{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Qin W"],"funding":["Simons Foundation","NICHD NIH HHS","NHLBI NIH HHS","Foundation for the National Institutes of Health","Foundation for the National Institutes of Health (Foundation for the National Institutes of Health, Inc.)","NIGMS NIH HHS"],"pagination":["5613"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11224239"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["15(1)"],"pubmed_abstract":["Advancements in CRISPR technology, particularly the development of base editors, revolutionize genetic variant research. When combined with model organisms like zebrafish, base editors significantly accelerate and refine in vivo analysis of genetic variations. However, base editors are restricted by protospacer adjacent motif (PAM) sequences and specific editing windows, hindering their applicability to a broad spectrum of genetic variants. Additionally, base editors can introduce unintended mutations and often exhibit reduced efficiency in living organisms compared to cultured cell lines. Here, we engineer a suite of adenine base editors (ABEs) called ABE-Ultramax (Umax), demonstrating high editing efficiency and low rates of insertions and deletions (indels) in zebrafish. The ABE-Umax su"],"journal":["Nature communications"],"pubmed_title":["ABE-ultramax for high-efficiency biallelic adenine base editing in zebrafish."],"pmcid":["PMC11224239"],"funding_grant_id":["R01GM136741","P50 HD109861","R01HL151576","R01 HL151576","P50HD109861","R01 GM136741"],"pubmed_authors":["Mourrain P","Liu Y","Varshney GK","Liang F","Varshney P","Zhang Y","Huang K","Qin W","Lin SJ","Petree C","Li L"],"additional_accession":[]},"is_claimable":false,"name":"ABE-ultramax for high-efficiency biallelic adenine base editing in zebrafish.","description":"Advancements in CRISPR technology, particularly the development of base editors, revolutionize genetic variant research. When combined with model organisms like zebrafish, base editors significantly accelerate and refine in vivo analysis of genetic variations. However, base editors are restricted by protospacer adjacent motif (PAM) sequences and specific editing windows, hindering their applicability to a broad spectrum of genetic variants. Additionally, base editors can introduce unintended mutations and often exhibit reduced efficiency in living organisms compared to cultured cell lines. Here, we engineer a suite of adenine base editors (ABEs) called ABE-Ultramax (Umax), demonstrating high editing efficiency and low rates of insertions and deletions (indels) in zebrafish. The ABE-Umax su","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Jul","modification":"2025-04-22T12:04:53.534Z","creation":"2025-04-06T00:11:31.492Z"},"accession":"S-EPMC11224239","cross_references":{"pubmed":["38965236"],"doi":["10.1038/s41467-024-49943-1"]}}