Keywords: BCL11A; fetal globin; gene addition; genome engineering; sickle cell anemia;
مقالات ISI (ترجمه نشده)
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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: HbF; Beta-thalassemia carriers; HPFH; BCL11A; HMIP; HBG2; KLF1 loci
Keywords: AI haplotype; Arab-Indian haplotype; ANOVA; Analysis of variance; ARMS-PCR; Amplification refractory mutation system-polymerase chain reaction; BCL11A; B-cell lymphoma/leukemia 11A; CSSCD; Co-operative study of sickle cell disease; DNA; Deoxyribonucleic a
Keywords: Adox; adenosine-2â²,3â²-dialdehyde; BCL11A; B-cell lymphoma/leukemia A; CID; chemical inducer of dimerization; CoREST; REST-co-repressor; DNMT; DNA methyltransferase; EKLF; erythroid Krüppel-like factor; FoP; friend of PRMT1 (protein arginine methyltra
Keywords: Sickle cell; Fetal hemoglobin; Haplotype; BCL11A;
Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability
Keywords: 2p16.1-p15 duplication; BCL11A; Intellectual disability;
miR-146a induces apoptosis in neuroblastoma cells by targeting BCL11A
Keywords: miR-146a; BCL11A; Neuroblastoma; Apoptosis;
Modifying effect of XmnI, BCL11A, and HBS1L-MYB on clinical appearances: A study on β-thalassemia and hemoglobin E/β-thalassemia patients in Indonesia
Keywords: BCL11A; HBS1L-MYB; Modifier effect; Thalassemia; XmnI
Brain malformations in a patient with deletion 2p16.1: A refinement of the phenotype to BCL11A
Keywords: 2p15-16.1 microdeletion syndrome; BCL11A; Pontocerebellar hypoplasia; CASK
Genetic variant in the BCL11A (rs1427407), but not HBS1-MYB (rs6934903) loci associate with fetal hemoglobin levels in Indian sickle cell disease patients
Keywords: Sickle cell Disease; Fetal hemoglobin; India; BCL11A; HBS1-MYB;
The influence of the BCL11A polymorphism on the phenotype of patients with beta thalassemia could be affected by the beta globin locus control region and/or the Xmn1-HBG2 genotypic background
Keywords: Beta thalassemia; BCL11A; 5′HS4; Beta globin LCR; Xmn1-HBG2
The XmnI Gγ polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 β-thalassemia intermedia patients
Keywords: Thalassemia intermedia; Fetal hemoglobin; XmnI polymorphism; BCL11A; HBS1L-MYB
Binding patterns of BCL11A in the globin and GATA1 loci and characterization of the BCL11A fetal hemoglobin locus
Keywords: BCL11A; GATA1; HbF; ChIP; Hemoglobinopathies
BCL11A-dependent recruitment of SIRT1 to a promoter template in mammalian cells results in histone deacetylation and transcriptional repression
Keywords: SIRT1; Bcl11a; CTIP1; Evi9; Transcriptional repression; Histone deacetylase;