会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 2. 发明授权
    • Treatment or prophylaxis of ischemic heart disease
    • 治疗或预防缺血性心脏病
    • US07026293B2
    • 2006-04-11
    • US09752724
    • 2001-01-03
    • Masafumi Kitakaze
    • Masafumi Kitakaze
    • A61K38/00A61K38/24C07K14/00
    • A61K38/2242
    • The present invention provides a pharmaceutical composition and a method for reducing an infarct region resulting from the ischemic necrosis of cells, especially, a pharmaceutical composition and a method for suppressing ischemia-reperfusion injury in the treatment of ischemic heart disease. The pharmaceutical composition and the method utilize a substance, as an active ingredient, which can increase intracellular cGMP production by acting on a natriuretic peptide receptor, and which has the effect of reducing an infarct region. The substance is preferably a natriuretic peptide. The present invention is particularly useful for the treatment or prophylaxis of ischemic disease.
    • 本发明提供了一种药物组合物和减少由细胞缺血性坏死引起的梗死区域的方法,特别是药物组合物和用于治疗缺血性心脏病的局部缺血再灌注损伤的方法。 药物组合物和方法利用作为活性成分的物质,其可以通过作用于利尿钠肽受体而增加细胞内cGMP产生,并且具有减少梗死区域的作用。 该物质优选为利尿钠肽。 本发明特别可用于治疗或预防缺血性疾病。
    • 8. 发明申请
    • Method for diagnosing arrhythmogenic right ventricular dysplasia
    • 诊断心律失常性右室发育不良的方法
    • US20050273871A1
    • 2005-12-08
    • US10860601
    • 2004-06-04
    • Yoshihiro AsanoSeiji TakashimaMasafumi Kitakaze
    • Yoshihiro AsanoSeiji TakashimaMasafumi Kitakaze
    • A01K67/027C12Q1/68G01N33/68
    • G01N33/6875A01K2227/105A01K2267/03G01N2800/325
    • A specific strain of KK obese mice was found to show a phenotype peculiar to human arrythomogenic right ventricular dysplasia (ARVD), and Lamrl-functional transposon 1 (Lamr1-tp1) was determined to be responsible for this phenotype. Furthermore, the translation product of Lamr1-tp1 was shown to interact with HP1-alpha. Together with the knowledge that human ARVD loci are reported to exist close to the retroposons of Lamr1 or histone-modulating protein genes, aberrant interaction of mutant-LAMR1 and HP1-alpha seems to be a cause of ARVD. Thus, the present invention relates to methods for diagnosing ARVD. The present invention further relates to an animal model of ARVD, and cells transfected with mutant Lamr1 gene demonstrated to cause ARVD in the animal model. Moreover, the present invention relates to methods of screening for compounds suppressing ARVD using the animal model or the transfected cells.
    • 发现KK肥胖小鼠的特异性菌株显示了人类发生心律失常的右心室发育不良(ARVD)特有的表型,并确定了Lamr1功能转座子1(Lamr1-tp1)对该表型负责。 此外,Lamr1-tp1的翻译产物显示与HP1-α相互作用。 与知道人类ARVD基因座据报道存在于接近Lamr1或组蛋白调节蛋白基因的翻新细胞的突变体LAMR1和HP1-α的异常相互作用似乎是ARVD的原因。 因此,本发明涉及用于诊断ARVD的方法。 本发明还涉及ARVD的动物模型和在动物模型中被证实导致ARVD的突变体Lamr1基因转染的细胞。 此外,本发明涉及使用动物模型或转染细胞筛选抑制ARVD的化合物的方法。