K-Ras(V14I) recapitulates Noonan syndrome in mice

Noonan syndrome (NS) is an autosomal dominant genetic disorder characterized by short stature, craniofacial dysmorphism, and congenital heart defects. NS also is associated with a risk for developing myeloproliferative disorders (MPD), including juvenile myelomonocytic leukemia (JMML). Mutations res...

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Detaylı Bibliyografya
Yayımlandı:Proc Natl Acad Sci U S A
Asıl Yazarlar: Hernández-Porras, Isabel, Fabbiano, Salvatore, Schuhmacher, Alberto J., Aicher, Alexandra, Cañamero, Marta, Cámara, Juan Antonio, Cussó, Lorena, Desco, Manuel, Heeschen, Christopher, Mulero, Francisca, Bustelo, Xosé R., Guerra, Carmen, Barbacid, Mariano
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: National Academy of Sciences 2014
Konular:
Biological Sciences
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4246321/
https://ncbi.nlm.nih.gov/pubmed/25359213
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1418126111
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