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7 in total

1. Assembly of recently translated full-length and C-terminal truncated human gamma-globin chains with a pool of alpha-globin chains to form Hb F in a cell-free system.

Authors: Kazuhiko Adachi; Yi Zhao; Vinaysagar Lakka; Mitchell J Weiss; Saul Surrey
Journal: Arch Biochem Biophys Date: 2007-03-16 Impact factor: 4.013

2. Posttranscriptional defects in beta-globin messenger RNA metabolism in beta-thalassemia: abnormal accumulation of beta-messenger RNA precursor sequences.

Authors: E J Benz; A L Scarpa; B L Tonkonow; H A Pearson; A K Ritchey
Journal: J Clin Invest Date: 1981-12 Impact factor: 14.808

3. Studies in porphyria. VII. Induction of uroporphyrinogen-I synthase and expression of the gene defect of acute intermittent porphyria in mitogen-stimulated human lymphocytes.

Authors: S Sassa; G L Zalar; A Kappas
Journal: J Clin Invest Date: 1978-02 Impact factor: 14.808

4. Alpha-globin gene deletion causes alpha-thalassemia syndromes in two German families.

Authors: J Horst; E U Griese; E Kleihauer; E Kohne
Journal: Hum Genet Date: 1984 Impact factor: 4.132

5. Heterogeneity of the alpha-globin gene defects in German alpha-thalassemia affected families.

Authors: E U Griese; E Kohne; J Horst
Journal: Hum Genet Date: 1985 Impact factor: 4.132

Review 6. Thalassemic hemoglobinopathies.

Authors: M H Steinberg; J G Adams
Journal: Am J Pathol Date: 1983-12 Impact factor: 4.307

7. Relative stability of alpha- and beta-globin messenger RNAs in homozygous beta+ thalassemia.

Authors: A W Nienhuis; P Turner; E J Benz
Journal: Proc Natl Acad Sci U S A Date: 1977-09 Impact factor: 11.205

7 in total