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    • 1. 发明申请
    • Method for analyzing a nucleic acid
    • 分析核酸的方法
    • US20070178452A1
    • 2007-08-02
    • US10277951
    • 2002-10-21
    • Pascal BouffardJohn HerrmannChunli HuangMichael JeffersJingfang JuLuca RastelliJuliette ShimketsJan SimonsBruce Taillon
    • Pascal BouffardJohn HerrmannChunli HuangMichael JeffersJingfang JuLuca RastelliJuliette ShimketsJan SimonsBruce Taillon
    • C12Q1/68G06F19/00
    • C12N15/1096C12Q2600/158G16B30/00
    • Disclosed is a method in which DNA sequences derived from microsome-associated mRNA sequences in a mixed sample or in an arrayed single sequence clone can be determined and classified without sequencing. The methods make use of information on the presence of carefully chosen target subsequences, typically of length from 4 to 8 base pairs, and preferably the length between target subsequences in a sample DNA sequence together with DNA sequence databases containing lists of sequences likely to be present in the sample to determine a sample sequence. The preferred method uses restriction endonucleases to recognize target subsequences and cut the sample sequence. Then carefully chosen recognition moieties are ligated to the cut fragments, the fragments amplified, and the experimental observation made. Polymerase chain reaction (PCR) is the preferred method of amplification. Another embodiment of the invention uses information on the presence or absence of carefully chosen target subsequences in a single sequence clone together with DNA sequence databases to determine the clone sequence. Computer implemented methods are provided to analyze the experimental results and to determine the sample sequences in question and to carefully choose target subsequences in order that experiments yield a maximum amount of information
    • 公开了可以确定和分类来自混合样品或排列单序列克隆中的微粒体相关mRNA序列的DNA序列而不进行测序的方法。 这些方法利用关于精确选择的目标子序列的存在的信息,通常长度为4至8个碱基对,优选样品DNA序列中目标子序列之间的长度以及含有可能存在的序列的DNA序列数据库 在样品中确定样品序列。 优选的方法是使用限制性核酸内切酶识别目标子序列并切割样品序列。 然后仔细选择识别部分连接到切割片段,扩增片段,并进行实验观察。 聚合酶链反应(PCR)是优选的扩增方法。 本发明的另一个实施方案使用关于在单个序列克隆中与DNA序列数据库一起存在或不存在仔细选择的目标子序列的信息来确定克隆序列。 提供计算机实现的方法来分析实验结果并确定所讨论的样本序列,并仔细选择目标子序列,以便实验产生最大量的信息
    • 10. 发明授权
    • Methods of prevention and treatment of inflammatory bowel disease
    • 预防和治疗炎症性肠病的方法
    • US06982250B2
    • 2006-01-03
    • US10011364
    • 2001-11-16
    • Henry LichensteinMichael Jeffers
    • Henry LichensteinMichael Jeffers
    • A61K38/00C07K17/00
    • C07K14/50A61K38/00C07K14/49C07K14/51C07K14/52
    • The present invention is based upon methods of treating inflammatory conditions in the intestinal tract of mammals using growth factor related polypeptides. The invention includes methods of reducing the morality rate or delaying mortality in a subject suffering from an inflammatory pathology. Methods of using fibroblast growth factor-CX (FGF-CX) polynucleotide sequences and the FGF-CX polypeptides encoded by such nucleic acid sequences, or variants, fragments and homologs thereof, are claimed in the invention. Similarly, methods of using FCTRX polynucleotide sequences and the FCTRX polypeptides encoded by such nucleic acid sequences, or variants, fragments and homologs thereof, alone or in combination, are also claimed in the invention. FCTRX collectively refers to any of six variant FCTRX sequences, variously designated FCTR1, FCTR2, FCTR3, FCTR4, FCTR5 and FCTR6.
    • 本发明是基于使用生长因子相关多肽治疗哺乳动物肠道炎症状况的方法。 本发明包括降低患有炎性病理学的受试者的道德率或延缓死亡率的方法。 在本发明中要求使用成纤维细胞生长因子CX(FGF-CX)多核苷酸序列和由这种核酸序列编码的FGF-CX多肽或其变体,片段和同系物的方法。 类似地,在本发明中还要求保护使用FCTRX多核苷酸序列和由此类核酸序列编码的FCTRX多肽,或其变体,片段和同源物单独或组合使用的方法。 FCTRX统称为六种变体FCTRX序列中的任何一种,分别为FCTR1,FCTR2,FCTR3,FCTR4,FCTR5和FCTR6。