Home > Publications database > Tyrosinase immunohistochemistry can be employed for the diagnosis of atypical teratoid/rhabdoid tumours of the tyrosinase subgroup (ATRT-TYR). > print |
001 | 143578 | ||
005 | 20240229123016.0 | ||
024 | 7 | _ | |a 10.1111/nan.12560 |2 doi |
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100 | 1 | _ | |a Hasselblatt, Martin |b 0 |
245 | _ | _ | |a Tyrosinase immunohistochemistry can be employed for the diagnosis of atypical teratoid/rhabdoid tumours of the tyrosinase subgroup (ATRT-TYR). |
260 | _ | _ | |a Oxford [u.a.] |c 2020 |b Wiley-Blackwell |
336 | 7 | _ | |a article |2 DRIVER |
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336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1597225956_3553 |2 PUB:(DE-HGF) |x Letter |
336 | 7 | _ | |a ARTICLE |2 BibTeX |
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500 | _ | _ | |a 2020 Feb;46(2):186-189 |
520 | _ | _ | |a 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. |
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700 | 1 | _ | |a Thomas, Christian |b 1 |
700 | 1 | _ | |a Nemes, Karolina |b 2 |
700 | 1 | _ | |a Monoranu, Camelia-Maria |b 3 |
700 | 1 | _ | |a Riemenschneider, Markus J |b 4 |
700 | 1 | _ | |a Koch, Arend |b 5 |
700 | 1 | _ | |a Sumerauer, David |b 6 |
700 | 1 | _ | |a Hauser, Peter |b 7 |
700 | 1 | _ | |a Paulus, Werner |b 8 |
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700 | 1 | _ | |a Frühwald, Michael C |b 11 |
773 | _ | _ | |a 10.1111/nan.12560 |g p. nan.12560 |0 PERI:(DE-600)2008293-9 |n 2 |p 186-189 |t Neuropathology & applied neurobiology |v 46 |y 2020 |x 1365-2990 |
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