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CRISPR/Cas9-mediated gene editing in human tripronuclear zygotes

Protein & cell, 2015-05, Vol.6 (5), p.363-372

2015

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Role of Nitric Oxide Carried by Hemoglobin in Cardiovascular Physiology: Developments on a Three-Gas Respiratory Cycle

Circulation research, 2020-01, Vol.126 (1), p.129-158

2020

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Alpha-thalassaemia

Orphanet journal of rare diseases, 2010-05, Vol.5 (1), p.13-13, Article 13

2010

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How we diagnose and manage altered oxygen affinity hemoglobin variants

American journal of hematology, 2019-05, Vol.94 (5), p.597-603

2019

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Post-translational transformation of methionine to aspartate is catalyzed by heme iron and driven by peroxide: a novel subunit-specific mechanism in hemoglobin

The Journal of biological chemistry, 2014-08, Vol.289 (32), p.22342-22357

2014

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Gene Duplication and the Evolution of Hemoglobin Isoform Differentiation in Birds

The Journal of biological chemistry, 2012-11, Vol.287 (45), p.37647-37658

2012

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Hb Chapel Hill or Alpha2 74(EF3) Asp>Gly, a mildly unstable variant found in a Chinese family

Hematology (Luxembourg), 2023-12, Vol.28 (1), p.2187154-2187154

2023

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Clinical impact of glycated albumin as another glycemic control marker

Endocrine Journal, 2010, Vol.57(9), pp.751-762

2010

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Heterogeneity between Two α Subunits of α 2 β 2 Human Hemoglobin and O 2 Binding Properties: Raman, 1 H Nuclear Magnetic Resonance, and Terahertz Spectra

Biochemistry (Easton), 2017-11, Vol.56 (46), p.6125-6136

2017

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Hemoglobin beta Kanagawa [c.443A>C; p.(Ter148Serext21)]: A novel β‐globin gene mutation causing dominantly inherited β‐thalassemia

Pediatric blood & cancer, 2019-09, Vol.66 (9), p.e27871-n/a

2019

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Potential new approaches to the management of the Hb Bart's hydrops fetalis syndrome: the most severe form of α-thalassemia

Hematology, 2018-11, Vol.2018 (1), p.353-360

2018

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Hemoglobin(βC93A)-Albumin Cluster: Mutation of Cysteine-β93 to Alanine Allows Moderate Reduction of O 2 Affinity by Inositol Hexaphosphate

Chembiochem : a European journal of chemical biology, 2019-07, Vol.20 (13), p.1684-1687

2019

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Mozhaisk haemoglobin variant effects on leukocyte differential channel using the Sysmex XN series

Clinical chemistry and laboratory medicine, 2019-11, Vol.57 (12), p.e324-e327

2019

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Severe thalassemia syndrome caused by Hemoglobin Pak Num Po AEBart’s disease: A hematological, molecular, and diagnostic aspects

International journal of laboratory hematology, 2020-08, Vol.42 (4), p.e173-e176

2020

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Hemoglobin Kirklareli (α H58L), a New Variant Associated with Iron Deficiency and Increased CO Binding

The Journal of biological chemistry, 2017-02, Vol.292 (6), p.2542-2555

2017

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Peripheral blood smear and hemoglobin electrophoresis of unsuspected hemoglobin Bart's hydrops fetalis in a newborn

International journal of laboratory hematology, 2022-02, Vol.44 (1), p.53-54

2022

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Gel filtration of dilute human embryonic hemoglobins reveals basis for their increased oxygen binding

Analytical biochemistry, 2017-02, Vol.519, p.38-41

2017

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Fetal Cardiac Cellular Damage Caused by Anemia in Utero in Hb Bart's Disease

Current molecular medicine, 2021-01, Vol.21 (2), p.165-175

2021

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Optimizing chronic transfusion therapy for survivors of hemoglobin Barts hydrops fetalis

Blood, 2016-03, Vol.127 (9), p.1208-1211

2016

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CRISPR/Cas9 gene correction of HbH-CS thalassemia-induced pluripotent stem cells

Annals of hematology, 2019-12, Vol.98 (12), p.2661-2671

2019

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Effect of Mutations on mRNA and Globin Stability: The Cases of Hb Bernalda/Groene Hart and Hb Southern Italy

Genes, 2020-07, Vol.11 (8), p.870

2020

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Outcomes of haemoglobin Bart's hydrops fetalis following intrauterine transfusion in Ontario, Canada

Archives of disease in childhood. Fetal and neonatal edition, 2021-01, Vol.106 (1), p.51-56

2021

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High oxygen affinity hemoglobins

La revue de medecine interne, 2017-02, Vol.38 (2), p.106-112

Mangin, O.

2017

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Hemoglobinopathy testing: the significance of accuracy and pitfalls in HbA 2 determination

International journal of laboratory hematology, 2017-02, Vol.39 (1), p.e23

2017

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Glycation rate of haemoglobins S, C, D, E, J and G, and analytical interference on the measurement of HbA1c with affinity chromatography and capillary electrophoresis

Clinical chemistry and laboratory medicine, 2015-08, Vol.53 (9), p.e207

2015

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CRISPR/Cas9-mediated gene editing in human tripronuclear zygotes

Role of Nitric Oxide Carried by Hemoglobin in Cardiovascular Physiology: Developments on a Three-Gas Respiratory Cycle

Alpha-thalassaemia

How we diagnose and manage altered oxygen affinity hemoglobin variants

Post-translational transformation of methionine to aspartate is catalyzed by heme iron and driven by peroxide: a novel subunit-specific mechanism in hemoglobin

Gene Duplication and the Evolution of Hemoglobin Isoform Differentiation in Birds

Hb Chapel Hill or Alpha2 74(EF3) Asp>Gly, a mildly unstable variant found in a Chinese family

Clinical impact of glycated albumin as another glycemic control marker

Heterogeneity between Two α Subunits of α 2 β 2 Human Hemoglobin and O 2 Binding Properties: Raman, 1 H Nuclear Magnetic Resonance, and Terahertz Spectra

Hemoglobin beta Kanagawa [c.443A>C; p.(Ter148Serext21)]: A novel β‐globin gene mutation causing dominantly inherited β‐thalassemia

Potential new approaches to the management of the Hb Bart's hydrops fetalis syndrome: the most severe form of α-thalassemia

Hemoglobin(βC93A)-Albumin Cluster: Mutation of Cysteine-β93 to Alanine Allows Moderate Reduction of O 2 Affinity by Inositol Hexaphosphate

Mozhaisk haemoglobin variant effects on leukocyte differential channel using the Sysmex XN series

Severe thalassemia syndrome caused by Hemoglobin Pak Num Po AEBart’s disease: A hematological, molecular, and diagnostic aspects

Hemoglobin Kirklareli (α H58L), a New Variant Associated with Iron Deficiency and Increased CO Binding

Peripheral blood smear and hemoglobin electrophoresis of unsuspected hemoglobin Bart's hydrops fetalis in a newborn

Gel filtration of dilute human embryonic hemoglobins reveals basis for their increased oxygen binding

Fetal Cardiac Cellular Damage Caused by Anemia in Utero in Hb Bart's Disease

Optimizing chronic transfusion therapy for survivors of hemoglobin Barts hydrops fetalis

CRISPR/Cas9 gene correction of HbH-CS thalassemia-induced pluripotent stem cells

Effect of Mutations on mRNA and Globin Stability: The Cases of Hb Bernalda/Groene Hart and Hb Southern Italy

Outcomes of haemoglobin Bart's hydrops fetalis following intrauterine transfusion in Ontario, Canada

High oxygen affinity hemoglobins

Hemoglobinopathy testing: the significance of accuracy and pitfalls in HbA 2 determination

Glycation rate of haemoglobins S, C, D, E, J and G, and analytical interference on the measurement of HbA1c with affinity chromatography and capillary electrophoresis

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