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    • 81. 发明申请
    • MOBILE ROBOT INTERNAL POSITION ERROR CORRECTION SYSTEM
    • 移动机器人内部位置错误校正系统
    • WO1995022041A1
    • 1995-08-17
    • PCT/US1995001859
    • 1995-02-14
    • THE REGENTS OF THE UNIVERSITY OF MICHIGAN
    • THE REGENTS OF THE UNIVERSITY OF MICHIGANBORENSTEIN, Johann
    • G01C21/12
    • G01C21/12G05D1/0255G05D1/0272
    • An improved device and method for performing accurate mobile robot dead-reckoning by performing Internal Position Error Correction (IPEC) which corrects systematic as well as non-systematic dead-reckoning errors. A first variation utilizes a smart encoder trailer (22) which adapts an existing dead-reckoning mobile robot (20). A second variation (71) provides a pair of robotic vehicles (72, 74) coupled with a compliant linkage (76) which monitors relative positioning between the vehicles (72, 74) in order to perform internal position error correction. A third and final variation utilizes a pair of decoupled mobile robotic vehicles (110, 112), each performing dead-reckoning, further provided with individual transmitter (122, 124) and receiver (126, 128) arrays which determine relative positioning therebetween in order to perform internal position error correction.
    • 一种改进的设备和方法,用于通过执行内部位置误差校正(IPEC)来执行精确的移动机器人推算,其校正系统和非系统的推算误差。 第一变型使用智能编码器拖车(22),其适应现有的推算机器人(20)。 第二变型(71)提供一对机器人车辆(72,74),该机器人车辆与顺应性联动装置(76)联接,该顺应联动装置监测车辆(72,74)之间的相对定位,以执行内部位置误差校正。 第三和最后的变型使用一对解耦的移动机器人车辆(110,112),每一个执行推算,进一步提供有单独的发射器(122,124)和接收器(126,128)阵列,其依次确定它们之间的相对定位 执行内部位置误差校正。
    • 85. 发明申请
    • METHOD FOR GENERATING CHROMOSOME REGION-SPECIFIC PROBES
    • 用于产生染色体区域特异性探针的方法
    • WO1993011265A1
    • 1993-06-10
    • PCT/US1992010429
    • 1992-12-03
    • THE REGENTS OF THE UNIVERSITY OF MICHIGAN
    • THE REGENTS OF THE UNIVERSITY OF MICHIGANTRENT, Jeffrey, M.MELTZER, Paul, S.
    • C12Q01/68
    • C12N15/1093C12Q1/6841C12Q1/6853C12Q1/6876C12Q2600/156G01T1/1648G21K1/025
    • The present invention provides rapid, reproducible procedures for generating chromosome region-specific probes (CRSPs) for diagnostic and research applications. Region-specific probes are provided by direct in vitro enzymatic amplification (PCR) of microdissected chromosomal or hyridized DNA from the chromosomal region of interest, followed by labelling for in situ hybridization to metaphase chromosomes and interphase nuclei. CRSP specificity can be further enhanced using a linker-based strategy, wherein linkered DNA (LDNA) sequences prepared from DNA libraries are hybridized to chromosomal DNA in situ, microdissected from the chromosomal region of interest and then directly amplified using the linker as primer. These procedures make it possible to generate a vast number of chromosome region-specific probes without microchemical manipulation after dissection and provide means for identifying cryptic chromosomal alterations previously not amenable to routine cytogenetic analysis. Probes generated by the methods of the present invention can also be used for screening any DNA library of interest.
    • 本发明提供用于产生用于诊断和研究应用的染色体区特异性探针(CRSP)的快速,可再现的程序。 区域特异性探针通过目的染色体区域的显微切割染色体或杂交DNA的直接体外酶扩增(PCR)提供,然后进行标记用于中期染色体和间期核的原位杂交。 可以使用基于接头的策略进一步提高CRSP特异性,其中由DNA文库制备的接头DNA(LDNA)序列原位杂交到染色体DNA,并从感兴趣的染色体区域显微切割,然后使用接头作为引物直接扩增。 这些程序使得可以在解剖后产生大量的染色体区域特异性探针而不进行微量化学操作,并提供用于鉴定以前不适合于常规细胞遗传学分析的隐性染色体改变的方法。 通过本发明的方法产生的探针也可以用于筛选目的的任何DNA文库。
    • 86. 发明申请
    • TREATMENT OF CYSTIC FIBROSIS
    • CYSTIC FIBROSIS的治疗
    • WO1993007265A1
    • 1993-04-15
    • PCT/US1992008346
    • 1992-09-30
    • THE REGENTS OF THE UNIVERSITY OF MICHIGAN
    • THE REGENTS OF THE UNIVERSITY OF MICHIGANCOLLINS, Francis, S.DRUMM, Mitchell, L.DAWSON, David, C.WILKINSON, Daniel, W.
    • C12N15/00
    • A61K45/06A61K38/00C07K14/4712
    • Cystic fibrosis (CF), a lethal genetic disease associated with a defect in Cl transport, is caused by mutations in the gene coding for cystic fibrosis transmembrane conductance regulator (CFTR). Surprisingly, not only wild type CFTR, but several naturally-occurring CFTR mutants carrying a defect in the first nucleotide binding fold (NFB1) all expressed cAMP-activatable Cl currents. Treatment of the CFTR mutants with appropriate concentrations of methylxanthine phosphodiesterase inhibitor (which increases cAMP levels) activated Cl conductance to near wild type levels. The present invention thus provides a new avenue for treating cystic fibrosis by the administration of therapeutically effective amounts of compounds which elevate cAMP levels. Dosage and patient responsiveness to treatment, as well as relative efficacies of the compounds being or to be administered can also be determined in accordance with the methods of present invention.
    • 囊性纤维化(CF)是与C1转运缺陷相关的致命遗传疾病,由编码囊性纤维化跨膜传导调节因子(CFTR)的基因突变引起。 令人惊讶的是,不仅野生型CFTR,而是在第一核苷酸结合折叠(NFB1)中携带缺陷的几种天然存在的CFTR突变体都表达cAMP可激活的Cl电流。 用适当浓度的甲基黄嘌呤磷酸二酯酶抑制剂(其增加cAMP水平)处理CFTR突变体将Cl电导活化到接近野生型水平。 因此,本发明通过施用治疗有效量的提高cAMP水平的化合物来提供治疗囊性纤维化的新途径。 治疗的剂量和患者反应性以及正在或将被给予的化合物的相对功效也可以根据本发明的方法来确定。