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Literature DB >> 4505416

Induction of -globin synthesis in the -thalassaemia of Ferrara.

F Conconi, P T Rowley, L Del Senno, S Pontremoli, S Volpato.

Abstract

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Year: 1972 PMID： 4505416 DOI： 10.1038/newbio238083a0

Source DB: PubMed Journal: Nat New Biol ISSN： 0090-0028

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9 in total

1. Partial mispairing and crossing-over between beta 0 and delta genes as the origin of the delta beta 0 thalassemia gene. A single mutational event hypothesis.

Authors: J M Cantú; B Ibarra; G Vaca; M L Ramirez; J Sánchez-Corona
Journal: Hum Genet Date: 1979-06-19 Impact factor: 4.132

2. Beta-Thalassaemia types in southern Sardinia.

Authors: A Cao; M Furbetta; A Ximenes; A Angius; C Rosatelli; T Tuveri; M T Scalas; A M Falchi; L Maccioni; M A Melis; R Galanello
Journal: J Med Genet Date: 1981-06 Impact factor: 6.318

Review 3. The molecular basis of disorders of human hemoglobin synthesis.

Authors: F Ramirez; J G Mears; A Bank
Journal: Mol Cell Biochem Date: 1980-08-16 Impact factor: 3.396

4. Hemoglobin messenger RNA from human bone marrow. Isolation and translation in homozygous and heterozygous beta-thalassemia.

Authors: A W Nienhuis; P H Canfield; W F Anderson
Journal: J Clin Invest Date: 1973-07 Impact factor: 14.808

Induction of -globin synthesis in the -thalassaemia of Ferrara.

1. Partial mispairing and crossing-over between beta 0 and delta genes as the origin of the delta beta 0 thalassemia gene. A single mutational event hypothesis.

2. Beta-Thalassaemia types in southern Sardinia.

Review 3. The molecular basis of disorders of human hemoglobin synthesis.

4. Hemoglobin messenger RNA from human bone marrow. Isolation and translation in homozygous and heterozygous beta-thalassemia.

5. Discrimination between messenger ribonucleic acids by a mammalian translation initiation factor.

6. Quantitative deficiency of chain-specific globin messenger ribonucleic acids in the thalassemia syndromes.

7. Human globin gene analysis for a patient with beta-o/delta beta-thalassemia.

8. Demonstration of non-functional beta-globin mRNA in homozygous beta (0) thalassemia.

9. Further evidence of a quantitative deficiency of chain-specific globin mRNA in the thalassemia syndromes.