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蛋白质与细胞:英文版, ISSN 1674-800X, 2017, Volume 8, Issue 11, pp. 811 - 822
Journal Article
Hemoglobin, ISSN 0363-0269, 01/2017, Volume 41, Issue 1, pp. 61 - 64
β-Thalassemia (β-thal) caused by mutations on the HBB gene is the most common single-gene disorder in the world. In this study, the HBB gene mutation was... 
Hamadan, Iran | HBB mutations | thalassemia | beta-Thalassemia - epidemiology | Cross-Sectional Studies | Introns | Gene Frequency | Humans | beta-Thalassemia - genetics | Genotype | beta-Globins - genetics | Phenotype | Codon | Alleles | Polymorphism, Single Nucleotide | Mutation | Iran - epidemiology | Iran - ethnology | Amino Acid Substitution
Journal Article
Journal of Clinical and Experimental Investigations, ISSN 1309-8578, 09/2016, Volume 7, Issue 4, pp. 265 - 268
Introduction: Beta-thalassemia is the most common autosomal recessive disease. More than 200 different mutations determined in beta-globin gene. Beta... 
HBB | Beta Thalassemia | Beta-globin
Journal Article
HEMOGLOBIN, ISSN 0363-0269, 2017, Volume 41, Issue 1, pp. 61 - 64
-Thalassemia (-thal) caused by mutations on the HBB gene is the most common single-gene disorder in the world. In this study, the HBB gene mutation was... 
Hamadan | thalassemia | Iran | HBB mutations | BIOCHEMISTRY & MOLECULAR BIOLOGY | SPECTRUM | BETA-THALASSEMIA | HEMATOLOGY
Journal Article
Cytokine, ISSN 1043-4666, 02/2014, Volume 65, Issue 2, pp. 217 - 221
The chronic inflammatory state in sickle cell anemia (SCA) is associated with several factors such as the following: endothelial damage; increased production... 
Inflammation | Sickle cell anemia | HBBS gene haplotype | Cytokines | HBB | S gene haplotype | NORTHEAST | ACTIVATION | HEMOLYSIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | IMMUNOLOGY | CELL BIOLOGY | TUMOR-NECROSIS-FACTOR | AMPLIFICATION | GLOBIN GENE-CLUSTER | DISEASE | DIVERSITY | EXPRESSION
Journal Article
Hemoglobin, ISSN 0363-0269, 01/2016, Volume 40, Issue 1, pp. 25 - 28
Journal Article
Croatica Chemica Acta, ISSN 0011-1643, 2018, Volume 91, Issue 1, pp. 121 - 124
We have evaluated theoretically in the gas-phase (MP2/aug-cc-pVTZ) the hydrogen-bond basicity of simple carbenes and vinylidenes and compared them to the... 
Gas-phase MP2 calculations | Β scale of HBB | Hydrogen-bond basicity (HBB) | Carbenes | N-heterocyclic carbenes | hydrogen-bond basicity (HBB) | beta scale of HBB | carbenes | SCALES | ATOMS | CHEMISTRY, MULTIDISCIPLINARY | SINGLET | ACIDITY | Hydrogen-ion concentration | Hydrogen | Hydrogen bonding | β scale of HBB
Journal Article
Journal of Natural Science, Biology and Medicine, ISSN 0976-9668, 01/2019, Volume 10, Issue 1, pp. 97 - 102
Journal Article
European Journal of Haematology, ISSN 0902-4441, 06/2018, Volume 100, Issue 6, pp. 529 - 535
Hemoglobinopathies are the most common autosomal recessive disorders and are mostly inherited in a recessive manner. However, certain mutations can affect the... 
unstable hemoglobin variants | dominant beta‐thalassemia | HBB gene | bioinformatics | hemolytic anemia | dominant beta-thalassemia | PHENOTYPE | EXON-2 | GENE | PREDICT | THALASSEMIA | DISEASE | SERVICE | HEMATOLOGY | WEB SERVER | EPIDEMIOLOGY | Histidine | Heme | Computer applications | Hemoglobin | Thalassemia | Mutation | Bioinformatics
Journal Article
Hemoglobin, ISSN 0363-0269, 07/2018, Volume 42, Issue 4, pp. 236 - 242
Hemoglobinopathies and thalassemias are the most commonly encountered monogenic disorders of blood in humans, posing a major genetic and public health problem... 
Hb S (HBB: c.20A>T)- β-thal | β-Thalassemia (β-thal) haplotype analysis | mutation | Hb F | α-Thalassemia (α-thal) | IVS-I-5 (G>C) (HBB: c.95 + 5G>C) | IVS-I-5 (G>C) (HBB: c.95 + 5G>C)
Journal Article
Archives of Medical Science, ISSN 1734-1922, 01/2018, Volume 14, Issue 1, pp. 230 - 236
Introduction: Elevated HbA2 (hemoglobin A2) level is considered the most reliable hematological parameter for the detection of β-thalassemia carriers. However,... 
Saudi Arabia | KLF1 gene | Borderline HbA2 | Variations | HBA1 gene | Β-thalassemia carrier | HBA2 gene | HBB gene | Genes | borderline HbA2 | variations | β-thalassemia carrier | Basic Research
Journal Article
Human Mutation, ISSN 1059-7794, 10/2013, Volume 34, Issue 10, pp. 1361 - 1365
ABSTRACT We describe the molecular etiology of β+‐thalassemia that is caused by the insertion of the full‐length transposable element LINE‐1 (L1) into the... 
LINE‐1 | epigenetic repression | HBB | β‐thalassemia | β‐globin | β-globin | LINE-1 | Epigenetic repression | β-thalassemia
Journal Article