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    • 2. 发明申请
    • DIAGNOSIS, PREVENTION AND TREATMENT OF ULCERATIVE COLITIS, AND CLINICAL SUBTYPES THEREOF, USING HISTONE H1
    • 诊断,预防和治疗精神分裂症及其临床亚型,使用HISTONE H1
    • WO1997038713A1
    • 1997-10-23
    • PCT/US1997006987
    • 1997-04-11
    • THE REGENTS OF THE UNIVERSITY OF CALIFORNIACEDARS-SINAI MEDICAL CENTER
    • THE REGENTS OF THE UNIVERSITY OF CALIFORNIACEDARS-SINAI MEDICAL CENTERBRAUN, JonathanTARGAN, Stephan, R.EGGENA, Mark
    • A61K39/00
    • G01N33/564A61K39/0008
    • The present invention provides a method of diagnosing ulcerative colitis (UC) in a subject suspected of having inflammatory bowel disease by obtaining a sample from the individual; contacting the sample with human histone H1, or pANCA-reactive fragment thereof, under conditions suitable to form a complex of human histone H1, or pANCA-reactive fragment thereof, and antibody to human histone H1; and detecting the presence or absence of the complex, where the presence of the complex indicates that the individual has UC. The invention also provides related methods of diagnosing a perinuclear anti-neutrophil cytoplasmic antibody positive (pANCA-positive) clinical subtype of UC in a patient with UC. In addition, the invention further provides methods of determining susceptibility to UC in an individual. The invention further provides methods of inducing tolerance in a pANCA-positive patient with UC by administering an effective dose of histone H1, or tolerogenic fragment thereof, to the pANCA-positive patient with UC. Compositions of histone H1, or fragment thereof, combined with a tolerogizing molecule also are provided.
    • 本发明提供一种通过从个体获得样品来诊断疑似患有炎症性肠病的受试者的溃疡性结肠炎(UC)的方法; 在适于形成人组蛋白H1或其pANCA反应性片段的复合物和人组蛋白H1的抗体的条件下,将样品与人组蛋白H1或其pANCA反应性片段接触; 并检测复合物的存在或不存在,其中复合物的存在表明个体具有UC。 本发明还提供了在UC患者中诊断UC的核周抗中性粒细胞胞质抗体阳性(pANCA阳性)临床亚型的相关方法。 此外,本发明还提供了确定个体对UC的易感性的方法。 本发明进一步提供了通过向具有UC的pANCA阳性患者施用有效剂量的组蛋白H1或其耐受性片段来诱导具有UC的pANCA阳性患者的耐受性的方法。 还提供组蛋白H1或其片段的组合物与耐受性分子组合。
    • 7. 发明申请
    • ESTROGEN RESPONSE ELEMENT BINDING PROTEINS AND NUCLEOTIDES ENCODING THEREFOR
    • 雌激素反应元件结合蛋白和核苷酸编码
    • WO1997029184A1
    • 1997-08-14
    • PCT/US1997002208
    • 1997-02-12
    • CEDARS-SINAI MEDICAL CENTER
    • CEDARS-SINAI MEDICAL CENTERADAMS, John, S.
    • C12N05/12
    • C07K14/47A61K38/00
    • The invention relates to the discovery and purification of novel estrogen response element binding proteins. Estrogen response element binding proteins are distinct from the estrogen receptor and other intracellular receptors, e.g. estrogen receptor. Estrogen response element binding proteins can interfere with the biological activity of the estrogen receptor and other related intracellular receptor proteins. One aspect of the invention is to provide purified estrogen response element binding proteins. Another aspect of the invention is to provide antibodies capable of binding to the estrogen response element binding proteins of the invention. Another aspect of the invention is to provide assays for the detection or screening of therapeutic compounds that interfere with the interaction between estrogen response element binding protein and estrogen response elements.
    • 本发明涉及新型雌激素反应元件结合蛋白的发现和纯化。 雌激素反应元件结合蛋白不同于雌激素受体和其他细胞内受体,例如 雌激素受体。 雌激素反应元件结合蛋白可能干扰雌激素受体和其他相关胞内受体蛋白的生物活性。 本发明的一个方面是提供纯化的雌激素反应元件结合蛋白。 本发明的另一方面是提供能够结合本发明的雌激素反应元件结合蛋白的抗体。 本发明的另一方面是提供用于检测或筛选干扰雌激素反应元件结合蛋白和雌激素反应元件之间的相互作用的治疗化合物的测定。
    • 8. 发明申请
    • INTRACELLULAR VITAMIN D BINDING PROTEIN
    • 细胞维生素D结合蛋白
    • WO1997028688A1
    • 1997-08-14
    • PCT/US1997002213
    • 1997-02-12
    • CEDARS-SINAI MEDICAL CENTER
    • CEDARS-SINAI MEDICAL CENTERADAMS, John, S.
    • A01N37/18
    • C07K14/57A61K38/00
    • The invention relates to the discovery and purification of novel intracellular vitamin D binding proteins (IDBPs) and the isolation of polynucleotide sequences encoding the proteins. IDBPs are of interest because they mediate the vitamin D resistance, i.e., insensitivity, observed in new world primates. IDBPs are distinct from the vitamin D receptor and other intracellular receptors, e.g. estrogen receptor. One aspect of the invention is to provide purified IDBPs as pharmaceutical compositions to affect steroid hormone activity. Another aspect of the invention provides polynucleotides encoding the IDBPs of the invention for use in altering the expression of IDBPs. Yet another aspect of the invention is to provide assays for the detection or screening of therapeutic compounds that interfere with the interaction between IDBP and vitamin D (or other ligands that bind to IDBP), and the use of such compounds as pharmaceutical compositions.
    • 本发明涉及新型细胞内维生素D结合蛋白(IDBPs)的发现和纯化以及编码蛋白质的多核苷酸序列的分离。 IDBPs是有意义的,因为它们介导在新世界灵长类动物中观察到的维生素D抗性,即不敏感性。 IDBPs不同于维生素D受体和其他细胞内受体,例如。 雌激素受体。 本发明的一个方面是提供纯化的IDBPs作为影响类固醇激素活性的药物组合物。 本发明的另一方面提供编码本发明的IDBPs的多核苷酸,用于改变IDBP的表达。 本发明的另一方面是提供用于检测或筛选干扰IDBP和维生素D(或与IDBP结合的其它配体)之间的相互作用的治疗化合物的测定,以及使用这些化合物作为药物组合物。
    • 9. 发明申请
    • FIBER-OPTIC ENDODONTIC APPARATUS AND METHOD
    • 光纤内置装置及方法
    • WO1995008962A1
    • 1995-04-06
    • PCT/US1994010973
    • 1994-09-28
    • CEDARS-SINAI MEDICAL CENTER
    • CEDARS-SINAI MEDICAL CENTERVARI, Sandor, G.
    • A61C05/02
    • A61B5/0088A61C5/40A61C19/004A61L2/10
    • An endodontic apparatus and related method for the instant detection of the anatomical structure of a tooth and for the restoration of a dead or severely decayed tooth using induced fluorescence spectroscopy. A root canal probe having an optical fiber through its center transmits excitation light into the tooth's root canal. The excitation light induces the tissue within the root canal to fluoresce. The fluorescent light is collected by the optical fiber and transmitted back to a sensor that generates electrical signals indicative of the intensity of light within predetermined wavelength bands. The electrical signals are processed to identify the tissues within the root canal. The probe may include a slightly conical metal surface having flutes for shaving and removing dentin from within the root canal. Using the fluorescent emission properties of the tissues of components of a tooth, the entrance of the root canal is located. The root canal is cleaned and shaped and the apex of the root canal located using the difference between the fluorescence spectrum of the apex and the root canal. The root canal is sealed and filled by a light cure restorative delivered into the root canal through a tube. The light cure restorative is activated by light transmitted into the root canal by an optical fiber. The light activation and polymerization of the light cure restorative can be controlled by monitoring the intensitity of the restorative's fluorescence spectrum.
    • 用于立即检测牙齿的解剖结构并使用诱导荧光光谱法恢复死亡或严重衰退的牙齿的根管装置和相关方法。 通过其中心具有光纤的根管探针将激发光透射到牙齿的根管中。 激发光诱导根管内的组织发荧光。 荧光灯由光纤收集并传输回传感器,该传感器产生指示预定波长带内的光强度的电信号。 处理电信号以识别根管内的组织。 探针可以包括略微锥形的金属表面,其具有用于剃刮的槽纹和从根管内去除牙本质。 使用牙齿组分的组织的荧光发射特性,定位根管的入口。 根管被清洁和成形,根管的顶点使用顶点的荧光光谱与根管之间的差异来定位。 根管被密封并由通过管输送到根管中的光固化修复剂填充。 光固化修复剂由通过光纤传播到根管中的光激活。 可以通过监测恢复性荧光光谱的强度来控制光固化修复剂的光活化和聚合。
    • 10. 发明申请
    • METHOD AND APPARATUS FOR RESTENOSIS TREATMENT
    • 用于保留治疗的方法和装置
    • WO1993004735A1
    • 1993-03-18
    • PCT/US1992007447
    • 1992-09-04
    • CEDARS-SINAI MEDICAL CENTERHESS, Robert, L.SHEFER, ArieEIGLER, Neal, L.WHITING, James, S.
    • CEDARS-SINAI MEDICAL CENTER
    • A61N05/00
    • A61N5/1002A61B2017/22068A61M2025/1047A61N2005/1004A61N2005/1023
    • Method and apparatus (10) for treatment and post-treatment of the stenosed region (14) of an artery (12) after reduction of the region by angioplasty or other means by applying a radioactive dose (30) to said reduced region of the artery by positioning a radioactive dose to the reduced region is disclosed. Low dose, local ionizing irradiation (38) is delivered to the site of an intravascular intervention to prevent and/or minimize excessive cell proliferation. The irradiating source may be located external to the site or may involve a source located within the vessel. The low dose, local ionizing irradiation may also be delivered during the interventional session or thereafter, preferably within 72 hours of the intervention, in a single dose or a fractionated dose, and alone or in combination with at least one radiosensitizing agent.
    • 用于通过血管成形术或其他手段减少该区域的动脉(12)的狭窄区域(14)进行治疗和后处理的方法和装置(10),其通过对所述动脉的所述减少区域施加放射性剂量(30) 公开了将放射性剂量定位到还原区域。 将低剂量局部电离辐射(38)输送到血管内干预部位,以预防和/或最小化过度的细胞增殖。 照射源可以位于该场所的外部,或者可以涉及位于容器内的源。 低剂量局部电离照射也可以在介入治疗期间或其后,优选在干预的72小时内以单一剂量或分次剂量,单独或与至少一种放射增敏剂组合递送。