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rdf:type |
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|
lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2005-7-1
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pubmed:abstractText |
Phenotype-driven screening of a great pool of randomly mutant mice and subsequent selection of animals showing symptoms equivalent to human kidney diseases may result in the generation of novel suitable models for the study of the pathomechanisms and the identification of genes involved in kidney dysfunction.
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pubmed:language |
eng
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pubmed:journal |
|
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pubmed:citationSubset |
IM
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pubmed:chemical |
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|
pubmed:status |
MEDLINE
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|
pubmed:issn |
1660-2129
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pubmed:author |
|
|
pubmed:issnType |
Electronic
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|
pubmed:volume |
100
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
e143-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15849479-Albuminuria,
pubmed-meshheading:15849479-Alkylating Agents,
pubmed-meshheading:15849479-Animals,
pubmed-meshheading:15849479-Disease Models, Animal,
pubmed-meshheading:15849479-Ethylnitrosourea,
pubmed-meshheading:15849479-Female,
pubmed-meshheading:15849479-Male,
pubmed-meshheading:15849479-Mice,
pubmed-meshheading:15849479-Mice, Inbred C3H,
pubmed-meshheading:15849479-Mutagenesis,
pubmed-meshheading:15849479-Pedigree,
pubmed-meshheading:15849479-Phenotype,
pubmed-meshheading:15849479-Proteinuria
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pubmed:year |
2005
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pubmed:articleTitle |
Large-scale albuminuria screen for nephropathy models in chemically induced mouse mutants.
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pubmed:affiliation |
Institute of Molecular Animal Breeding and Biotechnology, Ludwig Maximilians University, Munich, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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