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Sample GSM663754 Query DataSets for GSM663754
Status Public on Jan 31, 2011
Title T034, human gonadotrope/null cell tumor, biological rep 10
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: M
subclass: Null
invasive: Yes
recurrent: Yes
scan_date: 2005-04-15
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) [email protected]
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 9.48976
1053_at 6.24625
117_at 1.67553
121_at 5.32788
1294_at 5.31028
1316_at 4.60878
1405_i_at 2.88895
1431_at 2.92822
1438_at 1.72786
1487_at 4.46552
1494_f_at 2.29212
1552256_a_at 6.62338
1552257_a_at 9.08689
1552261_at 2.09308
1552263_at 4.93622
1552264_a_at 6.83206
1552266_at 2.79958
1552269_at 2.26809
1552272_a_at 2.06645
1552274_at 7.78545

Total number of rows: 38932

Table truncated, full table size 711 Kbytes.




Supplementary file Size Download File type/resource
GSM663754.CEL.gz 4.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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