is associated with HbF expression intergenic region on chromosome 6q23 HBS1L-MYB A 3-bp deletion in the

No abstract is available for this paper.

• Publication year

  2013

• Venue

  Unknown venue

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers

  No identifiers available.

• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

• MicroRNA-15a and -16-1 act via MYB to elevate fetal hemoglobin expression in human trisomy 13

  2011cited by this paper
• Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia.

  2011cited by this paper
• Genomics. 1000 Genomes Project gives new map of genetic diversity.

  2010cited by this paper
• MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

  2010cited by this paper
• A map of human genome variation from population-scale sequencing

  2010cited by this paper
• Transcription: Enhancers make non-coding RNA

  2010cited by this paper
• Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation

  2010cited by this paper
• Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.

  2010cited by this paper
• Genetic Variation on Chromosome 6 Influences F Cell Levels in Healthy Individuals of African Descent and HbF Levels in Sickle Cell Patients

  2009cited by this paper
• BCL11A represses HBG transcription in K562 cells.

  2009cited by this paper
• Erythroid GATA 1 function revealed by genome-wide analysis of transcription factor occupancy , histone modifications , and mRNA expression

  2009cited by this paper
• Amelioration of Sardinian beta0 thalassemia by genetic modifiers.

  2009cited by this paper
• The HBS1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells.

  2009cited by this paper
• Control of fetal hemoglobin: new insights emerging from genomics and clinical implications.

  2009cited by this paper
• A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium

  2009cited by this paper
• Perspectives on RUNX genes: An update

  2009cited by this paper
• Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

  2009cited by this paper
• A genome-wide association identified the common genetic variants influence disease severity in β0-thalassemia/hemoglobin E

  2009cited by this paper
• The UCSC Genome Browser database: update 2010

  2009cited by this paper
• ENCODE whole-genome data in the UCSC Genome Browser

  2009cited by this paper
• Discovering hematopoietic mechanisms through genome-wide analysis of GATA factor chromatin occupancy.

  2009cited by this paper
• Differential use of SCL/TAL-1 DNA-binding domain in developmental hematopoiesis.

  2008cited by this paper
• Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of β-thalassemia

  2008cited by this paper
• DNA polymorphisms at the BCL11A, HBS1L-MYB, and β-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease

  2008cited by this paper
• Molecular Hallmarks of Endogenous Chromatin Complexes Containing Master Regulators of Hematopoiesis

  2008cited by this paper
• Variation and heritability of Hb F and F‐cells among β‐thalassemia heterozygotes in Hong Kong

  2008cited by this paper
• The HBS1L-MYB intergenic region on chromosome 6q23 is a quantitative trait locus controlling fetal haemoglobin level in carriers of β-thalassaemia

  2008cited by this paper
• BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies.

  2008cited by this paper
• A T-to-G Transversion at Nucleotide −567 Upstream of HBG2 in a GATA-1 Binding Motif Is Associated with Elevated Hemoglobin F

  2008cited by this paper
• The Lim-only protein LMO2 acts as a positive regulator of erythroid differentiation.

  2007cited by this paper
• β‐Globin gene cluster polymorphisms are strongly associated with severity of HbE/β0‐thalassemia

  2007cited by this paper
• Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults

  2007cited by this paper
• Mechanisms of human gamma-globin transcriptional induction by apicidin involves p38 signaling to chromatin.

  2007cited by this paper
• A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15

  2007cited by this paper
• The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humans.

  2007cited by this paper
• cAMP differentially regulates gamma-globin gene expression in erythroleukemic cells and primary erythroblasts through c-Myb expression.

  2006cited by this paper
• cMYB is involved in the regulation of fetal hemoglobin production in adults.

  2006cited by this paper
• ESPERR: learning strong and weak signals in genomic sequence alignments to identify functional elements.

  2006cited by this paper
• Polymorphisms near a chromosome 6q QTL area are associated with modulation of fetal hemoglobin levels in sickle cell anemia.

  2004cited by this paper
• Identification of a TAL1 Target Gene Reveals a Positive Role for the LIM Domain-Binding Protein Ldb1 in Erythroid Gene Expression and Differentiation

  2003cited by this paper
• Induction of fetal hemoglobin expression by the histone deacetylase inhibitor apicidin.

  2003cited by this paper
• Chromatin immunoselection defines a TAL‐1 target gene

  1998cited by this paper
• Haplotype mapping of a major quantitative-trait locus for fetal hemoglobin production, on chromosome 6q23.

  1998cited by this paper
• The product of the mammalian orthologue of the Saccharomyces cerevisiae HBS1 gene is phylogenetically related to eukaryotic release factor 3 (eRF3) but does not carry eRF3‐like activity

  1998cited by this paper
• Prevalence and genotypes of α- and β-thalassemia carriers in Hong Kong : Implications for population screening

  1997cited by this paper
• The T cell leukemia oncoprotein SCL/tal-1 is essential for development of all hematopoietic lineages.

  1996cited by this paper
• Preferred sequences for DNA recognition by the TAL1 helix-loop-helix proteins

  1994cited by this paper
• DNA sequence variation associated with elevated fetal G gamma globin production.

  1985cited by this paper

• No citing papers are available for this paper.