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21. 发明授权

US07964377B2 Nucleic acid molecule encoding a fusion polypeptide capable of binding VEGF 有权
标题翻译：编码能够结合VEGF的融合多肽的核酸分子
公开(公告)号：US07964377B2
公开(公告)日：2011-06-21
申请号：US12334927
申请日：2008-12-15
申请人： Nicholas J. Papadopoulos , Samuel Davis , George D. Yancopoulos
发明人： Nicholas J. Papadopoulos , Samuel Davis , George D. Yancopoulos
IPC分类号： C12N15/62 , C12N15/63 , A61K38/18 , C07K14/00 , C07K14/71
CPC分类号： C07K14/71 , A61K38/00 , C07K16/22 , C07K19/00 , C07K2319/00 , C07K2319/30
摘要： Modified chimeric polypeptides with improved pharmacokinetics are disclosed. Specifically, modified chimeric Flt1 receptor polypeptides that have been modified in such a way as to improve their pharmacokinetic profile are disclosed. Also disclosed are methods of making and using the modified polypeptides including but not limited to using the modified polypeptides to decrease or inhibit plasma leakage and/or vascular permeability in a mammal.
摘要翻译：公开了具有改善的药代动力学的修饰的嵌合多肽。具体地，公开了已经以改善其药代动力学特征的方式修饰的修饰的嵌合Flt1受体多肽。还公开了制备和使用修饰的多肽的方法，包括但不限于使用修饰的多肽来降低或抑制哺乳动物的血浆渗透和/或血管通透性。

22. 发明授权

US07704500B2 Methods of inhibiting ascites formation with modified chimeric VEGF polypeptides 有权
标题翻译：用修饰的嵌合VEGF多肽抑制腹水形成的方法
公开(公告)号：US07704500B2
公开(公告)日：2010-04-27
申请号：US12102681
申请日：2008-04-14
申请人： Nicholas J. Papadopoulos , Samuel Davis , George D. Yancopoulos
发明人： Nicholas J. Papadopoulos , Samuel Davis , George D. Yancopoulos
IPC分类号： A61K38/18 , C07K14/71 , C12N15/62
CPC分类号： C07K14/71 , A61K38/00 , C07K16/22 , C07K19/00 , C07K2319/00 , C07K2319/30
摘要： Modified chimeric polypeptides with improved pharmacokinetics are disclosed. Specifically, modified chimeric Flt1 receptor polypeptides that have been modified in such a way as to improve their pharmacokinetic profile are disclosed. Also disclosed are methods of making and using the modified polypeptides including but not limited to using the modified polypeptides to decrease or inhibit plasma leakage and/or vascular permeability in a mammal.
摘要翻译：公开了具有改善的药代动力学的修饰的嵌合多肽。具体地，公开了已经以改善其药代动力学特征的方式修饰的修饰的嵌合Flt1受体多肽。还公开了制备和使用修饰的多肽的方法，包括但不限于使用修饰的多肽来降低或抑制哺乳动物的血浆渗透和/或血管通透性。

23. 发明申请

US20090155899A1 Modified Chimeric Polypeptides with Improved Pharmacokinetic Properties 有权
标题翻译：改进的嵌合多肽具有改善的药代动力学性质
公开(公告)号：US20090155899A1
公开(公告)日：2009-06-18
申请号：US12334927
申请日：2008-12-15
申请人： Nicholas J. Papadopoulos , Samuel Davis , George D. Yancopoulos
发明人： Nicholas J. Papadopoulos , Samuel Davis , George D. Yancopoulos
IPC分类号： C12N5/10 , C12N15/62 , C12N15/85 , C12N15/81 , C12N15/74 , C12N1/21 , C12N1/19
CPC分类号： C07K14/71 , A61K38/00 , C07K16/22 , C07K19/00 , C07K2319/00 , C07K2319/30
摘要： Modified chimeric polypeptides with improved pharmacokinetics are disclosed. Specifically, modified chimeric Flt1 receptor polypeptides that have been modified in such a way as to improve their pharmacokinetic profile are disclosed. Also disclosed are methods of making and using the modified polypeptides including but not limited to using the modified polypeptides to decrease or inhibit plasma leakage and/or vascular permeability in a mammal.
摘要翻译：公开了具有改善的药代动力学的修饰的嵌合多肽。具体地，公开了已经以改善其药代动力学特征的方式修饰的修饰的嵌合Flt1受体多肽。还公开了制备和使用修饰的多肽的方法，包括但不限于使用修饰的多肽来降低或抑制哺乳动物的血浆渗透和/或血管通透性。

24. 发明申请

US20090081217A1 Modified Chimeric Polypeptides with Improved Pharmacokinetic Properties 有权
公开(公告)号：US20090081217A1
公开(公告)日：2009-03-26
申请号：US12102666
申请日：2008-04-14
申请人： Nicholas J. Papadopoulos , Samuel Davis , George D. Yancopoulos
发明人： Nicholas J. Papadopoulos , Samuel Davis , George D. Yancopoulos
IPC分类号： A61K39/395 , C07K16/18
CPC分类号： C07K14/71 , A61K38/00 , C07K16/22 , C07K19/00 , C07K2319/00 , C07K2319/30
摘要： Modified chimeric polypeptides with improved pharmacokinetics are disclosed. Specifically, modified chimeric Flt1 receptor polypeptides that have been modified in such a way as to improve their pharmacokinetic profile are disclosed. Also disclosed are methods of making and using the modified polypeptides including but not limited to using the modified polypeptides to decrease or inhibit plasma leakage and/or vascular permeability in a mammal.

25. 发明申请

US20080194460A1 Modified Chimeric Polypeptides with Improved Pharmacokinetic Properties and Methods of Using Thereof 有权
标题翻译：改进的嵌合多肽具有改善的药代动力学性质及其使用方法
公开(公告)号：US20080194460A1
公开(公告)日：2008-08-14
申请号：US12102681
申请日：2008-04-14
申请人： Nicholas J. PAPADOPOULOS , Samuel Davis , George D. Yancopoulos
发明人： Nicholas J. PAPADOPOULOS , Samuel Davis , George D. Yancopoulos
IPC分类号： A61K38/00 , A61P43/00
CPC分类号： C07K14/71 , A61K38/00 , C07K16/22 , C07K19/00 , C07K2319/00 , C07K2319/30
摘要： Modified chimeric polypeptides with improved pharmacokinetics are disclosed. Specifically, modified chimeric Flt1 receptor polypeptides that have been modified in such a way as to improve their pharmacokinetic profile are disclosed. Also disclosed are methods of making and using the modified polypeptides including but not limited to using the modified polypeptides to decrease or inhibit plasma leakage and/or vascular permeability in a mammal.
摘要翻译：公开了具有改善的药代动力学的修饰的嵌合多肽。具体地，公开了已经以改善其药代动力学特征的方式修饰的修饰的嵌合Flt1受体多肽。还公开了制备和使用修饰的多肽的方法，包括但不限于使用修饰的多肽来降低或抑制哺乳动物的血浆渗透和/或血管通透性。

26. 发明授权

US06627415B1 TIE-2 ligands, methods of making and uses thereof 有权
标题翻译： TIE-2配体，其制备方法和用途
公开(公告)号：US06627415B1
公开(公告)日：2003-09-30
申请号：US09442717
申请日：1999-11-18
申请人： Samuel Davis , George D. Yancopoulos
发明人： Samuel Davis , George D. Yancopoulos
IPC分类号： C12N1519
CPC分类号： C07K14/515 , A61K38/00
摘要： The present invention provides for an isolated nucleic acid molecule encoding a human TIE-2 ligand. In addition, the invention provides for a receptorbody which specifically binds a human TIE-2 ligand. The invention also provides an antibody which specifically binds a human TIE-2 ligand. The invention further provides for an antagonist of human TIE-2. The invention further provides for a ligandbody which specifically binds TIE-2 receptor. The invention also provides for therapeutic compositions as well as a method of blocking blood vessel growth, a method of promoting neovascularization, a method of promoting the growth, differentiation or migration of cells expressing the TIE-2 receptor, including, but not limited to, hematopoietic precursor cells, a method of blocking the growth, differentiation or migration of cells expressing the TIE-2 receptor including, but not limited to, hematopoietic precursor cells, and a method of attenuating or preventing tumor growth in a human.
摘要翻译：本发明提供了编码人TIE-2配体的分离的核酸分子。此外，本发明提供了特异性结合人TIE-2配体的受体体。本发明还提供了特异性结合人TIE-2配体的抗体。本发明进一步提供人TIE-2的拮抗剂。本发明进一步提供了特异性结合TIE-2受体的配体体。本发明还提供治疗组合物以及阻断血管生长的方法，促进新生血管形成的方法，促进表达TIE-2受体的细胞的生长，分化或迁移的方法，包括但不限于，造血前体细胞，阻断表达TIE-2受体的细胞的生长，分化或迁移的方法，包括但不限于造血前体细胞，以及减弱或预防人类肿瘤生长的方法。

27. 发明授权

US6166185A Antibodies to human TIE-2 ligands 有权
标题翻译：人类TIE-2配体的抗体
公开(公告)号：US6166185A
公开(公告)日：2000-12-26
申请号：US162437
申请日：1998-09-28
申请人： Samuel Davis , JoAnne Bruno , Mitchell Goldfarb , Thomas H. Aldrich , Peter C. Maisonpierre , Czeslaw Radziejewski , Pamela F. Jones , George D. Yancopoulos
发明人： Samuel Davis , JoAnne Bruno , Mitchell Goldfarb , Thomas H. Aldrich , Peter C. Maisonpierre , Czeslaw Radziejewski , Pamela F. Jones , George D. Yancopoulos
IPC分类号： G01N33/50 , A61K38/00 , A61K38/17 , A61K39/395 , A61K47/48 , A61K48/00 , A61K51/00 , A61P9/10 , A61P29/00 , A61P31/04 , A61P35/00 , C07H21/04 , C07K20060101 , C07K14/47 , C07K14/515 , C07K14/705 , C07K16/28 , C07K19/00 , C12N20060101 , C12N5/06 , C12N5/10 , C12N15/00 , C12N15/02 , C12N15/09 , C12N15/12 , C12N15/19 , C12N15/62 , C12N15/63 , C12P21/02 , C12P21/08 , C12R1/91 , G01N33/53 , C07K16/18 , C07K16/22 , C07K16/24
CPC分类号： C07K14/515 , A61K38/00 , C07K2319/00
摘要： The present invention provides for an isolated nucleic acid molecule encoding a human TIE-2 ligand. In addition, the invention provides for a receptor body which specifically binds a human TIE-2 ligand. The invention also provides an antibody which specifically binds a human TIE-2 ligand. The invention further provides for an antagonist of human TIE-2. The invention also provides for therapeutic compositions as well as a method of blocking blood vessel growth, a method of promoting neovascularization, a method of promoting the growth or differentiation of a cell expressing the TIE-2 receptor, a method of blocking the growth or differentiation of a cell expressing the TIE-2 receptor and a method of attenuating or preventing tumor growth in a human.
摘要翻译：本发明提供了编码人TIE-2配体的分离的核酸分子。此外，本发明提供了特异性结合人TIE-2配体的受体体。本发明还提供了特异性结合人TIE-2配体的抗体。本发明进一步提供人TIE-2的拮抗剂。本发明还提供治疗组合物以及阻断血管生长的方法，促进新生血管形成的方法，促进表达TIE-2受体的细胞的生长或分化的方法，阻断生长或分化的方法的表达TIE-2受体的细胞以及减弱或预防人类肿瘤生长的方法。

28. 发明授权

US5426177A Ciliary neurotrophic factor receptor 失效
标题翻译：睫状神经营养因子受体
公开(公告)号：US5426177A
公开(公告)日：1995-06-20
申请号：US676647
申请日：1991-03-28
申请人： Samuel Davis , Stephen P. Squinto , Mark E. Furth , George D. Yancopoulos
发明人： Samuel Davis , Stephen P. Squinto , Mark E. Furth , George D. Yancopoulos
IPC分类号： A61K38/00 , C07K14/705 , C12Q1/68
CPC分类号： C12Q1/6883 , C07K14/705 , A61K38/00 , C07K2319/00 , C12Q2600/158 , Y10S530/839
摘要： The present invention relates to the ciliary neurotrophic factor (CNTF) receptor, and provides for CNTF receptor nucleic acid and amino acid sequences. It also relates to (i) assay systems for detecting CNTF activity; (ii) experimental model systems for studying the physiologic role of CNTF; (ii) diagnostic techniques for identifying CNTF-related neurologic conditions; (iv) therapeutic techniques for the treatment of CNTF-related neurologic and muscular conditions, and (v) methods for identifying molecules homologous to CNTF and CNTFR.
摘要翻译：本发明涉及睫状神经营养因子（CNTF）受体，并提供CNTF受体核酸和氨基酸序列。它还涉及（i）用于检测CNTF活性的测定系统; （ii）研究CNTF生理作用的实验模型系统; （ii）用于鉴定CNTF相关神经病症的诊断技术; （iv）用于治疗CNTF相关神经和肌肉病症的治疗技术，以及（v）用于鉴定与CNTF和CNTFR同源的分子的方法。

29. 发明授权

US5266490A Mammalian expression vector 失效
标题翻译：哺乳动物表达载体
公开(公告)号：US5266490A
公开(公告)日：1993-11-30
申请号：US678408
申请日：1991-03-28
申请人： Samuel Davis , George D. Yancopoulos
发明人： Samuel Davis , George D. Yancopoulos
IPC分类号： C07K14/48 , C07K14/71 , C07K14/82 , C12N15/85 , C12N15/79 , C12N15/12 , C12N15/18
CPC分类号： C12N15/85 , C07K14/48 , C07K14/71 , C07K14/82 , C07K2319/00 , C07K2319/41 , C07K2319/61 , C07K2319/75 , C12N2800/108
摘要： DNA plasmid expression vector, pCMX, enables cDNA expression cloning in mammalian cell culture. This novel expression vector exhibits a marked increase in gene expression when compared to its parental plasmid construction.
摘要翻译： DNA质粒表达载体pCMX能够在哺乳动物细胞培养物中进行cDNA表达克隆。当与其亲本质粒构建相比时，该新型表达载体表现出基因表达的显着增加。

30. 发明授权

US08084234B2 Isolated nucleic acid molecules encoding a fusion protein capable of binding VEGF 有权
标题翻译：分离编码能够结合VEGF的融合蛋白的核酸分子
公开(公告)号：US08084234B2
公开(公告)日：2011-12-27
申请号：US12715128
申请日：2010-03-01
申请人： Nicholas J. Papadopoulos , Samuel Davis , George D. Yancopoulos
发明人： Nicholas J. Papadopoulos , Samuel Davis , George D. Yancopoulos
IPC分类号： C12N15/62 , C12N15/63 , C07H21/00
CPC分类号： C07K14/71 , A61K38/00 , C07K16/22 , C07K19/00 , C07K2319/00 , C07K2319/30
摘要： Modified chimeric polypeptides with improved pharmacokinetics are disclosed. Specifically, modified chimeric Flt1 receptor polypeptides that have been modified in such a way as to improve their pharmacokinetic profile are disclosed. Also disclosed are methods of making and using the modified polypeptides including but not limited to using the modified polypeptides to decrease or inhibit plasma leakage and/or vascular permeability in a mammal.
摘要翻译：公开了具有改善的药代动力学的修饰的嵌合多肽。具体地，公开了已经以改善其药代动力学特征的方式修饰的修饰的嵌合Flt1受体多肽。还公开了制备和使用修饰的多肽的方法，包括但不限于使用修饰的多肽来降低或抑制哺乳动物的血浆渗透和/或血管通透性。

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