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1. 发明申请

US20130145396A1 DIGITAL TV AND METHOD FOR CONTROLLING SAME 有权
标题翻译：数字电视及其控制方法
公开(公告)号：US20130145396A1
公开(公告)日：2013-06-06
申请号：US13697719
申请日：2010-06-24
申请人： Chang Hun Sung , Hyun Sang Park , Taeg Il Cho , Woo Hyun Paik , Kwan Hee Lee
发明人： Chang Hun Sung , Hyun Sang Park , Taeg Il Cho , Woo Hyun Paik , Kwan Hee Lee
IPC分类号： H04N21/637
CPC分类号： H04N21/637 , G06F1/3203 , H04L12/12 , H04N5/63 , H04N21/4131 , H04N21/42204 , H04N21/4436 , H04N21/47 , H04N21/478 , H04N21/64322 , H04N21/6587 , Y02D50/00 , Y02D50/20 , Y02D50/40
摘要： Disclosed are a digital TV and a method for controlling same. The method for controlling a digital TV according to one embodiment of the present invention includes: displaying a user interface (UI) capable of selecting the standby mode for a power-off operation; and disconnecting the power source for a display panel so as to enter the standby mode when the standby mode is set through the UI in the power-off operation, and a power-off command is received. The standby mode includes a lower standby mode based on the operation of the digital TV and a network function, and the digital TV in the standby mode stops AV channel communication and performs SI channel communication.
摘要翻译：公开了一种数字电视及其控制方法。根据本发明的一个实施例的用于控制数字电视的方法包括：显示能够选择待机模式以进行断电操作的用户界面（UI）; 并且在断电操作中通过UI设置待机模式时，断开显示面板的电源以进入待机模式，并且接收掉电命令。待机模式包括基于数字电视的操作和网络功能的较低待机模式，待机模式中的数字电视停止AV信道通信并执行SI信道通信。

2. 发明授权

US07431922B2 Bioadhesive directed somatic cell therapy 有权
标题翻译：生物粘附定向体细胞治疗
公开(公告)号：US07431922B2
公开(公告)日：2008-10-07
申请号：US10382190
申请日：2003-03-05
申请人： Sun Uk Song , Youngsuk Yi , Kwan Hee Lee
发明人： Sun Uk Song , Youngsuk Yi , Kwan Hee Lee
IPC分类号： A61K48/00 , A01N63/00
CPC分类号： A61K9/0024 , A61K31/715 , A61K38/1841 , A61K38/1875 , A61K48/0041 , A61K48/005
摘要： The subject invention is related to a cell-mediated gene therapy treatment using a cell composition that includes bioadhesive material. The bioadhesive material allows targeted and localized delivery of therapeutic somatic cells to the site of interest.
摘要翻译：本发明涉及使用包括生物粘附材料的细胞组合物的细胞介导的基因治疗治疗。生物粘附材料允许治疗性体细胞靶向和局部递送到感兴趣的部位。

3. 发明授权

US07338655B1 Gene therapy using TGF-β 有权
标题翻译：使用TGF-β的基因治疗
公开(公告)号：US07338655B1
公开(公告)日：2008-03-04
申请号：US09707900
申请日：2000-11-08
申请人： Moon Jong Noh , Kyoung Ae Kang , Kwan Hee Lee
发明人： Moon Jong Noh , Kyoung Ae Kang , Kwan Hee Lee
IPC分类号： A01N65/00 , A01N63/00 , A01N43/04 , A61K31/70 , A61K48/00
CPC分类号： A61K48/00 , A61K31/70 , A61K38/1841
摘要： The subject invention is related to a cell-mediated gene therapy treatment for orthopedic disease using a member belonging to the transforming growth factor-β (TGF-β) superfamily. TGF-β gene therapy as a new treatment method for degenerative arthritis is demonstrated. After transfection of TGF-β cDNA expression vectors into fibroblasts (NIH 3T3-TGF-β1), the cells were injected into rabbit achilles tendon and knee joints with artificially-made cartilage defects. Intratendinous injections were performed to determine the optimal concentration for in vivo expression. Partially defected cartilage model was made to simulate degenerative arthritis of the knee joint. The partial cartilage defect treated with the cell-mediated gene therapy procedure was covered by newly formed hyaline cartilage which indicates that the cells survived and stimulated matrix formation in this area. Completely denuded cartilage areas were covered by fibrous collagen.
摘要翻译：本发明涉及使用属于转化生长因子-β（TGF-β）超家族的成员的骨科疾病的细胞介导的基因治疗治疗。证实了TGF-β基因治疗作为退行性关节炎的新治疗方法。将TGF-βcDNA表达载体转染到成纤维细胞（NIH 3T3-TGF-β1）后，将细胞注射到兔子跟腱和膝关节中，人工制造软骨缺损。进行Intratendinous注射以确定体内表达的最佳浓度。进行部分缺陷软骨模型，以模拟膝关节退行性关节炎。用细胞介导的基因治疗程序处理的部分软骨缺损被新形成的透明软骨覆盖，表明细胞存活并刺激了该区域的基质形成。完全剥落的软骨区域被纤维胶原覆盖。

4. 发明申请

US20060014288A1 NERVE REGENERATION 审中-公开
标题翻译：神经再生
公开(公告)号：US20060014288A1
公开(公告)日：2006-01-19
申请号：US11160446
申请日：2005-06-23
申请人： Chang Hwan Kim , Kwan Hee Lee
发明人： Chang Hwan Kim , Kwan Hee Lee
IPC分类号： A61K48/00 , C12N5/08 , C12N15/86
CPC分类号： A61K48/0058 , A61K35/30 , A61K38/1875 , A61K38/1883 , A61K48/00 , C12N2799/021 , C12N2799/022 , C12N2799/025 , C12N2799/027 , C12N2799/028 , A61K2300/00
摘要： The present application describes a method of regenerating nerve, which steps include generating a recombinant viral or plasmid vector comprising a DNA sequence encoding a member of a transforming growth factor superfamily of proteins operatively linked to a promoter; transfecting in vitro a population of cultured cells with the recombinant vector, resulting in a population of the cultured cells; and transplanting the transfected cells to an area near an injured nerve, such that expression of the DNA sequence within the area near the injured nerve causes regeneration of the nerve.
摘要翻译：本申请描述了再生神经的方法，该步骤包括产生重组病毒或质粒载体，其包含编码与启动子有效连接的蛋白质的转化生长因子超家族成员的DNA序列; 用重组载体体外转染培养的细胞群，导致培养细胞群体; 并将转染的细胞移植到受伤神经附近的区域，使得DNA序列在受伤神经附近的区域中的表达导致神经再生。

5. 发明授权

US07005127B2 Mixed-cell gene therapy 有权
公开(公告)号：US07005127B2
公开(公告)日：2006-02-28
申请号：US10382137
申请日：2003-03-05
申请人： Sun Uk Song , Youngsuk Yi , Kwan Hee Lee , Moon Jong Noh
发明人： Sun Uk Song , Youngsuk Yi , Kwan Hee Lee , Moon Jong Noh
IPC分类号： A61F48/00 , C12N5/10
CPC分类号： C12N5/0656 , A61K35/12 , A61K35/32 , A61K35/33 , A61K48/00 , A61K48/0008 , C12N5/0655 , C12N2501/15 , C12N2501/155 , C12N2502/13 , C12N2502/1317 , C12N2502/99 , C12N2510/02
摘要： The subject invention is directed to a mixed cell composition to generate a therapeutic protein at a target site by providing a first population of mammalian cells transfected or transduced with a gene that is sought to be expressed, and a second population of mammalian cells that have not been transfected or transduced with the gene, wherein endogenously existing forms of the second population of mammalian cells are decreased at the target site, and wherein generation of the therapeutic protein by the first population of mammalian cells at the target site stimulates the second population cells to induce a therapeutic effect.

6. 发明授权

US06957935B2 Cutting insert with curved cutting edge 失效
标题翻译：切割刀片具有弯曲的切削刃
公开(公告)号：US06957935B2
公开(公告)日：2005-10-25
申请号：US10362923
申请日：2001-08-16
申请人： Wook Jung Sung , Kwan Hee Lee , Yong Boo Lee , Young Heum Kim , Hak Kyu Kim , Kyung Bae Kim
发明人： Wook Jung Sung , Kwan Hee Lee , Yong Boo Lee , Young Heum Kim , Hak Kyu Kim , Kyung Bae Kim
IPC分类号： B23C9/00 , B23C5/20 , B23C5/10
CPC分类号： B23C5/202 , B23C2200/203 , B23C2200/283 , B23C2200/323 , Y10T407/23 , Y10T407/235 , Y10T407/245
摘要： A cutting insert for a milling machining adapted to be mounted on a milling cutter to carry out cutting operation and having primary and secondary cutting edges provided at sides of a rectangular body, each primary cutting edge having a curved line tangential to the adjacent secondary cutting edge, to reduce the cutting force and improve flatness of the side surface of a machined workpiece. The cutting insert includes an upper face, a bottom face and a plurality of side faces connecting the upper face and the bottom face. The primary cutting edge has chip breakers for guiding chip flow, primary cutting edge land faces and primary cutting edge clearance faces. The primary cutting edges enable a bottom surface and a side surface of a machined workpiece to have a right angle therebetween.
摘要翻译：一种用于铣削加工的切削刀片，其适于安装在铣刀上以执行切割操作并且具有设置在矩形体侧面的主切削刃和次切削刃，每个主切削刃具有与相邻次切削刃相切的曲线以减少切削力并提高被加工工件的侧面的平面度。切削刀片包括上表面，底面和连接上表面和底面的多个侧面。主切削刃具有用于引导切屑流动的切屑，主切削刃面和主切削刃间隙面。主切削刃使加工的工件的底表面和侧表面之间具有直角。

7. 发明授权

US06797703B1 Gene therapy using TGF-&bgr; 有权
标题翻译：使用TGF-β的基因治疗
公开(公告)号：US06797703B1
公开(公告)日：2004-09-28
申请号：US09702718
申请日：2000-11-01
申请人： Moon Jong Noh , Kyoung Ae Kang , Kwan Hee Lee
发明人： Moon Jong Noh , Kyoung Ae Kang , Kwan Hee Lee
IPC分类号： A61K3500
CPC分类号： A61K38/1841 , A61K35/12 , A61K48/00 , C07K14/495
摘要： The subject invention is related to a cell-mediated gene therapy treatment for orthopedic disease using a member belonging to the transforming growth factory-&bgr; (TGF-&bgr;) superfamily. TGF-&bgr; gene therapy as a new treatment method for degenerative arthritis is demonstrated. After transfection of TGF-&bgr; cDNA expression vectors into fibroblasts (NIH 3T3-TGF-&bgr;1), the cells were injected into rabbit achilles tendon and knee joints with artificially-made cartilage defects. Intratendinous injections were performed to determine the optimal concentration for in vivo expression. Partially defected cartilage model was made to simulate degenerative arthritis of the knee joint. The partial cartilage defect treated with the cell-mediated gene therapy procedure was covered by newly formed hyaline cartilage which indicates that the cells survived and stimulated matrix formation in this area. Completely denuded cartilage areas were covered by fibrous collagen.
摘要翻译：本发明涉及使用属于转化生长工厂-β（TGF-β）超家族的成员的骨科疾病的细胞介导的基因治疗治疗。证实了TGF-β基因治疗作为退行性关节炎的新治疗方法。将TGF-βcDNA表达载体转染到成纤维细胞（NIH 3T3-TGF-β1）后，将细胞注射到兔子跟腱和膝关节中，人工制造软骨缺损。进行Intratendinous注射以确定体内表达的最佳浓度。进行部分缺陷软骨模型，以模拟膝关节退行性关节炎。用细胞介导的基因治疗程序处理的部分软骨缺损被新形成的透明软骨覆盖，表明细胞存活并刺激了该区域的基质形成。完全剥落的软骨区域被纤维胶原覆盖。

8. 发明授权

US08190004B2 Recording/playing device and method for processing broadcast signal 有权
标题翻译：用于处理广播信号的记录/播放装置和方法
公开(公告)号：US08190004B2
公开(公告)日：2012-05-29
申请号：US12355283
申请日：2009-01-16
申请人： Kwan Hee Lee , Woo Hyun Paik
发明人： Kwan Hee Lee , Woo Hyun Paik
IPC分类号： H04N5/93 , H04N5/765
CPC分类号： H04N21/4408 , H04N5/775 , H04N5/781 , H04N5/85 , H04N5/907 , H04N9/7921 , H04N9/8205 , H04N21/4135 , H04N21/4325 , H04N21/43622
摘要： A recording/playing device and a method for processing a broadcast signal are disclosed. The device includes an external storage device, and a broadcast receiver. The external storage device includes at least one storage medium. And, the broadcast receiver includes a broadcast processor, an interface unit, and a record/play controlling unit. The broadcast processor receives a broadcast signal of a specific channel and demodulates and decodes the received broadcast signal. The interface unit is capable of being connected to the storage medium of the external storage device. And, the record/play controlling unit activates a record/play mode, when a connection with the storage medium of the external storage device is detected through the interface unit, and stores the demodulated broadcast signal in the storage medium of the external storage device through the interface unit, or reads and plays (or plays-back) the broadcast signal from the storage medium of the external storage device.
摘要翻译：公开了一种用于处理广播信号的记录/播放装置和方法。该设备包括外部存储设备和广播接收机。外部存储装置包括至少一个存储介质。并且，广播接收机包括广播处理器，接口单元和记录/播放控制单元。广播处理器接收特定信道的广播信号，并对所接收的广播信号进行解调和解码。接口单元能够连接到外部存储设备的存储介质。并且，当通过接口单元检测到与外部存储装置的存储介质的连接时，记录/播放控制单元激活记录/播放模式，并且将解调的广播信号存储在外部存储装置的存储介质中，通过接口单元，或从外部存储设备的存储介质读取和播放（或重放）广播信号。

9. 发明授权

US08058649B2 Thin-film transistor and method of manufacturing the same 有权
标题翻译：薄膜晶体管及其制造方法
公开(公告)号：US08058649B2
公开(公告)日：2011-11-15
申请号：US12399774
申请日：2009-03-06
申请人： Sung-Hoon Kim , Kwan Hee Lee , Sung-Hoon Yang , Young-Hoon Yoo
发明人： Sung-Hoon Kim , Kwan Hee Lee , Sung-Hoon Yang , Young-Hoon Yoo
IPC分类号： H01L29/00 , H01L21/00
CPC分类号： H01L27/1288 , H01L27/1214 , H01L29/04 , H01L29/78696
摘要： In one embodiment, a thin-film transistor (TFT) includes a gate electrode, a semiconductor pattern, first and second electrodes and a protective layer. The semiconductor pattern is formed on the gate electrode, and includes a first semiconductor layer deposited at a first deposition speed and a second semiconductor layer deposited at a second deposition speed faster than the first deposition speed. The first and second electrodes are spaced apart from each other on the semiconductor pattern. The protective layer is formed on the semiconductor pattern to cover the first and second electrodes, and makes contact with a channel region of the first semiconductor layer to form an interface with the first semiconductor layer. Thus, electrical characteristics of the TFT may be improved.
摘要翻译：在一个实施例中，薄膜晶体管（TFT）包括栅电极，半导体图案，第一和第二电极以及保护层。半导体图案形成在栅电极上，并且包括以第一沉积速度沉积的第一半导体层和以比第一沉积速度快的第二沉积速度沉积的第二半导体层。第一和第二电极在半导体图案上彼此间隔开。保护层形成在半导体图案上以覆盖第一和第二电极，并与第一半导体层的沟道区域接触以形成与第一半导体层的界面。因此，可以提高TFT的电特性。

10. 发明申请

US20100330053A1 MIXED-CELL GENE THERAPY 审中-公开
标题翻译：混合细胞基因治疗
公开(公告)号：US20100330053A1
公开(公告)日：2010-12-30
申请号：US12882027
申请日：2010-09-14
申请人： Sun Uk SONG , Youngsuk Yi , Kwan Hee Lee , Moon Jong Noh
发明人： Sun Uk SONG , Youngsuk Yi , Kwan Hee Lee , Moon Jong Noh
IPC分类号： A61K48/00 , A61P19/02 , A61P19/00
CPC分类号： C12N5/0656 , A61K35/12 , A61K35/32 , A61K35/33 , A61K48/00 , A61K48/0008 , C12N5/0655 , C12N2501/15 , C12N2501/155 , C12N2502/13 , C12N2502/1317 , C12N2502/99 , C12N2510/02
摘要： The subject invention is directed to a mixed cell composition to generate a therapeutic protein at a target site by providing a first population of mammalian cells transfected or transduced with a gene that is sought to be expressed, and a second population of mammalian cells that have not been transfected or transduced with the gene, wherein endogenously existing forms of the second population of mammalian cells are decreased at the target site, and wherein generation of the therapeutic protein by the first population of mammalian cells at the target site stimulates the second population cells to induce a therapeutic effect.
摘要翻译：本发明涉及一种混合细胞组合物，其通过提供用寻求表达的基因转染或转导的第一群哺乳动物细胞，以及第二组哺乳动物细胞，在靶位点产生治疗性蛋白质被转染或转导的基因，其中哺乳动物细胞的第二群体的内源存在形式在靶位点减少，并且其中在靶位点由哺乳动物细胞的第一群体产生治疗性蛋白质刺激第二群体细胞诱导治疗效果。

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