Works matching DE "MOLYBDENUM cofactor deficiency"
Results: 16
Molybdenum cofactor deficiency type B knock-in mouse models carrying patient-identical mutations and their rescue by singular AAV injections.
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- Human Genetics, 2019, v. 138, n. 4, p. 355, doi. 10.1007/s00439-019-01992-z
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- Article
Shared Sulfur Mobilization Routes for tRNA Thiolation and Molybdenum Cofactor Biosynthesis in Prokaryotes and Eukaryotes.
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- Biomolecules (2218-273X), 2017, v. 7, n. 1, p. 5, doi. 10.3390/biom7010005
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- Article
Mouse model for molybdenum cofactor deficiency type B recapitulates the phenotype observed in molybdenum cofactor deficient patients.
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- Human Genetics, 2016, v. 135, n. 7, p. 813, doi. 10.1007/s00439-016-1676-4
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ETHE1 and MOCS1 deficiencies: Disruption of mitochondrial bioenergetics, dynamics, redox homeostasis and endoplasmic reticulum-mitochondria crosstalk in patient fibroblasts.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-49014-2
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Identification and characterization of the rice pre‐harvest sprouting mutants involved in molybdenum cofactor biosynthesis.
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- New Phytologist, 2019, v. 222, n. 1, p. 275, doi. 10.1111/nph.15607
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- Article
Shared function and moonlighting proteins in molybdenum cofactor biosynthesis.
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- Biological Chemistry, 2017, v. 398, n. 9, p. 1009, doi. 10.1515/hsz-2017-0110
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- Article
Dimerization of the plant molybdenum insertase Cnx1E is required for synthesis of the molybdenum cofactor.
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- Biochemical Journal, 2017, v. 474, n. 1, p. 163, doi. 10.1042/BCJ20160846
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Oxygen reactivity of mammalian sulfite oxidase provides a concept for the treatment of sulfite oxidase deficiency.
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- Biochemical Journal, 2015, v. 469, n. 2, p. 211, doi. 10.1042/BJ20140768
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- Article
Metal insertion into the molybdenum cofactor: product-substrate channelling demonstrates the functional origin of domain fusion in gephyrin.
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- Biochemical Journal, 2013, v. 450, n. 1, p. 149, doi. 10.1042/BJ20121078
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- Article
Overexpression of a GmCnx1 Gene Enhanced Activity of Nitrate Reductase and Aldehyde Oxidase, and Boosted Mosaic Virus Resistance in Soybean.
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- PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0124273
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Using Next-Generation Sequencing to Identify a Mutation in Human MCSU that is Responsible for Type II Xanthinuria.
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- Cellular Physiology & Biochemistry (Karger AG), 2015, v. 35, n. 6, p. 2412, doi. 10.1159/000374042
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S-sulfocysteine/NMDA receptor-dependent signaling underlies neurodegeneration in molybdenum cofactor deficiency.
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- 2017
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- journal article
Detection of a Compact Folding Intermediate of Dimethyl Sulfoxide Reductase Secreted from a Molybdenum Cofactor-Deficient Mutant ofRhodobacter sphaeroidesf. sp. denitrificans.
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- Plant & Cell Physiology, 1997, v. 38, n. 11, p. 1286, doi. 10.1093/oxfordjournals.pcp.a029118
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Molybdate uptake by Agrobacterium tumefaciens correlates with the cellular molybdenum cofactor status.
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- Molecular Microbiology, 2016, v. 101, n. 5, p. 809, doi. 10.1111/mmi.13421
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- Article
T4 lysozyme‐facilitated crystallization of the human molybdenum cofactor‐dependent enzyme mARC.
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- Acta Crystallographica: Section F, Structural Biology Communications, 2018, v. 74, n. 6, p. 337, doi. 10.1107/S2053230X18006921
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The L-Cysteine Desulfurase NFS1 Is Localized in the Cytosol where it Provides the Sulfur for Molybdenum Cofactor Biosynthesis in Humans.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0060869
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- Article