11 Einträge gefunden

1. Phenotypic and genotypic overlap between mosaic NF2 and schwannomatosis in patients with multiple non-intradermal schwannomas

   1. Kehrer-Sawatzki, Hildegard
   2. Kluwe, Lan
   3. Friedrich, Reinhard E
   4. Summerer, Anna
   5. Schäfer, Eleonora
   6. Wahlländer, Ute
   7. Matthies, Cordula

   2018 - Forschungsinformationssystem des UKE
2. The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesis

   1. Kehrer-Sawatzki, Hildegard
   2. Farschtschi, Said
   3. Mautner, Victor-Felix
   4. Cooper, David N

   2017 - Forschungsinformationssystem des UKE
3. 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
4. Molecular heterogeneity in malignant peripheral nerve sheath tumors associated with neurofibromatosis type 1.

   1. Thomas, Laura
   2. Mautner, Viktor Felix
   3. Cooper, David N
   4. Upadhyaya, Meena

   2012 - Forschungsinformationssystem des UKE
5. 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
6. 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
7. Microarray-based copy number analysis of neurofibromatosis type-1 (NF1)-associated malignant peripheral nerve sheath tumors reveals a role for Rho-GTPase pathway genes in NF1 tumorigenesis.

   1. Upadhyaya, Meena
   2. Spurlock, Gill
   3. Thomas, Laura
   4. Thomas, Nick S T
   5. Richards, Mark
   6. Mautner, Viktor Felix
   7. Cooper, David N

   2012 - Forschungsinformationssystem des UKE
8. 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
9. 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
10. 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
11. 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