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The thermal decomposition of TC5 (TC5 = 3,9-bis(trimethylsilyl)tetracene) in vacuum has been studied by means of matrix-isolation infrared spectroscopy and density functional theory calculations. With the increase of temperature, a set of stable isomers π-stacked in layered domains are formed in a stepwise manner, followed by the spontaneous generation of benzene. These unusual isomers can survive up to ∼400 K, at which point they start to decompose via the formation of aromatic rings.Fluximplantation of human immunodeficiency virus (HIV)-infected cells in rhesus monkeys.
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Greenwich Historic District is a national historic district located at Greenwich, Davie County, South Carolina. It encompasses 95 contributing buildings in a predominantly residential section of the town. It was developed between about 1890 and 1935 and includes notable examples of Queen Anne, Colonial Revival, Neoclassical, Bungalow, American Craftsman, and American Foursquare style architecture. Notable buildings include the Prime O’Neil House (c. 1920), Sinkler-Hill-Black House (c. 1892), Joseph Mitchell (1892), James Mitchell House (c. 1890), W. A. Neswith House (c. 1894), James A. Smith House (1882), Joseph G. Harbin House (1880), and G. P. Cooper House (1904).

It was listed on the National Register of Historic Places in 2006.

References

Category:National Register of Historic Places in South Carolina
Category:Queen Anne architecture in South Carolina
Category:Colonial Revival architecture in South Carolina
Category:Buildings and structures in Davie County, South Carolina
Category:Historic districts on the National Register of Historic Places in South Carolina
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There is compelling evidence that immune system is centrally involved in the pathogenesis of autoantibody-associated disorders. Furthermore, genome wide searches identified autoimmunity-associated genes. We performed loss of heterozygosity (LOH) analysis in 64 multiple myeloma (MM) patients in 12 loci of lymphocyte and myeloma antigens and in the immunoglobulin heavy chain (IgH) intron 22 LOH hot spot. A significant LOH in the CDR3 region was observed in 23% of MM patients. Importantly, there was a tight association between LOH of the CDR3 region and a poor clinical outcome. Furthermore, a patient who had an LOH in both CDR3 and IgH gene intron 22 was found to have very bad prognosis. In conclusion, we have identified a MM patient who has a high percentage of LOH (19%) in the CDR3 region of the IgH gene. This patient may have the same genetic background as other MM patients who have a significant percentage of LOH at the CDR3 region. The loss of one allele of the IgH gene intron 22 might have a deleterious effect on lymph