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首页> 外文期刊>The anatomical record: advances in integrative anatomy and evolutionary biology >Historical Aspects of Gene Therapy and Stem Cell Therapy in the Treatment of Hearing and Balance Disorder
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Historical Aspects of Gene Therapy and Stem Cell Therapy in the Treatment of Hearing and Balance Disorder

机译:基因治疗与干细胞治疗听力和平衡障碍的历史方面

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摘要

ABSTRACT This review presents many but not all the major historical events that have led to our current understanding of gene and stem cell therapies for the treatment of hearing and balance disorders in animal models of these disorders. In order to better understand the application of these emerging therapies to the treatment of inner ear disorders in a clinical setting, it has been necessary to provide some genetic and pathobiology backgrounds from both animal models and clinical disorders. The current focus and goal of gene and stem cell therapies are directed toward understanding the effective treatment of animal models that mimic human disorders of hearing and balance. This approach not only addresses the most effective ways to deliver the gene or stem cell therapies to affected inner ears, it also provides an assessment of the efficacy of the applied therapy(s) in achieving either partial or full restoration of either hearing and/or balance within the animal models receiving these therapeutic interventions. This review also attempts to present a realistic assessment of how close the research fields of gene and stem cell therapies are to application for the treatment of human disorders in a clinical setting. Progress made in developing these novel therapies toward clinical applications would not have been possible without the many pioneering studies and discoveries achieved by the investigators cited in this review. There were also many other excellent studies performed by gifted investigators that were not able to be included within this review. Anat Rec, 303:390–407, 2020. ? 2019 American Association for Anatomy
机译:摘要此评价显示了许多但不是所有的主要历史事件,导致我们目前对基因和干细胞疗法的理解,以治疗这些疾病的动物模型中的听力和平衡障碍。为了更好地了解这些新出现的疗法在临床环境中治疗内耳疾病的应用,有必要提供来自动物模型和临床疾病的一些遗传和病理生物学背景。基因和干细胞疗法的目前的重点和目标旨在了解模仿人类听力和平衡的动物模型的有效治疗。这种方法不仅解决了将基因或干细胞疗法提供给受影响的内耳的最有效方法,还提供了对应用治疗的功效评估在实现听力和/或中的部分或完全恢复方面的疗效评估接受这些治疗干预的动物模型内的平衡。该评价还试图对基因和干细胞疗法的研究领域的研究如何施用临床环境中的人类疾病的临近。如果在本次审查中引用的调查人员实现的许多开创性的研究和发现,那么在发展这些新颖疗法方面取得了进展。还有许多其他优秀的研究表演,无法在本次审查中包含在内。 ANAT REC,303:390-407,2020。 2019年美国解剖学协会

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