Cargando…

Prevalence and Impact of HMOX1 Polymorphism (rs2071746: A > T) in Indian Sickle Cell Disease Patients

Introduction Fetal hemoglobin (HbF) levels play significant role in lowering down the morbidity and mortality in sickle cell disease (SCD) patients. Coinheritance of heme oxygenase-1 (HMOX1) rs2071746:A > T polymorphism may contribute to variable HbF levels in Indian SCD patients. Objective Thi...

Descripción completa

Detalles Bibliográficos
Autores principales:	Pandey, Hareram, Singh, Kanwaljeet, Ranjan, Ravi, Dass, Jasmita, Tyagi, Seema, Seth, Tulika, Saxena, Renu, Mahapatra, Manoranjan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Thieme Medical and Scientific Publishers Pvt. Ltd. 2023
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10539052/ https://www.ncbi.nlm.nih.gov/pubmed/37780888 http://dx.doi.org/10.1055/s-0043-1770068

Ejemplares similares

Immunophenotypic Profile of Multiple Myeloma: A Tertiary Care Centre Experience
por: Rath, Asish, et al.
Publicado: (2023)

Comparative analysis of the Sokal, Euro and European Treatment and Outcome Study score in prognostication of Indian chronic myeloid leukemia-chronic phase patients on imatinib
por: Chhikara, Sunita, et al.
Publicado: (2018)

Social and Financial Barriers to Optimum TKI Treatment in Patients with Chronic Myeloid Leukemia-A Knowledge-Attitudes-Practices Study from India
por: Gupta, Naveen, et al.
Publicado: (2021)

Hairy cell leukemia: A decade long experience of North Indian Hematology Center
por: Somasundaram, Venkatesan, et al.
Publicado: (2014)

Chronic myeloid leukemia with a rare fusion transcript, b2a3 (e13a3) BCR–ABL1: A report of four cases from India
por: Sazawal, Sudha, et al.
Publicado: (2019)

Hemostatic Abnormalities in COVID-19: An Update
por: Aggarwal, Mukul, et al.
Publicado: (2020)

PB2553: GENOTYPIC CHARACTERIZATION OF RARE INHERITED ANAEMIAS USING NEXT GENERATION SEQUENCING METHODS
por: Viswanathan, Ganesh Kumar, et al.
Publicado: (2023)

Transfusion practices during the COVID-19 pandemic: An experience from a hematology daycare in India
por: Senapati, Jayastu, et al.
Publicado: (2021)

Report of chronic myeloid leukemia in chronic phase from All India Institute of Medical Sciences, 1990-2010
por: Mishra, Pravas, et al.
Publicado: (2013)

Current state of non-hematologic cancer-associated thrombosis at a tertiary care hospital in India
por: Aggarwal, Mukul, et al.
Publicado: (2023)

Value of CD16/CD66b/CD45 in comparison to CD55/CD59/CD45 in diagnosis of paroxysmal nocturnal haemoglobinuria: An Indian experience
por: Kotru, Mrinalini, et al.
Publicado: (2017)

Influence of JAK2V617F allele burden on clinical phenotype of polycythemia vera patients: A study from India
por: Sazawal, Sudha, et al.
Publicado: (2019)

Cytogenetic profile of Indian patients with de novo myelodysplastic syndromes
por: Chaubey, Rekha, et al.
Publicado: (2011)

Aplastic Anaemia with Microfilaria in Marrow Aspirate
por: Tejwani, Narender, et al.
Publicado: (2012)

ATRA Induced Reactive Hemophagocytosis: a Case Report
por: Sharma, Monica, et al.
Publicado: (2011)

Genotypic influence of α-deletions on the phenotype of Indian sickle cell anemia patients
por: Pandey, Sanjay, et al.
Publicado: (2011)

Clinical Profile of Patients with Rare Inherited Coagulation Disorders: A Retrospective Analysis of 67 Patients from Northern India
por: Sharma, Sanjeev Kumar, et al.
Publicado: (2012)

Prevalence of Alpha Thalassemia in Microcytic Anemia: a Tertiary Care Experience from North India
por: Sharma, Monica, et al.
Publicado: (2015)

A paradigm shift: lineage switch from T-ALL to B/myeloid MPAL
por: Rath, Asish, et al.
Publicado: (2021)

Flow Cytometry as a Diagnostic Tool in Monoclonal Gammopathy of Renal Significance
por: Rath, Asish, et al.
Publicado: (2023)

Modulating Effect of the −158 (G)γ (C→T) Xmn1 Polymorphism in Indian Sickle Cell Patients
por: Pandey, Sanjay, et al.
Publicado: (2012)

Double heterozygous hemoglobin Q India/hemoglobin D Punjab hemoglobinopathy: Report of two rare cases
por: Mutreja, Deepti, et al.
Publicado: (2013)

Mild Bleeders: Diagnosis is Elusive in Large Number of Patients
por: Kotru, Mrinalini, et al.
Publicado: (2016)

Study of Bone Marrow Lymphocyte Subset in Acute Myeloid Leukemia
por: Dange, Prasad, et al.
Publicado: (2021)

Tele-Medicine Services in Hematological Practice During Covid Pandemic: Its Feasibility and Difficulties
por: Kumar, Pradeep, et al.
Publicado: (2020)

COVID-19 infection in patients with haematological disease - A tertiary centre experience from north India
por: Aggarwal, Mukul, et al.
Publicado: (2022)

Cytogenetics’ impact on the prognosis of acute myeloid leukemia
por: Gupta, Monika, et al.
Publicado: (2019)

Significance of heme oxygenase-1(HMOX1) gene on fetal hemoglobin induction in sickle cell anemia patients
por: Hariharan, Priya, et al.
Publicado: (2020)

Antithrombin III Deficiency in Indian Patients with Deep Vein Thrombosis: Identification of First India Based AT Variants Including a Novel Point Mutation (T280A) that Leads to Aggregation
por: Bhakuni, Teena, et al.
Publicado: (2015)

Trisomy Chromosome 6 as a Sole Cytogenetic Abnormality in Acute Myeloid Leukemia
por: Gupta, Monika, et al.
Publicado: (2015)

An unusual clonal cytogenetic abnormality with t(15;17)(p11;q21) in a patient with severe aplastic anemia
por: Sharma, Sanjeev K., et al.
Publicado: (2012)

Aberrant myeloid antigen co-expression is correlated with high percentages of CD34-positive cells among blasts of acute lymphoblastic leukemia patients: an Indian tertiary care center perspective
por: Sharma, Rahul Kumar, et al.
Publicado: (2014)

Prevalence of glutathione S-transferase gene deletions and their effect on sickle cell patients
por: Sanjay, Pandey, et al.
Publicado: (2012)

Optimization and Identification of Single Mutation in Hemoglobin Variants with 2,2,2 Trifluoroethanol Modified Digestion Method and Nano−LC Coupled MALDI MS/MS
por: Dasauni, Pushpanjali, et al.
Publicado: (2022)

Common Parasite With Uncommon Associations
por: Jain, Sonal, et al.
Publicado: (2011)

Association of HMOX1 and NQO1 Polymorphisms with Metabolic Syndrome Components
por: Martínez-Hernández, Angélica, et al.
Publicado: (2015)

Identification of HMOX1 as a Critical Ferroptosis-Related Gene in Atherosclerosis
por: Wu, Daiqian, et al.
Publicado: (2022)

Plasma cells with Auer rod-like inclusions in a patient with myeloma
por: Dass, Jasmita, et al.
Publicado: (2018)

Diamond Blackfan Anemia: a Tertiary Care Center Experience
por: Singh, Avinash Kumar, et al.
Publicado: (2013)

Genetic Analyses of Heme Oxygenase 1 (HMOX1) in Different Forms of Pancreatitis
por: Weis, Sebastian, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_jdulfnmc0i229s3va12mbbejkl