Literature DB >> 93487

Hereditary persistence of fetal haemoglobin (HPFH) and delta beta thalassaemia.

W G Wood, J B Clegg, D J Weatherall.   

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Year:  1979        PMID： 93487     DOI： 10.1111/j.1365-2141.1979.tb03784.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN： 0007-1048            Impact factor:   6.998


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  12 in total

1.  Translocation of an erythroid-specific hypersensitive site in deletion-type hereditary persistence of fetal hemoglobin.

Authors:  J T Elder; W C Forrester; C Thompson; D Mager; P Henthorn; M Peretz; T Papayannopoulou; M Groudine
Journal:  Mol Cell Biol       Date:  1990-04       Impact factor: 4.272

2.  A silent deletion in the beta-globin gene cluster.

Authors:  V E Tate; A V Hill; D K Bowden; J R Sadler; D J Weatherall; J B Clegg
Journal:  Nucleic Acids Res       Date:  1986-06-25       Impact factor: 16.971

3.  A fetal globin gene mutation in A gamma nondeletion hereditary persistence of fetal hemoglobin increases promoter strength in a nonerythroid cell.

Authors:  M W Rixon; R E Gelinas
Journal:  Mol Cell Biol       Date:  1988-02       Impact factor: 4.272

4.  Interaction of alpha- and delta beta o- thalassaemia: haematological features and globin chain synthesis analysis.

Authors:  R Galanello; M Furbetta; M A Melis; C Rosatelli; A Cao
Journal:  J Med Genet       Date:  1981-02       Impact factor: 6.318

5.  G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene.

Authors:  F S Collins; C J Stoeckert; G R Serjeant; B G Forget; S M Weissman
Journal:  Proc Natl Acad Sci U S A       Date:  1984-08       Impact factor: 11.205

6.  Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?

Authors:  S Ottolenghi; B Giglioni; R Taramelli; P Comi; U Mazza; G Saglio; C Camaschella; P Izzo; A Cao; R Galanello; E Gimferrer; M Baiget; A M Gianni
Journal:  Proc Natl Acad Sci U S A       Date:  1982-04       Impact factor: 11.205

7.  Genetic and molecular diversity in nondeletion Hb H disease.

Authors:  D R Higgs; L Pressley; B Aldridge; J B Clegg; D J Weatherall; A Cao; M G Hadjiminas; C Kattamis; A Metaxatou-Mavromati; E A Rachmilewitz; T Sophocleous
Journal:  Proc Natl Acad Sci U S A       Date:  1981-09       Impact factor: 11.205

8.  HIF prolyl hydroxylase inhibition results in endogenous erythropoietin induction, erythrocytosis, and modest fetal hemoglobin expression in rhesus macaques.

Authors:  Matthew M Hsieh; N Seth Linde; Aisha Wynter; Mark Metzger; Carol Wong; Ingrid Langsetmo; Al Lin; Reginald Smith; Griffin P Rodgers; Robert E Donahue; Stephen J Klaus; John F Tisdale
Journal:  Blood       Date:  2007-06-08       Impact factor: 22.113

9.  Delta beta (F)-thalassaemia in Sardinia.

Authors:  A Cao; M A Melis; R Galanello; A Angius; M Furbetta; P Giordano; L F Bernini
Journal:  J Med Genet       Date:  1982-06       Impact factor: 6.318

10.  Molecular characterization of a novel form of (A gamma delta beta)zero-thalassemia deletion with a 3' breakpoint close to those of HPFH-3 and HPFH-4: insights for a common regulatory mechanism.

Authors:  N P Anagnou; T Papayannopoulou; A W Nienhuis; G Stamatoyannopoulos
Journal:  Nucleic Acids Res       Date:  1988-07-11       Impact factor: 16.971
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