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Sample GSM663756 Query DataSets for GSM663756
Status Public on Jan 31, 2011
Title T119, human gonadotrope/null cell tumor, biological rep 12
Sample type RNA
 
Source name Human gonadotrope/null cell tumor collected at the time of transsphenoidal surgery
Organism Homo sapiens
Characteristics tissue (group): Gonadotrope tumor
gender: F
subclass: Null
invasive: Yes
recurrent: No
scan_date: 2009-10-23
Treatment protocol With informed consent, pituitary tumor samples were obtained from patients at University of Colorado Hospital at the time of transsphenoidal surgery. Portions of the specimens not used for histology and immunohistochemistry were placed in RNAlater and stored at -80C. Gonadotrope tumors were defined as demonstrating positive immunostaining for FSH, LH, or alpha subunit in greater than 5-10% of cells. Null cell adenomas were defined by gonadotropic staining for FSH, LH, or alpha subunit in less than 5-10% of cells. Normal pituitary glands used as controls were obtained at autopsy within 2 - 18 hours of death from University of Colorado Denver Pathology Department.
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol Microarray targets were prepared and labeled from 300ng of total RNA using the MessageAmp Premier RNA Amplification Kit (Applied Biosystems/Ambion, Austin, TX) following the manufactures instructions.
 
Hybridization protocol standard Affymetrix procedures
Scan protocol standard Affymetrix procedures, using the Affy GCS3000
Data processing Hybridization intensities were quantified and normalized across all arrays using the RMA algorithm with GC adjust available as an array processing tool on Partek® Genomics Suite™ 6.5 software (St.Louis, MS). Data were filtered to remove all genes considered absent, as determined by the Affymetrix GeneChip Operating Software (GCOS), in greater than 95% of all the samples (22 out of 23 total samples). Remaining transcripts (38,932 of 54,675) were used for all subsequent statistical and visual analysis. A mixed model ANOVA was employed to estimate the batch effect and the data were adjusted using the Partek Batch Remover™ tool available on Partek Genomics Suite.
 
Submission date Jan 31, 2011
Last update date Jan 31, 2017
Contact name Michael Edwards
E-mail(s) michael.edwards@ucdenver.edu
Phone 303-724-6054
Organization name UC Denver
Department Pulmonary
Street address 12700 East 19th Avenue, Box C272
City Aurora
State/province CO
ZIP/Postal code 80045
Country USA
 
Platform ID GPL570
Series (1)
GSE26966 Identification of Growth arrest and DNA-damage-inducible gene beta (GADD45beta) as a Novel Tumor Suppressor in Pituitary Gonadotrope Tumors
Relations
Reanalyzed by GSE68015
Reanalyzed by GSE94349

Data table header descriptions
ID_REF
VALUE GCRMA-calculated signal intensity (log2)

Data table
ID_REF VALUE
1007_s_at 9.36868
1053_at 6.51573
117_at 2.53375
121_at 5.11305
1294_at 4.07255
1316_at 4.79584
1405_i_at 3.03041
1431_at 2.61915
1438_at 1.81857
1487_at 4.86593
1494_f_at 2.45909
1552256_a_at 6.10056
1552257_a_at 8.91102
1552261_at 2.26742
1552263_at 5.58894
1552264_a_at 7.37057
1552266_at 3.06397
1552269_at 2.57731
1552272_a_at 2.60304
1552274_at 7.69655

Total number of rows: 38932

Table truncated, full table size 711 Kbytes.




Supplementary file Size Download File type/resource
GSM663756.CEL.gz 4.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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