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IVS-II-16 (G>C) (HBB: c.315+16G>C) or IVS-II-666 (C>T) (HBB: c.316-185C>T) Mutations Trigger an Hb S (HBB: c.20A>T)/β+-Thalassemia Phenotype in an Hb S Trait Patient

Hemoglobin, 2021-07, Vol.45 (4), p.225-227

2021

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Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India

Hemoglobin, 2019-03, Vol.43 (2), p.132-136

2019

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The Spectrum of β-Thalassemia Mutations in a Population from the Brazilian Amazon

Hemoglobin, 2016-01, Vol.40 (1), p.20-24

2016

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Sickle Cell Disease in the Kurdish Population of Northern Iraq

Hemoglobin, 2012-08, Vol.36 (4), p.333-342

2012

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Hb S/β-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics

Hemoglobin, 2020-01, Vol.44 (1), p.1-9

2020

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Can ketones compensate for deteriorating brain glucose uptake during aging? Implications for the risk and treatment of Alzheimer's disease

Annals of the New York Academy of Sciences, 2016-03, Vol.1367 (1), p.12-20

2016

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A ketogenic diet improves vascular hyperpermeability in type 2 diabetic mice by downregulating vascular pescadillo1 expression

Journal of cellular and molecular medicine, 2023-05, Vol.27 (10), p.1410-1422

2023

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Heterogeneity of βs gene haplotypes in patients with sickle cell disease (SCD) in Oman: A review of relevant publications

Acta bio-medica de l'Ateneo Parmense, 2022-08, Vol.93 (4)

2022

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The Prevalence of HBB Mutations among the Transfusion-Dependent and Non Transfusion-Dependent Hb E/β-Thalassemia Children in a Tertiary Center of West Bengal, India

Hemoglobin, 2021-05, Vol.45 (3), p.157-162

2021

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Transcriptional regulation of Hb‐α and Hb‐β through nuclear factor E2‐related factor‐2 (Nrf2) activation in human vaginal cells: A novel mechanism of cellular adaptability to oxidative stress

American journal of reproductive immunology (1989), 2017-06, Vol.77 (6), p.n/a

2017

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The Effect of Blood Transfusion on Growth of Patients with Hb E/β-Thalassemia

Hemoglobin, 2019-09, Vol.43 (4-5), p.264-272

2019

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Population Screening and Prevention Strategies for Thalassemias and other Hemoglobinopathies of Eastern India: Experience of 18,166 cases

Hemoglobin, 2015-11, Vol.39 (6), p.384-388

2015

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mTORC1 activation is not sufficient to suppress hepatic PPARα signaling or ketogenesis

The Journal of biological chemistry, 2021-07, Vol.297 (1), p.100884-100884, Article 100884

2021

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Hb E-β-Thalassemia in Five Indian States

Hemoglobin, 2016-09, Vol.40 (5), p.310-315

2016

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β-hydroxybutyrate impairs bovine oocyte maturation via pyruvate dehydrogenase (PDH) associated energy metabolism abnormality

Frontiers in pharmacology, 2023-08, Vol.14, p.1243243-1243243

2023

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The Effect of Nonsense Mediated Decay on Transcriptional Activity Within the Novel β-Thalassemia Mutation HBB: c.129delT

Hemoglobin, 2015-01, Vol.39 (5), p.334-339

2015

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Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region

Haematologica (Roma), 2015-05, Vol.100 (5), p.e166

2015

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Mutation Spectrum of β-Thalassemia and Other Hemoglobinopathies in Chittagong, Southeast Bangladesh

Hemoglobin, 2015-11, Vol.39 (6), p.389-392

2015

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β-hydroxybutyrate (β-HB) exerts anti-inflammatory and antioxidant effects in lipopolysaccharide (LPS)-stimulated macrophages in Liza haematocheila

Fish & shellfish immunology, 2020-12, Vol.107 (Pt B), p.444-451

2020

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Hemosiderosis causing liver cirrhosis in a patient with Hb S/beta thalassemia and no other known causes of hepatic disease

Hippokratia, 2017-01, Vol.21 (1), p.43-45

2017

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Clinical and Molecular Characteristics of Non-Transfusion-Dependent Thalassemia in Kuwait

Hemoglobin, 2015-09, Vol.39 (5), p.320-326

2015

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Molecular Characterization of a β-Thalassemia Intermedia Patient Presenting Inferior Vena Cava Thrombosis: Interaction of the β-Globin Erythroid Krüppel-Like Factor Binding Site Mutation with Hb E and α+-Thalassemia

Hemoglobin, 2014-12, Vol.38 (6), p.451-453

2014

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Optimizing the Dose of Hydroxyurea Therapy for Patients with β-Thalassemia Intermedia (Hb E-β-thalassemia): A Single Center Study from Eastern India

Hemoglobin, 2014-01, Vol.38 (1), p.44-48

2014

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Ketogenic diet ameliorates lipid dysregulation in type 2 diabetic mice by downregulating hepatic pescadillo 1

Molecular medicine (Cambridge, Mass.), 2022-01, Vol.28 (1), p.1-1, Article 1

2022

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Haemoglobin s interaction with Beta thalassaemia- a case report from assam, India

Journal of clinical and diagnostic research, 2014-09, Vol.8 (9), p.FD15-FD16

2014

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IVS-II-16 (G>C) (HBB: c.315+16G>C) or IVS-II-666 (C>T) (HBB: c.316-185C>T) Mutations Trigger an Hb S (HBB: c.20A>T)/β+-Thalassemia Phenotype in an Hb S Trait Patient

Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India

The Spectrum of β-Thalassemia Mutations in a Population from the Brazilian Amazon

Sickle Cell Disease in the Kurdish Population of Northern Iraq

Hb S/β-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics

Can ketones compensate for deteriorating brain glucose uptake during aging? Implications for the risk and treatment of Alzheimer's disease

A ketogenic diet improves vascular hyperpermeability in type 2 diabetic mice by downregulating vascular pescadillo1 expression

Heterogeneity of βs gene haplotypes in patients with sickle cell disease (SCD) in Oman: A review of relevant publications

The Prevalence of HBB Mutations among the Transfusion-Dependent and Non Transfusion-Dependent Hb E/β-Thalassemia Children in a Tertiary Center of West Bengal, India

Transcriptional regulation of Hb‐α and Hb‐β through nuclear factor E2‐related factor‐2 (Nrf2) activation in human vaginal cells: A novel mechanism of cellular adaptability to oxidative stress

The Effect of Blood Transfusion on Growth of Patients with Hb E/β-Thalassemia

Population Screening and Prevention Strategies for Thalassemias and other Hemoglobinopathies of Eastern India: Experience of 18,166 cases

mTORC1 activation is not sufficient to suppress hepatic PPARα signaling or ketogenesis

Hb E-β-Thalassemia in Five Indian States

β-hydroxybutyrate impairs bovine oocyte maturation via pyruvate dehydrogenase (PDH) associated energy metabolism abnormality

The Effect of Nonsense Mediated Decay on Transcriptional Activity Within the Novel β-Thalassemia Mutation HBB: c.129delT

Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region

Mutation Spectrum of β-Thalassemia and Other Hemoglobinopathies in Chittagong, Southeast Bangladesh

β-hydroxybutyrate (β-HB) exerts anti-inflammatory and antioxidant effects in lipopolysaccharide (LPS)-stimulated macrophages in Liza haematocheila

Hemosiderosis causing liver cirrhosis in a patient with Hb S/beta thalassemia and no other known causes of hepatic disease

Clinical and Molecular Characteristics of Non-Transfusion-Dependent Thalassemia in Kuwait

Molecular Characterization of a β-Thalassemia Intermedia Patient Presenting Inferior Vena Cava Thrombosis: Interaction of the β-Globin Erythroid Krüppel-Like Factor Binding Site Mutation with Hb E and α+-Thalassemia

Optimizing the Dose of Hydroxyurea Therapy for Patients with β-Thalassemia Intermedia (Hb E-β-thalassemia): A Single Center Study from Eastern India

Ketogenic diet ameliorates lipid dysregulation in type 2 diabetic mice by downregulating hepatic pescadillo 1

Haemoglobin s interaction with Beta thalassaemia- a case report from assam, India

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