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. Non-coding RNA ANRIL and the number of plexiform neurofibromas in patients with NF1 microdeletions.

   1. Mußotter, Tanja
   2. Kluwe, Lan
   3. Högel, Josef
   4. Nguyen, Rosa
   5. Cooper, David N
   6. Mautner, Viktor Felix
   7. Kehrer-Sawatzki, Hildegard

   2012 - Forschungsinformationssystem des UKE - frei zugänglich
3. 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
4. Extended runs of homozygosity at 17q11.2: an association with type-2 NF1 deletions?

   1. Roehl, Angelika C
   2. Cooper, David N
   3. Kluwe, Lan
   4. Helbrich, Andreas
   5. Wimmer, Katharina
   6. Högel, Josef
   7. Mautner, Viktor Felix

   2010 - 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