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Journal Articles

Phenotypes of Hb Okayama Mutation

Rudra Ray, PhD MSc, Ankita Biswas, Msc, Sunistha Bhattacharjee, Msc, Maitreyee Bhattacharyya, DM

Blood (2018) 132 (Supplement 1): 4898.

https://doi.org/10.1182/blood-2018-99-118079

Published: 2018

Journal Articles

Identification of a new VHL exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau disease

Marion Lenglet, Florence Robriquet, Klaus Schwarz, Carme Camps, Anne Couturier, David Hoogewijs, Alexandre Buffet, Samantha J. L. Knight, Sophie Gad, Sophie Couvé, Franck Chesnel, Mathilde Pacault, Pierre Lindenbaum, Sylvie Job, Solenne Dumont, Thomas Besnard, Marine Cornec, Helene Dreau, Melissa Pentony, Erika Kvikstad, Sophie Deveaux, Nelly Burnichon, Sophie Ferlicot, Mathias Vilaine, Jean-Michaël Mazzella, Fabrice Airaud, Céline Garrec, Laurence Heidet, Sabine Irtan, Elpis Mantadakis, Karim Bouchireb, Klaus-Michael Debatin, Richard Redon, Stéphane Bezieau, Brigitte Bressac-de Paillerets, Bin Tean Teh, François Girodon, Maria-Luigia Randi, Maria Caterina Putti, Vincent Bours, Richard Van Wijk, Joachim R. Göthert, Antonis Kattamis, Nicolas Janin, Celeste Bento, Jenny C. Taylor, Yannick Arlot-Bonnemains, Stéphane Richard, Anne-Paule Gimenez-Roqueplo, Holger Cario, Betty Gardie

Blood (2018) 132 (5): 469–483.

https://doi.org/10.1182/blood-2018-03-838235

Published: 2018

Includes: Supplemental data

Journal Articles

Systematic Assessment of GATA2 Genetic Variation Reveals the Presence of Novel Disease-Causing Synonymous Exonic Mutations

Blood (2017) 130 (Supplement 1): 2449.

https://doi.org/10.1182/blood.V130.Suppl_1.2449.2449

Published: 2017

Journal Articles

Structural and Functional Characterization of a Codon Optimized Coagulation Factor VIII

Svetlana A Shestopal, PhD, James H Kurasawa, MS, Jian-Jiang Hao, PhD, Elena Karnaukhova, PhD, Yideng Liang, PhD, Min Lin, PhD, Mikhail V Ovanesov, PhD, Timothy K Lee, PhD, John H McVey, PhD, Andrey G Sarafanov, PhD

Blood (2016) 128 (22): 3765.

https://doi.org/10.1182/blood.V128.22.3765.3765

Published: 2016

Journal Articles

Intron retention resulting from a silent mutation in the VWF gene that structurally influences the 5′ splice site

Hamideh Yadegari, Arijit Biswas, Mohammad Suhail Akhter, Julia Driesen, Vytautas Ivaskevicius, Natascha Marquardt, Johannes Oldenburg

Blood (2016) 128 (17): 2144–2152.

https://doi.org/10.1182/blood-2016-02-699686

Published: 2016

Includes: Supplemental data

Journal Articles

Generation of Cell Lines Harboring SETBP1 Mutations By the Crispr/Cas9 System

Nozomu Kawashima, MD, Yusuke Okuno, MD PhD, Yuko Sekiya, MD, Xinan Wang, Yinyan Xu, PhD, Atsushi Narita, MD, Sayoko Doisaki, MD, Michi Kamei, MD, Hideki Muramatsu, MD PhD, Masahiro Irie, MD PhD, Asahito Hama, MD PhD, Yoshiyuki Takahashi, MD, PhD, Seiji Kojima, MD PhD

Blood (2014) 124 (21): 4622.

https://doi.org/10.1182/blood.V124.21.4622.4622

Published: 2014

Journal Articles

Peroxiredoxin 6 (Prdx6) Is Associated with Changes in Autophagy in Myeloid and Non-Myeloid Cells

Michael Ellison, PhD, Gail Thurman, BA, Daniel R. Ambruso, MD

Blood (2014) 124 (21): 1407.

https://doi.org/10.1182/blood.V124.21.1407.1407

Published: 2014

Journal Articles

Prevalence and Clinical Impacts Of SETBP1 Mutation In East Asian Patients With MDS/MPN

Hyun-Woo Choi, MD, Hye-Ran Kim, PhD, Hwan-Young Kim, Ju-Heon Park, MD, Jae-Sook Ahn, Duck Cho, MD, PhD, Seung-Jung Kee, MD, PhD, Soo-Hyun Kim, MD, PhD, Jong-Hee Shin, MD, PhD, Soon-Pal Suh, MD, PhD, Dong-Wook Ryang, MD, PhD, Myung-Geun Shin, MD, PhD

Blood (2013) 122 (21): 2629.

https://doi.org/10.1182/blood.V122.21.2629.2629

Published: 2013

Journal Articles

Absence Of Mutation In Cereblon (CRBN) and DNA Damage Binding Protein 1 (DDB1) Genes In Myeloma Cells and Patients and Its Clinical Significance

Anjan Thakurta, PhD, Anita K Gandhi, PhD, Michelle Waldman, MS, Chad C. Bjorklund, Ph.D., Suzanne Lentzsch, MD, PhD, Stephen A Schey, MD, Yolanda Calle, PhD, Rajani Chelliah, BSc, MSc, Robert Z. Orlowski, M.D., Ph.D, Anup Madan, PhD, Yuhong Ning, Derek Mendy, B.S., Antonia Lopez-Girona, PhD, Peter H Schafer, PhD, Herve Avet-Loiseau, MD, Rajesh Chopra, MD

Blood (2013) 122 (21): 3139.

https://doi.org/10.1182/blood.V122.21.3139.3139

Published: 2013

Journal Articles

Single and Codon-Optimized Synonymous Mutations in Factor IX Alter Protein Properties

Sandra C. Tseng, Nobuko H. Katagiri, Ph.D., Vijaya L. Simhadri, Ph.D., Sujata Jha, M.S., Nathan C. Edwards, David B. Kopelman, Zuben E. Sauna, Ph.D., Michael Z. Stern, Ph.D., Ran Zichel, Ph.D., Anton A. Komar, Ph.D., Chava Kimchi-Sarfaty, Ph.D.

Blood (2011) 118 (21): 1185.

https://doi.org/10.1182/blood.V118.21.1185.1185

Published: 2011

Journal Articles

Chronic Lymphocytic Leukemia Patients with IGHV Genes Carrying Only Silent Mutations Have A Longer Time From Diagnosis to Initial Therapy Than Patients Expressing B-Cell Receptors with No Somatic Mutations

Matthew Kaufman, MD, Xiao J. Yan, MD, PhD, Emanuela M. Ghia, PhD, Donna Neuberg, ScD, Laura Z. Rassenti, Ph.D., Kostas Stamatopoulos, MD, Paolo Ghia, MD, PhD, David G Oscier, MD, Frederic Davi, MD, PhD, Richard Rosenquist, MD, PhD, Chrysoula Belessi, MD, Zadie Davis, PhD, Andreas Agathangelidis, Neil Kay, MD, John C. Byrd, MD, Jennifer R Brown, MD, PhD, Kanti R. Rai, M.D., Thomas J. Kipps, M.D., Ph.D, Nicholas Chiorazzi, M.D.

Blood (2011) 118 (21): 288.

https://doi.org/10.1182/blood.V118.21.288.288

Published: 2011

Journal Articles

Knockdown of N-cadherin suppresses the long-term engraftment of hematopoietic stem cells

Kentaro Hosokawa, Fumio Arai, Hiroki Yoshihara, Hiroko Iwasaki, Yuka Nakamura, Yumiko Gomei, Toshio Suda

Blood (2010) 116 (4): 554–563.

https://doi.org/10.1182/blood-2009-05-224857

Published: 2010

Includes: Supplemental data

Journal Articles

High Frequency of C-Terminal Frame-Shift Mutations of RUNX1 Gene in De Novo AML with Partial Tandem Duplication of MLL .

Chein-Fuang Huang, Lee-Yung Shih, Der-Cherng Liang, Sung-Tzu Liang, Jen-Fen Fu, Yu-Shu Shih, Chia-Ling Chang, Jo-Chuan Liu, Wen-Hsin Hsu, Chang-Liang Lai

Blood (2009) 114 (22): 3468.

https://doi.org/10.1182/blood.V114.22.3468.3468

Published: 2009

Journal Articles

Systematic Definition and Evolutionary Analsis of Macrophage Genes: Evidence for Novel Host Defense Genes.

Jennifer J. MacDonald, Angel W. Lee, M.D., Ph.D., David J. States, MD, PhD

Blood (2007) 110 (11): 3856.

https://doi.org/10.1182/blood.V110.11.3856.3856

Published: 2007

Journal Articles

Molecular Analysis of Immunoglobulin Variable Genes in HIV-Related Non-Hodgkin Lymphoma: Implications for Disease Pathogenesis and Histogenesis.

Daniela Capello, PhD, Eva Berra, PhD, Michaela Cerri, PhD, Annunziata Gloghini, PhD, Davide Rossi, MD, Luigi M. Larocca, MD, Antonino Carbone, MD, Gianluca Gaidano, MD, PhD

Blood (2005) 106 (11): 330.

https://doi.org/10.1182/blood.V106.11.330.330

Published: 2005

Journal Articles

Mutational Status of IgV H Genes in B-Cell Chronic Lymphocytic Leukemia (B-CLL) and Prognosis: Percent Mutations or Evaluation of Antigen-Driven Selection?

Valter Gattei, MD, Michele Dal, Bo BSci, Antonella Zucchetto, BSci, Dania Benedetti, BSci, Eva Zaina, Tech, Paola Nanni, Tech, Paolo Sonego, Giovanni Del Poeta, MD, Massimo Degan, BSci, Riccardo Bomben, BSci

Blood (2005) 106 (11): 2106.

https://doi.org/10.1182/blood.V106.11.2106.2106

Published: 2005

Journal Articles

Erratum for vol. 97, p. 2130

Blood (2001) 97 (11): 3678.

https://doi.org/10.1182/blood.V97.11.3678.h8003678_3678_3678

Published: 2001

Journal Articles

De Novo CD5 + Diffuse Large B-Cell Lymphomas Express VH Genes With Somatic Mutation

Masanori Taniguchi, Kouji Oka, Atsunori Hiasa, Motoko Yamaguchi, Toshiyuki Ohno, Kenkichi Kita, Hiroshi Shiku

Blood (1998) 91 (4): 1145–1151.

https://doi.org/10.1182/blood.V91.4.1145

Published: 1998

NARROW

Phenotypes of Hb Okayama Mutation

Identification of a new VHL exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau disease

Systematic Assessment of GATA2 Genetic Variation Reveals the Presence of Novel Disease-Causing Synonymous Exonic Mutations

Structural and Functional Characterization of a Codon Optimized Coagulation Factor VIII

Intron retention resulting from a silent mutation in the VWF gene that structurally influences the 5′ splice site

Generation of Cell Lines Harboring SETBP1 Mutations By the Crispr/Cas9 System

Peroxiredoxin 6 (Prdx6) Is Associated with Changes in Autophagy in Myeloid and Non-Myeloid Cells

Prevalence and Clinical Impacts Of SETBP1 Mutation In East Asian Patients With MDS/MPN

Absence Of Mutation In Cereblon (CRBN) and DNA Damage Binding Protein 1 (DDB1) Genes In Myeloma Cells and Patients and Its Clinical Significance

Single and Codon-Optimized Synonymous Mutations in Factor IX Alter Protein Properties

Chronic Lymphocytic Leukemia Patients with IGHV Genes Carrying Only Silent Mutations Have A Longer Time From Diagnosis to Initial Therapy Than Patients Expressing B-Cell Receptors with No Somatic Mutations

Knockdown of N-cadherin suppresses the long-term engraftment of hematopoietic stem cells

High Frequency of C-Terminal Frame-Shift Mutations of RUNX1 Gene in De Novo AML with Partial Tandem Duplication of MLL .

Systematic Definition and Evolutionary Analsis of Macrophage Genes: Evidence for Novel Host Defense Genes.

Molecular Analysis of Immunoglobulin Variable Genes in HIV-Related Non-Hodgkin Lymphoma: Implications for Disease Pathogenesis and Histogenesis.

Mutational Status of IgV H Genes in B-Cell Chronic Lymphocytic Leukemia (B-CLL) and Prognosis: Percent Mutations or Evaluation of Antigen-Driven Selection?

Erratum for vol. 97, p. 2130

De Novo CD5 + Diffuse Large B-Cell Lymphomas Express VH Genes With Somatic Mutation

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American Society of Hematology

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American Society of Hematology

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