Abstract |
Mutations in LKB1 lead to Peutz-Jeghers syndrome (PJS). However, only a subset of PJS patients harbours LKB1 mutations. We performed a mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADalpha, and MO25alpha, in 28 LKB1-negative PJS patients. No disease-causing mutations were detected in the studied genes in PJS patients from different European populations.
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Authors | P Alhopuro, P Katajisto, R Lehtonen, S K Ylisaukko-Oja, L Näätsaari, A Karhu, A M Westerman, J H P Wilson, F W M de Rooij, T Vogel, G Moeslein, I P Tomlinson, L A Aaltonen, T P Mäkelä, V Launonen |
Journal | British journal of cancer
(Br J Cancer)
Vol. 92
Issue 6
Pg. 1126-9
(Mar 28 2005)
ISSN: 0007-0920 [Print] England |
PMID | 15756273
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Adaptor Proteins, Signal Transducing
- Adaptor Proteins, Vesicular Transport
- Nuclear Proteins
- STRADA protein, human
- Transcription Factors
- SMARCA4 protein, human
- DNA Helicases
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Topics |
- Adaptor Proteins, Signal Transducing
(genetics)
- Adaptor Proteins, Vesicular Transport
(genetics)
- DNA Helicases
- Humans
- Introns
- Mutation
- Nuclear Proteins
(genetics)
- Peutz-Jeghers Syndrome
(genetics)
- Polymorphism, Genetic
- Transcription Factors
(genetics)
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