|
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.
|
|
|
Overall design |
sample was analysed by arrayCGH method using Agilent recommendations. Sample was labeled in Cy5 and co-hybridized with control DNA cy3 labeled.
|
|
|
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 |
|
|
Platforms (1) |
GPL10123 |
Agilent-022060 SurePrint G3 Human CGH Microarray 4x180K (Feature Number version) |
|
Samples (1) |
|
Relations |
BioProject |
PRJNA296360 |