Correlating power signatures with automated equipment
    11.
    发明授权
    Correlating power signatures with automated equipment 失效
    将功率签名与自动化设备相关联

    公开(公告)号:US07231317B2

    公开(公告)日:2007-06-12

    申请号:US10339515

    申请日:2003-01-08

    IPC分类号: G06F11/30

    摘要: A method and system for monitoring the activity of a system of one or more electro-mechanical components that receive electrical current from a power supply. The method and system samples an actual current supplied to the electro-mechanical component from the power supply. Next, the method and system reads a theoretical current for the activity of the system. A statistical value is computed from comparing the actual current and the theoretical current. This statistical value is compared to upper and lower threshold values. Depending upon this comparison, the system issues various output messages. Further, if this comparison indicates that one of the electro-mechanical components is failing, the method and system will shut that component down.

    摘要翻译: 一种用于监测从电源接收电流的一个或多个机电组件的系统的活动的方法和系统。 该方法和系统从电源对从机电组件提供的实际电流进行采样。 接下来,该方法和系统读取系统活动的理论电流。 通过比较实际电流和理论电流计算统计值。 将此统计值与上限和下限阈值进行比较。 根据这种比较,系统会发出各种输出信息。 此外,如果该比较表明机电组件之一发生故障,则该方法和系统将关闭该组件。

    Apparatus, system, and method for authorized remote access to a target system
    13.
    发明授权
    Apparatus, system, and method for authorized remote access to a target system 有权
    用于授权远程访问目标系统的装置,系统和方法

    公开(公告)号:US07302570B2

    公开(公告)日:2007-11-27

    申请号:US10644140

    申请日:2003-08-19

    IPC分类号: H04L9/00

    摘要: An apparatus, system, and method are provided for authorized remote access to a target system. The apparatus, system, and method include a security module and an authorization module that cooperate to authenticate a remote user using three passwords. The apparatus, system, and method selectively generate an encrypted key in response to a first password. The authorization module decrypts the encrypted key and determines a third password in response to authenticating a second password and identifying a remote user within an authorized user list. The third password is then used to gain secure, traceable, and in certain embodiments, restricted remote access to a target system.

    摘要翻译: 提供了用于授权远程访问目标系统的装置,系统和方法。 该装置,系统和方法包括一个安全模块和一个授权模块,用于使用三个密码进行远程用户认证。 装置,系统和方法响应于第一密码选择性地生成加密密钥。 授权模块解密加密的密钥并且响应于验证第二密码并识别授权用户列表中的远程用户来确定第三密码。 然后,第三个密码用于获得安全,可跟踪,并且在某些实施例中,限制了对目标系统的远程访问。

    Mitochondrial biology expression arrays
    14.
    发明申请
    Mitochondrial biology expression arrays 审中-公开
    线粒体生物学表达阵列

    公开(公告)号:US20060099578A1

    公开(公告)日:2006-05-11

    申请号:US10488619

    申请日:2002-08-30

    IPC分类号: C12Q1/68 C12M1/34

    摘要: This invention provides a library of genes involved in mitochondrial biology, arrays containing probes for genes involved in mitochondrial biology, methods for making such arrays, and methods of using such arrays. Genes and probe sequences involved in mitochondrial biology in humans and mice are provided. The arrays of this invention are useful for determining mitochondrial biology gene expression profiles. Mitochondrial biology gene expression profiles are useful for determining expression profiles diagnostic of physiological conditions; diagnosing physiological conditions; identifying biochemical pathways, genes, and mutations involved in physiological conditions; identify therapeutic agents useful for preventing and/or treating such physiological conditions; evaluating and/or monitoring the efficacy of such therapies, and creating and identifying animal models of human physiologic conditions. Arrays containing probes for all genes known to be involved in mitochondrial biology are provided, as well as arrays containing subsets of such probes.

    摘要翻译: 本发明提供了涉及线粒体生物学的基因文库,包含涉及线粒体生物学基因的探针的阵列,以及制备这种阵列的方法,以及使用这种阵列的方法。 提供了涉及人和小鼠线粒体生物学的基因和探针序列。 本发明的阵列可用于测定线粒体生物学基因表达谱。 线粒体生物学基因表达谱可用于确定生理条件诊断的表达谱; 诊断生理条件; 识别涉及生理条件的生物化学途径,基因和突变; 鉴定可用于预防和/或治疗这种生理状况的治疗剂; 评估和/或监测这些疗法的功效,以及创建和鉴定人类生理状况的动物模型。 提供了包含已知参与线粒体生物学的所有基因的探针的阵列,以及包含这种探针子集的阵列。

    Human mitochondrial dna polymorphisms, haplogroups, associations with physiological conditions, and genotyping arrays

    公开(公告)号:US20050123913A1

    公开(公告)日:2005-06-09

    申请号:US10488618

    申请日:2002-08-30

    摘要: This invention provides human mtDNA polymorphisms that are diagnostic of all the major human haplogroups and methods of diagnosing those haplogroups and selected subhaplogroups. This invention also provides methods for identifying evolutionarily significant mitochondrial DNA genes, nucleotide alleles, and amino acid alleles. Evolutionarily significant genes and alleles are identified using one or two populations of a single species. The process of identifying evolutionarily significant nucleotide alleles involves identifying evolutionarily significant genes and then evolutionarily significant nucleotide alleles in those genes, and identifying evolutionarily significant amino acid alleles involves identifying amino acids encoded by all nonsynonymous alleles. Synonymous codings of the nucleotide alleles encoding evolutionarily significant amino acid alleles of this invention are equivalent to the evolutionarily significant amino acid alleles disclosed herein and are included within the scope of this invention. Synonymous codings include alleles at neighboring nucleotide loci that are within the same codon. This invention also provides methods for associating haplogroups and evolutionarily significant nucleotide and amino acid alleles with predispositions to physiological conditions. Methods for diagnosing predisposition to LHON, and methods for diagnosing increased likelihood of developing blindness, centenaria, and increased longevity that are not dependent on the geographical location of the individual being diagnosed are provided herein. Diagnosis of an individual with a predisposition to an energy metabolism-related physiological condition is dependent on the geographic region of the individual. Physiological conditions diagnosable by the methods of this invention include healthy conditions and pathological conditions. Physiological conditions that are associated with haplogroups and with alleles provided by this invention include energetic imbalance, metabolic disease, abnormal energy metabolism, abnormal temperature regulation, abnormal oxidative phosphorylation, abnormal electron transport, obesity, amount of body fat, diabetes, hypertension, and cardiovascular disease.

    Computerized test preparation system employing individually tailored diagnostics and remediation
    19.
    发明授权
    Computerized test preparation system employing individually tailored diagnostics and remediation 失效
    计算机化测试准备系统采用单独定制的诊断和修复

    公开(公告)号:US06688889B2

    公开(公告)日:2004-02-10

    申请号:US09802312

    申请日:2001-03-08

    IPC分类号: G09B1100

    CPC分类号: G09B7/06

    摘要: A computerized test preparation system and methods are disclosed which assist an examinee to increase his learning and improve his performance on standardized academic or applied aptitude and achievement exams. Performance feedback information is provided to a user, including conventional information such as number of items correct and time elapsed, pinpoints substantive areas of a particular exam in which the user is either weak or strong, and offers diagnoses of, and remediation tailored to, a user's personal difficulties. By assessing a user's responses to given exam questions, through various distractor error patterns manifested in the incorrect answers to multiple-choice questions, or through coded categories of responses in the case of user responses to constrained open-ended items, a preliminary diagnosis of a user's deficits in knowledge and/or test taking skill is made. This preliminary diagnosis is subsequently refined utilizing additional examination questions. The refined diagnosis is then utilized to offer recommendations to an individual user to ameliorate the user's manifested error patterns. A user's response to this remediation is confirmed and reinforced using subsequent remediation activities.

    摘要翻译: 公开了一种计算机化的测试准备系统和方法,帮助受试者增加他的学习能力,提高他在标准化学术或应用能力和成就考试中的表现。 向用户提供性能反馈信息,包括常规信息,例如正确数量和经过时间的常规信息,确定用户弱或强的特定检查的实质性区域,并提供针对某一特定检查的诊断和修复 用户的个人困难。 通过评估用户对给定考试问题的回答,通过在多项选择问题的错误答案中表现的各种干扰误差模式,或通过用户对受限制的开放式项目的响应的编码类别的响应,初步诊断 进行用户的知识和/或考试技能缺陷。 随后使用额外的检查问题来改进初步诊断。 然后利用精细诊断为个人用户提供建议,以改善用户表现的错误模式。 使用后续修复活动确认和加强用户对此修复的响应。