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• W2047471344 endingPage "286" @default.
• W2047471344 startingPage "271" @default.
• W2047471344 abstract "Transgenic mice and Drosophila mutant studies demonstrate that the leukocyte common antigen-related (LAR) protein tyrosine phosphatase (PTPase) receptor is required for formation of neural networks. We assessed the hypothesis that alternative splicing of the LAR extracellular region contributes to this function by establishing temporospatial expression patterns of LAR isoforms containing an alternatively spliced extracellular nine amino acid segment (LAR alternatively spliced element-c; LASE-c). LASE-c was present in multiple alternatively spliced and truncated LAR transcripts. In contrast to LAR isoforms without LASE-c, levels of LAR transcripts and protein isoforms containing LASE-c were primarily present during development, suggesting a mechanism for developmental regulation of LAR function.In situanalysis demonstrated increasingly region- and cell-specific expression of LASE-c during maturation. Immunostaining revealed LASE-c-containing LAR protein along neurites and in growth cones. The discovery of highly regulated, temporospatial extracellular domain alternative splicing of LAR-type PTPase receptors points to a novel mechanism by which these receptors might influence network formation." @default.
• W2047471344 created "2016-06-24" @default.
• W2047471344 creator A5001857082 @default.
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• W2047471344 creator A5019824956 @default.
• W2047471344 creator A5025299288 @default.
• W2047471344 creator A5079616106 @default.
• W2047471344 date "1998-04-01" @default.
• W2047471344 modified "2023-10-11" @default.
• W2047471344 title "LAR Tyrosine Phosphatase Receptor: A Developmental Isoform Is Present in Neurites and Growth Cones and Its Expression Is Regional- and Cell-Specific" @default.
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• W2047471344 doi "https://doi.org/10.1006/mcne.1998.0663" @default.
• W2047471344 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9618218" @default.
• W2047471344 hasPublicationYear "1998" @default.
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