SABITALKS / Gene Therapy for Ion ChannelsSABITALKS / Gene Therapy for Ion ChannelsSABITALKS / Gene Therapy for Ion ChannelsSABITALKS / Gene Therapy for Ion Channels
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  • RESEARCH CENTERS
  • CORE FACILITIES
    • Advanced Microscopy
    • Cell Culture
    • Molecular Cell Biology
    • Proteomics
    • Drug Discovery
    • Bioinformatics
    • Biomaterials
    • Electrophysiology and Behavior
    • Cognitive Neuroscience
    • Animal House
  • PEOPLE
    • Administration
    • Group Leader
    • Transition Scientist
    • Early Career Researchers
    • Students
  • EVENTS
    • Event Calendar
    • Critical Mind
    • SABITALKS
    • InFocus
    • CROSSTALKS
    • MODAS WS
    • SABITA Podcast
    • Social
  • ABOUT US
    • Our Mission
    • Gender Equality Policy

SABITALKS / Gene Therapy for Ion Channels

Dr. Enes Akyüz from University of Wisconsin-Madison is going to be at SABITALKS on September 18, 2024 at 14:00. The event will take place in person. You can attend the event in person in Lecture Hall C-412.

Location: Istanbul Medipol University Kavacık North Campus: https://goo.gl/maps/JDDjygVtFLWiPiMJA

*Participants from outside SABITA must fill in the participation form.

SABITALKS PARTICIPATION FORM

Gene Therapy for Ion Channels

It will be about KCNJ13 nonsense mutation leading to channelopathy on Kir7.1 ion channel. This dysfunction of the channel lead LCA and we do gene therapy via enginereed tRNA.

Enes Akyüz

University of Wisconsin-Madison, Faculty of Medicine and Public Health

[email protected]

My key focus of research is channelopathy, defects in inwardly rectifying potassium channel 7.1 (Kir7.1) proteins, leading to congenital blindness. I am working on the mutations in retinal pigment epithelium Kir7.1 channels cause blindness such as Leber congenital amaurosis (LCA). I am currently doing several in-vitro (HEK293 and patient-derived induced pluripotent stem cells iPSC-RPE) and in-vivo (genetically engineered mouse) models to study cell, tissue, organ, and animal physiology. I am using techniques like patch-clamp, biological imaging, molecular techniques to repair Kir7.1 channel defects in the hope to treat blindness.

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