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1. 发明申请

US20090084148A1 TREATMENT OF ORGANIC MATTER SLUDGES 失效
标题翻译：有机物质处理
公开(公告)号：US20090084148A1
公开(公告)日：2009-04-02
申请号：US11917523
申请日：2006-07-14
申请人： Hendrik J. Venter , Carl Nieuwmeijer
发明人： Hendrik J. Venter , Carl Nieuwmeijer
IPC分类号： C05F7/00
CPC分类号： C05F3/00 , C05F7/00 , Y02A40/205 , Y02A40/213 , Y02P20/145 , Y02W10/37
摘要： A process for treating an organic matter sludge includes, in a mixing stage, mixing an organic matter sludge and particulate sterilized organic matter, to form an organic matter mixture. This mixture is dried in a drying stage to obtain a homogeneous particulate organic product.
摘要翻译：处理有机物污泥的方法包括在混合阶段中混合有机物污泥和颗粒灭菌的有机物，形成有机物混合物。将该混合物在干燥阶段干燥以获得均匀的颗粒状有机产物。

2. 发明申请

US20070037165A1 Polymorphisms in known genes associated with human disease, methods of detection and uses thereof 审中-公开
标题翻译：与人类疾病相关的已知基因的多态性，检测方法及其用途
公开(公告)号：US20070037165A1
公开(公告)日：2007-02-15
申请号：US10940774
申请日：2004-09-15
申请人： J. Venter , Jinghui Zhang , Xiangjun Liu , William Rowe , Anibal Cravchik , Francis Kalush , Ashwinikumar Naik , Gangadharan Subramanian , Trevor Woodage
发明人： J. Venter , Jinghui Zhang , Xiangjun Liu , William Rowe , Anibal Cravchik , Francis Kalush , Ashwinikumar Naik , Gangadharan Subramanian , Trevor Woodage
IPC分类号： C12Q1/68 , C07H21/04
CPC分类号： C12Q1/6883 , C12Q2600/156
摘要： The present invention is based on the discovery of novel polymorphisms (SNPs) in the genes known in the art to contribute to human disease. Such polymorphisms can lead to a variety of disorders that are mediated/modulated by a variant human disease associated protein. The present invention provides reagents used for detecting and expressing the variant nucleic acid/protein sequence as well as methods of identifying and using these variants.
摘要翻译：本发明是基于本领域已知的有助于人类疾病的基因中的新型多态性（SNP）的发现。这种多态性可导致由变异的人类疾病相关蛋白介导/调节的多种病症。本发明提供用于检测和表达变体核酸/蛋白质序列的试剂以及鉴定和使用这些变体的方法。

3. 发明申请

US20050147987A1 Polymorphisms in known genes associated with type II diabetes and obesity, methods of detection and uses thereof 审中-公开
标题翻译：与II型糖尿病和肥胖相关的已知基因的多态性，检测方法及其用途
公开(公告)号：US20050147987A1
公开(公告)日：2005-07-07
申请号：US10893315
申请日：2004-07-19
申请人： J. Venter , Jinghui Zhang , Xiangjun Liu , William Rowe , Anibal Cravchik , Francis Kalush , Ashwinikumar Naik , Gangadharan Subramanian , Trevor Woodage
发明人： J. Venter , Jinghui Zhang , Xiangjun Liu , William Rowe , Anibal Cravchik , Francis Kalush , Ashwinikumar Naik , Gangadharan Subramanian , Trevor Woodage
IPC分类号： C07H21/04 , C12Q1/68
CPC分类号： C12Q1/6883 , C07H21/04 , C12Q2600/156
摘要： The present invention is based on the discovery of novel polymorphisms (SNPs) in the genes known in the art to contribute to type II diabetes and obesity. Such polymorphisms can lead to a variety of disorders that are mediated/modulated by a variant type II diabetes and obesity associated protein. The present invention provides reagents used for detecting and expressing the variant nucleic acid/protein sequence as well as methods of identifying and using these variants.
摘要翻译：本发明基于本领域已知的用于II型糖尿病和肥胖症的基因中的新型多态性（SNP）的发现。这种多态性可导致由变异II型糖尿病和肥胖相关蛋白介导/调节的多种病症。本发明提供用于检测和表达变体核酸/蛋白质序列的试剂以及鉴定和使用这些变体的方法。

4. 发明申请

US20070269862A1 Installation of genomes or partial genomes into cells or cell-like systems 有权
标题翻译：将基因组或部分基因组安装到细胞或细胞样系统中
公开(公告)号：US20070269862A1
公开(公告)日：2007-11-22
申请号：US11644713
申请日：2006-12-22
申请人： John Glass , Lei Young , Carole Lartigue , Nacyra Assad-Garcia , Hamilton Smith , Clyde Hutchison , J. Venter
发明人： John Glass , Lei Young , Carole Lartigue , Nacyra Assad-Garcia , Hamilton Smith , Clyde Hutchison , J. Venter
IPC分类号： C12N15/87 , C12N5/06 , C12P21/04
CPC分类号： C12P21/02 , C12N2510/00
摘要： A method is provided for introducing a genome into a cell or cell-like system. The introduced genome may occur in nature, be manmade with or without automation, or may be a hybrid of naturally occurring and manmade materials. The genome is obtained outside of a cell with minimal damage. Materials such as a proteins, RNAs, polycations, nucleoid condensation proteins, or gene translation systems may accompany the genome. The genome is installed into a naturally occurring cell or into a manmade cell-like system. A cell-like system or synthetic cell resulting from the practice of the provided method may be designed and used to yield gene-expression products, such as desired proteins. By enabling the synthesis of cells or cell-like systems comprising a wide variety of genomes, accompanying materials and membrane types, the provided method makes possible a broader field of experimentation and bioengineering than has been available using prior art methods.
摘要翻译：提供了将基因组导入细胞或细胞样系统的方法。引入的基因组可以在自然界中发生，在有或没有自动化的情况下是人造的，或者可以是天然存在的和人造的材料的混合物。基因组以最小的损伤在细胞外获得。材料如蛋白质，RNAs，聚阳离子，核仁缩合蛋白或基因翻译系统可能伴随着基因组。将基因组安装到天然存在的细胞或人造细胞样系统中。可以设计并使用由所提供的方法的实践产生的细胞样系统或合成细胞来产生基因表达产物，例如所需的蛋白质。通过实现包含各种各样的基因组，伴随材料和膜类型的细胞或细胞样系统的合成，所提供的方法可能比使用现有技术方法可用的更广泛的实验和生物工程领域。

5. 发明申请

US20070037162A1 Polymorphisms in known genes associated with osteoporosis, methods of detection and uses thereof 审中-公开
标题翻译：与骨质疏松症相关的已知基因中的多态性，检测方法及其用途
公开(公告)号：US20070037162A1
公开(公告)日：2007-02-15
申请号：US10893319
申请日：2004-07-19
申请人： J. Venter , Jinghui Zhang , Xiangjun Liu , William Rowe , Anibal Cravchik , Francis Kalush , Ashwinikumar Naik , Gangadharan Subramanian , Trevor Woodage
发明人： J. Venter , Jinghui Zhang , Xiangjun Liu , William Rowe , Anibal Cravchik , Francis Kalush , Ashwinikumar Naik , Gangadharan Subramanian , Trevor Woodage
IPC分类号： C12Q1/68 , C07H21/04
CPC分类号： C12Q1/6883 , C12Q2600/156
摘要： The present invention is based on the discovery of novel polymorphisms (SNPs) in the genes known in the art to contribute to osteoporosis. Such polymorphisms can lead to a variety of disorders that are mediated/modulated by a variant osteoporosis associated protein. The present invention provides reagents used for detecting and expressing the variant nucleic acid/protein sequence as well as methods of identifying and using these variants.
摘要翻译：本发明基于本领域已知的有助于骨质疏松症的基因中的新型多态性（SNP）的发现。这种多态性可导致由变异性骨质疏松症相关蛋白介导/调节的多种病症。本发明提供用于检测和表达变体核酸/蛋白质序列的试剂以及鉴定和使用这些变体的方法。

6. 发明申请

US20050208558A1 Detection kits, such as nucleic acid arrays, for detecting the expression or 10,000 or more Drosophila genes and uses thereof 审中-公开
标题翻译：检测试剂盒，例如核酸阵列，用于检测表达或10,000或更多果蝇基因及其用途
公开(公告)号：US20050208558A1
公开(公告)日：2005-09-22
申请号：US11097143
申请日：2005-04-04
申请人： J. Venter , Mark Adams , Peter Li , Eugene Meyers
发明人： J. Venter , Mark Adams , Peter Li , Eugene Meyers
IPC分类号： C12M1/34 , C12Q1/68 , G06F19/00
CPC分类号： C12Q1/6888 , B01J2219/00378 , B01J2219/00691 , B01J2219/00722 , C12Q1/6837 , C12Q2600/158 , G16B30/00
摘要： The present invention is based on the sequencing and assembly of the Drosophila melanogaster genome. The present invention provides the primary nucleotide sequence of a large portion of the Drosophila melanogaster genome in a series of genomic and predicted transcript sequences. This information is provided in the form of sequences and annotation information and can be used to generate nucleic acid detection reagents and kits such a nucleic acid arrays.
摘要翻译：本发明基于黑腹果蝇基因组的测序和装配。本发明提供了一系列基因组和预测转录本序列中大部分黑腹果蝇基因组的主要核苷酸序列。该信息以序列和注释信息的形式提供，并且可用于产生核酸检测试剂和试剂盒，例如核酸阵列。

7. 发明授权

US4191227A Attachment for a power tool 失效
标题翻译：电动工具附件
公开(公告)号：US4191227A
公开(公告)日：1980-03-04
申请号：US900877
申请日：1978-04-28
申请人： Daniel J. J. Venter
发明人： Daniel J. J. Venter
IPC分类号： B25B21/00 , B25B23/10
CPC分类号： B25B23/10 , B25B21/00
摘要： An attachment for a power tool which permits a fastener being driven-in by the power tool to be held in a stable condition. The attachment includes a channel with an aperture in the web. The nose of the power tool fits in this aperture and can be secured therein. Each flange of the channel has a slot therein and a slide element passes through these aligned slots. The slide element has a keyhole opening therein formed by an aperture and a contiguous slot. The aperture is dimensioned to permit the head of a fastener to pass therethrough and the slot is dimensioned to receive the shank of the fastener. The head of the fastener cannot pass through the slot. By moving the slide element either the slot or the aperture therein can be aligned with the aperture in the web. A spacer can be provided for engaging the surface into which the fastener is to be driven. The spacer can be adjustable in position with respect to the channel.
摘要翻译：用于电动工具的附件，其允许紧固件由电动工具驱动以保持在稳定状态。附件包括在网中具有孔的通道。电动工具的鼻子装配在该孔中并可固定在其中。通道的每个凸缘在其中具有槽，并且滑动元件穿过这些对齐的槽。滑动元件具有其中由孔和连续槽形成的锁孔。孔的尺寸被设计成允许紧固件的头部穿过其中，并且狭槽的尺寸被设计成容纳紧固件的柄部。紧固件的头部不能通过狭槽。通过移动滑动元件，槽或其中的孔可以与幅材中的孔对准。可以设置间隔件用于接合紧固件将被驱动到的表面。间隔件可以在相对于通道的位置可调节。

8. 发明授权

US07785386B2 Treatment of organic matter sludges 失效
标题翻译：有机污泥的处理
公开(公告)号：US07785386B2
公开(公告)日：2010-08-31
申请号：US11917523
申请日：2006-07-14
申请人： Hendrik J. Venter , Carl Nieuwmeijer
发明人： Hendrik J. Venter , Carl Nieuwmeijer
IPC分类号： C05F7/00 , C05F3/00 , C02F1/66 , C02F1/00 , C05F11/00 , C05F5/00 , C05F3/02
CPC分类号： C05F3/00 , C05F7/00 , Y02A40/205 , Y02A40/213 , Y02P20/145 , Y02W10/37
摘要： A process for treating an organic matter sludge includes, in a mixing stage, mixing an organic matter sludge and particulate sterilized organic matter, to form an organic matter mixture. This mixture is dried in a drying stage to obtain a homogeneous particulate organic product.
摘要翻译：处理有机物污泥的方法包括在混合阶段中混合有机物污泥和颗粒灭菌的有机物，形成有机物混合物。将该混合物在干燥阶段干燥以获得均匀的颗粒状有机产物。

9. 发明申请

US20070219347A1 Neisseria genomic sequences and methods of their use 审中-公开
标题翻译：奈瑟氏球菌基因组序列及其使用方法
公开(公告)号：US20070219347A1
公开(公告)日：2007-09-20
申请号：US11711740
申请日：2007-02-26
申请人： Claire Fraser , Erin Hickey , Jeremy Peterson , Herve Tettelin , J. Venter , Vega Masignani , Cesira Galeotti , Marirosa Mora , Giulio Ratti , Maria Scarselli , Vincenzo Scarlato , Rino Rappuoli , Mariagrazia Pizza , Guido Grandi
发明人： Claire Fraser , Erin Hickey , Jeremy Peterson , Herve Tettelin , J. Venter , Vega Masignani , Cesira Galeotti , Marirosa Mora , Giulio Ratti , Maria Scarselli , Vincenzo Scarlato , Rino Rappuoli , Mariagrazia Pizza , Guido Grandi
IPC分类号： C07K14/22 , C07H21/04 , C07K16/12 , C07K4/04 , C07K7/00
CPC分类号： C07K14/22 , A61K38/00 , A61K2039/53 , C12Q1/6886 , C12Q1/689
摘要： The invention provides methods of obtaining immunogenic proteins from genomic sequences including Neisseria, including the amino acid sequences and the corresponding nucleotide sequences, as well as the genomic sequence of Neisseria meningitidis B. The proteins so obtained are useful antigens for vaccines, immunogenic compositions, and/or diagnostics
摘要翻译：本发明提供了从包括奈瑟氏球菌在内的基因组序列获得免疫原性蛋白质的方法，包括氨基酸序列和相应的核苷酸序列，以及脑膜炎奈瑟氏球菌B的基因组序列。如此获得的蛋白质是疫苗，免疫原性组合物和 /或诊断

10. 发明申请

US20050131222A1 Nucleotide sequence of the haemophilus influenzae Rd genome, fragments thereof, and uses thereof 审中-公开
标题翻译：流感嗜血杆菌Rd基因组的核苷酸序列，其片段及其用途
公开(公告)号：US20050131222A1
公开(公告)日：2005-06-16
申请号：US10981687
申请日：2004-11-05
申请人： Robert Fleischmann , Mark Adams , Owen White , Hamilton Smith , J. Venter
发明人： Robert Fleischmann , Mark Adams , Owen White , Hamilton Smith , J. Venter
IPC分类号： C07K14/285 , C07H21/04
CPC分类号： C07K14/285
摘要： The present invention provides the sequencing of the entire genome of Haemophilus influenzae Rd, SEQ ID NO:1. The present invention further provides the sequence information stored on computer readable media, and computer-based systems and methods which facilitate its use. In addition to the entire genomic sequence, the present invention identifies over 1700 protein encoding fragments of the genome and identifies, by position relative to a unique Not I restriction endonuclease site, any regulatory elements which modulate the expression of the protein encoding fragments of the Haemophilus genome.
摘要翻译：本发明提供了流感嗜血杆菌Rd，SEQ ID NO：1的整个基因组的测序。本发明还提供存储在计算机可读介质上的序列信息，以及便于其使用的基于计算机的系统和方法。除了整个基因组序列之外，本发明鉴定了基因组的超过1700个蛋白质编码片段，并且通过相对于独特的Not I限制性内切核酸酶位点的位置鉴定调节嗜血杆菌蛋白编码片段的表达的任何调节元件基因组

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