9 Einträge gefunden

1. 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
2. Analysis of crossover breakpoints yields new insights into the nature of the gene conversion events associated with large NF1 deletions mediated by nonallelic homologous recombination

   1. Bengesser, Kathrin
   2. Vogt, Julia
   3. Mussotter, Tanja
   4. Mautner, Victor-Felix
   5. Messiaen, Ludwine
   6. Cooper, David N
   7. Kehrer-Sawatzki, Hildegard

   2014 - Forschungsinformationssystem des UKE
3. Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder.

   1. Vogt, Julia
   2. Mussotter, Tanja
   3. Bengesser, Kathrin
   4. Claes, Kathleen
   5. Högel, Josef
   6. Chuzhanova, Nadia
   7. Fu, Chuanhua

   2012 - Forschungsinformationssystem des UKE
4. Tissue-specific differences in the proportion of mosaic large NF1 deletions are suggestive of a selective growth advantage of hematopoietic del(+/-) stem cells.

   1. Roehl, Angelika C
   2. Mussotter, Tanja
   3. Cooper, David N
   4. Kluwe, Lan
   5. Wimmer, Katharina
   6. Högel, Josef
   7. Zetzmann, Marion

   2012 - Forschungsinformationssystem des UKE
5. Internal tumor burden in neurofibromatosis Type I patients with large NF1 deletions.

   1. Kluwe, Lan
   2. Nguyen, Rosa
   3. Vogt, Julia
   4. Bengesser, Kathrin
   5. Mussotter, Tanja
   6. Friedrich, Reinhard
   7. Jett, Kimberly

   2012 - Forschungsinformationssystem des UKE
6. Dissecting the clinical phenotype associated with mosaic type-2 NF1 microdeletions.

   1. Kehrer-Sawatzki, Hildegard
   2. Vogt, Julia
   3. Mußotter, Tanja
   4. Kluwe, Lan
   5. Cooper, David N
   6. Mautner, Viktor Felix

   2012 - Forschungsinformationssystem des UKE
7. Monozygotic twins discordant for neurofibromatosis type 1 due to a postzygotic NF1 gene mutation.

   1. Vogt, Julia
   2. Kohlhase, Jürgen
   3. Morlot, Susanne
   4. Kluwe, Lan
   5. Mautner, Viktor Felix
   6. Cooper, David N
   7. Kehrer-Sawatzki, Hildegard

   2011 - Forschungsinformationssystem des UKE
8. Delineation of the clinical phenotype associated with non-mosaic type-2 NF1 deletions: two case reports.

   1. Vogt, Julia
   2. Nguyen, Rosa
   3. Kluwe, Lan
   4. Schuhmann, Martin
   5. Roehl, Angelika C
   6. Mußotter, Tanja
   7. Cooper, David N

   2011 - Forschungsinformationssystem des UKE - frei zugänglich
9. Intrachromosomal mitotic nonallelic homologous recombination is the major molecular mechanism underlying type-2 NF1 deletions.

   1. Roehl, Angelika C
   2. Vogt, Julia
   3. Mussotter, Tanja
   4. Zickler, Antje N
   5. Spöti, Helene
   6. Högel, Josef
   7. Chuzhanova, Nadia A

   2010 - Forschungsinformationssystem des UKE