The major splice variant of human 5-aminolevulinate synthase-2 contributes significantly to erythroid heme biosynthesis

Author:

Cox Timothy C,Sadlon Timothy J,Schwarz Quenten P,Matthews Christopher S,Wise Phillip D,Cox Liza L,Bottomley Sylvia S,May Brian K

Publisher

Elsevier BV

Subject

Cell Biology,Biochemistry

Reference41 articles.

1. The putative iron-responsive element in the human erythroid 5-aminolevulinate synthase mRNA mediates translational control;Bhasker;Journal of Biological Chemistry,1993

2. Human δ-aminolevulinate synthase: Assignment of the housekeeping gene to 3p21 and the erythroid-specific gene to the X chromosome;Bishop;Genomics,1990

3. Purification of 5-aminolevulinate synthase from liver mitochondria of chick embryo;Borthwick;European Journal of Biochemistry,1983

4. Bottomley, S. S. (1999). Sideroblastic anemias. In G. R. Lee, et al. (Eds.), Wintrobe’s clinical hematology (pp. 1022–1045). Baltimore, MD: Williams & Wilkins.

5. Molecular defects of erythroid 5-aminolevulinate synthase in X-linked sideroblastic anemia;Bottomley;Journal of Bioenergetics and Biomembranes,1995

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