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@ARTICLE{Hasselblatt:143578,
      author       = {M. Hasselblatt and C. Thomas and K. Nemes and C.-M.
                      Monoranu and M. J. Riemenschneider and A. Koch and D.
                      Sumerauer and P. Hauser and W. Paulus and P. Johann$^*$ and
                      M. Kool$^*$ and M. C. Frühwald},
      title        = {{T}yrosinase immunohistochemistry can be employed for the
                      diagnosis of atypical teratoid/rhabdoid tumours of the
                      tyrosinase subgroup ({ATRT}-{TYR}).},
      journal      = {Neuropathology $\&$ applied neurobiology},
      volume       = {46},
      number       = {2},
      issn         = {1365-2990},
      address      = {Oxford [u.a.]},
      publisher    = {Wiley-Blackwell},
      reportid     = {DKFZ-2019-01158},
      pages        = {186-189},
      year         = {2020},
      note         = {2020 Feb;46(2):186-189},
      abstract     = {Atypical teratoid/rhabdoid tumour (ATRT) is a malignant
                      brain tumour mainly occurring in young children [1].
                      Mutations of chromatin remodelling complex member
                      SMARCB1/INI1 or (rarely) SMARCA4/BRG1 are the sole recurrent
                      genetic lesions [2, 3]. On an epigenetic level, however,
                      ATRT is a heterogeneous disease comprised of three different
                      molecular subgroups (ATRT-TYR, ATRT-SHH and ATRT-MYC). This
                      article is protected by copyright. All rights reserved.},
      subtyp        = {Letter},
      cin          = {B062 / HD01},
      ddc          = {610},
      cid          = {I:(DE-He78)B062-20160331 / I:(DE-He78)HD01-20160331},
      pnm          = {312 - Functional and structural genomics (POF3-312)},
      pid          = {G:(DE-HGF)POF3-312},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:31077608},
      doi          = {10.1111/nan.12560},
      url          = {https://inrepo02.dkfz.de/record/143578},
}