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- Cooper, David N
- Mautner, Viktor Felix 14
- Kehrer-Sawatzki, Hildegard 13
- Kluwe, Lan 12
- Vogt, Julia 7
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17 Einträge gefunden
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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
- Bengesser, Kathrin
- Vogt, Julia
- Mussotter, Tanja
- Mautner, Victor-Felix
- Messiaen, Ludwine
- Cooper, David N
- Kehrer-Sawatzki, Hildegard
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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.
- Upadhyaya, Meena
- Spurlock, Gill
- Thomas, Laura
- Thomas, Nick S T
- Richards, Mark
- Mautner, Viktor Felix
- Cooper, David N
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Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder.
- Vogt, Julia
- Mussotter, Tanja
- Bengesser, Kathrin
- Claes, Kathleen
- Högel, Josef
- Chuzhanova, Nadia
- Fu, Chuanhua
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Tissue-specific differences in the proportion of mosaic large NF1 deletions are suggestive of a selective growth advantage of hematopoietic del(+/-) stem cells.
- Roehl, Angelika C
- Mussotter, Tanja
- Cooper, David N
- Kluwe, Lan
- Wimmer, Katharina
- Högel, Josef
- Zetzmann, Marion
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Dissecting the clinical phenotype associated with mosaic type-2 NF1 microdeletions.
- Kehrer-Sawatzki, Hildegard
- Vogt, Julia
- Mußotter, Tanja
- Kluwe, Lan
- Cooper, David N
- Mautner, Viktor Felix
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Molecular heterogeneity in malignant peripheral nerve sheath tumors associated with neurofibromatosis type 1.
2012 - Forschungsinformationssystem des UKE -
Non-coding RNA ANRIL and the number of plexiform neurofibromas in patients with NF1 microdeletions.
- Mußotter, Tanja
- Kluwe, Lan
- Högel, Josef
- Nguyen, Rosa
- Cooper, David N
- Mautner, Viktor Felix
- Kehrer-Sawatzki, Hildegard
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Delineation of the clinical phenotype associated with non-mosaic type-2 NF1 deletions: two case reports.
- Vogt, Julia
- Nguyen, Rosa
- Kluwe, Lan
- Schuhmann, Martin
- Roehl, Angelika C
- Mußotter, Tanja
- Cooper, David N
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A novel third type of recurrent NF1 microdeletion mediated by nonallelic homologous recombination between LRRC37B-containing low-copy repeats in 17q11.2.
- Bengesser, Kathrin
- Cooper, David N
- Steinmann, Katharina
- Kluwe, Lan
- Chuzhanova, Nadia A
- Wimmer, Katharina
- Tatagiba, Marcos
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Extended runs of homozygosity at 17q11.2: an association with type-2 NF1 deletions?
- Roehl, Angelika C
- Cooper, David N
- Kluwe, Lan
- Helbrich, Andreas
- Wimmer, Katharina
- Högel, Josef
- Mautner, Viktor Felix
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Type 2 NF1 deletions are highly unusual by virtue of the absence of nonallelic homologous recombination hotspots and an apparent preference for female mitotic recombination.
- Steinmann, Katharina
- Cooper, David N
- Kluwe, Lan
- Chuzhanova, Nadia A
- Senger, Cornelia
- Serra, Eduard
- Lazaro, Conxi