RPTPζ/phosphacan is abnormally glycosylated in a model of muscle-eye-brain disease lacking functional POMGnT1
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O-Mannosylation and human diseaseNeurodevelopmental Changes in Excitatory Synaptic Structure and Function in the Cerebral Cortex of Sanfilippo Syndrome IIIA MiceMammalian O-mannosylation of cadherins and plexins is independent of protein O-mannosyltransferases 1 and 2.Brevican knockdown reduces late-stage glioma tumor aggressiveness.Neurons and glia modify receptor protein-tyrosine phosphatase ζ (RPTPζ)/phosphacan with cell-specific O-mannosyl glycans in the developing brain.A Sulfated Glycosaminoglycan Linkage Region is a Novel Type of Human Natural Killer-1 (HNK-1) Epitope Expressed on Aggrecan in Perineuronal Nets.Protein O-Mannosylation in the Murine Brain: Occurrence of Mono-O-Mannosyl Glycans and Identification of New SubstratesUnderstanding human glycosylation disorders: biochemistry leads the charge.Mining the O-mannose glycoproteome reveals cadherins as major O-mannosylated glycoproteins.KSGal6ST is essential for the 6-sulfation of galactose within keratan sulfate in early postnatal brain.Postnatal Gene Therapy Improves Spatial Learning Despite the Presence of Neuronal Ectopia in a Model of Neuronal Migration Disorder.Dissecting the molecular basis of the role of the O-mannosylation pathway in disease: α-dystroglycan and forms of muscular dystrophy.Glycan susceptibility factors in autism spectrum disorders.Induction of Antibodies Directed Against Branched Core O-Mannosyl Glycopeptides-Selectivity Complimentary to the ConA Lectin.Chondroitin sulfates and their binding molecules in the central nervous system.Recent advancements in understanding mammalian O-mannosylation.A novel splice variant of the protein tyrosine phosphatase PTPRJ that encodes for a soluble protein involved in angiogenesis.Synthesis of a glycopeptide vaccine conjugate for induction of antibodies recognizing O-mannosyl glycopeptides.Perineuronal net degradation in epilepsy.Major glycan structure underlying expression of the Lewis X epitope in the developing brain is O-mannose-linked glycans on phosphacan/RPTPβ.
P2860
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P2860
RPTPζ/phosphacan is abnormally glycosylated in a model of muscle-eye-brain disease lacking functional POMGnT1
description
2012 nî lūn-bûn
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2012年の論文
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2012年論文
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2012年論文
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2012年論文
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2012年論文
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2012年論文
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2012年论文
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name
RPTPζ/phosphacan is abnormally ...... ase lacking functional POMGnT1
@en
type
label
RPTPζ/phosphacan is abnormally ...... ase lacking functional POMGnT1
@en
prefLabel
RPTPζ/phosphacan is abnormally ...... ase lacking functional POMGnT1
@en
P2093
P2860
P1433
P1476
RPTPζ/phosphacan is abnormally ...... ase lacking functional POMGnT1
@en
P2093
P2860
P356
10.1016/J.NEUROSCIENCE.2012.06.026
P407
P577
2012-06-19T00:00:00Z