Works matching DE "FETAL hemoglobin"
Results: 1109
COMPREHENSIVE ANALYSIS OF α- AND β-THALASSEMIA GENOTYPES AND HEMATOLOGIC PHENOTYPES.
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- Journal of Medical Biochemistry, 2025, v. 44, n. 1, p. 93, doi. 10.5937/jomb0-51740
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- Article
EVALUATION OF HEMOGLOBINOPATHIES WITH CAPILLARY ZONE ELECTROPHORESIS.
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- Turkish Journal of Biochemistry / Turk Biyokimya Dergisi, 2023, v. 48, p. 80
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- Article
INVESTIGATION OF BCL11A (rs1427407) and HMIP (rs9399137) SNPs ASSOCIATED WITH HIGH HbF LEVELS IN β-THALASSEMIA.
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- 2023
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- Abstract
Iron Overload Induces Apoptosis and Cytoprotective Autophagy Regulated by ROS Generation in Mc3t3-E1 Cells.
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- Biological Trace Element Research, 2021, v. 199, n. 10, p. 3781, doi. 10.1007/s12011-020-02508-x
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- Article
A novel rhombic shaped photonic crystal bio-sensor for identifying disorders in the blood samples.
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- Optical & Quantum Electronics, 2023, v. 55, n. 4, p. 1, doi. 10.1007/s11082-023-04584-4
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- Article
Enhanced sensitivity of surface plasmon resonance biosensor for the selective detection of immunoglobin (IgG).
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- Optical & Quantum Electronics, 2022, v. 54, n. 12, p. 1, doi. 10.1007/s11082-022-04213-6
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- Article
Is chronic use of hydroxyurea safe for patients with sickle cell anemia? An account of genotoxicity and mutagenicity.
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- Environmental & Molecular Mutagenesis, 2019, v. 60, n. 3, p. 302, doi. 10.1002/em.22260
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- Article
Optical coherence tomography (OCT) and OCT angiography allow early identification of sickle cell maculopathy in children and correlate it with systemic risk factors.
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- Graefe's Archive of Clinical & Experimental Ophthalmology, 2020, v. 258, n. 11, p. 2551, doi. 10.1007/s00417-020-04764-y
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- Article
Correction to: Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease.
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- 2019
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- Correction Notice
Mutate and observe: utilizing deep neural networks to investigate the impact of mutations on translation initiation.
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- Bioinformatics, 2023, v. 39, n. 6, p. 1, doi. 10.1093/bioinformatics/btad338
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- Article
Patient Death in Beam Sickle Cell Trial Attributed to Conditioning Regimen.
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- GEN Biotechnology, 2024, v. 3, n. 6, p. 328, doi. 10.1089/genbio.2024.0061
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- Article
Ten Years at Vertex: An Interview with David Altshuler.
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- GEN Biotechnology, 2024, v. 3, n. 5, p. 274, doi. 10.1089/genbio.2024.0050
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- Article
Characterization of the interactions between Codanin-1 and C15Orf41, two proteins implicated in congenital dyserythropoietic anemia type I disease.
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- BMC Molecular & Cell Biology, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12860-020-00258-1
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- Article
Spontaneous Retroperitoneal Hematoma Treated with Percutaneous Transarterial Embolization in COVID-19 Era: Diagnostic Findings and Procedural Outcome.
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- Tomography: A Journal for Imaging Research, 2022, v. 8, n. 3, p. 1228, doi. 10.3390/tomography8030101
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- Article
Comparison of Hb A<sub>1c</sub> Quantification in the Presence of Hemoglobin Variants of an HPLC Assay with an Enzymatic Assay.
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- Journal of Applied Laboratory Medicine, 2023, v. 8, n. 6, p. 1127, doi. 10.1093/jalm/jfad053
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- Article
Optimizing Measurement and Interpretation of the G6PD/Hb Ratio.
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- Journal of Applied Laboratory Medicine, 2021, v. 6, n. 5, p. 1251, doi. 10.1093/jalm/jfab008
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- Article
Study of some biochemical parameters such as (Total serum bilirubin, Serum GOT, Serum GPT, Serum calcium and Serum ferritin) in thalassemia Patients.
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- Diyala Journal of Medicine, 2018, v. 15, n. 2, p. 9, doi. 10.26505/djm.15024010327
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- Article
Correlations between glycosylated hemoglobin and glucose levels in Chinese older adults with newly diagnosed type 2 diabetes mellitus.
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- Turkish Journal of Medical Sciences, 2022, v. 52, n. 4, p. 1207, doi. 10.55730/1300-0144.5425
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- Article
Burkitt Leukemia in a Child with Beta Thalassemia Major.
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- Journal of Kerman University of Medical Sciences, 2022, v. 29, n. 1, p. 91, doi. 10.22062/jkmu.2022.91868
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- Article
Transient Neonatal Diabetes Mellitus with an Unknown Cause in a 1-Month-Old Infant: A Case Report.
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- Healthcare (2227-9032), 2024, v. 12, n. 13, p. 1257, doi. 10.3390/healthcare12131257
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- Article
The Practices of Anaesthesiologists in the Management of Patients with Sickle Cell Disease: Empirical Evidence from Cameroon.
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- Healthcare (2227-9032), 2021, v. 9, n. 12, p. 1617, doi. 10.3390/healthcare9121617
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- Article
Nonsurgical Approaches for Managing Hypersplenism in Thalassemia.
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- Journal of Applied Hematology, 2024, v. 15, n. 4, p. 259, doi. 10.4103/joah.joah_94_24
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- Article
Estimated Level of Plasma Micro RNA-210 in Beta Thalassemia Patients and Its Relation to Hemoglobin F Level and Disease Severity.
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- Journal of Applied Hematology, 2023, v. 14, n. 3, p. 208, doi. 10.4103/joah.joah_42_23
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- Article
The Relationship between Maternal Anti-A\-B Titers and the Severity of Positive Direct Antiglobulin Test ABO-Hemolytic Disease of the Newborn in a Syrian Population.
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- Journal of Applied Hematology, 2023, v. 14, n. 2, p. 108, doi. 10.4103/joah.joah_101_22
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- Article
Fetal Hemoglobin Inducer Activity of Moringa oleifera, Curcuma aueruginosa Roxb., and Artocarpus altilis Based on the Gamma Globin Expression.
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- Journal of Applied Hematology, 2023, v. 14, n. 1, p. 17, doi. 10.4103/joah.joah_74_22
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- Article
Drug therapy in patients with severe forms of sickle cell anemia: A nonrandomized clinical trial of combining l-carnitine with hydroxycarbamide therapy.
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- Journal of Applied Hematology, 2022, v. 13, n. 4, p. 237, doi. 10.4103/joah.joah_23_22
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- Article
Detection of BCL11A, HMIP, and XmnI polymorphisms among anemic pregnant women in hospital Universiti Sains Malaysia.
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- Journal of Applied Hematology, 2022, v. 13, n. 4, p. 183, doi. 10.4103/joah.joah_22_22
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- Article
Treatment of acute erythroleukaemia with high‐dose cytarabine in a cat with feline leukaemia virus infection.
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- Veterinary Medicine & Science, 2022, v. 8, n. 1, p. 9, doi. 10.1002/vms3.646
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- Article
Report on the Relative Affinity Constant (M) of Hemoglobin for Carbon Monoxide in the Animal World: A Comparative Review with a Meta-Analysis Based on a Systematic Review.
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- Journal of Evolutionary Biochemistry & Physiology, 2019, v. 55, n. 5, p. 348, doi. 10.1134/S0022093019050028
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- Article
Establishment of haemoglobin A<sub>2</sub> reference intervals in Pretoria, South Africa: A retrospective secondary data analysis.
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- African Journal of Laboratory Medicine, 2022, v. 11, n. 1, p. 1, doi. 10.4102/ajlm.v11i1.1841
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- Article
Operational analysis of the national sickle cell screening programme in the Republic of Uganda.
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- African Journal of Laboratory Medicine, 2021, v. 10, n. 1, p. 1, doi. 10.4102/ajlm.v10i1.1303
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- Article
Prevalence and risk factors for red blood cell alloimmunisation among sickle cell patients in Mwanza City, Tanzania.
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- African Journal of Laboratory Medicine, 2020, v. 9, n. 1, p. 1, doi. 10.4102/ajlm.v9i1.823
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- Article
Haematological indices of sickle cell patients with chronic leg ulcers on compression therapy.
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- African Journal of Laboratory Medicine, 2020, v. 9, n. 1, p. 1, doi. 10.4102/ajlm.v9i1.1037
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- Article
Applied research won't flourish without basic science.
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- eLife, 2024, p. 1, doi. 10.7554/eLife.102368
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- Article
Inhibition of LATS kinases reduces tumorigenicity and increases the sensitivity of human chronic myelogenous leukemia cells to imatinib.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-54728-z
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- Article
Evaluating sheep hemoglobins with MD simulations as an animal model for sickle cell disease.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-023-50707-y
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- Article
Mutational analysis of hemoglobin genes and functional characterization of detected variants, through in-silico analysis, in Pakistani beta-thalassemia major patients.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-35481-1
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- Article
Mutational analysis of hemoglobin genes and functional characterization of detected variants, through in-silico analysis, in Pakistani beta-thalassemia major patients.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-35481-1
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- Article
High throughput human genotyping for variants associated with malarial disease outcomes using custom targeted amplicon sequencing.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-39233-z
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- Article
Molecular basis of non-deletional HPFH in Thailand and identification of two novel mutations at the binding sites of CCAAT and GATA-1 transcription factors.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-39173-8
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- Article
DETERMINATION THE EFFECT OF IRON OVERLOAD ON VITAMIN D AND THE PERCENTAGE OF EACH BLOOD GROUPS IN PATIENTS WITH THALASSEMIA.
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- Periódico Tchê Química, 2020, v. 17, n. 36, p. 223, doi. 10.52571/ptq.v17.n36.2020.239_periodico36_pgs_223_237.pdf
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- Article
MARCADORES ÓSSEOS METABÓLICOS BIOQUÍMICOS E HORMÔNIO DA PARATIREOIDE EM PACIENTES COM β-TALASSEMIA MAIOR NA PROVÍNCIA DE MISAN/IRAQUE.
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- Periódico Tchê Química, 2020, v. 17, n. 35, p. 65, doi. 10.52571/ptq.v17.n35.2020.06_al-zuhairy_pgs_65_72.pdf
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- Article
Piceatannol bolsteres fetal haemoglobin formation in K562 cells via p38 map kinase activation and ERK inactivation.
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- Journal of BioScience & Biotechnology, 2015, v. 4, n. 2, p. 231
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- Article
The prevalence and genetic disorders spectrum of thalassemia among breast cancer patients in Jiangxi province, China.
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- Frontiers in Genetics, 2022, v. 13, p. 01, doi. 10.3389/fgene.2022.1001369
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- Article
Case Report: The third-generation sequencing confirmed a novel 7.2Kb deletion at β-globin gene in a patient with rare β-thalassemia.
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- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.984996
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- Article
Induction of Fetal Hemoglobin by Introducing Natural Hereditary Persistence of Fetal Hemoglobin Mutations in the γ-Globin Gene Promoters for Genome Editing Therapies for β-Thalassemia.
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- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.881937
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- Article
Outcome of Hydroxyurea Use in SCD and Evaluation of Patients' Perception and Experience in Nigeria.
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- Frontiers in Genetics, 2022, p. 1, doi. 10.3389/fgene.2022.826132
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- Article
Epigenetic and Transcriptional Control of Erythropoiesis.
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- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.805265
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- Article
Adiponectin and Disease Severity in Sickle Cell Anemia Patients Attending a Tertiary Health Institution in Nnewi, Southeast Nigeria.
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- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.799425
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- Article
Barriers to Therapeutic Use of Hydroxyurea for Sickle Cell Disease in Nigeria: A Cross-Sectional Survey.
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- Frontiers in Genetics, 2022, v. 12, p. 1, doi. 10.3389/fgene.2021.765958
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- Article