Source:http://linkedlifedata.com/resource/pubmed/id/10461199
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
1999-10-18
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pubmed:abstractText |
Several different mutant genes in humans, mice and Drosophila, most of which were identified initially on the basis of reduced pigmentation, have been associated with defects of multiple cytoplasmic organelles - melanosomes, lysosomes and granules. Recent discoveries show that several of these mutations directly affect components in the pathway of organelle-specific protein trafficking, and provide new insights into the relationships of these pathways in mammals, flies and yeast.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0168-9525
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
337-40
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pubmed:dateRevised |
2005-11-16
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pubmed:meshHeading |
pubmed-meshheading:10461199-Animals,
pubmed-meshheading:10461199-Drosophila,
pubmed-meshheading:10461199-Humans,
pubmed-meshheading:10461199-Mice,
pubmed-meshheading:10461199-Mutation,
pubmed-meshheading:10461199-Organelles,
pubmed-meshheading:10461199-Pigmentation Disorders,
pubmed-meshheading:10461199-Proteins,
pubmed-meshheading:10461199-Saccharomyces cerevisiae
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pubmed:year |
1999
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pubmed:articleTitle |
Multi-organellar disorders of pigmentation: intracellular traffic jams in mammals, flies and yeast.
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pubmed:affiliation |
Human Medical Genetics Program, University of Colorado Health Sciences Center, 4200 East Ninth Avenue, B161, Denver, CO 80262, USA. richard.spritz@uchsc.edu
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pubmed:publicationType |
Journal Article,
Review
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