Literature DB >> 985635

Abnormal or absent beta mRNA in betao Ferrara and gene deletion in delta beta thalassaemia.

F Ramirez, J V O'Donnell, P A Marks, A Bank, S Musumeci, G Schilirò, G Pizzarelli, G Russo, B Luppis, R Gambino.   

Abstract

In patients with betao thalassaemia from Ferrara, beta globin mRNA sequences are either absent or structurally abnormal while in betao thalassaemia in Catania, beta globin mRNA sequences are present. In deltabeta thalassaemia there is a deletion of beta-like globin genes, while in betao Catania DNA, no beta globin gene deletion is detectable.

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Year:  1976        PMID： 985635     DOI： 10.1038/263471a0

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


  23 in total

1.  Deletion of the A gamma-globin gene in G gamma-delta beta-thalassemia.

Authors:  S H Orkin; B P Alter; C Altay
Journal:  J Clin Invest       Date:  1979-09       Impact factor: 14.808

2.  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

3.  Heterogeneity of DNA fragments associated with the sickle-globin gene.

Authors:  J Feldenzer; J G Mears; A L Burns; C Natta; A Bank
Journal:  J Clin Invest       Date:  1979-09       Impact factor: 14.808

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

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

Authors:  J G Adams; M H Steinberg; M V Newman; W T Morrison; E J Benz; R Iyer
Journal:  Proc Natl Acad Sci U S A       Date:  1981-01       Impact factor: 11.205

8.  Restriction endonuclease mapping of gamma-delta-beta-globin region in G gamma (beta)+ HPFH and a Chinese A gamma HPFH variant.

Authors:  M Farquhar; R Gelinas; B Tatsis; J Murray; M Yagi; R Mueller; G Stamatoyannopoulos
Journal:  Am J Hum Genet       Date:  1983-07       Impact factor: 11.025

Review 9.  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

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

Authors:  J Enssle; W Kugler; M W Hentze; A E Kulozik
Journal:  Proc Natl Acad Sci U S A       Date:  1993-11-01       Impact factor: 11.205
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