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Introduction to the Thalassemia Syndromes: Molecular Medicine's Index Case

Hematology/oncology clinics of North America, 2023-04, Vol.37 (2), p.245-259

Benz, Jr, Edward J

2023

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Molecular and phenotype characterization of an elongated β‐globin variant produced by HBB:C.313delA

International journal of laboratory hematology, 2021-12, Vol.43 (6), p.1620-1627

2021

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Laboratory diagnosis of thalassemia

International journal of laboratory hematology, 2016-05, Vol.38 (S1), p.32-40

2016

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Beta‐thalassemia and the advent of new interventions beyond transfusion and iron chelation

British journal of clinical pharmacology, 2022-08, Vol.88 (8), p.3610-3626

2022

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The α-globin chain of hemoglobin potentiates tissue plasminogen activator induced hyperfibrinolysis in vitro

The journal of trauma and acute care surgery, 2022-01, Vol.92 (1), p.159-166

2022

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Hemoglobin β-Globin Variants In Hispanic Patients: An Institutional Experience From Dallas, Texas

Hemoglobin, 2023-07, Vol.47 (4), p.167-171

2023

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A New Hemoglobin Variant: Hb Jiujiang [α18(A16)Gly→Cys, HBA2 : c.55G>T]

Hemoglobin, 2021-07, Vol.45 (4), p.254-255

2021

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Mild α-Thalassemia Caused by a Mosaic α-Globin Gene Mutation

Hemoglobin, 2021-03, Vol.45 (2), p.140-141

2021

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Evidence for embryonic haemoglobins from Sparus aurata under normal and hypoxic conditions

Fish physiology and biochemistry, 2019-06, Vol.45 (3), p.943-954

2019

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Hemoglobin Reims—a rare alpha globin chain variant and its interaction with beta thalassemia

Journal of hematopathology, 2022-12, Vol.15 (4), p.265-269

2022

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Reverse Phase-high-performance Liquid Chromatography (RP-HPLC) Analysis of Globin Chains from Human Erythroid Cells

Bio-protocol, 2021-01, Vol.11 (2), p.e3899-e3899

2021

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Reduction and alkylation of proteins in preparation of two-dimensional map analysis: Why, when, and how?

Electrophoresis, 2001-06, Vol.22 (10), p.2046-2057

2001

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Diagnostic challenges posed by a rare alpha globin chain variant Hb Fontainebleau in a pregnant female and its potential effects in her children in view of multiple globin gene defects in her husband

Indian journal of pathology & microbiology, 2019-04, Vol.62 (2), p.323-325

2019

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Imbalanced globin chain synthesis determines erythroid cell pathology in thalassemic mice

Haematologica (Roma), 2009-09, Vol.94 (9), p.1211-1219

2009

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Development of a capillary zone electrophoresis method for rapid determination of human globin chains in α and β-thalassemia subjects

Blood cells, molecules, & diseases, 2015-06, Vol.55 (1), p.62-67

2015

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Relative proteome quantification of alpha, beta, gamma and delta globin chains in early eluting peaks of Bio-Rad variant II ® CE-HPLC of hemoglobin from healthy and beta-thalassemia subjects in Malaysia

Biochemistry and biophysics reports, 2019-07, Vol.18, p.100635-100635, Article 100635

2019

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Approaches for Analysis of Erythroid Cell Parameters and Hemoglobinopathies in Mouse Models

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1698, p.103

2018

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Immunostick Test for Detecting ζ-Globin Chains and Screening of the Southeast Asian α-Thalassemia 1 Deletion

Biological procedures online, 2019-08, Vol.21 (1), p.15-15, Article 15

2019

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The Effect of Mir-451 Upregulation on Erythroid Lineage Differentiation of Murine Embryonic Stem Cells

Cell journal (Yakhteh), 2016-07, Vol.18 (2), p.165-178

2016

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Development of a fluorescence immunochromatographic assay for the detection of zeta globin in the blood of (−−SEA) α-thalassemia carriers

Blood cells, molecules, & diseases, 2012-10, Vol.49 (3-4), p.128-132

2012

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Improvements in phenotype studies of hemoglobin disorders brought by advances in reversed-phase chromatography of globin chains

International journal of laboratory hematology, 2015-04, Vol.37 (2), p.279-286

2015

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Hemoglobin Wayne Trait with Incidental Polycythemia

Annals of clinical and laboratory science, 2017-01, Vol.47 (1), p.96-98

2017

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Detection of Compound Heterozygous Sickle Cell-β + Thalassaemia in a Patient with Extreme Weakness, Mild Jaundice and Moderate Anaemia - A Case Report

Journal of clinical and diagnostic research, 2017-05, Vol.11 (5), p.ED07

2017

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Two New γ Chain Variants: Hb F-Augusta GA [Gγ59(E3)Lys → Arg; HBG2: c.179A > G] and Hb F-Port Royal-II [Aγ125(H3)Glu → Ala; HBG1: c.377A > C]

Hemoglobin, 2014-10, Vol.38 (5), p.376-380

2014

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α/β-Globin mRNA ratio determination by multiplex quantitative real-time reverse transcription-polymerase chain reaction as an indicator of globin gene function

Clinical biochemistry, 2007-12, Vol.40 (18), p.1373-1377

2007

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Introduction to the Thalassemia Syndromes: Molecular Medicine's Index Case

Molecular and phenotype characterization of an elongated β‐globin variant produced by HBB:C.313delA

Laboratory diagnosis of thalassemia

Beta‐thalassemia and the advent of new interventions beyond transfusion and iron chelation

The α-globin chain of hemoglobin potentiates tissue plasminogen activator induced hyperfibrinolysis in vitro

Hemoglobin β-Globin Variants In Hispanic Patients: An Institutional Experience From Dallas, Texas

A New Hemoglobin Variant: Hb Jiujiang [α18(A16)Gly→Cys, HBA2 : c.55G>T]

Mild α-Thalassemia Caused by a Mosaic α-Globin Gene Mutation

Evidence for embryonic haemoglobins from Sparus aurata under normal and hypoxic conditions

Hemoglobin Reims—a rare alpha globin chain variant and its interaction with beta thalassemia

Reverse Phase-high-performance Liquid Chromatography (RP-HPLC) Analysis of Globin Chains from Human Erythroid Cells

Reduction and alkylation of proteins in preparation of two-dimensional map analysis: Why, when, and how?

Diagnostic challenges posed by a rare alpha globin chain variant Hb Fontainebleau in a pregnant female and its potential effects in her children in view of multiple globin gene defects in her husband

Imbalanced globin chain synthesis determines erythroid cell pathology in thalassemic mice

Development of a capillary zone electrophoresis method for rapid determination of human globin chains in α and β-thalassemia subjects

Relative proteome quantification of alpha, beta, gamma and delta globin chains in early eluting peaks of Bio-Rad variant II ® CE-HPLC of hemoglobin from healthy and beta-thalassemia subjects in Malaysia

Approaches for Analysis of Erythroid Cell Parameters and Hemoglobinopathies in Mouse Models

Immunostick Test for Detecting ζ-Globin Chains and Screening of the Southeast Asian α-Thalassemia 1 Deletion

The Effect of Mir-451 Upregulation on Erythroid Lineage Differentiation of Murine Embryonic Stem Cells

Development of a fluorescence immunochromatographic assay for the detection of zeta globin in the blood of (−−SEA) α-thalassemia carriers

Improvements in phenotype studies of hemoglobin disorders brought by advances in reversed-phase chromatography of globin chains

Hemoglobin Wayne Trait with Incidental Polycythemia

Detection of Compound Heterozygous Sickle Cell-β + Thalassaemia in a Patient with Extreme Weakness, Mild Jaundice and Moderate Anaemia - A Case Report

Two New γ Chain Variants: Hb F-Augusta GA [Gγ59(E3)Lys → Arg; HBG2: c.179A > G] and Hb F-Port Royal-II [Aγ125(H3)Glu → Ala; HBG1: c.377A > C]

α/β-Globin mRNA ratio determination by multiplex quantitative real-time reverse transcription-polymerase chain reaction as an indicator of globin gene function

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