Radiation Safety and You

Automi e Linguaggi Regolari

Enolase catalyzed βγ-αβ isomerization of 2-phospho-3-butenoic acid to (Z)-phosphoenol-α-ketobutyrate

Site-Specific Insertion of 3-Aminotyrosine into Subunit α2 of E. coli Ribonucleotide Reductase:  Direct Evidence for Involvement of Y 730 and Y 731 in Radical Propagation

Forward and Reverse Electron Transfer with the Y 356 DOPA-β2 Heterodimer of E. coli Ribonucleotide Reductase

Site-Specific Replacement of Y 356 with 3,4-Dihydroxyphenylalanine in the β2 Subunit of E. coli Ribonucleotide Reductase

Use of 2,3,5-F 3 Y-β2 and 3-NH 2 Y-α2 To Study Proton-Coupled Electron Transfer in Escherichia coli Ribonucleotide Reductase

Further Identification of The Hyperunstable α-Globin Chain Variant Hb Heraklion [codons 36/37 (–CCC); Pro→0 (α1)] in Greek Cases With Co-Inherited α + -Thalassemia Mutations

A Rare Thalassemic Syndrome Caused by Interaction of Hb Adana [α59(E8)Gly→Asp] with an α + -Thalassemia Deletion: Clinical Aspects in Two Cases

First Observation of Hb Taybe [Codons 38/39 (−Acc) Thr→0 (α1)] In Greece: Clinical and Hematological Findings in Patients With Co-Inherited α + -Thalassemia Mutations

Observation of a Rare Hemoglobin Variant [Hb Lulu Island, β107(G9)Gly→Asp, G G C→G A C] Co-Inherited With a β + -Thalassemia Mutation [IVS-I-110 (G→A)] or in the Heterozygous

β + -Thalassemia Trait Due to a Novel Mutation in the β-Globin Gene Promoter: −26 (A>C) [HBB c.−76A>C]

Association of Mild and Severely Unstable α Chain Variants: The First Observation of a Compound Heterozygote with Hb Setif [α94(G1)Asp→Tyr (α2)] and Hb Agrinio [α29(B10)Leu→Pro