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Complex Interactions in Regulation of Haematopoiesis-An Unexplored Iron Mine

Genes, 2021-08, Vol.12 (8), p.1270

2021

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Molecular insights into placental iron transfer mechanisms and maternofetal regulation

Archives of gynecology and obstetrics, 2024, Vol.309 (1), p.63-77

2024

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A novel δ-globin gene mutation (HBD: c.323G>A) masking the diagnosis of β-thalassemia: a first report from India

International journal of hematology, 2012-05, Vol.95 (5), p.570-572

2012

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Comparison of telomere length in patients with bone marrow failure syndromes and healthy controls

European journal of haematology, 2024-05, Vol.112 (5), p.810-818

2024

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Treosulfan Exposure Predicts Thalassemia‐Free Survival in Patients with Beta Thalassemia Major Undergoing Allogeneic Hematopoietic Cell Transplantation

Clinical pharmacology and therapeutics, 2024-01, Vol.115 (1), p.116-125

2024

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Pharmacokinetics and Pharmacodynamics of Treosulfan in Patients With Thalassemia Major Undergoing Allogeneic Hematopoietic Stem Cell Transplantation

Clinical pharmacology and therapeutics, 2018-09, Vol.104 (3), p.575-583

2018

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Spectrum of ELANE mutations in congenital neutropenia: a single-centre study in patients of Indian origin

Journal of clinical pathology, 2018-12, Vol.71 (12), p.1046

2018

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Iron homeostasis: new players, newer insights

European journal of haematology, 2008-12, Vol.81 (6), p.411-424

2008

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Association of growth differentiation factor 15 (GDF15) polymorphisms with serum GDF15 and ferritin levels in β-thalassemia

Annals of hematology, 2014-12, Vol.93 (12), p.2093-2095

2014

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Molecular Characterization of G6PD Deficiency: Report of Three Novel G6PD Variants

Indian journal of hematology & blood transfusion, 2020-04, Vol.36 (2), p.349-355

2020

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A novel splice site mutation c.2278 (−1) G>C in the TMPRSS6 gene causes deletion of the substrate binding site of the serine protease resulting in refractory iron deficiency anaemia

British journal of haematology, 2009-12, Vol.147 (5), p.766-769

2009

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Two novel missense mutations in iron transport protein transferrin causing hypochromic microcytic anaemia and haemosiderosis: molecular characterization and structural implications

British journal of haematology, 2013-11, Vol.163 (3), p.404-407

2013

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Clinical, Hematological and Molecular Analysis of Homozygous Hb E (HBB: c.79G > A) in the Indian Population

Hemoglobin, 2016-01, Vol.40 (1), p.16-19

2016

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Identification of rare and novel deletions that cause (δβ)0-thalassaemia and hereditary persistence of foetal haemoglobin in Indian population

European journal of haematology, 2014-06, Vol.92 (6), p.514-520

2014

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Characterization of Clinical and Laboratory Profiles of the Deletional α2-Globin Gene Polyadenylation Signal Sequence (AATAAA > AATA- -) in an Indian Population

Hemoglobin, 2015, Vol.39 (6), p.415-418

2015

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A Novel 26 bp Deletion [HBB: c.20_45del26bp] in Exon 1 of the β-Globin Gene Causing β-Thalassemia Major

Hemoglobin, 2012-02, Vol.36 (1), p.98-102

2012

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Early Immune Reconstitution Is Similar in Patients with and without Acute GvHD Undergoing Haploidentical HCT with Post-Transplant Cyclophosphamide As Gvhd Prophylaxis

Transplantation and cellular therapy, 2024-02, Vol.30 (2), p.S312-S313

2024

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T-Cell Reconstitution Can be a Predictive Biomarker for Severe Acute GvHD in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation with a Treosulfan/Fludarabine Conditioning Regimen

Transplantation and cellular therapy, 2024-02, Vol.30 (2), p.S67-S68

2024

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Hb Showa-Yakushiji [beta110(G12)Leu-->Pro] in four unrelated patients from west Bengal

Hemoglobin, 2005, Vol.29 (1), p.19-25

2005

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Association of growth differentiation factor 15 (GDF15) polymorphisms with serum GDF15 and ferritin levels in [beta]-thalassemia

Annals of hematology, 2014-12, Vol.93 (12), p.2093

2014

Volltextzugriff (PDF)

Characterization of Clinical and Laboratory Profiles of the Deletional α 2-Globin Gene Polyadenylation Signal Sequence (AATA AA > AATA– –) in an Indian Population

Hemoglobin, 2015-11, Vol.39 (6), p.415-418

2015

Volltextzugriff (PDF)

A novel [delta]-globin gene mutation (HBD: c.323G>A) masking the diagnosis of [beta]-thalassemia: a first report from India

International journal of hematology, 2012-05, Vol.95 (5), p.570

2012

Volltextzugriff (PDF)

Identification of rare and novel deletions that cause ( δβ ) 0 ‐thalassaemia and hereditary persistence of foetal haemoglobin in I ndian population

European journal of haematology, 2014-06, Vol.92 (6), p.514-520

2014

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Molecular Analysis of WASP Gene - First Report from India

Blood, 2007-11, Vol.110 (11), p.3217-3217

2007

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Analysis of β Globin Mutations in the Indian Population: Presence of Rare and Novel Mutations and Region Wise Heterogeneity

Blood, 2007-11, Vol.110 (11), p.3822-3822

2007

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Complex Interactions in Regulation of Haematopoiesis-An Unexplored Iron Mine

Molecular insights into placental iron transfer mechanisms and maternofetal regulation

A novel δ-globin gene mutation (HBD: c.323G>A) masking the diagnosis of β-thalassemia: a first report from India

Comparison of telomere length in patients with bone marrow failure syndromes and healthy controls

Treosulfan Exposure Predicts Thalassemia‐Free Survival in Patients with Beta Thalassemia Major Undergoing Allogeneic Hematopoietic Cell Transplantation

Pharmacokinetics and Pharmacodynamics of Treosulfan in Patients With Thalassemia Major Undergoing Allogeneic Hematopoietic Stem Cell Transplantation

Spectrum of ELANE mutations in congenital neutropenia: a single-centre study in patients of Indian origin

Iron homeostasis: new players, newer insights

Association of growth differentiation factor 15 (GDF15) polymorphisms with serum GDF15 and ferritin levels in β-thalassemia

Molecular Characterization of G6PD Deficiency: Report of Three Novel G6PD Variants

A novel splice site mutation c.2278 (−1) G>C in the TMPRSS6 gene causes deletion of the substrate binding site of the serine protease resulting in refractory iron deficiency anaemia

Two novel missense mutations in iron transport protein transferrin causing hypochromic microcytic anaemia and haemosiderosis: molecular characterization and structural implications

Clinical, Hematological and Molecular Analysis of Homozygous Hb E (HBB: c.79G > A) in the Indian Population

Identification of rare and novel deletions that cause (δβ)0-thalassaemia and hereditary persistence of foetal haemoglobin in Indian population

Characterization of Clinical and Laboratory Profiles of the Deletional α2-Globin Gene Polyadenylation Signal Sequence (AATAAA > AATA- -) in an Indian Population

A Novel 26 bp Deletion [HBB: c.20_45del26bp] in Exon 1 of the β-Globin Gene Causing β-Thalassemia Major

Early Immune Reconstitution Is Similar in Patients with and without Acute GvHD Undergoing Haploidentical HCT with Post-Transplant Cyclophosphamide As Gvhd Prophylaxis

T-Cell Reconstitution Can be a Predictive Biomarker for Severe Acute GvHD in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation with a Treosulfan/Fludarabine Conditioning Regimen

Hb Showa-Yakushiji [beta110(G12)Leu-->Pro] in four unrelated patients from west Bengal

Association of growth differentiation factor 15 (GDF15) polymorphisms with serum GDF15 and ferritin levels in [beta]-thalassemia

Characterization of Clinical and Laboratory Profiles of the Deletional α 2-Globin Gene Polyadenylation Signal Sequence (AATA AA > AATA– –) in an Indian Population

A novel [delta]-globin gene mutation (HBD: c.323G>A) masking the diagnosis of [beta]-thalassemia: a first report from India

Identification of rare and novel deletions that cause ( δβ ) 0 ‐thalassaemia and hereditary persistence of foetal haemoglobin in I ndian population

Molecular Analysis of WASP Gene - First Report from India

Analysis of β Globin Mutations in the Indian Population: Presence of Rare and Novel Mutations and Region Wise Heterogeneity

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