Publications by authors named "Timo Keskinen"

Claim this Profile
G
Genetic Correction of the Most Common Mutation Causing Primary Hyperoxaluria Restores Enzyme Localization and Oxalate Metabolism.
Timo Keskinen, Sami Jalil, Irem Gümüşoğlu, Juhana Juutila, Nadim Kestilä

J Inherit Metab Dis· January 2026

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic and functional correction of argininosuccinate lyase deficiency using CRISPR adenine base editors.
Sami Jalil, Timo Keskinen, Juhana Juutila, Rocio Sartori Maldonado, Liliya Euro

Am J Hum Genet· April 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
CRISPR correction of the Finnish ornithine delta-aminotransferase mutation restores metabolic homeostasis in iPSC from patients with gyrate atrophy.
Rocio Maldonado, Sami Jalil, Timo Keskinen, Anni I Nieminen, Mervi E Hyvönen

Mol Genet Metab Rep· June 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Simultaneous high-efficiency base editing and reprogramming of patient fibroblasts.
Sami Jalil, Timo Keskinen, Rocío Maldonado, Joonas Sokka, Ras Trokovic

Stem Cell Reports· December 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis