The chemical heterogeneity of fetal hemoglobin (Hb F) due to variable ratios of the Gγ and Aγ globin subunits reflects genetic complexity because of common dimorphisms such as Hb F Sardegna (or Aγ75(E19) Ile>Thr; also known as AγT) in Caucasians, and common variants such the Gγ globin variant, Hb F Malta I (or Gγ117(G19) His>Arg) that is in tight linkage disequilibrium with the β globin variant Hb Valletta (or β87(F3) Thr>Pro) and is found in 1.8% of neonates from Malta.peer-reviewe
Aim: In humans, fetal hemoglobin (HbF) production is controlled by many intricate mechanisms that, t...
Haploinsufficiency for the erythroid-specific transcription factor KLF1 is associated with hereditar...
Craig, J E ; Rochette, J ; Sampietro, M ; Wilkie, A O ; Barnetson, R ; Hatton, C S ; Demenais, F ; T...
SummaryFetal hemoglobin (Hb F) and fetal cell (FC) levels in adults show considerable variation and ...
Molecular analysis has revealed that a variety of hemoglobin molecules are produced in humans. All a...
Human hemoglobin genes are located in α and β globin gene clusters in chromosomes 16 and 11, respect...
Fetal hemoglobin (Hb F), formed by two alpha globin chains (α) and two gamma chains (γ) (α2 γ2), has...
Hereditary persistence of fetal hemoglobin (HPFH) is a rare hereditary condition resulting in elevat...
Increased γ-globin production and consequent fetal hemoglobin (Hb F, α2γ2) formation is an important...
The major hemoglobin component found in the blood of humans at birth is fetal hemoglobin, hemoglobin...
Hereditary persistence of fetal hemoglobin (HPFH) is characterized by persistent high levels of feta...
Fetal hemoglobin (HbF), the predominant hemoglobin in the fetus, is a mixture of two molecular speci...
This thesis investigated the extent to which genetic factors underlie the variations observed in fet...
We genotyped single nucleotide polymorphisms (SNPs) in: (1) the β-globin gene-like cluster, (2) quan...
Hereditary persistence of fetal hemoglobin (HPFH) is an important hemoglobin disorder. It is n ted t...
Aim: In humans, fetal hemoglobin (HbF) production is controlled by many intricate mechanisms that, t...
Haploinsufficiency for the erythroid-specific transcription factor KLF1 is associated with hereditar...
Craig, J E ; Rochette, J ; Sampietro, M ; Wilkie, A O ; Barnetson, R ; Hatton, C S ; Demenais, F ; T...
SummaryFetal hemoglobin (Hb F) and fetal cell (FC) levels in adults show considerable variation and ...
Molecular analysis has revealed that a variety of hemoglobin molecules are produced in humans. All a...
Human hemoglobin genes are located in α and β globin gene clusters in chromosomes 16 and 11, respect...
Fetal hemoglobin (Hb F), formed by two alpha globin chains (α) and two gamma chains (γ) (α2 γ2), has...
Hereditary persistence of fetal hemoglobin (HPFH) is a rare hereditary condition resulting in elevat...
Increased γ-globin production and consequent fetal hemoglobin (Hb F, α2γ2) formation is an important...
The major hemoglobin component found in the blood of humans at birth is fetal hemoglobin, hemoglobin...
Hereditary persistence of fetal hemoglobin (HPFH) is characterized by persistent high levels of feta...
Fetal hemoglobin (HbF), the predominant hemoglobin in the fetus, is a mixture of two molecular speci...
This thesis investigated the extent to which genetic factors underlie the variations observed in fet...
We genotyped single nucleotide polymorphisms (SNPs) in: (1) the β-globin gene-like cluster, (2) quan...
Hereditary persistence of fetal hemoglobin (HPFH) is an important hemoglobin disorder. It is n ted t...
Aim: In humans, fetal hemoglobin (HbF) production is controlled by many intricate mechanisms that, t...
Haploinsufficiency for the erythroid-specific transcription factor KLF1 is associated with hereditar...
Craig, J E ; Rochette, J ; Sampietro, M ; Wilkie, A O ; Barnetson, R ; Hatton, C S ; Demenais, F ; T...