Theodoros Georgomanolis

Koeln, NW, Germany

Last Updated: 09/26/2026

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Found 17 publications

The risk of nephrotic range proteinuria and kidney failure in primary laminopathies is genotype-specific.

The risk of nephrotic range proteinuria and kidney failure in primary laminopathies is genotype-specific.

Journal: JCI insight
Published: July 16, 2026

Cardiolipin preserves Treg metabolic fitness and immune homeostasis in the gut.

Cardiolipin preserves Treg metabolic fitness and immune homeostasis in the gut.

Journal: Nature metabolism
Published: May 07, 2025

Novel netrin-1-Unc5b-Klf4 axis balances AT2 survival in experimental bronchopulmonary dysplasia.

Novel netrin-1-Unc5b-Klf4 axis balances AT2 survival in experimental bronchopulmonary dysplasia.

Journal: American journal of respiratory cell and molecular biology
Published: April 23, 2025

Tissue-specific adaptations to cytochrome c oxidase deficiency shape physiological outcomes.

Tissue-specific adaptations to cytochrome c oxidase deficiency shape physiological outcomes.

Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: July 31, 2024

2-hydroxyglutarate mediates whitening of brown adipocytes coupled to nuclear softening upon mitochondrial dysfunction.

2-hydroxyglutarate mediates whitening of brown adipocytes coupled to nuclear softening upon mitochondrial dysfunction.

Journal: Nature metabolism
Published: July 09, 2024

Mitochondrial metabolism sustains DNMT3A-R882-mutant clonal haematopoiesis.

Mitochondrial metabolism sustains DNMT3A-R882-mutant clonal haematopoiesis.

Journal: Nature
Published: March 19, 2024

Autophagy regulator ATG5 preserves cerebellar function by safeguarding its glycolytic activity.

Autophagy regulator ATG5 preserves cerebellar function by safeguarding its glycolytic activity.

Journal: Nature metabolism
Published: February 02, 2024

Single-cell genomics highlight MYC-associated metabolic activation and altered cell interactions in T-prolymphocytic leukemia progression.

Single-cell genomics highlight MYC-associated metabolic activation and altered cell interactions in T-prolymphocytic leukemia progression.

Journal: Nature communications
Published: November 15, 2023

Biallelic loss-of-function variants of ZFTRAF1 cause neurodevelopmental disorder with microcephaly and hypotonia.

Biallelic loss-of-function variants of ZFTRAF1 cause neurodevelopmental disorder with microcephaly and hypotonia.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 31, 2023

NIK/MAP3K14 in hepatocytes orchestrates NASH to hepatocellular carcinoma progression via JAK2/STAT5 inhibition.

NIK/MAP3K14 in hepatocytes orchestrates NASH to hepatocellular carcinoma progression via JAK2/STAT5 inhibition.

Journal: Molecular metabolism
Published: July 21, 2022

Remodeling of the endothelial cell transcriptional program via paracrine and DNA-binding activities of MPO.

Remodeling of the endothelial cell transcriptional program via paracrine and DNA-binding activities of MPO.

Journal: iScience
Published: July 04, 2022

Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signaling.

Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signaling.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 29, 2021
Showing 1-12 of 17

Last Updated: 09/26/2026