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    Article

    The primacy of NF1 loss as the driver of tumorigenesis in neurofibromatosis type 1-associated plexiform neurofibromas

    Neurofibromatosis type 1 (NF1) is a common tumor-predisposition disorder due to germline mutations in the tumor suppressor gene NF1. A virtually pathognomonic finding of NF1 is the plexiform neurofibroma (PN), a ...

    A Pemov, H Li, R Patidar, N F Hansen, S Sindiri, S W Hartley, J S Wei in Oncogene (2017)

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    Somatic mutational landscape of AML with inv(16) or t(8;21) identifies patterns of clonal evolution in relapse leukemia

    R Sood, N F Hansen, F X Donovan, B Carrington, D Bucci, B Maskeri, A Young in Leukemia (2016)

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    The DNA sequence and analysis of human chromosome 6

    Chromosome 6 is a metacentric chromosome that constitutes about 6% of the human genome. The finished sequence comprises 166,880,988 base pairs, representing the largest chromosome sequenced so far. The entire ...

    A. J. Mungall, S. A. Palmer, S. K. Sims, C. A. Edwards, J. L. Ashurst, L. Wilming in Nature (2003)

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    An SNP map of human chromosome 22

    The human genome sequence will provide a reference for measuring DNA sequence variation in human populations. Sequence variants are responsible for the genetic component of individuality, including complex cha...

    J. C. Mullikin, S. E. Hunt, C. G. Cole, B. J. Mortimore, C. M. Rice, J. Burton in Nature (2000)