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Thrombocytopenia and kidney disease in mice with a mutation in the C1galt1 gene
An N-ethyl-N-nitrosourea mutagenesis screen in mice was performed to isolate regulators of circulating platelet number. We report here recessive thrombocytopenia and kidney disease in plt1 mice, which is the result of a severe but partial loss-of-function mutation in the gene encoding glycoprotein-N...
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| Hlavní autoři: | , , , , , , , , , , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
2006
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1637601/ https://ncbi.nlm.nih.gov/pubmed/17062753 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0607872103 |
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