelos, PhD, Student, Raquel Ciuvalschi Maia, Sr., MD, PhD

Blood (2008) 112 (11): 5049.

https://doi.org/10.1182/blood.V112.11.5049.5049

Published: 2008

Journal Articles

Genetic Evidence That an 11 Amino Acid β-Hairpin Loop in the Cytoplasmic Domain of Band 3 Is Responsible for at Least 50% of Ankyrin Binding in Mouse Erythrocytes.

Nicholas O. Markham, BA, Erin M. Parry, BA, Marko Stefanovic, BS, Patrick G. Gallagher, MD, Philip S. Low, PhD, David M. Bodine, PhD

Blood (2005) 106 (11): 1659.

https://doi.org/10.1182/blood.V106.11.1659.1659

Published: 2005

Journal Articles

Molecular Genetics of Hereditary Prothrombin Deficiency in Indian Patients: Identification of a Novel Ala362→Thr (Prothrombin Vellore 1) Mutation by Conformation Sensitive Gel Electrophoresis.

G Jayandharan, R.V. Shaji, Auro Viswabandhya, Sukesh C. Nair, Joy Mammen, Biju George, Vikram Mathews, Mammen Chandy, Alok Srivastava

Blood (2004) 104 (11): 1037.

https://doi.org/10.1182/blood.V104.11.1037.1037

Published: 2004

Journal Articles

Immunoglobulin Heavy Chain (IgH) Gene Somatic Hypermutation Status Using Homoduplex-Separated RT-PCR Products.

Melissa A. Melan, PhD, Kenneth A. Foon, MD, Stanley M. Marks, MD, Jeffrey A. Kant, MD PhD

Blood (2004) 104 (11): 4813.

https://doi.org/10.1182/blood.V104.11.4813.4813

Published: 2004

Journal Articles

Conversion of the active to latent plasminogen activator inhibitor from human endothelial cells

EG Levin, L Santell

Blood (1987) 70 (4): 1090–1098.

https://doi.org/10.1182/blood.V70.4.1090.1090

Published: 1987

NARROW

TFDP3 and DDX53 are Highly Re-Expressed after One Cycle of Azacitidine in Myelodysplastic Syndrome Patients Achieving Complete Response: A Cancer Testis Antigen RNA-Seq Screening

Dissecting the Role of Individual Bcl-2 Members in Response and Resistance to Ibrutinib or Venetoclax in CLL

Severe Reduction of Free ADAMTS13, Unbound to Von Willebrand Factor, in Plasma Milieu Is a Unique Feature of HELLP Syndrome

Differentially Expressed Protein Patterns in Chronic Lymphocytic Leukemia (CLL) after Thymosin beta4 (Tb4) and Lenalidomide (Len) Treatment: Two-Dimensional Gel Electrophoresis (2DE) Analysis

Rapid Simultaneous Detection of Multiple Micro-Ribonucleic Acids By Surface Plasmon Resonance Array in Cell Lysates of Myelodysplastic Syndromes Patients

Development of 99mTcHYNIC-Tocilizumab as Imaging Agent In Multiple Myeloma

AML in Israel: Younger Age at Diagnosis Does Not Improve Prognosis.

MDR1 gene Polymorphisms Are Related to Efflux-Independent P-Glycoprotein Overexpression in Brazilian AML Patients

Genetic Evidence That an 11 Amino Acid β-Hairpin Loop in the Cytoplasmic Domain of Band 3 Is Responsible for at Least 50% of Ankyrin Binding in Mouse Erythrocytes.

Molecular Genetics of Hereditary Prothrombin Deficiency in Indian Patients: Identification of a Novel Ala362→Thr (Prothrombin Vellore 1) Mutation by Conformation Sensitive Gel Electrophoresis.

Immunoglobulin Heavy Chain (IgH) Gene Somatic Hypermutation Status Using Homoduplex-Separated RT-PCR Products.

Conversion of the active to latent plasminogen activator inhibitor from human endothelial cells

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American Society of Hematology

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American Society of Hematology

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