Abstract:
A system and method for updating a system that controls files executed on a workstation. The workstation includes a workstation management module configured to detect the launch of an application. A workstation application server receives data associated with the application from the workstation. This data can include a hash value. The application server module can determine one or more categories to associate with the application by referencing an application inventory database or requesting the category from an application database factory. The application database factory can receive applications from multiple application server modules. The application database factory determines whether the application was previously categorized by the application database factory and provides the category to the application server module. Once the application server module has the category, it forwards a hash/policy table to the workstation management module. Upon receipt of the hash/policy table, the workstation management module applies the policy that is associated with the launched application to control access to the application on the workstation.
Abstract:
There are several different applications where it is desirable to increase the amount of material that can be introduced to the surface of a microresonator that has whispering gallery modes. The use of a porous surface on the microresonator permits greater amounts of the material to be captured on or near the surface of the microresonator, resulting in an increased optical interaction between the material and the light propagating in the whispering gallery mode(s) of the microresonator.
Abstract:
The present invention relates to the identification, isolation and purification of the catalytic domain of the human effector checkpoint protein kinase (hChk1). A 1.7Å crystal structure of the hChk1 kinase domain in the active conformation is reported herein. The kinase domain of hChk1 and its associated crystal structure is described for use in the discovery, identification and characterization of inhibitors of hChk1. This structure provides a three-dimensional description of the binding site of the hChk1 for structure-based design of small molecule inhibitors thereof as therapeutic agents. Inhibitors of hChk1 find utility in the treatment of hyperproliferative disorders such as HIV and cancer.
Abstract:
A two-part connector structure (22, 32) includes a male connector part (32) and a female connector part (22) which are mutually engageable to open fluid communication between the connector parts (22, 32). For example, the connector parts (22, 32) may be used to establish fluid communication between a container (12) and a conduit (14). The connector parts (22, 32) are disengageable from one another to discontinue fluid communication between them, and also to close communication between ambient and each of the container and the conduit. The male connector part (32) includes a mounting structure (32a) for supporting on the female connector part (22), and also includes a guide structure (44) effective to guide a male portion (36) of the male connector part (32) into engagement with the female connector part (22). A handnut (34) of the male connector part (32), and is effective upon manual rotation to cause axial relative movement of the male probe portion (36) into or out of engagement with the female connector part (32). This invention provides a connector structure (22, 32) with considerably lowered manual engagement and disengagement forces, along with increased convenience and ease of use.
Abstract:
Poly(vinylamine)-based superabsorbent gels are disclosed. The superabsorbent gels either comprise a mixture of a poly(vinylamine) polymer and an acidic water-absorbing polymer, like polyacrylic acid, or comprise a salt of a poly(vinylamine) polymer. An improved method of preparing poly(vinylamine), and improved diaper cores, also are disclosed.
Abstract:
Aminosterol compounds are described that are useful as inhibitors of the sodium/proton exchanger (NHE). Methods of using such aminosterols compounds are also disclosed, including those employing compounds that are inhibitors of a spectrum of NHEs as well as those using compounds that are inhibitors of only one specific NHE. Advantageous screening techniques and assays for evaluating a compound's therapeutic activity are also disclosed.
Abstract:
A hermetically sealed, nonrotatable closure for a bottle having a cylindrical body containing liquid and having an integral tubular neck formed with a free open end, comprises an annular flange on the tubular neck. A flexible stopper mounts on the flange. A cup shaped cap has a flat top wall with peripherally integral pliable skirt in which is an internal beveled ridge. The ridge engages the flange to lock the cap on the neck of the bottle. The top wall of the cap has a central hole to expose the stopper which can be pierced by a hypodermic needle to extract the liquid from the bottle while the cap remains unbroken on the neck of the bottle. Inside the skirt of the cap are circumferentially spaced teeth which engage in circumferential slots in the annular flange to cooperate with the ridge in preventing axial movement on the cap and stopper on the bottle. Radial webs separate the slots in the annular flange and engage in stalls defined by flat radial walls of the spaced teeth to prevent the cap and stopper from rotating on the tubular neck of the bottle.
Abstract:
Methods and systems of maintaining, evaluating, and providing therapy to a lung ex vivo. The methods and systems involve positioning the lung in an ex vivo perfusion circuit; circulating a perfusion fluid through the lung, the fluid entering the lung through a pulmonary artery interface and leaving the lung through a left atrial interface; and ventilating the lung by flowing a ventilation gas through a tracheal interface. Maintaining the lung for extended periods involves causing the lung to rebreath a captive volume of air, and reaching an equilibrium state between the perfusion fluid and the ventilation gas. Evaluating the gas exchange capability of the lung involves deoxygenating the perfusion fluid and measuring a time taken to reoxygenate the perfusion fluid by ventilating the lung with an oxygenation gas.
Abstract:
Methods and systems of maintaining, evaluating, and providing therapy to a lung ex vivo. The methods and systems involve positioning the lung in an ex vivo perfusion circuit; circulating a perfusion fluid through the lung, the fluid entering the lung through a pulmonary artery interface and leaving the lung through a left atrial interface; and ventilating the lung by flowing a ventilation gas through a tracheal interface. Maintaining the lung for extended periods involves causing the lung to rebreath a captive volume of air, and reaching an equilibrium state between the perfusion fluid and the ventilation gas. Evaluating the gas exchange capability of the lung involves deoxygenating the perfusion fluid and measuring a time taken to reoxygenate the perfusion fluid by ventilating the lung with an oxygenation gas.
Abstract:
Methods and systems of maintaining, evaluating, and providing therapy to a lung ex vivo. The methods and systems involve positioning the lung in an ex vivo perfusion circuit; circulating a perfusion fluid through the lung, the fluid entering the lung through a pulmonary artery interface and leaving the lung through a left atrial interface; and ventilating the lung by flowing a ventilation gas through a tracheal interface. Maintaining the lung for extended periods involves causing the lung to rebreath a captive volume of air, and reaching an equilibrium state between the perfusion fluid and the ventilation gas. Evaluating the gas exchange capability of the lung involves deoxygenating the perfusion fluid and measuring a time taken to reoxygenate the perfusion fluid by ventilating the lung with an oxygenation gas.