摘要:
A method of making a reclosable plastic bag (38) having a fin seal (35) which provides a weakness area (23, 80, 81, 84, 86) that extends into at least one side of the fin seal (35). Perforation axes (19, 20) for opening the reclosable plastic bag (38) may be aligned with the weakness area (23, 80, 81, 84, 86). A reclosable bag (38) made in accordance with the method is also disclosed.
摘要:
The present invention is directed to a method and system for allowing a user to control the user interface environment and specifically a sidebar within the user interface environment. The method controls tiles within a sidebar to respond to a manipulation request by a system user or by an application to manipulate a selected tile. The method includes determining a current status of the selected tile and selecting an appropriate rule for manipulating the tile based on the status of the tile and an identity of the manipulation requestor. One rule set is provided for the application and another rule set is provided for the user. The method further includes manipulating the selected tile in accordance with the appropriate rule. The user rules allow insertion of the tile in most, if not all cases, whereas the application rules may prohibit insertion of the selected tile.
摘要:
Methods of making slide-zippered reclosable packages are provided. In one embodiment, a pair of opposing film extensions are provided on each package between which a zipper and slider are attached. In another embodiment, sliders are inserted on to zippered packages output from a form-fill-seal machine or the like. In yet another embodiment, during package formation a reclosable zipper is sealed to each package and then a slider is inserted on to the zipper. In yet another embodiment, during package formation a reclosable zipper is sealed to each package and a slider is inserted on to each zipper, either before or after zipper sealing.
摘要:
The present invention is directed to a method and system for use in a computing environment to present and provide access to user information. The system may include a sidebar for hosting a plurality of tiles. Applications may be minimized and inserted into the sidebar upon minimization. Selected features of the application remain available through a tile when the application is represented by a tile in the sidebar. The system may also include user interface tools for allowing a user to command placement of a selected application into the sidebar. The application may include an available feature selection module for allowing an application to provide at least a sub-set of a full feature set upon minimization. An insertion module may be provided for inserting the tile into the user interface.
摘要:
A transaction process system (10) provides for data transactions between parties. In a credit card transaction, the parties are the merchant (20), acquiring bank (24), card association (34), issuing bank (14), and cardholder (12). A transaction processing center (30) is positioned between the acquiring bank and the card association. The transaction processing center provides data processing channels for message-based processing (72) and filed-based processing (76). The file-based processing uses an incoming queue (80) and outgoing queue (84) to simplify the interface. The transaction processing center also provides for currency conversions and account reconciliation on a per transaction basis. The transaction processing center uses a scheduler (160) to efficiently manage the data processing resources and an account reconciliation processor (200) to identify discrepancies and initiate corrective action.
摘要:
Inhibitors of parasitic dihydroorotate dehydrogenase enzyme (DHOD) are candidate therapeutics for treating malaria. Illustrative of such therapeutic agents include the compound: and a triazolopyrimidine class of compounds that conform to Formula IX: and their solvates, stereoisomers, tautomers and pharmaceutically acceptable salts.
摘要:
The present invention provides methods of treating cancer by administering a compound of Formula I, optionally as a pharmaceutically acceptable salt, solvate and/or hydrate thereof, in combination with other cancer treatments.
摘要:
Described herein are compounds, pharmaceutical compositions and methods for the inhibition of RAF kinae mediated signaling. Said compounds, pharmaceutical compositions and methods have utility in the treatment of human disease and disorders.
摘要:
This invention is based on the discovery that the administration of a sphingosine-1-phosphate receptor antagonist (S1P) and at least one chemotherapeutic agent selected from the the group of antimicrotubule agents provides an unexpectedly superior treatment for cancer. Antimicrobial agents such as the taxane compounds are known in the art, for example, paclitaxel (available as TAXOL® from Bristol-Myers Squibb, Princeton, N.J.), docetaxel (available as TAXOTERE® from Sanofi-aventis, Bridgewater, N.J.) and the like and other compounds that act as antimicrotubule agents, such as Vincristine (ONCOVIN®, VINCASAR PFS®, VCR), Vinblastin (VELBAN®, VELSAR®) and Vinorelbine, and similar compounds. The present invention also provides methods of modulating the growth of selected cell populations, such as cancer cells, by administering a therapeutically effective amount of at least one sphingosine-1-phosphate 1 (S1P1R) receptor antagonists, and at least one antimicrotubule agent.
摘要:
A nucleic acid delivery complex is provided which comprises a condensed polypeptide/nucleic acid complex and a cationic lipid wherein the complex comprises (a) a nucleic acid sequence of interest (NOI); and (b) one or more viral nucleic acid packaging polypeptides, or derivatives thereof, said polypeptides or derivatives thereof being (i) capable of binding to the NOI; and (ii) capable of condensing the NOI; and wherein the NOI is heterologous to the polypeptide. Also provided is a method of introducing an NOI into a cell using the delivery vector.