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    • 4. 发明授权
    • Method of inducing cell death using West Nile virus capsid protein
    • 使用西尼罗病毒衣壳蛋白诱导细胞死亡的方法
    • US07348138B2
    • 2008-03-25
    • US10966576
    • 2004-10-14
    • David B. WeinerJoo-Sung YangKaruppiah Muthumani
    • David B. WeinerJoo-Sung YangKaruppiah Muthumani
    • C12Q1/70A61K39/12
    • A61K38/162A61K48/00A61K2039/53C07K14/005C07K2319/02C12N2740/16222C12N2770/24122C12N2770/24322G01N33/56983G01N2469/20Y02A50/394
    • This invention provides methods of inducing cell death with Flavivirus or Pestivirus capsid protein, such as West Nile virus (WNV) capsid protein, and functional fragments thereof. The invention also provides methods of treating patients suffering from diseases characterized by hyperproliferating cells by administering pharmaceutical compositions comprising WNV or other virus including Flavivirus or Pestivirus capsid or other protein or a nucleic acid molecule encoding the same. Methods of identifying compounds which have anti-viral and/or anti-WNV and/or anti-Flavivirus and/or anti-Pestivirus capsid or other protein activity are disclosed. The invention also provides vaccine compositions comprising capsid or other proteins, or fragments thereof, or nucleic acids encoding same, from WNV or other virus including Flavivirus or Pestivirus and a pharmaceutically acceptable carrier. The invention also provides diagnostic methods and kits for identifying individuals exposed to WNV or other viruses including Flavivirus or Pestivirus.
    • 本发明提供了用黄病毒或瘟病毒衣壳蛋白(例如西尼罗河病毒(WNV)衣壳蛋白)及其功能片段诱导细胞死亡的方法。 本发明还提供了通过施用包含WNV或其它病毒(包括黄病毒或瘟病毒衣壳或其他蛋白质)的药物组合物或其编码的核酸分子来治疗患有特征在于过度增殖细胞的疾病的患者的方法。 公开了鉴定具有抗病毒和/或抗WNV和/或抗黄病毒和/或抗瘟病毒衣壳或其它蛋白质活性的化合物的方法。 本发明还提供包含衣壳或其它蛋白质或其片段,或编码其的核酸的疫苗组合物,来自WNV或其它病毒,包括黄病毒或瘟病毒和药学上可接受的载体。 本发明还提供用于鉴定暴露于WNV或其它病毒(包括黄病毒或瘟病毒)的个体的诊断方法和试剂盒。
    • 6. 发明授权
    • Highly expressible genes
    • 高度可表达的基因
    • US06733994B2
    • 2004-05-11
    • US09971806
    • 2001-10-04
    • David B. WeinerJoo-Sung Yang
    • David B. WeinerJoo-Sung Yang
    • C12P2102
    • A61K38/162A61K48/00A61K2039/53C07K14/005C07K2319/02C12N2740/16222C12N2770/24122C12N2770/24322G01N33/56983G01N2469/20Y02A50/394
    • The present invention provides methods of producing protein in a recombinant expression system that comprises translation of mRNA transcribed from a heterologous DNA sequence in the expression system, said method comprising the steps of predicting the secondary structure of mRNA transcribed from a native heterologous DNA sequence; modifying the native heterologous DNA sequence to produce a modified heterologous DNA sequence wherein mRNA transcribed from the modified heterologous DNA sequence has a secondary structure having increased free energy compared to that of the secondary structure of the mRNA transcribed from the native heterologous DNA sequence; and using the modified heterologous DNA sequence in the recombinant expression system for protein production. The invention also provides injectable pharmaceutical compositions comprising a nucleic acid molecule that includes a modified coding sequence. The invention also provides recombinant viral vectors comprising a nucleic acid molecule that includes a modified coding sequence.
    • 本发明提供了在重组表达系统中产生蛋白质的方法,该重组表达系统包括从表达系统中异源DNA序列转录的mRNA的翻译,所述方法包括预测从天然异源DNA序列转录的mRNA的二级结构的步骤; 修饰天然异源DNA序列以产生修饰的异源DNA序列,其中从修饰的异源DNA序列转录的mRNA具有与从天然异源DNA序列转录的mRNA的二级结构相比具有增加的自由能的二级结构; 并在重组表达系统中使用修饰的异源DNA序列进行蛋白质生产。 本发明还提供了包含核酸分子的可注射药物组合物,其包含修饰的编码序列。 本发明还提供包含核酸分子的重组病毒载体,其包含修饰的编码序列。