Beverly hills hotel history
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The Beverly Hills Hotel
Famous California hotel
The Beverly Hills Hotel, also called the Beverly Hills Hotel and Bungalows,[1] is located on Sunset Boulevard in Beverly Hills, California. One of the world's best-known hotels, it is closely associated with Hollywood film stars, rock stars, and celebrities. The hotel has 210 guest rooms and suites and 23 bungalows and the exterior bears the hotel's signature pink and green colors.
The Beverly Hills Hotel was established in May 1912, before the city itself was incorporated. The original owners were Margaret J. Anderson, a wealthy widow, and her son, Stanley S. Anderson, who had been managing the Hollywood Hotel. The original hotel was designed by Pasadena architect Elmer Grey in the Mediterranean Revival style. From 1928 to 1932, the hotel was owned by the Interstate Company. In 1941, Hernando Courtright, a vice president of the Bank of America, purchased the hotel with friends including Irene Dunne, Loretta Young, and Harry Warner. Courtright established the Polo Lounge, which is considered to be one of the premi
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The NF-κB transcription factor is activated via different key inflammatory pathways and typically results in the fast expression of several proinflammatory genes as well as negative feedback loop genes to prevent excessive inflammation. In the current report, we describe that infection of cells with the porcine alphaherpesvirus pseudorabies virus (PRV) triggers a gradual and persistent aberrant activation of NF-κB, which does not result in expression of hallmark proinflammatory or negative feedback loop genes. In addition, although PRV-induced NF-κB activation shares some mechanistic features with canonical NF-κB activation, it also shows remarkable differences; e.g., it is largely independent of the canonical IκB kinase (IKK) and even renders infected cells resistant to canonical NF-κB activation by the inflammatory cytokine TNF-α. Aberrant PRV-induced NF-κB activation may therefore paradoxically serve as a viral immune evasion strategy and may represent an important tool to unravel currently unknown mechanisms and consequences of NF-κB activation.
KEYWORDS: NF-κB, evasion, h
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