Keywords: β-تالاسمی; β-Thalassemia; β-Globin; Gene transfer; Hemichromes; New therapies; Trap ligands;
مقالات ISI β-تالاسمی (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: β-تالاسمی; Transferrin therapy; Anemia; Hypotransferrinemia; β-thalassemia; Oxidative stress; Non-transferrin bound iron;
Keywords: β-تالاسمی; β-thalassemia; colony-forming cell assay; cryopreservation; density-gradient separation; erythrocyte lysis by ACK buffer; hematopoietic stem and progenitor cell; in vitro expansion; lentiviral transduction;
Keywords: β-تالاسمی; Biosensor; Bimetallic nanoparticles; Methylene blue; β-Thalassemia; Polymerase chain reaction;
Keywords: β-تالاسمی; Chronic myeloid leukemia; Atrial fibrillation; β-Thalassemia; Decision making; Treatment switch; Patients' decision;
Keywords: β-تالاسمی; β-Thalassemia; Skeletal changes; Sinonasal; Paransal sinuses; Pediatric sinusitis; Chronic sinusitis;
Keywords: β-تالاسمی; Iron metabolism; Ineffective erythropoiesis; Hereditary hemochromatosis; β-Thalassemia; Hepcidin/minihepcidins; Lipid nanoparticle siRNA/antisense oligonucleotide;
Keywords: β-تالاسمی; Ovarian tissue transplantation; fertility preservation; ovarian tissue cryopreservation; live birth; β-thalassemia;
Calibration by commutable control materials is able to reduce inter-method differences of current high-performance methods for HbA2
Keywords: β-تالاسمی; HbA2; Multicenter evaluation; β-Thalassemia; Commutability; Harmonization; Standardization;
Prenatal diagnosis of a case with SEA-HPFH deletion thalassemia with whole HBB gene deletion
Keywords: β-تالاسمی; β-Thalassemia; Deletion; Hereditary persistence of fetal hemoglobinemia (HPFH);
A novel and efficient protocol for Surface Plasmon Resonance based detection of four β-thalassemia point mutations in blood samples and salivary swabs
Keywords: β-تالاسمی; Surface Plasmon Resonance; Biosensor; Biacore⢠X100; β-thalassemia; Single point mutation;
Emerging spread of β-thalassemia trait in Nigeria
Keywords: β-تالاسمی; Chronic anaemia; β-Thalassemia; Haemoglobin F; Haemoglobin A2; Iron deficiency anaemia;
A universal locked nucleic acid-integrated X-shaped DNA probe design for amplified fluorescence detection of single-nucleotide variant
Keywords: β-تالاسمی; Single-nucleotide variant; X-shaped DNA probe; Locked nucleic acid; Toehold-mediated strand-displacement reaction; β-thalassemia; Fluorescence detection;
Identifying targets for gene therapy of β-globin disorders using quantitative modeling approach
Keywords: β-تالاسمی; Hybrid functional Petri net; Quantitative modeling; Cell illustrator; β-thalassemia; Sickle cell disease; Fetal-to-adult hemoglobin switching network;
Hypermethylation of 28S ribosomal RNA in β-thalassemia trait carriers
Keywords: β-تالاسمی; Fibrillarin; Ribosome biogenesis; β-Thalassemia; rRNA methylation;
Left ventricle remodeling in patients with β-thalassemia major. An emerging differential diagnosis with left ventricle noncompaction disease
Keywords: β-تالاسمی; Magnetic resonance imaging; Left ventricle non compaction; β-thalassemia; Cardiomyopathy; Heart failure;
Serum YKL-40 in young patients with β-thalassemia major: Relation to hepatitis C virus infection, liver stiffness by transient elastography and cardiovascular complications
Keywords: β-تالاسمی; β-thalassemia; YKL-40; Liver fibrosis; Transient elastography; Hepatitis C; Cardiac disease; Iron overload;
Hématopoïèse extra-médullaire symptomatique au cours des β-thalassémies : étude rétrospective monocentrique
Keywords: β-تالاسمی; Anémie; β-thalassémie; Hématopoïèse extra-médullaire; Anemia; β-thalassemia; Extramedullary hematopoiesis;
Iron Overload Leading to Torsades de Pointes in β-Thalassemia and Long QT Syndrome
Keywords: β-تالاسمی; Long QT; β-thalassemia; Iron overload;
CRISPR/Cas9 system and its applications in human hematopoietic cells
Keywords: β-تالاسمی; CRISPR-Cas9; Hematopoietic cells; HIV; β-Thalassemia; Sickle cell disease;
Determination of deferasirox in human plasma by short-end injection and sweeping with a field-amplified sample stacking and micellar electrokinetic chromatography
Keywords: β-تالاسمی; BGE; background electrolyte; CE; capillary electrophoresis; DFX; deferasirox; EOF; electroosmotic flow; FASS; field-amplified sample stacking; HPLC; high-performance liquid chromatography; LOD; limit of detection; LOQ; limit of quantitation; MEKC; micella
Peripheral expression of hepcidin gene in Egyptian β-thalassemia major
Keywords: β-تالاسمی; ALT; Alanine aminotransferases; AST; Aspartate aminotransferases; BMP6; bone morphogenetic protein 6; cDNA; Complementary DNA; ERFE; erythroferrone; Hb; hemoglobin; HCV; Hepatitis C Virus; MCV; mean corpuscular volume; MEIA; microparticle enzyme immunoass
Incidence of hemoglobinopathies and thalassemias in Northern Alberta. Establishment of reference intervals for HbF and HbA2
Keywords: β-تالاسمی; CE-HPLC; cation-exchange high performance liquid chromatography; CI; confidence intervals; Hb; hemoglobin; HPFH; Hereditary Persistence of HbF; RI; reference interval; Hemoglobinopathy screening; β-Thalassemia; α-Thalassemia; HbF reference interval; Hem
β-Thalassemia and Polycythemia vera: Targeting chronic stress erythropoiesis
Keywords: β-تالاسمی; β-Thalassemia; Polycythemia vera; Chronic stress erythropoiesis; Iron metabolism; Macrophages;
Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGH
Keywords: β-تالاسمی; α-Thalassemia; β-Thalassemia; δβ-Thalassemia; Hereditary persistence of fetal hemoglobin (HPFH); Array CGH; Multiplex ligation-dependent probe amplification (MLPA); KLF1-gene;
Identification of candidate genes involved in clinical variability among Tunisian patients with β-thalassemia
Keywords: β-تالاسمی; STR; Short tandem repeats; TM; β-thalassemia major; TI; β-thalassemia intermedia; MCC; maternal cells contamination; PND; prenatal diagnosis; Hb; hemoglobine; β-thalassemia; Short tandem repeats; Clinical expression variation;
Hemoglobinopathies in India-Clinical and Laboratory Aspects
Keywords: β-تالاسمی; β-thalassemia; α-thalassemia; Epidemiology; Molecular mutations; Molecular methods; Prenatal diagnosis;
Natural and vaccine-induced immunity to Neisseria meningitidis serogroup C in asplenic patients with β-thalassemia
Keywords: β-تالاسمی; Meningococcal C conjugate vaccine; β-Thalassemia; Children; Splenectomy;
Extramedullary hematopoiesis: A rare occurrence in the sinonasal tract
Keywords: β-تالاسمی; β-Thalassemia; Chronic myeloproliferative disorder; Extramedullary hematopoiesis; Nasal endoscopy; Sinonasal tract;
Noninvasive Approaches to Prenatal Diagnosis of Hemoglobinopathies Using Fetal DNA in Maternal Plasma
Keywords: β-تالاسمی; Noninvasive prenatal diagnosis; Plasma DNA; Digital PCR; β-Thalassemia; Circulating nucleic acids;
Anemia, Ineffective Erythropoiesis, and Hepcidin: Interacting Factors in Abnormal Iron Metabolism Leading to Iron Overload in β-Thalassemia
Keywords: β-تالاسمی; β-Thalassemia; Ineffective erythropoiesis; Iron overload; Splenomegaly; Hepcidin; Jak2;
Haplotype analysis of beta thalassemia patients in Western Iran
Keywords: β-تالاسمی; Haplotype; β-thalassemia; Mutation; XmnI site; Western Iran;
Rodzina obciÄ
żona talasemiÄ
β - opis przypadku
Keywords: β-تالاسمی; talasemia β; dziecko; homozygota; mutacja IVS-I-6(T>C); β-thalassemia; child; homozygote; mutation IVS-I-6(T>C);
Natural and vaccine-induced immunity against Haemophilus influenzae type b in patients with β-thalassemia
Keywords: β-تالاسمی; Hib immunity; Conjugate vaccine; Immunologic memory; β-Thalassemia;
Neurological complications in β-thalassemia
Keywords: β-تالاسمی; β-Thalassemia; Neurophysiological; Neurological; Neuropsychological; Complications; Subclinical; Abnormalities; Neurotoxicity; Evoked potentials; Nerve conduction velocities;
Detection of known thalassemia point mutations by snapback single-strand conformation polymorphism: The feasibility analysis
Keywords: β-تالاسمی; SSCP; β-Thalassemia; α-Thalassemia; Point mutation; Haemoglobinopathy; Monogenic disease; PCR; PAGE; Silver stain; Prenatal diagnosis;
Elevated plasma chemokine CCL18/PARC in β-thalassemia
Keywords: β-تالاسمی; β-Thalassemia; CCL18/PARC; Chemokines;
A humanized mouse model for a common β0-thalassemia mutation
Keywords: β-تالاسمی; Bacterial artificial chromosomes; Hemoglobin; β-Thalassemia; 4-bp deletion mutation; Transgenic mice; Knockout mice; Gene correction; HbF induction;
Enhancement of growth and survival and alterations in Bcl-family proteins in β-thalassemic erythroid progenitors by novel short-chain fatty acid derivatives
Keywords: β-تالاسمی; Growth; Survival; Bcl-family protein; β-thalassemia; Erythroid; Fatty acid;