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Titlebook: Selenium; Its Molecular Biolog Dolph L. Hatfield Book 2001 Springer Science+Business Media New York 2001 Amino acid.Mammalia.aging.cancer.d

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楼主: Amalgam
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Identity, evolution and function of selenoproteins and selenoprotein genese (MSGS), allow recognition of selenoproteins through identification of SECIS elements and homology analyses of Sec-flanking areas. Identification of new selenoprotein sequences may lead to an understanding of many biological and health-related properties of selenium.
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Introductioner [reviewed in 1]. Thus, it was quite surprising when Schwarz and Foltz reported in 1957 [2] that selenium prevented liver necrosis in rats. This finding and a report that selenium was important in anaerobic growth of . when grown on glucose [3] provided evidence that selenium was an important micronutrient for mammals and for certain bacteria.
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Introductionammals. In the 1930s, this element was found to be responsible for severe illnesses that had been documented, primarily in livestock, many years earlier [reviewed in 1]. Thus, it was quite surprising when Schwarz and Foltz reported in 1957 [2] that selenium prevented liver necrosis in rats. This fin
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Mammalian selenocysteine tRNA-O-ribosyl moiety at position 34. The tRNAs are 90 nucleotides in length making them the longest eukaryotic tRNAs sequenced to date. Both tRNAs decode UGA and arise from a single copy gene. The primary transcript is generated unlike that of any known tRNA as transcription begins at the first nucleot
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SECIS binding proteinsng the .-acting factors that are thought to be required for selenocysteine (Sec) insertion are RNA binding proteins that interact with the SECIS element. In addition to several proteins which bind non-specifically, this element is specifically bound by SECIS binding protein 2 (SBP2), and this intera
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