Severe Hypomyelination and Developmental Defects Are Caused in Mice Lacking Protein Arginine Methyltransferase 1 (PRMT1) in the Central Nervous System
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Arginine Methylation by PRMT1 Regulates Muscle Stem Cell Fate.Emerging Role for Methylation in Multiple Sclerosis: Beyond DNA.Asymmetric Arginine Dimethylation Modulates Mitochondrial Energy Metabolism and Homeostasis in Caenorhabditis elegans.Chromatin remodeling and epigenetic regulation of oligodendrocyte myelination and myelin repair.PRMT1 regulates astrocytic differentiation of embryonic neural stem/precursor cells.PRMT-5 converts monomethylarginines into symmetrical dimethylarginines in Caenorhabditis elegans.Simultaneous ablation of prmt-1 and prmt-5 abolishes asymmetric and symmetric arginine dimethylations in Caenorhabditis elegans.Angiodysplasia in embryo lacking protein arginine methyltransferase 1 in vascular endothelial cells.
P2860
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P2860
Severe Hypomyelination and Developmental Defects Are Caused in Mice Lacking Protein Arginine Methyltransferase 1 (PRMT1) in the Central Nervous System
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2015 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
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2015 թվականի դեկտեմբերին հրատարակված գիտական հոդված
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年论文
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Severe Hypomyelination and Dev ...... in the Central Nervous System
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Severe Hypomyelination and Dev ...... in the Central Nervous System
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Severe Hypomyelination and Dev ...... in the Central Nervous System
@ast
Severe Hypomyelination and Dev ...... in the Central Nervous System
@en
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Severe Hypomyelination and Dev ...... in the Central Nervous System
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Severe Hypomyelination and Dev ...... in the Central Nervous System
@en
P2093
P2860
P356
P1476
Severe Hypomyelination and Dev ...... in the Central Nervous System
@en
P2093
Akihiko Kanou
Akiyoshi Fukamizu
Junji Ishida
Kazuya Murata
Misuzu Hashimoto
Yoshitoshi Kasuya
P2860
P304
P356
10.1074/JBC.M115.684514
P407
P577
2015-12-04T00:00:00Z