|
| Status |
Public on Sep 19, 2015 |
| Title |
Simultaneous amplification and mutation of KRAS: a therapeutic target in a rare subgroup of glioblastoma? |
| Organism |
Homo sapiens |
| Experiment type |
Genome variation profiling by genome tiling array
|
| Summary |
We describe the case of a glioblostoma multiform in a 66 year old female patient showing both amplification and mutation (exon 3; codon 61) of KRAS.
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| Overall design |
sample was analysed by arrayCGH method using Agilent recommendations. Sample was labeled in Cy5 and co-hybridized with control DNA cy3 labeled.
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| Contributor(s) |
Pedeutour-Braccini Z, Almairac F, Saada-Bouzid E, Duranton-Tanneur V, Kubiniek V, Pedeutour F, Burel-Vandenbos F |
| Citation missing |
Has this study been published? Please login to update or notify GEO. |
| Submission date |
Sep 18, 2015 |
| Last update date |
Sep 21, 2015 |
| Contact name |
Thibault FABAS |
| Organization name |
CHU Nice
|
| Lab |
Génétiques des Tumeurs Solides
|
| Street address |
28 av Valombrose
|
| City |
NICE |
| ZIP/Postal code |
06107 |
| Country |
France |
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| Platforms (1) |
| GPL10123 |
Agilent-022060 SurePrint G3 Human CGH Microarray 4x180K (Feature Number version) |
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| Samples (1) |
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| Relations |
| BioProject |
PRJNA296360 |
