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http://purl.uniprot.org/citations/3402356http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/3402356http://www.w3.org/2000/01/rdf-schema#comment"The lipids of white matter and peripheral nerve from neurological mutant mice with possible myelin abnormalities were analyzed by thin-layer chromatography and quantitated by densitometry. Eight mutants had major abnormalities in the central nervous system (CNS) and/or peripheral nervous system (PNS) tissues examined (optic nerve, and trigeminal and sciatic nerves). In the optic nerve of axJ/axJ, there were increases of 20-30% in the levels of the major phospholipids; peripheral nerve was normal. In bc3J/bc3J CNS, the major phospholipids and cholesterol were increased by 25-40%; the PNS was normal. In myd/myd CNS, there were increases of about 20% in the levels of both forms of cerebrosides and in the major phospholipids; in the PNS the lipids were normal. ot/ot CNS had 20-40% reductions of all the glycolipids and minor alterations in some of the phospholipids and cholesterol; the PNS had 20% losses of both forms of cerebrosides. In the PNS of ji/ji, there were decreases of 10-40% among the glycolipids and of 15-25% in three of the major phospholipids; the CNS was virtually normal. In the PNS of dtJ/dtJ, vb/vb and wr/wr, almost all lipids were significantly decreased. The CNS of dtJ/dtJ and vb/vb were normal; wr/wr had minor reductions of certain glycolipids and phospholipids. Six mutants had relatively minor lipid abnormalities in their myelinated tissues. In cr/cr PNS, there were elevated levels of the cerebrosides and major phospholipids; the CNS was virtually normal. In db/db CNS and PNS, there were reduced levels of the nonhydroxy forms of cerebroside and sulfatide. The major change in htr/htr was the elevation of all the glycolipids in the CNS. In the CNS of Lc/+, nonhydroxy cerebroside was reduced. In shm/shm PNS, nonhydroxy sulfatide was elevated and there were small decreases in some of the phospholipids. wl/wl CNS showed decreases among most of the glycolipids. Mutants homozygous for du, mto, spa and tg had virtually normal lipid levels in both the optic and peripheral nerves. Cholesterol ester, lysophospholipids and other unusual lipid species were not detected in any of the mutants. The plasmalogen forms of ethanolamine and choline phosphatides were at normal levels in all mutants that otherwise had significant alterations among their lipids. Although many alterations in lipid composition were found in these mutants, the changes were moderate compared to the classical myelin mutants and indicate that none of the mutants are severely myelin-deficient.(ABSTRACT TRUNCATED AT 400 WORDS)"xsd:string
http://purl.uniprot.org/citations/3402356http://purl.org/dc/terms/identifier"doi:10.1159/000111963"xsd:string
http://purl.uniprot.org/citations/3402356http://purl.uniprot.org/core/author"Davisson M.T."xsd:string
http://purl.uniprot.org/citations/3402356http://purl.uniprot.org/core/author"Brown B.J."xsd:string
http://purl.uniprot.org/citations/3402356http://purl.uniprot.org/core/author"Kirschner D.A."xsd:string
http://purl.uniprot.org/citations/3402356http://purl.uniprot.org/core/author"Ganser A.L."xsd:string
http://purl.uniprot.org/citations/3402356http://purl.uniprot.org/core/author"Kerner A.L."xsd:string
http://purl.uniprot.org/citations/3402356http://purl.uniprot.org/core/date"1988"xsd:gYear
http://purl.uniprot.org/citations/3402356http://purl.uniprot.org/core/name"Dev Neurosci"xsd:string
http://purl.uniprot.org/citations/3402356http://purl.uniprot.org/core/pages"123-140"xsd:string
http://purl.uniprot.org/citations/3402356http://purl.uniprot.org/core/title"A survey of neurological mutant mice. II. Lipid composition of myelinated tissue in possible myelin mutants."xsd:string
http://purl.uniprot.org/citations/3402356http://purl.uniprot.org/core/volume"10"xsd:string
http://purl.uniprot.org/citations/3402356http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/3402356
http://purl.uniprot.org/citations/3402356http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/3402356
http://purl.uniprot.org/uniprot/#_A0A087WRP2-mappedCitation-3402356http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/3402356
http://purl.uniprot.org/uniprot/#_A0A5F8MPG7-mappedCitation-3402356http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/3402356
http://purl.uniprot.org/uniprot/#_A0A5F8MPY7-mappedCitation-3402356http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/3402356
http://purl.uniprot.org/uniprot/#_A0A1Y7VM63-mappedCitation-3402356http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/3402356
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http://purl.uniprot.org/uniprot/#_A0A498WGS3-mappedCitation-3402356http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/3402356
http://purl.uniprot.org/uniprot/#_A0A411P8U6-mappedCitation-3402356http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/3402356
http://purl.uniprot.org/uniprot/#_F7C9S1-mappedCitation-3402356http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/3402356
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http://purl.uniprot.org/uniprot/#_E9Q2N3-mappedCitation-3402356http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/3402356