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Journal Articles

Relationship of Host Genetic Factors with Severe Malaria in Nigerian Children

Olukemi Amodu, PhD, Binal N. Shah, Subulade Ademola, PhD, Bamidele Tayo, PhD, Victor R Gordeuk, MD

Blood (2019) 134 (Supplement_1): 942.

https://doi.org/10.1182/blood-2019-132190

Published: 2019

Journal Articles

Smooth Muscle Cytochrome b5 Reductase 3 Deficiency Accelerates Pulmonary Hypertension Development in Sickle Cell Mice

Katherine Wood, PhD BA, Brittany Durgin, PhD, Heidi M Schmidt, BSE, Scott Hahn, Jeffrey Baust, Tim Bachman, Dario A. Vitturi, PhD, Samit Ghosh, Solomon Fiifi Ofori-Acquah, Ana Mora, MD, Mark T Gladwin, MD, Adam Straub, PhD

Blood (2019) 134 (Supplement_1): 3619.

https://doi.org/10.1182/blood-2019-124159

Published: 2019

Journal Articles

Congenital Methemoglobinemia Under Diagnosed Condition with Variiable Therapeurtic Options

Mohamed A. Yassin, MBBS,MSc,CABM,FACP,MSC, Dina Sameh Soliman, PhD

Blood (2017) 130 (Supplement 1): 4746.

https://doi.org/10.1182/blood.V130.Suppl_1.4746.4746

Published: 2017

Journal Articles

Host Genetic Factors in Glucose-6-Phosphate Dehydrogenase and Cytochrome B5 Reductase 3 Affect the Susceptibility of Developing Severe Malarial Anemia

Binal N. Shah, PhD, Philip E Thuma, N. Scott Reading, PhD, Josef T. Prchal, MD, Victor R. Gordeuk, MD

Blood (2016) 128 (22): 2438.

https://doi.org/10.1182/blood.V128.22.2438.2438

Published: 2016

Journal Articles

A Novel EPO Gene Mutation In a Family With Autosomal Dominant Polycythemia

Felipe R Lorenzo V, PhD, Rebecca Margraf, PhD, Sabina Swierczek, PhD, Kimberly Hickman, Karl Voelkerding, MD, Josef Prchal, MD

Blood (2013) 122 (21): 950.

https://doi.org/10.1182/blood.V122.21.950.950

Published: 2013

Journal Articles

Methemoglobinemia In Rhesus Monkeys Due To M-Hemoglobinopathy

Osheiza Abdulmalik, DVM, MS, Larry Handt, DVM, MS, Martin Safo, PhD, Mary M Patterson, MS, DVM, Ping Wang, Caitlin A Fitzgerald, BS, Urs Giger, PD Dr. med. vet. MS FVH

Blood (2013) 122 (21): 4696.

https://doi.org/10.1182/blood.V122.21.4696.4696

Published: 2013

Journal Articles

Cytochrome B5 Reductase T116S Polymorphism Is Associated with Decreased Risk of Severe Anemia Among Zambian Children with Malaria

Victor R. Gordeuk, MD, Mehdi Nouraie, PhD, Xiaomei Niu, PhD, Jessica Nachel DelBove, Josef T. Prchal, MD

Blood (2010) 116 (21): 4233.

https://doi.org/10.1182/blood.V116.21.4233.4233

Published: 2010

Journal Articles

Cytochrome b5 Reductase T116S Mutation and Hemolysis in Sickle Cell Disease.

Mehdi Nouraie, Noel S. Reading, PhD, Andrew Campbell, Caterina Minniti, M.D., Sohail R Rana, MD, Lori Luchtman-Jones, MD, Craig Sable, Niti Dham, MD, Gregory Ensing, Gregory J Kato, Mark Gladwin, MD, Oswaldo L Castro, MD, Josef T. Prchal, MD, Victor R. Gordeuk, MD

Blood (2009) 114 (22): 903.

https://doi.org/10.1182/blood.V114.22.903.903

Published: 2009

Journal Articles

Type I Methemoglobinemia Caused by the Cytochrome b5 Reductase 806C>T Mutation Is Present in the Indigenous Evenk People of Yakutia.

Tatyana Burtseva, Tatiana Ammosova, PhD, Josef T. Prchal, MD, Vyacheslav Chasnyk, MD, Sergei Nekhai, PhD, Victor R. Gordeuk, MD

Blood (2009) 114 (22): 2588.

https://doi.org/10.1182/blood.V114.22.2588.2588

Published: 2009

Journal Articles

Identification of Two Novel Mutations in the CYB5R3 Gene in Five Cases of Type I Methemoglobinemia

Felipe R. Lorenzo, V, MD, PhD, Roberto H Nussenzveig, PhD, John D Phillips, PhD, Stanley L. Schrier, MD, Josef T. Prchal, MD

Blood (2008) 112 (11): 3854.

https://doi.org/10.1182/blood.V112.11.3854.3854

Published: 2008

Journal Articles

A Novel Heterologous Expression System for Characterization of Individual NADH-Cytochrome b 5 Reductase Variants in Recessive Congenital Methemoglobinemia.

Melanie J. Percy, PhD, L. J. Crowley, PhD, C. A. Davis, PhD, J. Boudreaux, MD, D. M. Layton, MD, M. F. McMullin, MD, T. R. Lappin, PhD, M. J. Barber, DPhil

Blood (2005) 106 (11): 1676.

https://doi.org/10.1182/blood.V106.11.1676.1676

Published: 2005

Journal Articles

The First Indian Mutation of NADH-Cytochrome b5 Reductase as a Cause for Type 1 Methemoglobinemia.

Hima B. Lingam, MD, Roberto H. Nussenveig, PhD, Qiqing Zhu, PhD, Naijie Jing, PhD, Josef T. Prchal, MD

Blood (2005) 106 (11): 1677.

https://doi.org/10.1182/blood.V106.11.1677.1677

Published: 2005

Journal Articles

Heterogeneity of Molecular Biology of Methemoglobinemia; Study of Eight Consecutive Patients.

Jey Maran, M.D., Yongli Guan, Ching-Nan Ou, Ph.D, Josef T. Prchal, M.D.

Blood (2004) 104 (11): 1587.

https://doi.org/10.1182/blood.V104.11.1587.1587

Published: 2004

Journal Articles

Familial idiopathic methemoglobinemia revisited: original cases reveal 2 novel mutations in NADH-cytochrome b5 reductase

Melanie J. Percy, Matthew J. S. Gillespie, Geraldine Savage, Anne E. Hughes, Mary Frances McMullin, Terry R. J. Lappin

Blood (2002) 100 (10): 3447–3449.

https://doi.org/10.1182/blood-2002-05-1405

Published: 2002

Journal Articles

Seven new mutations in the nicotinamide adenine dinucleotide reduced–cytochrome b 5 reductase gene leading to methemoglobinemia type I

Jan Dekker, Michel H. M. Eppink, Rob van Zwieten, Thea de Rijk, Angel F. Remacha, Lap Kay Law, Albert M. Li, Kam Lau Cheung, Willem J. H. van Berkel, Dirk Roos

Blood (2001) 97 (4): 1106–1114.

https://doi.org/10.1182/blood.V97.4.1106

Published: 2001

Journal Articles

Serine-proline replacement at residue 127 of NADH-cytochrome b5 reductase causes hereditary methemoglobinemia, generalized type

Y Kobayashi, Y Fukumaki, T Yubisui, J Inoue, Y Sakaki

Blood (1990) 75 (7): 1408–1413.

https://doi.org/10.1182/blood.V75.7.1408.1408

Published: 1990

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Relationship of Host Genetic Factors with Severe Malaria in Nigerian Children

Smooth Muscle Cytochrome b5 Reductase 3 Deficiency Accelerates Pulmonary Hypertension Development in Sickle Cell Mice

Congenital Methemoglobinemia Under Diagnosed Condition with Variiable Therapeurtic Options

Host Genetic Factors in Glucose-6-Phosphate Dehydrogenase and Cytochrome B5 Reductase 3 Affect the Susceptibility of Developing Severe Malarial Anemia

A Novel EPO Gene Mutation In a Family With Autosomal Dominant Polycythemia

Methemoglobinemia In Rhesus Monkeys Due To M-Hemoglobinopathy

Cytochrome B5 Reductase T116S Polymorphism Is Associated with Decreased Risk of Severe Anemia Among Zambian Children with Malaria

Cytochrome b5 Reductase T116S Mutation and Hemolysis in Sickle Cell Disease.

Type I Methemoglobinemia Caused by the Cytochrome b5 Reductase 806C>T Mutation Is Present in the Indigenous Evenk People of Yakutia.

Identification of Two Novel Mutations in the CYB5R3 Gene in Five Cases of Type I Methemoglobinemia

A Novel Heterologous Expression System for Characterization of Individual NADH-Cytochrome b 5 Reductase Variants in Recessive Congenital Methemoglobinemia.

The First Indian Mutation of NADH-Cytochrome b5 Reductase as a Cause for Type 1 Methemoglobinemia.

Heterogeneity of Molecular Biology of Methemoglobinemia; Study of Eight Consecutive Patients.

Familial idiopathic methemoglobinemia revisited: original cases reveal 2 novel mutations in NADH-cytochrome b5 reductase

Seven new mutations in the nicotinamide adenine dinucleotide reduced–cytochrome b 5 reductase gene leading to methemoglobinemia type I

Serine-proline replacement at residue 127 of NADH-cytochrome b5 reductase causes hereditary methemoglobinemia, generalized type

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