11 Einträge gefunden

1. Evidence for a low-penetrant extended phenotype of rhabdoid tumor predisposition syndrome type 1 from a kindred with gain of SMARCB1 exon 6

   1. Kordes, Uwe
   2. Mautner, Victor-Felix
   3. Oyen, Florian
   4. Hagel, Christian
   5. Hartmann, Christian
   6. Heuser, Michael
   7. Frühwald, Michael

   2021 - Forschungsinformationssystem des UKE
2. 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
3. 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
4. Poorly differentiated chordoma with SMARCB1/INI1 loss: a distinct molecular entity with dismal prognosis

   1. Hasselblatt, Martin
   2. Thomas, Christian
   3. Hovestadt, Volker
   4. Schrimpf, Daniel
   5. Johann, Pascal
   6. Bens, Susanne
   7. Oyen, Florian

   2016 - Forschungsinformationssystem des UKE
5. SMARCA4-mutated atypical teratoid/rhabdoid tumors are associated with inherited germline alterations and poor prognosis

   1. Hasselblatt, Martin
   2. Nagel, Inga
   3. Oyen, Florian
   4. Bartelheim, Kerstin
   5. Russell, Robert B
   6. Schüller, Ulrich
   7. Junckerstorff, Reimar

   2014 - Forschungsinformationssystem des UKE
6. Identifying molecular markers for the sensitive detection of residual atypical teratoid rhabdoid tumor cells

   1. Vu-Han, Tu-Lan
   2. Frühwald, Michael C
   3. Hasselblatt, Martin
   4. Kerl, Kornelius
   5. Nagel, Inga
   6. Obser, Tobias
   7. Oyen, Florian

   2014 - Forschungsinformationssystem des UKE
7. High-resolution genomic analysis suggests the absence of recurrent genomic alterations other than SMARCB1 aberrations in atypical teratoid/rhabdoid tumors.

   1. Hasselblatt, Martin
   2. Isken, Sarah
   3. Linge, Anna
   4. Eikmeier, Kristin
   5. Jeibmann, Astrid
   6. Oyen, Florian
   7. Nagel, Inga

   2013 - Forschungsinformationssystem des UKE
8. Nonsense mutation and inactivation of SMARCA4 (BRG1) in an atypical teratoid/rhabdoid tumor showing retained SMARCB1 (INI1) expression.

   1. Hasselblatt, Martin
   2. Gesk, Stefan
   3. Oyen, Florian
   4. Rossi, Sabrina
   5. Viscardi, Elisabetta
   6. Giangaspero, Felice
   7. Giannini, Caterina

   2011 - Forschungsinformationssystem des UKE
9. Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome.

   1. Schneppenheim, Reinhard
   2. Frühwald, Michael C
   3. Gesk, Stefan
   4. Hasselblatt, Martin
   5. Jeibmann, Astrid
   6. Kordes, Uwe
   7. Kreuz, Markus

   2010 - Forschungsinformationssystem des UKE
10. Clinical and molecular features in patients with atypical teratoid rhabdoid tumor or malignant rhabdoid tumor.

    1. Kordes, Uwe
    2. Gesk, Stefan
    3. Frühwald, Michael Christoph
    4. Graf, Norbert
    5. Leuschner, Ivo
    6. Hasselblatt, Martin
    7. Jeibmann, Astrid

    2010 - Forschungsinformationssystem des UKE
11. Cribriform neuroepithelial tumor (CRINET): a nonrhabdoid ventricular tumor with INI1 loss and relatively favorable prognosis.

    1. Hasselblatt, Martin
    2. Oyen, Florian
    3. Gesk, Stefan
    4. Kordes, Uwe
    5. Brigitte, Wrede
    6. Bergmann, Markus
    7. Schmid, Hansjörg

    2009 - Forschungsinformationssystem des UKE