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The CRISPR Vision Program: Nonviral Genome Editing Platforms to Treat Inherited Retinal Channelopath — Krishanu Saha (UNIVERSITY O

PROJECT SUMMARY/ABSTRACT – OVERALL The genome editing community is celebrating the ten-year anniversary of landmark CRISPR papers in 2022. What is notable to many in the field is tremendous technologi

Project titleThe CRISPR Vision Program: Nonviral Genome Editing Platforms to Treat Inherited Retinal Channelopath
Project number1U19NS132296-01
PI nameKrishanu Saha
InstitutionUNIVERSITY OF WISCONSIN-MADISON
Funding mechanismU19
AgencyNINDS
Award amount$6.16M
Fiscal year2023
Project start2023-05-16T00:00:00
Project end2028-04-30T00:00:00
AbstractPROJECT SUMMARY/ABSTRACT – OVERALL The genome editing community is celebrating the ten-year anniversary of landmark CRISPR papers in 2022. What is notable to many in the field is tremendous technologi
Key terms<Academia><Address><Adeno-Associated Viruses><Adverse Experience><Adverse event><Affect><Animal Mode

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