Matti Myllykoski

Oulu, 90014, Finland

Last Updated: 09/26/2026

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Found 26 publications

The molecular basis for acetylhistidine synthesis by HisAT/NAT16.

The molecular basis for acetylhistidine synthesis by HisAT/NAT16.

Journal: Nature communications

Published: October 31, 2024

Molecular mechanism of HNF-1A-mediated HNF4A gene regulation and promoter-driven HNF4A-MODY diabetes.

Molecular mechanism of HNF-1A-mediated HNF4A gene regulation and promoter-driven HNF4A-MODY diabetes.

Journal: JCI insight

Published: September 28, 2023

N-terminal cysteine acetylation and oxidation patterns may define protein stability.

N-terminal cysteine acetylation and oxidation patterns may define protein stability.

Journal: Nature communications

Published: August 17, 2023

Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosis.

Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosis.

Journal: Haematologica

Published: February 10, 2023

(R)-2-Hydroxyglutarate Inhibits KDM5 Histone Lysine Demethylases to Drive Transformation in IDH-Mutant Cancers.

(R)-2-Hydroxyglutarate Inhibits KDM5 Histone Lysine Demethylases to Drive Transformation in IDH-Mutant Cancers.

Journal: Cancer discovery

Published: July 20, 2022

HIDEA syndrome is caused by biallelic, pathogenic, rare or founder P4HTM variants impacting the active site or the overall stability of the P4H-TM protein.

HIDEA syndrome is caused by biallelic, pathogenic, rare or founder P4HTM variants impacting the active site or the overall stability of the P4H-TM protein.

Journal: Clinical genetics

Published: June 02, 2022

Structure of transmembrane prolyl 4-hydroxylase reveals unique organization of EF and dioxygenase domains.

Structure of transmembrane prolyl 4-hydroxylase reveals unique organization of EF and dioxygenase domains.

Journal: The Journal of biological chemistry

Published: October 24, 2020

Biallelic loss-of-function P4HTM gene variants cause hypotonia, hypoventilation, intellectual disability, dysautonomia, epilepsy, and eye abnormalities (HIDEA syndrome).

Biallelic loss-of-function P4HTM gene variants cause hypotonia, hypoventilation, intellectual disability, dysautonomia, epilepsy, and eye abnormalities (HIDEA syndrome).

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

Published: November 24, 2018

Molecular structure and function of myelin protein P0 in membrane stacking.

Molecular structure and function of myelin protein P0 in membrane stacking.

Journal: Scientific reports

Published: August 22, 2018

Crystallographic home-source X-ray data for the atomic-resolution experimental phasing of the Shank3 SH3 domain structure from pseudomerohedrally twinned crystals.

Crystallographic home-source X-ray data for the atomic-resolution experimental phasing of the Shank3 SH3 domain structure from pseudomerohedrally twinned crystals.

Journal: Data in brief

Published: July 07, 2018

High-affinity heterotetramer formation between the large myelin-associated glycoprotein and the dynein light chain DYNLL1.

High-affinity heterotetramer formation between the large myelin-associated glycoprotein and the dynein light chain DYNLL1.

Journal: Journal of neurochemistry

Published: July 05, 2018

Cancer-associated 2-oxoglutarate analogues modify histone methylation by inhibiting histone lysine demethylases.

Cancer-associated 2-oxoglutarate analogues modify histone methylation by inhibiting histone lysine demethylases.

Journal: Journal of molecular biology

Published: May 14, 2018

Showing 1-12 of 26

Last Updated: 09/26/2026