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Cure for thalassemia major - from allogeneic hematopoietic stem cell transplantation to gene therapy

Haematologica (Roma), 2017-02, Vol.102 (2), p.214-223

2017

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RNA expression of genes involved in cytarabine metabolism and transport predicts cytarabine response in acute myeloid leukemia

Pharmacogenomics, 2015-07, Vol.16 (8), p.877-890

2015

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Cytidine deaminase genetic variants influence RNA expression and cytarabine cytotoxicity in acute myeloid leukemia

Pharmacogenomics, 2012-02, Vol.13 (3), p.269-282

2012

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Screening of genetic variants in ELANE mutation negative congenital neutropenia by next generation sequencing

Journal of clinical pathology, 2020-06, Vol.73 (6), p.322-327

2020

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Novel frameshift variant (c.409dupG) in SLC25A38 is a common cause of congenital sideroblastic anaemia in the Indian subcontinent

Journal of clinical pathology, 2021-03, Vol.74 (3), p.157-162

2021

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Glutathione S-transferase M1 polymorphism: a risk factor for hepatic venoocclusive disease in bone marrow transplantation

Blood, 2004-09, Vol.104 (5), p.1574-1577

2004

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Molecular characterization of factor IX gene mutations in 53 patients with haemophilia B in India

Thrombosis and haemostasis, 2005-10, Vol.94 (4), p.883

2005

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Sitosterolemia: Four Cases of an Uncommon Cause of Hemolytic Anemia (Mediterranean Stomatocytosis with Macrothrombocytopenia)

Indian journal of hematology & blood transfusion, 2021-01, Vol.37 (1), p.157-161

2021

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Slow parasite clearance, absent K13-propeller gene polymorphisms and adequate artesunate levels among patients with malaria: A pilot study from southern India

The National medical journal of India, 2019-07, Vol.32 (4), p.200-206

2019

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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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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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Interaction of Hemoglobin E with Other Abnormal Hemoglobins

Acta haematologica, 2011-01, Vol.126 (4), p.246-248

2011

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Molecular basis of Wiskott-Aldrich syndrome in patients from India

European journal of haematology, 2012-10, Vol.89 (4), p.356-360

2012

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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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Rapid detection of β-globin gene mutations and polymorphisms by temporal temperature gradient gel electrophoresis

Clinical chemistry (Baltimore, Md.), 2003-05, Vol.49 (5), p.777-781

2003

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HIV-2 subtype circulating in India (south)

Journal of acquired immune deficiency syndromes (1999), 2003-06, Vol.33 (2), p.219-222

2003

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Compound Heterozygosity for Hb E and Hb Lepore-Hollandia in India; First Report and Potential Diagnostic Pitfalls

Hemoglobin, 2005, Vol.29 (3), p.221-224

2005

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Role Of Stress Responsive Genes Responsible In Molecular Switch From Adaptive Phase To Apoptosis In HbE−β Thalassemia

Blood, 2013-11, Vol.122 (21), p.3447-3447

2013

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Hyperbilirubinemia in Homozygous HbE Disease Is Associated with the UGT1A1 Gene Polymorphism

Hemoglobin, 2005, Vol.29 (3), p.189-195

2005

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High Expression of p53 and Growth Differentiation Factor-15 in Beta-Thalassemia

Blood, 2012-11, Vol.120 (21), p.2130-2130

2012

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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

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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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Hb Lepore in the Indian Population

Hemoglobin, 2003-01, Vol.27 (1), p.7-14

2003

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Genetic Diagnosis of Inherited Bleeding Disorders in 1250 Probands From India: A Single Centre Experience

Blood, 2012-11, Vol.120 (21), p.1127-1127

2012

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Prenatal diagnosis of Glanzmann thrombasthenia

The National medical journal of India, 2003-07, Vol.16 (4), p.207-208

2003

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Cure for thalassemia major - from allogeneic hematopoietic stem cell transplantation to gene therapy

RNA expression of genes involved in cytarabine metabolism and transport predicts cytarabine response in acute myeloid leukemia

Cytidine deaminase genetic variants influence RNA expression and cytarabine cytotoxicity in acute myeloid leukemia

Screening of genetic variants in ELANE mutation negative congenital neutropenia by next generation sequencing

Novel frameshift variant (c.409dupG) in SLC25A38 is a common cause of congenital sideroblastic anaemia in the Indian subcontinent

Glutathione S-transferase M1 polymorphism: a risk factor for hepatic venoocclusive disease in bone marrow transplantation

Molecular characterization of factor IX gene mutations in 53 patients with haemophilia B in India

Sitosterolemia: Four Cases of an Uncommon Cause of Hemolytic Anemia (Mediterranean Stomatocytosis with Macrothrombocytopenia)

Slow parasite clearance, absent K13-propeller gene polymorphisms and adequate artesunate levels among patients with malaria: A pilot study from southern India

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

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

Interaction of Hemoglobin E with Other Abnormal Hemoglobins

Molecular basis of Wiskott-Aldrich syndrome in patients from India

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

Rapid detection of β-globin gene mutations and polymorphisms by temporal temperature gradient gel electrophoresis

HIV-2 subtype circulating in India (south)

Compound Heterozygosity for Hb E and Hb Lepore-Hollandia in India; First Report and Potential Diagnostic Pitfalls

Role Of Stress Responsive Genes Responsible In Molecular Switch From Adaptive Phase To Apoptosis In HbE−β Thalassemia

Hyperbilirubinemia in Homozygous HbE Disease Is Associated with the UGT1A1 Gene Polymorphism

High Expression of p53 and Growth Differentiation Factor-15 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

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

Hb Lepore in the Indian Population

Genetic Diagnosis of Inherited Bleeding Disorders in 1250 Probands From India: A Single Centre Experience

Prenatal diagnosis of Glanzmann thrombasthenia

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