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Disambiguation of "Schuhmacher, Maren Kirstin"

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Author Correction: Sequence specificity analysis of the SETD2 protein lysine methyltransferase and discovery of a SETD2 super-substrate

, , , , , , , , and . Communications Biology, (2020)Correction to: https://doi.org/10.1038/s42003-020-01223-6.
DOI: 10.1038/s42003-020-01351-z

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Maren Neubrand University of Stuttgart

Dr. Maren Scheel University of Stuttgart

 

Other publications of authors with the same name

The Legionella pneumophila Methyltransferase RomA Methylates Also Non-histone Proteins during Infection, , , , , , and . Journal of Molecular Biology, 430 (13): 1912--1925 (June 2018)Investigation of H2AX methylation by the SUV39H2 protein lysine methyltransferase, , and . FEBS letters, 590 (12): 1713-1719 (2016)Analysis of the Substrate Specificity of the SMYD2 Protein Lysine Methyltransferase and Discovery of Novel Non-Histone Substrates, , , , , and . ChemBioChem, 21 (1-2): 256-264 (2019)A loss-of-function variant in SUV39H2 identified in autism-spectrum disorder causes altered H3K9 trimethylation and dysregulation of protocadherin $\beta$-cluster genes in the developing brain, , , , , , , , , and 18 other author(s). Molecular Psychiatry, 26 (12): 7550--7559 (Dec 1, 2021)Biochemical characterization and identification of novel substrates of protein lysine methyltransferases. Universität Stuttgart, Stuttgart, Dissertation, (2019)Globally altered epigenetic landscape and delayed osteogenic differentiation in H3.3-G34W-mutant giant cell tumor of bone, , , , , , , , , and 23 other author(s). Nature Communications, 11 (1): 5414 (Oct 27, 2020)The H3.3 G34W oncohistone mutation increases K36 methylation by the protein lysine methyltransferase NSD1, , , , , , and . Biochimie, 198 (July): 86-91 (2022)The methyltransferase METTL9 mediates pervasive 1-methylhistidine modification in mammalian proteomes, , , , , , , , , and 18 other author(s). Nature Communications, 12 (1): 891 (Feb 9, 2021)Sequence specificity analysis of the SETD2 protein lysine methyltransferase and discovery of a SETD2 super-substrate, , , , , , , , and . Communications Biology, 3 (1): 511 (Sep 16, 2020)A loss-of-function variant in SUV39H2 identified in autism-spectrum disorder causes altered H3K9 trimethylation and dysregulation of protocadherin β-cluster genes in the developing brain, , , , , , , , , and 18 other author(s). Molecular psychiatry, (2021)