METHOD AND APPARATUS FOR DISPLAYING CHARACTER STRING
    1.
    发明申请
    METHOD AND APPARATUS FOR DISPLAYING CHARACTER STRING 审中-公开
    用于显示字符串的方法和装置

    公开(公告)号:US20080143741A1

    公开(公告)日:2008-06-19

    申请号:US11945571

    申请日:2007-11-27

    IPC分类号: G09G5/00

    CPC分类号: G06F17/211

    摘要: A method and an apparatus are provided for displaying a character string when the character string is being input. The method includes: grouping a plurality of positions for inputting characters into a plurality of position groups; configuring display format of the characters to be input for every position group; and responding to input of the character string, displaying the input character string with the configured display format. The methods and apparatus will facilitate a user reading character strings, and verifying character strings while inputting them.

    摘要翻译: 提供了一种方法和装置,用于在输入字符串时显示字符串。 该方法包括:将用于输入字符的多个位置分组成多个位置组; 配置要为每个位置组输入的字符的显示格式; 响应输入的字符串,以配置的显示格式显示输入的字符串。 方法和装置将方便用户读取字符串,并在输入字符串时验证字符串。

    Subunit-selective nucleic acid inhibitors of glutamate receptors
    3.
    发明授权
    Subunit-selective nucleic acid inhibitors of glutamate receptors 有权
    亚基选择性谷氨酸受体核酸抑制剂

    公开(公告)号:US09200286B2

    公开(公告)日:2015-12-01

    申请号:US13810572

    申请日:2011-07-15

    摘要: Inhibitors of AMPA-type glutamate ion channels are useful as biochemical probes for structure-function studies and as drug candidates for a number of neurological disorders and diseases. Disclosed herein is the identification of an RNA inhibitor or aptamer by an in vitro evolution approach and characterization of its mechanism of inhibition on the sites of interaction by equilibrium binding and on the receptor channel-opening rate by a laser-pulse photolysis technique. The aptamer of the invention is a noncompetitive inhibitor of AMPA-type glutamate ion channels, one that selectively inhibits the GluA2Qflip AMPA receptor subunit without any effect on other AMPA receptor subunits or on kainate or NMDA receptors. Furthermore, the aptamer preferentially inhibits the closed-channel state of GluA2Qflip with a KI=1.5 μM or by ˜15-fold over the open-channel state. The potency and selectivity of this aptamer rival those of small molecule inhibitors. Together, these properties make the aptamers of the present invention promising water-soluble, highly potent, GluA2 subunit-selective drugs.

    摘要翻译: AMPA型谷氨酸离子通道的抑制剂可用作结构功能研究的生物化学探针和许多神经障碍和疾病的候选药物。 本文公开了通过体外进化方法鉴定RNA抑制剂或适体,并通过激光脉冲光解技术通过平衡结合和受体通道开放速率表征其抑制作用位点的机制。 本发明的适体是AMPA型谷氨酸离子通道的非竞争性抑制剂,其选择性地抑制GluA2Qflip AMPA受体亚基而对其它AMPA受体亚基或红藻氨酸或NMDA受体没有任何作用。 此外,适体优先抑制GluA2Qflip的闭通道状态,KI =1.5μM或比开放通道状态约〜15倍。 该适配体的效力和选择性与小分子抑制剂的效力和选择性相当。 这些性质一起使得本发明的适体具有潜在的水溶性,高效的GluA2亚基选择性药物。

    Ultraviolet and High-Performance Liquid Chromatography Methods for the Evaluation of Sunscreen Efficacy
    4.
    发明申请
    Ultraviolet and High-Performance Liquid Chromatography Methods for the Evaluation of Sunscreen Efficacy 审中-公开
    紫外线和高效液相色谱法评估防晒功效

    公开(公告)号:US20130183765A1

    公开(公告)日:2013-07-18

    申请号:US13823028

    申请日:2011-09-13

    申请人: Zhen Huang

    发明人: Zhen Huang

    IPC分类号: G01N21/63

    摘要: Disclosed are compositions which can mimic DNA and/or RNA in cells of a subject and methods of using them as a substrate in testing efficacy of one or more compositions in reducing and/or preventing radiation, such as ultraviolet (UV) radiation-caused DNA and/or RNA damage of said subject. Also disclosed are systems related to the disclosed methods.

    摘要翻译: 公开了可以模拟受试者细胞中的DNA和/或RNA的组合物以及在测试一种或多种组合物在减少和/或预防辐射中的功效(例如紫外线(UV)辐射引起的DNA)中使用它们作为底物的方法 和/或所述受试者的RNA损伤。 还公开了与所公开的方法相关的系统。

    Indoor Unit of Air Conditioner
    6.
    发明申请
    Indoor Unit of Air Conditioner 审中-公开
    室内空调机组

    公开(公告)号:US20130035028A1

    公开(公告)日:2013-02-07

    申请号:US13638607

    申请日:2011-03-25

    IPC分类号: F25D17/06 F24H3/06 F24F7/06

    摘要: An indoor unit of air conditioner comprises a panel body (2) enclosing side portions and a top portion of the air conditioner, a rear shell enclosing a rear portion of the air conditioner, and the front panel (1) arranged in the front of the air conditioner and closely connected to the panel body (2). The rear shell, the panel body (2) and the front panel (1) form an inner chamber of the air conditioner in which a heat exchanger, a control element and a fan component are provided. Side surfaces of the indoor unit of air conditioner are of a U shape structure, and the front, the rear and the bottom surfaces of the lower portion of the indoor unit of air conditioner are formed by more than one curved surface.

    摘要翻译: 空调机的室内机包括封闭侧部的面板体(2)和空调机的顶部,包围空调机的后部的后壳以及配置在空调机的前方的前面板(1) 空调,并紧密连接到面板主体(2)。 后壳体,面板体(2)和前面板(1)形成空调机的内室,其中设置有热交换器,控制元件和风扇部件。 空调机的室内机的侧面为U形结构,空调机的室内机的下部的前表面,后表面和底面由多于一个的曲面形成。

    Synthesis of selenium-derivatized nucleosides, nucleotides, phosphoramidites, triphosphates and nucleic acids
    7.
    发明授权
    Synthesis of selenium-derivatized nucleosides, nucleotides, phosphoramidites, triphosphates and nucleic acids 有权
    硒衍生的核苷,核苷酸,亚磷酰胺,三磷酸和核酸的合成

    公开(公告)号:US08354524B2

    公开(公告)日:2013-01-15

    申请号:US13172559

    申请日:2011-06-29

    申请人: Zhen Huang

    发明人: Zhen Huang

    摘要: The present invention provides selenium derivatives of nucleosides, nucleoside phosphoramidites, nucleotides, nucleotide triphosphates, oligonucleotides, polynucleotides, and larger nucleic acids and methods for their synthesis. Selenium derivatives of both ribonucleic acids and deoxyribonucleic acids, as well as methods for their synthesis, crystallization and uses in structural determinations, particularly by X-ray crystallographic techniques are disclosed. The selenium derivatives of the present invention are also useful as food supplements.

    摘要翻译: 本发明提供了核苷,核苷亚磷酰胺,核苷酸,核苷酸三磷酸,寡核苷酸,多核苷酸和较大的核酸的硒衍生物及其合成方法。 公开了核糖核酸和脱氧核糖核酸的硒衍生物,以及它们的合成,结晶和用于结构测定的方法,特别是通过X射线晶体学技术。 本发明的硒衍生物也可用作食品添加剂。

    ONU WITH WIRELESS CONNECTIVITY CAPABILITY
    8.
    发明申请
    ONU WITH WIRELESS CONNECTIVITY CAPABILITY 有权
    ONU具有无线连接能力

    公开(公告)号:US20120243871A1

    公开(公告)日:2012-09-27

    申请号:US13053925

    申请日:2011-03-22

    申请人: Zhen Huang David Hood

    发明人: Zhen Huang David Hood

    IPC分类号: H04J14/00

    摘要: The embodiments herein relate to a method in an optical network unit (103), referred to as an ONU, for providing wireless connectivity capability to the ONU (103). The ONU (103) is comprised in a communications network (100). The ONU (103) is interconnected to an optical line terminal (101), referred to as an OLT, via a wireline communications link (104) and a wireless communications link (113). The ONU (103) is configured to support a sleep mode. The ONU (103) obtains information about entry into the sleep mode. The ONU (103) identifies whether the wireless communications link (113) is activated or deactivated, and activates the wireless communications link (113) if the wireless communications link (113) is identified as deactivated. The ONU (103) enters sleep mode, and provides wireless connectivity capability to the ONU (103) by means of the wireless communications link during the sleep mode.

    摘要翻译: 本文的实施例涉及用于向ONU(103)提供无线连接能力的光网络单元(103)中的称为ONU的方法。 ONU(103)包括在通信网络(100)中。 ONU(103)经由有线通信链路(104)和无线通信链路(113)互连到被称为OLT的光线路终端(101)。 ONU(103)被配置为支持睡眠模式。 ONU(103)获取关于进入睡眠模式的信息。 如果无线通信链路(113)被识别为去激活,则ONU(103)识别无线通信链路(113)是否被激活或去激活,并激活无线通信链路(113)。 ONU(103)进入睡眠模式,并且在睡眠模式期间通过无线通信链路向ONU(103)提供无线连接能力。

    Novel Compounds and Derivatizations of DNAs and RNAs on the Nucleobases of Pyrimidines for Function, Structure and Therapeutics
    9.
    发明申请
    Novel Compounds and Derivatizations of DNAs and RNAs on the Nucleobases of Pyrimidines for Function, Structure and Therapeutics 有权
    关于功能,结构和治疗的嘧啶核苷酸的DNA和RNAs的新型化合物和衍生物

    公开(公告)号:US20120070825A1

    公开(公告)日:2012-03-22

    申请号:US13321544

    申请日:2010-05-20

    申请人: Zhen Huang

    发明人: Zhen Huang

    CPC分类号: C07H21/00 C07H19/06

    摘要: Disclosed are compounds of formula (I), a derivative, or a tautomer thereof, or a pharmaceutically acceptable salt of said compound or said tautomer. Also disclosed are methods of preparing compound of formula (I), a derivative, or a tautomer thereof, or a pharmaceutically acceptable salt of said compound or said tautomer. Further disclosed are methods of conducting drug discovery and research comprises applying the compound of formula (I), a derivative, or a tautomer thereof, or a pharmaceutically acceptable salt of said compound or said tautomer in an investigation.

    摘要翻译: 公开了式(I)的化合物,其衍生物或互变异构体,或所述化合物或所述互变异构体的药学上可接受的盐。 还公开了制备式(I)化合物,其衍生物或其互变异构体或所述化合物或所述互变异构体的药学上可接受的盐的方法。 进一步披露的是进行药物发现和研究的方法包括在调查中应用式(I)化合物,其衍生物或互变异构体,或所述化合物或所述互变异构体的药学上可接受的盐。

    Nucleic acid inhibitors of glutamate receptors
    10.
    发明授权
    Nucleic acid inhibitors of glutamate receptors 有权
    谷氨酸受体的核酸抑制剂

    公开(公告)号:US08076467B2

    公开(公告)日:2011-12-13

    申请号:US12578231

    申请日:2009-10-13

    CPC分类号: C12N15/115 C12N2310/16

    摘要: The present invention relates to novel nucleic acid ligands or aptamers that bind to and inhibit the activation of the α-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) subtype of ionotropic glutamate receptors. Also disclosed is a novel combination of technologies, i.e., SELEX and laser pulse photolysis for the selection and screening of aptamers that inhibit receptor function and are useful therefore, in the treatment of diseases associated with excessive activation of ionotropic glutamate receptors.

    摘要翻译: 本发明涉及结合并抑制离子型谷氨酸受体的α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)亚型的活化的新型核酸配体或适体。 还公开了技术的新型组合,即SELEX和激光脉冲光解用于选择和筛选抑制受体功能的适体,因此可用于治疗与离子型谷氨酸受体的过度活化相关的疾病。