Imre F. Schene

Uppsalalaan 8, 3584, CT
Utrecht, UT, Netherlands

Last Updated: 09/26/2026

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Found 17 publications

Functional characterization of BAP1 mutations in genome edited cholangiocarcinoma organoids: Role in cell death and drug responses.

Functional characterization of BAP1 mutations in genome edited cholangiocarcinoma organoids: Role in cell death and drug responses.

Journal: iScience

Published: July 07, 2025

Misidentification of neural cell identity in liver-derived organoid systems.

Misidentification of neural cell identity in liver-derived organoid systems.

Journal: Stem cell reports

Published: December 16, 2023

Isoleucine-to-valine substitutions support cellular physiology during isoleucine deprivation.

Isoleucine-to-valine substitutions support cellular physiology during isoleucine deprivation.

Journal: Nucleic acids research

Published: September 15, 2022

A comprehensive transcriptomic comparison of hepatocyte model systems improves selection of models for experimental use.

A comprehensive transcriptomic comparison of hepatocyte model systems improves selection of models for experimental use.

Journal: Communications biology

Published: June 17, 2022

Bi-allelic variants in NAE1 cause intellectual disability, ischiopubic hypoplasia, stress-mediated lymphopenia and neurodegeneration.

Bi-allelic variants in NAE1 cause intellectual disability, ischiopubic hypoplasia, stress-mediated lymphopenia and neurodegeneration.

Journal: American journal of human genetics

Published: February 09, 2022

The potential and limitations of intrahepatic cholangiocyte organoids to study inborn errors of metabolism.

The potential and limitations of intrahepatic cholangiocyte organoids to study inborn errors of metabolism.

Journal: Journal of inherited metabolic disease

Published: June 18, 2021

Mutation-specific reporter for optimization and enrichment of prime editing.

Mutation-specific reporter for optimization and enrichment of prime editing.

Journal: Nature communications

Published: May 26, 2021

Treatment of ARS deficiencies with specific amino acids.

Treatment of ARS deficiencies with specific amino acids.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: March 18, 2021

Correction: Aminoacyl-tRNA synthetase deficiencies in search of common themes.

Correction: Aminoacyl-tRNA synthetase deficiencies in search of common themes.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: September 16, 2020

Human extrahepatic and intrahepatic cholangiocyte organoids show region-specific differentiation potential and model cystic fibrosis-related bile duct disease.

Human extrahepatic and intrahepatic cholangiocyte organoids show region-specific differentiation potential and model cystic fibrosis-related bile duct disease.

Journal: Scientific reports

Published: June 22, 2020

Prime editing for functional repair in patient-derived disease models.

Prime editing for functional repair in patient-derived disease models.

Journal: Nature communications

Published: May 30, 2020

Misdiagnosis of CTX due to propofol: The interference of total intravenous propofol anaesthesia with bile acid profiling.

Misdiagnosis of CTX due to propofol: The interference of total intravenous propofol anaesthesia with bile acid profiling.

Journal: Journal of inherited metabolic disease

Published: June 26, 2019

Showing 1-12 of 17

Last Updated: 09/26/2026