Abstract: A system may provide an eco-feedback and gaming platform for home energy management. The system may generate daily energy scores for a plurality of households. The system may prepare a community energy conservation game in which community conservation goals and participation thresholds are generated. The system may execute the game by receiving time series date from each of the households and rewards the households for participating in achieving the community goal.

Abstract: Systems for fabricating nanofiber yarn at rates of at least 30 m/min (1.8 kilometers (km)/hour (hr)) using a “false twist” nanofiber yarn spinner and a false twist spinning technique are disclosed. In a false twist spinning technique, a twist is introduced to nanofibers in a strand by twisting the nanofibers at points between ends of the strand. This is in contrast to the “true twist” technique where one end of a strand is fixed and the opposing end of the strand is rotated to introduce the twist to intervening portions of yarn.

Abstract: Provided are methods of treatment comprising administering to a subject in need thereof a therapeutically effective amount of encapsulated cells to an affected tissue or organ.

Abstract: A mouthwash composition for inhibiting the buildup of plaque on dental surfaces and preventing dental diseases consisting essentially of an aqueous solution of alkali metal chlorides as active agents wherein the active agents include 0.5 % to 8.0 % by weight of at least one of the alkali metal chlorides including CaCl2, MgCl2 and KCl, with the balance being water.

Abstract: The present invention relates to a method of administering a compound of Formula I: wherein R1 is hydrogen or C1-6-alkyl; R2 is C1-6-alkyl or adamantyl; R3 is C1-6-alkyl or hydroxy; or R2 and R3 taken together are —(CR6R7)n—; R4 is C2-8-alkyl, C2-8-alkenyl, C2-8-alkynyl, —OCH2R5 or C2-8-alkanoyl, or hydrogen when R3 is hydroxy; R5 is C1-6-alkyl, C2-6-alkenyl or C2-6-alkynyl; R6 and R7 are hydrogen or C1-6-alkyl; Y is oxygen or sulfur; and n is 3, 4, or 5, or a pharmaceutically acceptable salts of carboxylic acid of formula I, wherein said method comprises the step of admixing said compound in solid form with a topical carrier to form a topical formulation within seven days prior to first topical administration of said compound.

Abstract: The present invention relates to a method of administering a compound of Formula I: wherein R1 is hydrogen or C1-6-alkyl; R2 is C1-6-alkyl or adamantyl; R3 is C1-6-alkyl or hydroxy; or R2 and R3 taken together are —(CR6R7)n—; R4 is C2-8-alkyl, C2-8-alkenyl, C2-8-alkynyl, —OCH2R5 or C2-8-alkanoyl, or hydrogen when R3 is hydroxy; R5 is C1-6-alkyl, C2-6-alkenyl or C2-6-alkynyl; R6 and R7 are hydrogen or C1-6-alkyl; Y is oxygen or sulfur; and n is 3, 4, or 5, or a pharmaceutically acceptable salts of carboxylic acid of formula I, wherein said method comprises the step of admixing said compound in solid form with a topical carrier to form a topical formulation within seven days prior to first topical administration of said compound.

Abstract: The present invention relates to a method of administering a compound of Formula I: 1