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Literature DB >> 4817859

Absence of messenger RNA for beta globin chain in beta(0) thalassaemia.

B G Forget, E J Benz, A Skoultchi, C Baglioni, D Housman.

Abstract

Entities: Gene

Mesh：

Substances：
RNA, Messenger
Globins
DNA

Year: 1974 PMID： 4817859 DOI： 10.1038/247379a0

Source DB: PubMed Journal: Nature ISSN： 0028-0836 Impact factor: 49.962

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Cited

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21 in total

1. Globin synthesis in fractionated Normoblasts of beta-thalassemia heterozygotes.

Authors: W G Wood; G Stamatoyannopoulos
Journal: J Clin Invest Date: 1975-03 Impact factor: 14.808

2. Molecular cloning of human epsilon-globin gene.

Authors: N J Proudfoot; F E Baralle
Journal: Proc Natl Acad Sci U S A Date: 1979-11 Impact factor: 11.205

3. 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

4. The structure of the human beta-globin gene in beta-thalassaemia.

Authors: R A Flavell; R Bernards; J M Kooter; E de Boer; P F Little; G Annison; R Williamson
Journal: Nucleic Acids Res Date: 1979-06-25 Impact factor: 16.971

5. Defects in DNA and globin messenger RNA in homozygotes for hemoglobin Lepore.

Authors: F Ramirez; J G Mears; U Nudel; A Bank; L Luzzatto; G DiPrisco; R D'Avino; G Pepe; L Camardella; R Gambino; R Cimino; N Quattrin
Journal: J Clin Invest Date: 1979-04 Impact factor: 14.808

6. Hemoglobin Indianapolis (beta 112[G14] arginine). An unstable beta-chain variant producing the phenotype of severe beta-thalassemia.

Authors: J G Adams; L A Boxer; R L Baehner; B G Forget; G A Tsistrakis; M H Steinberg
Journal: J Clin Invest Date: 1979-05 Impact factor: 14.808

Absence of messenger RNA for beta globin chain in beta(0) thalassaemia.

1. Globin synthesis in fractionated Normoblasts of beta-thalassemia heterozygotes.

2. Molecular cloning of human epsilon-globin gene.

3. 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.

4. The structure of the human beta-globin gene in beta-thalassaemia.

5. Defects in DNA and globin messenger RNA in homozygotes for hemoglobin Lepore.

6. Hemoglobin Indianapolis (beta 112[G14] arginine). An unstable beta-chain variant producing the phenotype of severe beta-thalassemia.

7. beta-Thalassemia present in cis to a new beta-chain structural variant, Hb Vicksburg [beta 75 (E19)Leu leads to 0].

Review 8. Nonsense-mediated decay in genetic disease: friend or foe?

Review 9. The molecular basis of disorders of human hemoglobin synthesis.

10. Determination of mRNA fate by different RNA polymerase II promoters.