Associated Papers
Mapping cryptic phosphorylation sites in the human proteome.
Gasparotto D et al.
The Embo Journal, 2025
41044218 (PubMed )
Supplement: 44318_2025_567_MOESM5_ESM.xlsx › Table
Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates.
de Leng WW et al.
Clinical Genetics, 2007
Frequency and spectrum of cancers in the Peutz-Jeghers syndrome.
Hearle N et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2006
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
Aretz S et al.
Human Mutation, 2005
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