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Patched1 haploinsufficiency severely impacts intermediary metabolism in the skin of Ptch1(+/−)/ODC transgenic mice

The study of dominantly heritable cancers has provided insights about tumor development. Gorlin syndrome (GS) is an autosomal dominant disorder wherein affected individuals develop multiple basal cell carcinomas (BCCs) of the skin. We developed a murine model of Ptch1 haploinsufficiency on an ornith...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Li, Changzhao, Mishra, Bharat, Kashyap, Mahendra, Weng, Zhiping, Andrabi, Shaida A., Mukhtar, Shahid M., Kim, Arianna L., Bickers, David R., Kopelovich, Levy, Athar, Mohammad
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2019
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6737076/
https://ncbi.nlm.nih.gov/pubmed/31506465
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-49470-w
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