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- 2020
-
Mark
The Rare IL22RA2 Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1, -2 and -3 and Is Associated with Risk for Multiple Sclerosis
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- Contribution to journal › Article
- 2019
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Mark
Mutations in the mitochondrial tryptophanyl-tRNA synthetase cause growth retardation and progressive leukoencephalopathy
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- Contribution to journal › Article
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Mark
DNA aptamers for the recognition of HMGB1 from Plasmodium falciparum
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- Contribution to journal › Article
- 2018
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Mark
Crystal Structures and Inhibitor Interactions of Mouse and Dog MTH1 Reveal Species-Specific Differences in Affinity
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- Contribution to journal › Article
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Mark
Mechanism of Peptide Binding and Cleavage by the Human Mitochondrial Peptidase Neurolysin
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- Contribution to journal › Article
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Mark
Sequence, Structure, and Expression of Opsins in the Monochromatic Stomatopod Squilla empusa
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- Contribution to journal › Article
- 2017
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Mark
Identification and characterization of a novel botulinum neurotoxin
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- Contribution to journal › Article
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Mark
Methylation of human eukaryotic elongation factor alpha (eEF1A) by a member of a novel protein lysine methyltransferase family modulates mRNA translation
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- Contribution to journal › Article
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Mark
The novel lysine specific methyltransferase METTL21B affects mRNA translation through inducible and dynamic methylation of Lys-165 in human eukaryotic elongation factor 1 alpha (eEF1A)
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- Contribution to journal › Article
- 2016
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Mark
Mitochondrial DNA triplication and punctual mutations in patients with mitochondrial neuromuscular disorders
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- Contribution to journal › Article