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Disambiguation of "Weirich, Sara"

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Somatic cancer mutations in the MLL1 histone methyltransferase modulate its enzymatic activity and dependence on the WDR5/RBBP5/ASH2L complex

, , and . Molecular oncology, 11 (4): 373-387 (2017)
DOI: 10.1002/1878-0261.12041

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Dr. rer. nat. Sara Weirich University of Stuttgart

Univ. -Prof. Dr. rer. nat. Sara Kleindienst University of Stuttgart

Sara Bender University of Stuttgart

Neslihan Sarac University of Stuttgart

Sara Dula University of Stuttgart

 

Other publications of authors with the same name

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)Specificity of the SUV4–20H1 and SUV4–20H2 protein lysine methyltransferases and methylation of novel substrates, , and . Journal of Molecular Biology, 428 (11): 2344--2358 (June 2016)The Legionella pneumophila Methyltransferase RomA Methylates Also Non-histone Proteins during Infection, , , , , , and . Journal of Molecular Biology, 430 (13): 1912--1925 (June 2018)A functional LSD1 coregulator screen reveals a novel transcriptional regulatory cascade connecting R-loop homeostasis with epigenetic regulation, , , , , , , , , and 3 other author(s). Nucleic Acids Research, 49 (8): 4350-4370 (April 2021)Distinct specificities of the HEMK2 protein methyltransferase in methylation of glutamine and lysine residues, , , , , , , , and . Protein science : a publication of the Protein Society, 33 (2): e4897--e4897 (February 2024)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)Recognition of nonproline N-terminal residues by the Pro/N-degron pathway, , , , , , , and . PNAS, 117 (25): 14158-14167 (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)Activity and specificity of the human SUV39H2 protein lysine methyltransferase, , , , and . Biochimica et biophysica acta, 1849 (1): 55-63 (2015)