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    • 43. 发明申请
    • SYSTEMS AND METHODS FOR RECOVERING INFORMATION FROM NAND GATES ARRAY MEMORY SYSTEMS
    • 用于从NAND门阵列存储器系统恢复信息的系统和方法
    • US20110055626A1
    • 2011-03-03
    • US12910132
    • 2010-10-22
    • Qing YangWeijun Xiao
    • Qing YangWeijun Xiao
    • G06F11/14
    • G06F11/1008G06F11/0727G06F11/073G06F11/0793G06F11/1076
    • A method is disclosed for recovering data associated with a damaged file stored in a NAND gate array memory. The method includes the steps of: identifying all meta data associated with the damaged file; identifying each logical block address of all identified meta data; collecting all physical block addresses associated with one of the identified logical block addresses or the identified meta data; counting in a replace table (ReplTable) a number of matches to a physical block address of the damaged file for each physical block address of the damaged file; choosing a block in a linked list that corresponds to the physical block address of the block in the linked list; and linking all chosen blocks to form a replicated file.
    • 公开了一种用于恢复与存储在NAND门阵列存储器中的损坏文件相关联的数据的方法。 该方法包括以下步骤:识别与损坏文件相关联的所有元数据; 识别所有识别的元数据的每个逻辑块地址; 收集与所识别的逻辑块地址之一相关联的所有物理块地址或所识别的元数据; 在替换表(ReplTable)中计数与损坏文件的每个物理块地址的损坏文件的物理块地址的匹配数; 在链表中选择与链表中的块的物理块地址对应的块; 并链接所有选定的块以形成复制文件。
    • 47. 发明授权
    • Live, avirulent strain of V. anguillarum that protects fish against infection by virulent V. anguillarum and method of making the same
    • 鳗鱼的活的无毒力菌株,可保护鱼类免受毒性鳗鱼的感染及其制作方法
    • US06913757B1
    • 2005-07-05
    • US10780347
    • 2004-02-17
    • David R. Nelson
    • David R. Nelson
    • A61K39/106C07K14/28
    • A61K39/107C07K14/28Y02A50/472
    • The present invention comprises the identification, characterization and sequencing of a gene within the V. anguillarum genome, the mugA gene, a live, attenuated strain of V. anguillarum which comprises a mutated mugA gene, methods of making the strain, vaccines comprising the strain and methods of making such vaccines and administering the vaccines to animals. The invention further comprises vaccines comprised of proteins encoded by the mugA gene, to methods of making such vaccines and administering the vaccines to animals, to vectors comprised of the attenuated strain of V.anguillarum and additional immunizing materials, methods of making the vectors and methods of administering the vectors to animals. Also disclosed are probes, passive vaccines and monoclonal antibodies for the detection and prevention of vibriosis.
    • 本发明包括对鳗弧菌基因组中的基因的鉴定,表征和测序,其包含变异的mugA基因的mugA基因,鳗弧菌的活的,减毒的菌株,制备菌株的方法,包含菌株的疫苗 以及制备这种疫苗并将疫苗给予动物的方法。 本发明还包括由mugA基因编码的蛋白质组成的疫苗,制备这样的疫苗和向动物施用疫苗的方法,包括由镰刀菌的减毒株和另外的免疫材料组成的载体,制备载体的方法和方法 向动物施用载体。 还公开了用于检测和预防弧菌病的探针,被动疫苗和单克隆抗体。
    • 48. 发明授权
    • Process to prepare pyrimidine nucleosides
    • 制备嘧啶核苷的方法
    • US6121438A
    • 2000-09-19
    • US327739
    • 1999-06-08
    • Elie AbushanabPalle V. P. Pragnacharyulu
    • Elie AbushanabPalle V. P. Pragnacharyulu
    • C07H19/06C07H19/073
    • C07H19/06
    • A process for the production of a compound of the formula: ##STR1## wherein R.sub.1 is hydrogen, alkyl C.sub.1 -C.sub.16 substituted alkyl, aryl, substituted aryl, aralkyl, substituted aralkyls, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cyano, carboxy, carboxy esters, carboxamido, N-mono substituted and N,N-disubstituted carboxamido with alkyl, aralkyl and aryl groups; R.sub.2 is hydrogen, alkyl C.sub.1 -C.sub.16 substituted alkyl, aryl, substituted aryl, aralkyl, substituted aralkyls, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl; R.sub.3 is alkyl C.sub.2 -C.sub.6, branched alkyl, aryl C.sub.2 -C.sub.6, substituted aryl and R.sub.4 is halogen or H. A condensation reaction is effected between compounds of the formulae: ##STR2## to form a novel compound of the formula: ##STR3## Compound (2) is acylated with a compound of the formula:R.sub.3 COClto form a novel compound of the formula: ##STR4## Compound (3) is mixed with pyridine and is reacted with thionyl chloride to form compound (4) and compound (4) is dehalogenated to form compound (5).
    • 制备下式化合物的方法:其中R 1是氢,烷基C 1 -C 16取代的烷基,芳基,取代的芳基,芳烷基,取代的芳烷基,烯基,取代的烯基,炔基,取代的炔基,氰基,羧基,羧基酯 芳基,芳烷基和芳基; N,N-二取代的甲酰氨基; R2是氢,烷基C1-C16取代的烷基,芳基,取代的芳基,芳烷基,取代的芳烷基,烯基,取代的烯基,炔基,取代的炔基; R3是烷基C2-C6,支链烷基,芳基C2-C6,取代的芳基,R4是卤素或H.在下式化合物之间进行缩合反应:形成下式的新型化合物:化合物(2)被酰化 与下式的化合物反应形成下式化合物:化合物(3)与吡啶混合并与亚硫酰氯反应形成化合物(4),化合物(4)脱卤以形成化合物(5) 。