7 Einträge gefunden

1. SMARCB1-deficient and SMARCA4-deficient Malignant Brain Tumors With Complex Copy Number Alterations and TP53 Mutations May Represent the First Clinical Manifestation of Li-Fraumeni Syndrome

   1. Hasselblatt, Martin
   2. Thomas, Christian
   3. Federico, Aniello
   4. Nemes, Karolina
   5. Johann, Pascal D
   6. Bison, Brigitte
   7. Bens, Susanne

   2022 - Forschungsinformationssystem des UKE
2. ATRT-SHH comprises three molecular subgroups with characteristic clinical and histopathological features and prognostic significance

   1. Federico, Aniello
   2. Thomas, Christian
   3. Miskiewicz, Katarzyna
   4. Woltering, Niklas
   5. Zin, Francesca
   6. Nemes, Karolina
   7. Bison, Brigitte

   2022 - Forschungsinformationssystem des UKE - frei zugänglich
3. Low-grade diffusely infiltrative tumour (LGDIT), SMARCB1-mutant: A clinical and histopathological distinct entity showing epigenetic similarity with ATRT-MYC

   1. Hasselblatt, Martin
   2. Thomas, Christian
   3. Federico, Aniello
   4. Bens, Susanne
   5. Hellström, Mats
   6. Casar-Borota, Olivera
   7. Kordes, Uwe

   2022 - Forschungsinformationssystem des UKE - frei zugänglich
4. Transposable element insertion as a mechanism of SMARCB1 inactivation in atypical teratoid/rhabdoid tumor

   1. Thomas, Christian
   2. Oehl-Huber, Kathrin
   3. Bens, Susanne
   4. Soschinski, Patrick
   5. Koch, Arend
   6. Nemes, Karolina
   7. Oyen, Florian

   2021 - Forschungsinformationssystem des UKE - frei zugänglich
5. Inhibition of nuclear export restores nuclear localization and residual tumor suppressor function of truncated SMARCB1/INI1 protein in a molecular subset of atypical teratoid/rhabdoid tumors

   1. Pathak, Rajiv
   2. Zin, Francesca
   3. Thomas, Christian
   4. Bens, Susanne
   5. Gayden, Tenzin
   6. Karamchandani, Jason
   7. Dudley, Roy W

   2021 - Forschungsinformationssystem des UKE - frei zugänglich
6. Two molecularly distinct atypical teratoid/rhabdoid tumors (or tumor components) occurring in an infant with rhabdoid tumor predisposition syndrome 1

   1. Thomas, Christian
   2. Knerlich-Lukoschus, Friederike
   3. Reinhard, Harald
   4. Johann, Pascal D
   5. Sturm, Dominik
   6. Sahm, Felix
   7. Bens, Susanne

   2019 - Forschungsinformationssystem des UKE
7. Germline variants in SMARCB1 and other members of the BAF chromatin-remodeling complex across human disease entities:a meta-analysis

   1. Holsten, Till
   2. Bens, Susanne
   3. Oyen, Florian
   4. Nemes, Karolina
   5. Hasselblatt, Martin
   6. Kordes, Uwe
   7. Siebert, Reiner

   2018 - Forschungsinformationssystem des UKE