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EP 159: Engineering macrophages to tackle rare disease with Noam Baumatz of Noga Therapeutics

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Manage episode 447802745 series 2631947
内容由Sano Genetics提供。所有播客内容(包括剧集、图形和播客描述)均由 Sano Genetics 或其播客平台合作伙伴直接上传和提供。如果您认为有人在未经您许可的情况下使用您的受版权保护的作品,您可以按照此处概述的流程进行操作https://zh.player.fm/legal
0:00 Intro to The Genetics Podcast

01:00 Welcome to Noam and discussion of his motivation to drive rare disease forward

03:00 Noam’s daughter Noga’s experience of rare disease, including an 8 to 12 month journey to diagnosis

05:10 How the experience of his daughter receiving a genetic diagnosis motivated Noam to take change into his own hands

10:12 How meeting other families impacted by rare disease led Noam to work on gene therapy for children living with primary immune deficiencies

12:33 How Noga Therapeutics is aiming to reprogram blood stem cells and the potential impact on rare diseases

15:22 Why it’s not yet possible to use the technology to correct gain of function mutations

17:42 How Noga’s program is aiding treatment of multiple primary immune deficiencies

22:25 The techniques the company uses in XLA to modify stem cells and enable expression of a functional copy of the BTK gene

26:30 Why gene therapies don’t always provide a comprehensive solution or cure

28:10 Bridging the gap between transformative therapies and the cost of delivering drugs to very small ultra-rare disease populations

34:41 Noam’s history working in traditional Chinese medicine

39:53 The importance of thinking holistically about health, from understanding g genetic root causes to considering how genes impact whole organ systems

43:15 The collaborative nature of the rare disease community and how parents who want to use their personal experience to further research and advocacy can connect with Noam

44:37 Closing remarks

  continue reading

188集单集

Artwork
icon分享
 
Manage episode 447802745 series 2631947
内容由Sano Genetics提供。所有播客内容(包括剧集、图形和播客描述)均由 Sano Genetics 或其播客平台合作伙伴直接上传和提供。如果您认为有人在未经您许可的情况下使用您的受版权保护的作品,您可以按照此处概述的流程进行操作https://zh.player.fm/legal
0:00 Intro to The Genetics Podcast

01:00 Welcome to Noam and discussion of his motivation to drive rare disease forward

03:00 Noam’s daughter Noga’s experience of rare disease, including an 8 to 12 month journey to diagnosis

05:10 How the experience of his daughter receiving a genetic diagnosis motivated Noam to take change into his own hands

10:12 How meeting other families impacted by rare disease led Noam to work on gene therapy for children living with primary immune deficiencies

12:33 How Noga Therapeutics is aiming to reprogram blood stem cells and the potential impact on rare diseases

15:22 Why it’s not yet possible to use the technology to correct gain of function mutations

17:42 How Noga’s program is aiding treatment of multiple primary immune deficiencies

22:25 The techniques the company uses in XLA to modify stem cells and enable expression of a functional copy of the BTK gene

26:30 Why gene therapies don’t always provide a comprehensive solution or cure

28:10 Bridging the gap between transformative therapies and the cost of delivering drugs to very small ultra-rare disease populations

34:41 Noam’s history working in traditional Chinese medicine

39:53 The importance of thinking holistically about health, from understanding g genetic root causes to considering how genes impact whole organ systems

43:15 The collaborative nature of the rare disease community and how parents who want to use their personal experience to further research and advocacy can connect with Noam

44:37 Closing remarks

  continue reading

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