{"title":"线粒体治疗:热带病治疗管理的新概念","authors":"V. Wiwanitkit","doi":"10.15761/imm.1000348","DOIUrl":null,"url":null,"abstract":"Mitochondria is an important cellular organelle. This organelle plays important role regarding intracellular energy. Of interest, this organelle has its specific set of genetic components. At present, several medical disorders, such as Parkinson disease, are proven for their rooted causes as mitochondrial disorders [1]. In mitochondrial disease, mutations in genes in the mitochondrial DNA (mtDNA) that encode structural mitochondrial proteins or proteins involved in mitochondrial function is observed and this is the basic rooted pathogenesis of the clinical problem [1].","PeriodicalId":94322,"journal":{"name":"Integrative molecular medicine","volume":"59 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mitochrondrial therapy: A new concept for therapeutic management for tropical diseases\",\"authors\":\"V. Wiwanitkit\",\"doi\":\"10.15761/imm.1000348\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Mitochondria is an important cellular organelle. This organelle plays important role regarding intracellular energy. Of interest, this organelle has its specific set of genetic components. At present, several medical disorders, such as Parkinson disease, are proven for their rooted causes as mitochondrial disorders [1]. In mitochondrial disease, mutations in genes in the mitochondrial DNA (mtDNA) that encode structural mitochondrial proteins or proteins involved in mitochondrial function is observed and this is the basic rooted pathogenesis of the clinical problem [1].\",\"PeriodicalId\":94322,\"journal\":{\"name\":\"Integrative molecular medicine\",\"volume\":\"59 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Integrative molecular medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15761/imm.1000348\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Integrative molecular medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15761/imm.1000348","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Mitochrondrial therapy: A new concept for therapeutic management for tropical diseases
Mitochondria is an important cellular organelle. This organelle plays important role regarding intracellular energy. Of interest, this organelle has its specific set of genetic components. At present, several medical disorders, such as Parkinson disease, are proven for their rooted causes as mitochondrial disorders [1]. In mitochondrial disease, mutations in genes in the mitochondrial DNA (mtDNA) that encode structural mitochondrial proteins or proteins involved in mitochondrial function is observed and this is the basic rooted pathogenesis of the clinical problem [1].