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  1. No Access

    Article

    Maternal but not paternal transmission of 15q11–13–linked nondeletion Angelman syndrome leads to phenotypic expression

    Angelman syndrome (AS) may result from either maternally inherited deletions of chromosome 15q11–13 or from paternal uniparental disomy for chromosome 15. This is in contrast to Prader–Willi syndrome (PWS), wh...

    J. Wagstaff, J.H.M. Knoll, K.A. Glatt, Y.Y. Shugart, A. Sommer… in Nature Genetics (1992)

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    Article

    The major lung cancer-derived mutants of ERBB2 are oncogenic and are associated with sensitivity to the irreversible EGFR/ERBB2 inhibitor HKI-272

    Mutations in the ERBB2 gene were recently found in approximately 2% of primary non-small cell lung cancer (NSCLC) specimens; however, little is known about the functional consequences and the relevance to respons...

    Y Minami, T Shimamura, K Shah, T LaFramboise, K A Glatt, E Liniker, C L Borgman… in Oncogene (2007)