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公开(公告)号:US20240166735A1
公开(公告)日:2024-05-23
申请号:US18350287
申请日:2023-07-11
发明人: Jae Young SEONG , Jong Ik HWANG , Woong SUN , Eun Bee CHO , Won-Ki KIM
IPC分类号: C07K16/24 , A61K38/17 , A61K48/00 , C07K14/47 , C07K16/18 , C12N15/113 , C12Q1/6886 , G01N33/577 , G01N33/68 , A61K39/00
CPC分类号: C07K16/24 , A61K38/1709 , A61K48/00 , C07K14/4701 , C07K14/4702 , C07K16/18 , C12N15/113 , C12Q1/6886 , G01N33/577 , G01N33/6896 , A61K2039/505 , C07K2317/31 , C07K2317/54 , C07K2317/55 , C07K2317/76 , C12N2310/11 , C12N2310/141 , C12Q2600/156 , G01N2333/47
摘要: The present invention relates to the pharmaceutical use of FAM19A5 involved in regulating gliogenesis, and more specifically, to the use of FAM19A5 in the prevention, diagnosis, or treatment of central nervous system injuries, degenerative brain diseases, or central nervous system diseases, FAM19A5 being spread in the neural stem cells in vertebrates and regulating gliogenesis.
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公开(公告)号:US20170226152A1
公开(公告)日:2017-08-10
申请号:US15299931
申请日:2016-10-21
申请人: CEM Corporation
发明人: JONATHAN M. COLLINS
IPC分类号: C07K1/04 , C07K1/14 , C07K1/06 , C07K14/575 , C07K14/605 , C07K14/815 , C07K14/635 , C07K14/59 , C07K14/705 , C07K14/645 , C07K14/005 , C12N7/00 , C07K14/47 , C07K7/08 , C07K7/16 , C07K14/46 , B01J19/12 , C07K1/107
CPC分类号: C07K1/045 , B01J19/126 , B01J2204/005 , B01J2219/00058 , B01J2219/0879 , B01J2219/1248 , C07K1/04 , C07K1/063 , C07K1/1075 , C07K1/14 , C07K7/08 , C07K7/16 , C07K14/005 , C07K14/463 , C07K14/4701 , C07K14/4723 , C07K14/575 , C07K14/57572 , C07K14/59 , C07K14/605 , C07K14/635 , C07K14/645 , C07K14/705 , C07K14/815 , C12N7/00 , C12N2740/16322
摘要: An improved method of deprotection in solid phase peptide synthesis is disclosed. In particular the deprotecting composition is added in high concentration and small volume to the mixture of the coupling solution, the growing peptide chain, and any excess activated acid from the preceding coupling cycle, and without any draining step between the coupling step of the previous cycle and the addition of the deprotection composition for the successive cycle. Thereafter, the ambient pressure in the vessel is reduced with a vacuum pull to remove the deprotecting composition without any draining step and without otherwise adversely affecting the remaining materials in the vessel or causing problems in subsequent steps in the SPPS cycle.
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公开(公告)号:US06620403B2
公开(公告)日:2003-09-16
申请号:US09841669
申请日:2001-04-24
申请人: Roman Perez-Soler
发明人: Roman Perez-Soler
IPC分类号: A61K4900
CPC分类号: A61K49/0008 , A01K2217/05 , C07K14/4701
摘要: A method of evaluating the chemosensitivity of a tumor to an anti-tumor agent in vivo is provided. The method comprises extracting a portion of a tumor from a human host and inserting the portion of the tumor into an immunodeficient mouse. The tumor portion is permitted to grow to a minimum preselected size to form a test tumor. An amount of an anti-tumor agent is administered to the immunodeficient mouse sufficient to determine whether the anti-tumor agent is effective in treating the test tumor. The anti-tumor activity of the anti-tumor agent on the test tumor is assessed.
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公开(公告)号:US20020031473A1
公开(公告)日:2002-03-14
申请号:US09841669
申请日:2001-04-24
发明人: Roman Perez-Soler
IPC分类号: A61K049/00 , A01K067/00
CPC分类号: A61K49/0008 , A01K2217/05 , C07K14/4701
摘要: A method of evaluating the chemosensitivity of a tumor to an anti-tumor agent in vivo is provided. The method comprises extracting a portion of a tumor from a human host and inserting the portion of the tumor into an immunodeficient mouse. The tumor portion is permitted to grow to a minimum preselected size to form a test tumor. An amount of an anti-tumor agent is administered to the immunodeficient mouse sufficient to determine whether the anti-tumor agent is effective in treating the test tumor. The anti-tumor activity of the anti-tumor agent on the test tumor is assessed.
摘要翻译: 提供了一种在体内评估肿瘤对抗肿瘤剂的化学敏感性的方法。 该方法包括从人宿主中提取肿瘤的一部分并将该部分肿瘤插入免疫缺陷小鼠。 允许肿瘤部分生长至最小预选大小以形成测试肿瘤。 向免疫缺陷小鼠施用足量的抗肿瘤剂量以确定抗肿瘤剂是否有效治疗试验肿瘤。 评估抗肿瘤剂对测试肿瘤的抗肿瘤活性。
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公开(公告)号:US20170121401A1
公开(公告)日:2017-05-04
申请号:US15404011
申请日:2017-01-11
发明人: Jae Young SEONG , Jong Ik Hwang , Woong Sun , Eun Bee Cho , Won-Ki Kim
IPC分类号: C07K16/24 , G01N33/577 , G01N33/68
CPC分类号: C07K16/24 , A61K38/1709 , A61K48/00 , A61K2039/505 , C07K14/4701 , C07K14/4702 , C07K16/18 , C07K2317/31 , C07K2317/54 , C07K2317/55 , C07K2317/76 , C12N15/113 , C12N2310/11 , C12N2310/141 , C12Q1/6886 , C12Q2600/156 , G01N33/577 , G01N33/6896 , G01N2333/47
摘要: The present invention relates to the pharmaceutical use of FAM19A5 involved in regulating gliogenesis, and more specifically, to the use of FAM19A5 in the prevention, diagnosis, or treatment of central nervous system injuries, degenerative brain diseases, or central nervous system diseases, FAM19A5 being spread in the neural stem cells in vertebrates and regulating gliogenesis.
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6.
公开(公告)号:US20150118230A1
公开(公告)日:2015-04-30
申请号:US14378505
申请日:2013-02-15
发明人: Jae Young Seong , Jong Ik Hwang , Woong Sun , Eun Bee Cho , Won-Ki Kim
IPC分类号: A61K48/00 , C07K16/18 , C12N15/113
CPC分类号: C07K16/24 , A61K38/1709 , A61K48/00 , A61K2039/505 , C07K14/4701 , C07K14/4702 , C07K16/18 , C07K2317/31 , C07K2317/54 , C07K2317/55 , C07K2317/76 , C12N15/113 , C12N2310/11 , C12N2310/141 , C12Q1/6886 , C12Q2600/156 , G01N33/577 , G01N33/6896 , G01N2333/47
摘要: The present invention relates to the pharmaceutical use of FAM19A5 involved in regulating gliogenesis, and more specifically, to the use of FAM19A5 in the prevention, diagnosis, or treatment of central nervous system injuries, degenerative brain diseases, or central nervous system diseases, FAM19A5 being spread in the neural stem cells in vertebrates and regulating gliogenesis.
摘要翻译: 本发明涉及涉及调节胶质发生的FAM19A5的药物用途,更具体地说,涉及使用FAM19A5预防,诊断或治疗中枢神经系统损伤,退行性脑病或中枢神经系统疾病,FAM19A5为 在脊椎动物的神经干细胞中扩散并调节胶质细胞发生。
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公开(公告)号:US07947804B1
公开(公告)日:2011-05-24
申请号:US09556178
申请日:2000-04-20
申请人: Olga Bandman , Preeti Lal , Karl J. Guegler , Purvi Shah , Neil C. Corley
发明人: Olga Bandman , Preeti Lal , Karl J. Guegler , Purvi Shah , Neil C. Corley
CPC分类号: C07K14/4701 , A61K38/00
摘要: The invention provides three human vesicle trafficking proteins (VTP) and polynucleotides which identify and encode VTP. The invention also provides expression vectors, host cells, agonists, antibodies and antagonists. The invention also provides methods for preventing and treating disorders associated with expression of VTP.
摘要翻译: 本发明提供了三种人囊泡运输蛋白(VTP)和识别和编码VTP的多核苷酸。 本发明还提供表达载体,宿主细胞,激动剂,抗体和拮抗剂。 本发明还提供了预防和治疗与VTP表达相关的疾病的方法。
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公开(公告)号:US20030143583A1
公开(公告)日:2003-07-31
申请号:US10261517
申请日:2002-10-01
IPC分类号: C12Q001/68 , G06F019/00 , G01N033/48 , G01N033/50 , C07H021/04 , C12N009/22 , C12P021/02 , C12N005/06
CPC分类号: C12N15/11 , C07K14/4701 , C07K14/4702 , C07K2319/00 , C12N15/85 , C12N2830/002
摘要: The present invention is directed to a novel Afx response element comprising the nucleotide sequence AACATGTT, said nucleotide sequence having a DNA binding site for the human fork head transkription factor Afx. The invention also relates to the use of the Afx response element in the screening for genes as diabetes drug targets and in the bioinformatic analysis of the human genome, said genes in turn being useful in other screening methods for compounds modifying the insulin receptor signaling pathway. A further aspect of the invention is a vector construct comprising the novel nucleotide sequence, a host cell transformed with said vector construct as well as the fusion protein expressed by said host cell.
摘要翻译: 本发明涉及包含核苷酸序列AACATGTT的新型Afx应答元件,所述核苷酸序列具有人叉头转录因子Afx的DNA结合位点。 本发明还涉及Afx应答元件在筛选基因作为糖尿病药物靶标和在人类基因组的生物信息学分析中的用途,所述基因又可用于修饰胰岛素受体信号通路的化合物的其它筛选方法。 本发明的另一方面是载体构建体,其包含新的核苷酸序列,用所述载体构建体转化的宿主细胞以及由所述宿主细胞表达的融合蛋白。
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公开(公告)号:US20240279330A1
公开(公告)日:2024-08-22
申请号:US18542152
申请日:2023-12-15
IPC分类号: C07K16/28 , A61K38/00 , A61K39/00 , A61K47/68 , B82Y5/00 , C07K7/08 , C07K14/47 , C07K14/77 , C07K16/18 , C07K16/30
CPC分类号: C07K16/28 , A61K39/0008 , A61K39/001 , A61K47/6849 , B82Y5/00 , C07K7/08 , C07K14/4701 , C07K14/77 , C07K16/18 , C07K16/30 , A61K38/00 , A61K2039/505 , A61K2039/6031 , A61K2039/6056 , C07K2317/34 , C07K2317/622 , C07K2319/00 , C07K2319/01 , C07K2319/21 , C07K2319/22 , C07K2319/23 , C07K2319/33 , C07K2319/41 , C07K2319/43 , C07K2319/74
摘要: Peptides that specifically bind erythrocytes are described. These are provided as peptidic ligands having sequences that specifically bind, or as antibodies or fragments thereof that provide specific binding, to erythrocytes. The peptides may be prepared as molecular fusions with therapeutic agents, tolerizing antigens, or targeting peptides. Immunotolerance may be created by use of the fusions and choice of an antigen on a substance for which tolerance is desired. Fusions with targeting peptides direct the fusions to the target, for instance a tumor, where the erythrocyte-binding ligands reduce or entirely eliminate blood flow to the tumor by recruiting erythrocytes to the target.
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公开(公告)号:US11884721B2
公开(公告)日:2024-01-30
申请号:US17143731
申请日:2021-01-07
IPC分类号: A61K39/00 , A61K47/68 , B82Y5/00 , C07K14/47 , C07K16/18 , C07K16/28 , C07K16/30 , C07K7/08 , C07K14/77 , A61K38/00
CPC分类号: C07K16/28 , A61K39/001 , A61K39/0008 , A61K47/6849 , B82Y5/00 , C07K7/08 , C07K14/4701 , C07K14/77 , C07K16/18 , C07K16/30 , A61K38/00 , A61K2039/505 , A61K2039/6031 , A61K2039/6056 , C07K2317/34 , C07K2317/622 , C07K2319/00 , C07K2319/01 , C07K2319/22 , C07K2319/23 , C07K2319/33 , C07K2319/41 , C07K2319/43 , C07K2319/74 , A61K2039/57 , A61K2039/577
摘要: Peptides that specifically bind erythrocytes are described. These are provided as peptidic ligands having sequences that specifically bind, or as antibodies or fragments thereof that provide specific binding, to erythrocytes. The peptides may be prepared as molecular fusions with therapeutic agents, tolerizing antigens, or targeting peptides. Immunotolerance may be created by use of the fusions and choice of an antigen on a substance for which tolerance is desired. Fusions with targeting peptides direct the fusions to the target, for instance a tumor, where the erythrocyte-binding ligands reduce or entirely eliminate blood flow to the tumor by recruiting erythrocytes to the target.
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