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Red ochre, typically derived from iron oxides and hematite, has been used since Pleistocene times for a range of different applications, practical as well as symbolic, including cave paintings and use in prehistoric burials. The importance to discover new methods for provenance determination, based on non-destructive portable techniques, represents a new challenge in the field of diagnostics of cultural heritage. This study presents the data obtained from the analysis of several non-flaked tools and ochre-stained bones, showing evidence of ochre processing at the Mesolithic site of S'omu e S'Orku in Sardinia (Italy). To investigate the provenance of the ochre (hematite phase) found on a massive stone from the site and also used to cover the bones, we propose three distinct approaches derived from high-resolution Raman spectra of ochres, aiming to identify the maximum number of observables that can be reconducted to unicity criteria. The reliability of this method enables the development of an automatic algorithm of Artificial Intelligence able to recognize the provenance of raw materials used in a range of activities. Furthermore, this study sheds light on one of the earliest and most distinctive Mesolithic burials uncovered in Sardinia to date, providing valuable insights into the human colonization of the island and the symbolic practices of its inhabitants during the Holocene epoch., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved.)

Background: Methylmalonic aciduria combined with homocystinuria (MMA-HC) is the biochemical trait of a metabolic disorder resulting from impaired conversion of dietary cobalamin (cbl, or vitamin B12) to its two metabolically active forms. Effects on urinary purine and pyrimidine levels have not been described for this condition., Methods: Urine samples were collected from three patients with methylmalonic aciduria combined with homocystinuria and from 70 healthy subjects. Urinary purine and pyrimidine levels were quantitated by the use of LC/UV-Vis and LC/ESI/MS., Results: Higher urine levels of pyrimidines were detected with both methods in patients compared to controls., Conclusion: Methylmalonic aciduria with homocystinuria is due to deficiency of the enzyme, cobalamin reductase. The enzyme defect leads to altered hepatic metabolism, which appears to modify circulating pyrimidine levels., (Copyright 2010 Elsevier B.V. All rights reserved.)

Tyramine, an important plant intermediate, was found to be a substrate for two proteins, a copper amine oxidase and a peroxidase from Euphorbia characias latex. The oxidation of tyramine took place by two different mechanisms: oxidative deamination to p-hydroxyphenylacetaldehyde by the amine oxidase and formation of di-tyramine by the peroxidase. The di-tyramine was further oxidized at the two amino groups by the amino oxidase, whereas p-hydroxyphenylacetaldehyde was transformed to di-p-hydroxyphenylacetaldehyde by the peroxidase. Data obtained in this study indicate a new interesting scenario in the metabolism of tyramine.

The human beta globin locus spans an 80-kb chromosomal region encompassing both the five expressed globin genes and the cis-acting elements that direct their stage-specific expression during ontogeny. Sequences proximal to the genes and in the locus control region, 60 kb upstream of the adult beta globin gene, are required for developmental regulation. Transgenic studies have shown that altering the structural organization of the locus disrupts the normal pattern of globin gene regulation. Procedures for introducing yeast artificial chromosomes (YACs) containing large genetic loci now make it possible to define the sequences required for stage-restricted gene expression in constructs that preserve the integrity of the beta globin locus. We demonstrate that independent YAC transgenic lines exhibit remarkably similar patterns of globin gene expression during development. The switch from gamma to beta globin predominant expression occurs between day 11.5 and 12.5 of gestation, with no more than twofold differences in human beta globin mRNA levels between lines. Human beta globin mRNA levels were twofold to fourfold lower than that of mouse betamaj, revealing potentially significant differences in the regulatory sequences of the two loci. These findings provide an important basis for studying regulatory elements within the beta globin locus.