5 Einträge gefunden

1. 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
2. Characterization of the nonallelic homologous recombination hotspot PRS3 associated with type-3 NF1 deletions.

   1. Zickler, Antje M
   2. Hampp, Stephanie
   3. Messiaen, Ludwine
   4. Bengesser, Kathrin
   5. Mussotter, Tanja
   6. Roehl, Angelika C
   7. Wimmer, Katharina

   2012 - Forschungsinformationssystem des UKE
3. 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
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. 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