Role of Lkb1, the causative gene of Peutz–Jegher's syndrome, in embryogenesis and polyposis

Peutz–Jeghers syndrome (PJS) is a dominantly inherited human disorder characterized by gastrointestinal hamartomatous polyposis and mucocutaneous melanin pigmentation. LKB1 (STK11) serine/threonine kinase is the product of the causative gene of PJS, which has been mapped to chromosome 19p13.3. Howev...

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Detalhes bibliográficos
Main Authors: Jishage, Kou-ichi, Nezu, Jun-ichi, Kawase, Yosuke, Iwata, Takamitsu, Watanabe, Miho, Miyoshi, Akio, Ose, Asuka, Habu, Kiyoshi, Kake, Takei, Kamada, Nobuo, Ueda, Otoya, Kinoshita, Michiko, Jenne, Dieter E., Shimane, Miyuki, Suzuki, Hiroshi
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2002
Assuntos:
Biological Sciences
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC124396/
https://ncbi.nlm.nih.gov/pubmed/12060709
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.122254599
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