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The Fly in the Cathedral: How a Small Group of Cambridge Scientists Won the Race to Split the Atom by Brian Cathcart 288pp, Viking, £14.99 Out of the 40 or so centuries of human civilisation, the 20th, as we designate it, was without doubt one of the very worst, a period during which mankind disgraced itself on a hitherto undreamed-of scale and with maniacal ingenuity.
We designate it improved BSR (IBSR).
Thus, we designate it as HzCR-1.
These are the common structural characteristics of MITEs [ 44], thus we designate it as HzMITE1.
Our analysis of the genomic sequence at this locus reveals that it is actually a retrotransposed pseudogene of the VENTX gene (formerly VENTX2); thus we designate it VENTXP7.
The gene copy on the plus strand (site 4) corresponds to the originally sequenced ADH gene from F. × ananassa [ 20], in recognition of which we designate it ADH-1.
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We designated it the ancestral lineage, since its members are genetically closer to the progenitor M. marinum in sequence composition, order and orientation.
We designated it muNS-Mi, and characterized the role that its four different domains (Coil1, Coil2, Intercoil and C-Tail) play in inclusion formation.
We designated it SGIV-miR-homoHSV as one novel viral miRNA.
This result confirmed that the 80 91 residue of hTNF-α was a novel epitope, and we designated it as YG1.
Analysis of the domain composition of the 635-residue muNS protein produced the following results: i) the region comprising residues 448 to 635 constitutes the minimal muNS portion able to form inclusions; we designated it muNS-Mi.
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