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Kornel Labun

Showing results (11-20 of 14) with videos related to

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Bioinformatics (Oxford, England)|June 12, 2016
RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing dataTomasz Stokowy, Mateusz Garbulowski, Torunn Fiskerstrand, et al.
Nucleic Acids Research|February 27, 2026
A novel Dual-guide CRISPR-Cas13 strategy improves specificity for single-nucleotide variant detectionAraceli Aguilar-González, Ismael Martos-Jamai, Iris Ramos-Hernández, et al.
Elife|December 13, 2021
Rapid genome editing by CRISPR-Cas9-POLD3 fusionGanna Reint, Zhuokun Li, Kornel Labun, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 14, 2025
Precision T cell correction platform for Inborn Errors of ImmunityKatariina Mamia, Solrun Kolbeinsdottir, Kornel Labun, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Bioinformatics (Oxford, England)|June 12, 2016
RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing dataTomasz Stokowy, Mateusz Garbulowski, Torunn Fiskerstrand, et al.
Nucleic Acids Research|February 27, 2026
A novel Dual-guide CRISPR-Cas13 strategy improves specificity for single-nucleotide variant detectionAraceli Aguilar-González, Ismael Martos-Jamai, Iris Ramos-Hernández, et al.
Elife|December 13, 2021
Rapid genome editing by CRISPR-Cas9-POLD3 fusionGanna Reint, Zhuokun Li, Kornel Labun, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 14, 2025
Precision T cell correction platform for Inborn Errors of ImmunityKatariina Mamia, Solrun Kolbeinsdottir, Kornel Labun, et al.
Pageof 2