The human fetal globin genes consist of the first mammalian genomic loci for which gene conversion was reported. To date, 14 gene conversions have been described in the human Gγ- and Aγ-globin genes, the vast majority of which are restricted to the coding sequences. Here, we provide evidence for three new gene conversion events in the 5′ regulatory region of the human fetal globin genes, identified during a large genetic screening effort in adult individuals with high fetal hemoglobin (Hb) levels. The sequence variations, resulting from these conversion events, are transcriptionally silent polymorphisms that do not contribute to increased fetal Hb levels. Our results suggest that the 5′ regulatory region of the human fetal globin genes is a...
The fetal to adult hemoglobin switch is a developmental process by which fetal hemoglobin becomes si...
In normal humans the fetal stage-specific gamma-globin genes are silenced after birth and not expres...
The fetal hemoglobin (HbF) levels and betaS-globin gene haplotypes of 125 sickle cell anemia patient...
Increased γ-globin production and consequent fetal hemoglobin (Hb F, α2γ2) formation is an important...
Human hemoglobin genes are located in α and β globin gene clusters in chromosomes 16 and 11, respect...
Chromatin structure is tightly intertwined with transcription regulation. Here we compared the chrom...
Chromatin structure is tightly intertwined with transcription regulation. Here we compared the chrom...
Human hemoglobin genes are located in α and β globin gene clusters in chromosomes 16 and 1...
The fetal hemoglobin (HbF) levels and ßS-globin gene haplotypes of 125 sickle cell anemia patients f...
textabstractIncreased fetal hemoglobin (Hb F; α2γ2) production in adults can ameliorate the clinical...
The globin chain synthetic pattern and the extent of DNA methylation within embryonic, fetal, and ad...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Ci...
Hereditary persistence of fetal hemoglobin (HPFH) is an important hemoglobin disorder. It is n ted t...
The globin chain synthetic pattern and the extent of DNA methylation within embryonic, fetal, and ad...
Fetal hemoglobin (HbF), encoded by the HBG2 and HBG1 genes, is the best-known genetic modulator of s...
The fetal to adult hemoglobin switch is a developmental process by which fetal hemoglobin becomes si...
In normal humans the fetal stage-specific gamma-globin genes are silenced after birth and not expres...
The fetal hemoglobin (HbF) levels and betaS-globin gene haplotypes of 125 sickle cell anemia patient...
Increased γ-globin production and consequent fetal hemoglobin (Hb F, α2γ2) formation is an important...
Human hemoglobin genes are located in α and β globin gene clusters in chromosomes 16 and 11, respect...
Chromatin structure is tightly intertwined with transcription regulation. Here we compared the chrom...
Chromatin structure is tightly intertwined with transcription regulation. Here we compared the chrom...
Human hemoglobin genes are located in α and β globin gene clusters in chromosomes 16 and 1...
The fetal hemoglobin (HbF) levels and ßS-globin gene haplotypes of 125 sickle cell anemia patients f...
textabstractIncreased fetal hemoglobin (Hb F; α2γ2) production in adults can ameliorate the clinical...
The globin chain synthetic pattern and the extent of DNA methylation within embryonic, fetal, and ad...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Ci...
Hereditary persistence of fetal hemoglobin (HPFH) is an important hemoglobin disorder. It is n ted t...
The globin chain synthetic pattern and the extent of DNA methylation within embryonic, fetal, and ad...
Fetal hemoglobin (HbF), encoded by the HBG2 and HBG1 genes, is the best-known genetic modulator of s...
The fetal to adult hemoglobin switch is a developmental process by which fetal hemoglobin becomes si...
In normal humans the fetal stage-specific gamma-globin genes are silenced after birth and not expres...
The fetal hemoglobin (HbF) levels and betaS-globin gene haplotypes of 125 sickle cell anemia patient...