textabstractWe have cloned the single beta-globin gene from an Italian patient who is a double heterozygote for beta o/delta beta o thalassaemia. RNA isolated from nucleated red cells from this patient can be translated in vitro to give detectable levels of A gamma- G gamma and alpha-globin, but no beta-globin. S1-mapping transcription studies show that beta-globin mRNA is present at about 1-3% of the level of alpha- and gamma-globin mRNA. In addition, the expression of this gene has been studied by reversed genetics. SV40-plasmid-beta o-globin gene recombinants have been transfected into Hela cells and analysed for beta-globin mRNA. In contrast to the results obtained with mRNA isolated directly from the blood of this patient, in the trans...
In this study, we sought to clarity the molecular basis of a dominant inherited beta-thalassemia, fo...
The silent carrier of (beta) thalassemia has a decreased (beta)/(alpha) globin synthesis ratio, but ...
We have introduced into murine erythroleukaemia (MEL) cells a series of human globin gene cosmids an...
We have cloned the single p-globin gene from an Italian patient who is a double heterozygote for (3°...
We have studied the structure and transcription of a cloned human beta-globin gene from a fetus diag...
A number of cases of beta0 thalassemia have been examined for the presence or absence of beta-globin...
The alpha-like and beta-like subunits of human hemoglobin are encoded by a small family of genes tha...
The ɑ-like and β-like subunits of human hemoglobin are encoded by a small family of genes that are d...
A cloned library of large, random embryonic human DNA fragments was constructed and screened for β-g...
textabstractThe DNA spanning two large deletions in the human beta-globin gene cluster (gamma beta-t...
A family was studied in which two inherited defects of the non-alpha-globin cluster segregate: Greek...
A Southern Italian patient homozygous for hemoglobin Lepore disease synthesizes approximately 3% Lep...
Aim: While the phenotype for heterozygous beta-thalassaemia is straightforward, it is more difficult...
In this study we have carried out alpha- and beta-globin gene analysis and defined the beta-globin g...
textabstractWe have used restriction endonuclease mapping to study a deletion involving the beta-glo...
In this study, we sought to clarity the molecular basis of a dominant inherited beta-thalassemia, fo...
The silent carrier of (beta) thalassemia has a decreased (beta)/(alpha) globin synthesis ratio, but ...
We have introduced into murine erythroleukaemia (MEL) cells a series of human globin gene cosmids an...
We have cloned the single p-globin gene from an Italian patient who is a double heterozygote for (3°...
We have studied the structure and transcription of a cloned human beta-globin gene from a fetus diag...
A number of cases of beta0 thalassemia have been examined for the presence or absence of beta-globin...
The alpha-like and beta-like subunits of human hemoglobin are encoded by a small family of genes tha...
The ɑ-like and β-like subunits of human hemoglobin are encoded by a small family of genes that are d...
A cloned library of large, random embryonic human DNA fragments was constructed and screened for β-g...
textabstractThe DNA spanning two large deletions in the human beta-globin gene cluster (gamma beta-t...
A family was studied in which two inherited defects of the non-alpha-globin cluster segregate: Greek...
A Southern Italian patient homozygous for hemoglobin Lepore disease synthesizes approximately 3% Lep...
Aim: While the phenotype for heterozygous beta-thalassaemia is straightforward, it is more difficult...
In this study we have carried out alpha- and beta-globin gene analysis and defined the beta-globin g...
textabstractWe have used restriction endonuclease mapping to study a deletion involving the beta-glo...
In this study, we sought to clarity the molecular basis of a dominant inherited beta-thalassemia, fo...
The silent carrier of (beta) thalassemia has a decreased (beta)/(alpha) globin synthesis ratio, but ...
We have introduced into murine erythroleukaemia (MEL) cells a series of human globin gene cosmids an...