Abstract:
In one embodiment, the present invention includes a method for securing tissue to bone, including drilling a bone hole into the bone; passing a filament through the tissue, the filament including a first end, a second end and a length therebetween, the second end having a loop; passing the first end of the filament through the loop of the filament; pulling on the first end of the filament such that the loop travels along the length of the filament and to the tissue; passing an anchor along the length of the filament, from the first end towards the loop and tissue; engaging the loop with a distal end of the anchor; positioning the distal end of the anchor, with the loop of the filament, into the bone hole; and securing the anchor in the bone.
Abstract:
Systems and methods that regulate range of access to personal information of a mobile unit's owner. The access control component can designate granularity for access levels and/or a spectrum of access modes—(as opposed to a binary choice of full access or no access at all). Such access can be based on a spectrum and/or discrete trust relationship between the owner and user of the mobile unit. A profile definition component can exploit an owner's trust relationships to designate levels of security. The profile definition component can further define a profile based on a set of applications, such as entertainment mode, browser mode, and the like.
Abstract:
Various technologies pertaining to authenticating a password in a manner that prevents offline dictionary attacks are described. A protected module, which can be a hardware security module, a trusted platform module, or the like, is in communication with an authentication server. The protected module comprises a key that is restricted to the protected module. The key is employed in connection with authenticating the password on the protected module.
Abstract:
Compounds of formula (I) or pharmaceutically acceptable salts thereof, are opioid receptor modulators, e.g. mu-opioid receptor antagonists, neutral antagonists or inverse agonists, and are useful inter alia for the treatment of obesity.
Abstract:
Compounds of formula (I): or pharmaceutically acceptable salts thereof, are GPCR agonists and are useful as for the treatment of obesity and diabetes.
Abstract:
Compounds of formula (I): or pharmaceutically acceptable salts thereof, are GPCR agonists and are useful as for the treatment of obesity and diabetes.
Abstract:
Compounds of Formula (I) or pharmaceutically acceptable salts or N-oxides thereof, are agonists of GPR116 and are useful for the treatment of obesity, and for the treatment of diabetes.
Abstract:
A method, apparatus, and article of manufacture for an application programming interface (API) on a client computer that enables access to architectural project information stored across the internet on a server site. The server site maintains an organization for the architectural information in the form of containers for storing, managing, and sharing files for one or more architectural projects, wherein the files comprise drawings, documents, communications, and tasks related to the architectural projects. The API of the invention permits third parties to create custom clients or permit direct access to a site hosted on a server. Such an API operates with both thick (.exe) and thin (.html) clients. The API establishes/obtains a connection between the client and the server to enable such access. For example, if the user desires to store a file on the server site, the user selects the appropriate server site/folder from within an application program executing the API. The API may then require the user to logon and confirms that the user has appropriate access permissions to work with the server site/folder. Once confirmed, the connection session is established. During the session, the user may access and download files as desired while maintaining the storage structure of architectural information stored on the server site.
Abstract:
The present invention relates to an improved process for preparing 4-substituted resorcinol derivatives, and intermediate compounds useful in the preparation of such resorcinol derivatives.