Genetic defects underlying Peutz–Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates

LKB1/STK11 germline inactivations are identified in the majority (66–94%) of Peutz–Jeghers syndrome (PJS) patients. Therefore, defects inother genes or so far unidentified ways of LKB1 inactivation may cause PJS. The genes encoding the MARK proteins, homologues of the Par1 polarity protein that asso...

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Detaylı Bibliyografya
Asıl Yazarlar: de Leng, WWJ, Jansen, M, Carvalho, R, Polak, M, Musler, AR, Milne, ANA, Keller, JJ, Menko, FH, de Rooij, FWM, Iacobuzio-Donahue, CA, Giardiello, FM, Weterman, MAJ, Offerhaus, GJA
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2007
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2714539/
https://ncbi.nlm.nih.gov/pubmed/17924967
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1399-0004.2007.00907.x
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