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Journal Articles

Genetics of Monosomy 7 and Del(7q) in MDS Informs Potential Therapeutic Targets

Cassandra M Kerr, MS, Vera Adema, PhD, Wencke Walter, PhD, Stephan Hutter, PhD, Christina A. Snider, BA, Yasunobu Nagata, MD PhD, Manja Meggendorfer, PhD, Claudia Haferlach, MD, Valeria Visconte, PhD, Mikkael A. Sekeres, MD MS, Thomas Laframboise, PhD, Torsten Haferlach, MD, Jaroslaw P. Maciejewski, MD PhD

Blood (2019) 134 (Supplement_1): 1703.

https://doi.org/10.1182/blood-2019-126866

Published: 2019

Journal Articles

GWAS of Osmotic Hemolysis in 12,352 Healthy Blood Donors Identifies Red Cell Genetic Variants Associated with Steady State Hemolysis in Patients with Sickle Cell Disease

Grier Page, PhD BS, MS, Tamir Kanias, PhD, Marion C. Lanteri, PhD, Yuelong Guo, PhD, Alan E. Mast, MDPhD, Richard G. Cable, MD, Bryan R Spencer, MPH, Joseph Kiss, MD, Stacey Endres, MPH, Donald Brambilla, PhD, Seyed Mehdi Nouraie, PhD MD, Victor R. Gordeuk, MD, Steven Kleinman, MD, Mark T Gladwin, MD, Michael Paul Busch, MD PhD

Blood (2017) 130 (Supplement 1): 1117.

https://doi.org/10.1182/blood.V130.Suppl_1.1117.1117

Published: 2017

Journal Articles

Cellular Hydration and Oxidation As Phenotype Modifiers in Sickle Cell Anemia

Mary A Risinger, PhD, Neha Dagaonkar, Georgios E Christakopoulos, MD, Jie Liu, PhD, Katie Giger Seu, PhD, Diamantis G Konstantinidis, BSc, PhD, Charles T Quinn, MD, Satheesh Chonat, MD, Clinton H Joiner, MD PhD, Kejian Zhang, MD, Theodosia A Kalfa, MD PhD

Blood (2016) 128 (22): 2446.

https://doi.org/10.1182/blood.V128.22.2446.2446

Published: 2016

Journal Articles

The Human Kell Blood Group Binds the Erythroid 4.1R Protein: New Insights into the 4.1R-Dependent Red Cell Membrane Complex

Slim Azouzi, Emmanuel Collec, Narla Mohandas, DSc, Xiuli An, MD PhD, Yves Colin Aronovicz, Caroline Le Van Kim

Blood (2015) 126 (23): 3334.

https://doi.org/10.1182/blood.V126.23.3334.3334

Published: 2015

Journal Articles

Mature erythrocyte membrane homeostasis is compromised by loss of the GATA1-FOG1 interaction

Atsushi Hasegawa, Ritsuko Shimizu, Narla Mohandas, Masayuki Yamamoto

Blood (2012) 119 (11): 2615–2623.

https://doi.org/10.1182/blood-2011-09-382473

Published: 2012

Includes: Supplemental data

Journal Articles

A New Case of KLF1 G973A Mutation and Congenital Dyserythropoeitic Anemia (CDA)- Further Definition of Emerging New Syndrome and Possible Association with Gonadal Dysgenesis

Yaddanapudi Ravindranath, MD, Gerald Goyette, BS, Steven Buck, MS, Manisha Gadgeel, MD, Alan Dombkowski, Ph.D, Laurence A. Boxer, MD, Patrick G. Gallagher, MD, Robert M Johnson, Ph.D

Blood (2011) 118 (21): 2101.

https://doi.org/10.1182/blood.V118.21.2101.2101

Published: 2011

Journal Articles

Case Report of Erythroid Transcription Factor EKLF Mutation Causing a Rare Form of Congenital Dyserythropoetic Anemia in a Patient of Taiwanese Origin

W. Beau Mitchell, MD, Merlin Nithya Gnanapragasam, PhD, Julie A Jaffray, MD, James J. Bieker, PhD, Deepa Manwani, MD

Blood (2011) 118 (21): 2154.

https://doi.org/10.1182/blood.V118.21.2154.2154

Published: 2011

Journal Articles

A Novel EKLF Mutation in a Patient with Dyserythropoietic Anemia: The First Association of EKLF with Disease in Man.

Belinda K Singleton, Victoria SS Fairweather, Winnie Lau, Stephen F Parsons, Nicholas M Burton, Jan Frayne, R. Leo Brady, David J Anstee

Blood (2009) 114 (22): 162.

https://doi.org/10.1182/blood.V114.22.162.162

Published: 2009

Journal Articles

The water channel aquaporin-1 partitions into exosomes during reticulocyte maturation: implication for the regulation of cell volume

Lionel Blanc, Jing Liu, Michel Vidal, Joel Anne Chasis, Xiuli An, Narla Mohandas

Blood (2009) 114 (18): 3928–3934.

https://doi.org/10.1182/blood-2009-06-230086

Published: 2009

Includes: Supplemental data

Journal Articles

C1GALT1C1 ( COSMC ) Mutations in Four Individuals with Tn+ Phenotype.

Vanja Karamatic Crew, PhD, Carole Green, FIBMS, Stephen Parsons, PhD, Belinda K. Singleton, PhD, Geoff Daniels, PhD, David J. Anstee, PhD

Blood (2007) 110 (11): 1727.

https://doi.org/10.1182/blood.V110.11.1727.1727

Published: 2007

Journal Articles

Regulators of Erythrocyte Volume as Modifiers in Sickle Cell Disease: The Gardos Channel.

Charles Tian, Maureen Okam, MD, Seth L. Alper, MD PhD, Martin H. Steinberg, MD, Carlo Brugnara, MD, Patrick G. Gallagher, MD

Blood (2007) 110 (11): 3387.

https://doi.org/10.1182/blood.V110.11.3387.3387

Published: 2007

Journal Articles

Genetic Polymorphisms Associated with Priapism in Sickle Cell Disease.

Laine Elliott, BS, Allison E. Ashley-Koch, PhD, Jude Jonassaint, RN, Jennifer Price, BS, Jason Galloway, BS, Kenneth I. Ataga, MBBS, Marc C. Levesque, MD, J. Brice Weinberg, MD, James R. Eckman, MD, Eugene P. Orringer, MD, Jeffery M. Vance, MD, PhD, Marilyn J. Telen, MD

Blood (2006) 108 (11): 789.

https://doi.org/10.1182/blood.V108.11.789.789

Published: 2006

Journal Articles

A Differentiation Block in Erythroid Cells Lacking Erythroid Krupple-Like Factor (EKLF).

Patrick G. Gallagher, MD, Murat O. Arcasoy, MD, Serena E. Vayda, BS, Holly K. Dressman, PhD, James J. Bieker, PhD, David M. Bodine, PhD

Blood (2005) 106 (11): 526.

https://doi.org/10.1182/blood.V106.11.526.526

Published: 2005

Journal Articles

Priapism in SCD: Clinical and Genetic Correlations.

Allison E. Ashley-Koch, PhD, Laura M. De Castro, MD, Felicia Lennon-Graham, MBA, Jude Jonassaint, RN, Terry L. Jackson, BS, Jennifer Price, BS, Jason Galloway, BS, Susan Jones, RN, Eldrida Randall, BS, Charles Packman, MD, Charles Knupp, MD, James R. Eckman, MD, Rupa Redding-Lallinger, MD, Eugene P. Orringer, MD, Jeffery M. Vance, MD, Marilyn J. Telen, MD

Blood (2005) 106 (11): 3174.

https://doi.org/10.1182/blood.V106.11.3174.3174

Published: 2005

Journal Articles

A band 3–based macrocomplex of integral and peripheral proteins in the RBC membrane

Lesley J. Bruce, Roland Beckmann, M. Leticia Ribeiro, Luanne L. Peters, Joel A. Chasis, Jean Delaunay, Narla Mohandas, David J. Anstee, Michael J.A. Tanner

Blood (2003) 101 (10): 4180–4188.

https://doi.org/10.1182/blood-2002-09-2824

Published: 2003

Journal Articles

A Single Mutation Inside the NPA Motif of Aquaporin-1 Found in a Colton-Null Phenotype

Stany Chrétien, Jean Pierre Cartron, Manuel de Figueiredo

Blood (1999) 93 (11): 4021–4023.

https://doi.org/10.1182/blood.V93.11.4021

Published: 1999

NARROW

Genetics of Monosomy 7 and Del(7q) in MDS Informs Potential Therapeutic Targets

GWAS of Osmotic Hemolysis in 12,352 Healthy Blood Donors Identifies Red Cell Genetic Variants Associated with Steady State Hemolysis in Patients with Sickle Cell Disease

Cellular Hydration and Oxidation As Phenotype Modifiers in Sickle Cell Anemia

The Human Kell Blood Group Binds the Erythroid 4.1R Protein: New Insights into the 4.1R-Dependent Red Cell Membrane Complex

Mature erythrocyte membrane homeostasis is compromised by loss of the GATA1-FOG1 interaction

A New Case of KLF1 G973A Mutation and Congenital Dyserythropoeitic Anemia (CDA)- Further Definition of Emerging New Syndrome and Possible Association with Gonadal Dysgenesis

Case Report of Erythroid Transcription Factor EKLF Mutation Causing a Rare Form of Congenital Dyserythropoetic Anemia in a Patient of Taiwanese Origin

A Novel EKLF Mutation in a Patient with Dyserythropoietic Anemia: The First Association of EKLF with Disease in Man.

The water channel aquaporin-1 partitions into exosomes during reticulocyte maturation: implication for the regulation of cell volume

C1GALT1C1 ( COSMC ) Mutations in Four Individuals with Tn+ Phenotype.

Regulators of Erythrocyte Volume as Modifiers in Sickle Cell Disease: The Gardos Channel.

Genetic Polymorphisms Associated with Priapism in Sickle Cell Disease.

A Differentiation Block in Erythroid Cells Lacking Erythroid Krupple-Like Factor (EKLF).

Priapism in SCD: Clinical and Genetic Correlations.

A band 3–based macrocomplex of integral and peripheral proteins in the RBC membrane

A Single Mutation Inside the NPA Motif of Aquaporin-1 Found in a Colton-Null Phenotype

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American Society of Hematology

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American Society of Hematology

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