摘要:
The invention relates to an improved process for the manufacture of substituted 2-cyanocinnamic esters. This novel economical process provides products in high purity and yields.
摘要:
The invention relates to an improved process for the manufacture of substitute 2-cyanocinnamic esters. This novel economical process provides products in high purity and yields.
摘要:
The invention relates to an improved process for the manufacture of substituted 2-cyanocinnamic esters. This novel economical process provides products in high purity and yields.
摘要:
In certain embodiments this invention pertains to the discovery that inhibition of the expression and/or activity of eukaryotic initiation factor 4A (eIF4A) inhibits the aging process. Accordingly, in certain embodiments, methods are provided for inhibiting/slowing aging. The methods typically involve administering to a mammal an agent that inhibits the expression and/or activity of eukaryotic initiation factor 4A (eIF4A) in an amount sufficient to inhibit expression or activity of EIF4A, where the agent is not resveratrol.
摘要:
Methods for genotyping polymorphisms using allele specific probes are disclosed. A training set is used to generate a model for each polymorphism to be interrogated. The training set is used to obtain an estimate of the asymmetry between an intensity measurement for a first allele and an intensity measurement for a second allele of the same polymorphism. The intensity measurement obtained for a test sample is adjusted using the estimate of asymmetry prior to using the intensity measurements to make a genotyping call. In preferred embodiments the adjustment is applied to polymorphisms that have a likelihood of being heterozygous that is above a specified threshold.
摘要:
Methods of identifying allele-specific changes in genomic DNA copy number are disclosed. Methods for identifying homozygous deletions and genetic amplifications are disclosed. An array of probes designed to detect presence or absence of a plurality of different sequences is also disclosed. The probes are designed to hybridize to sequences that are predicted to be present in a reduced complexity sample. The methods may be used to detect copy number changes in cancerous tissue compared to normal tissue. The methods may be used to diagnose cancer and other diseases associated with chromosomal anomalies.
摘要:
A method, programmed medium and system are provided for implementing a prebuilt and encrypted personal identification information (PII) profile which resides only on a user's computer and is prevented from being permanently stored in a server's database. In an exemplary embodiment, when a user visits a web site and creates a new account, the site submits a request to query the user's profile using an extension to the HTTP protocol. The user is prompted by the user's browser to grant the site permission to do so and the site automatically uploads a non-personal identifying number (ID) to the user's system to create an account. All personal information remains on the user's computer within the user's encrypted PII profile and is not allowed to be stored in the server's storage. Therefore, each time the user purchases something, the site must again request to query the user's profile for the user's name, credit card information and/or billing address or other information, rather than keeping that information in the web site's datastore.
摘要:
A method and apparatus for performing driver configuration operations without a system reboot is disclosed. In one embodiment, a network server's adapter driver receives a request to change a configuration of a selected instance of a plurality of instances. In response, the adapter driver may then determine if there is data flow through the selected instance. If there is no data flow through the selected instance, the method includes blocking subsequent data flow and subsequent information requests issued to the adapter driver. The selected instance may then be reinitializing without rebooting the server.
摘要:
Methods of identifying allele-specific changes in genomic DNA copy number are disclosed. Methods for identifying homozygous deletions and genetic amplifications are disclosed. An array of probes designed to detect presence or absence of a plurality of different sequences is also disclosed. The probes are designed to hybridize to sequences that are predicted to be present in a reduced complexity sample. The methods may be used to detect copy number changes in cancerous tissue compared to normal tissue. The methods may be used to diagnose cancer and other diseases associated with chromosomal anomalies.
摘要:
A method, programmed medium and system are provided for implementing a prebuilt and encrypted personal identification information (PII) profile which resides only on a user's computer and is prevented from being permanently stored in a server's database. When a user visits a web site and creates a new account, the site submits a request to query the user's profile using an extension to the HTTP protocol. The user is prompted by the user's browser to grant the site permission to do so and the site automatically uploads a non-personal identifying number (ID) to the user's system to create an account. User-selected fields of the PII are transmitted to the server for processing a user-requested transaction. All personal information remains on the user's computer within the user's encrypted PII profile and is deleted at the server after the completion of the requested transaction.