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Organotypic specificity of key RET adaptor-docking sites in the pathogenesis of neurocristopathies and renal malformations in mice

The receptor tyrosine kinase ret protooncogene (RET) is implicated in the pathogenesis of several diseases and in several developmental defects, particularly those in neural crest–derived structures and the genitourinary system. In order to further elucidate RET-mediated mechanisms that contribute t...

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書誌詳細
主要な著者: Jain, Sanjay, Knoten, Amanda, Hoshi, Masato, Wang, Hongtao, Vohra, Bhupinder, Heuckeroth, Robert O., Milbrandt, Jeffrey
フォーマット: Artigo
言語:Inglês
出版事項: American Society for Clinical Investigation 2010
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オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2827965/
https://ncbi.nlm.nih.gov/pubmed/20160347
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI41619
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