Detailed longitudinal sampling of glioma stem cells in situ reveals Chr7 gain and Chr10 loss as repeated events in primary tumor formation and recurrence

Author:

Baysan Mehmet1ORCID,Woolard Kevin2,Cam Margaret C.3,Zhang Wei4,Song Hua4,Kotliarova Svetlana5,Balamatsias Demosthenes6,Linkous Amanda6,Ahn Susie4,Walling Jennifer7,Belova Galina I.8,Fine Howard A.6

Affiliation:

1. Department of Computer Science & Engineering; Istanbul Sehir University; Istanbul 34662 Turkey

2. Department of Pathology; Microbiology, and Immunology, University of California; Davis CA

3. Office of Science and Technology Resources, National Cancer Institute, National Institutes of Health; Bethesda MD

4. Neuro-Oncology Branch; National Cancer Institute, National Institutes of Health; Bethesda MD

5. Center for Scientific Review, National Institutes of Health; Bethesda MD

6. Sandra and Edward Meyer Cancer Center, Weill Cornell Medical College; New York NY

7. Cancer Genetics Branch, National Cancer Institute, National Institutes of Health; Bethesda MD

8. Office of The Clinical Director, National Cancer Institute, National Institutes of Health; Bethesda MD

Publisher

Wiley

Subject

Cancer Research,Oncology

Reference49 articles.

1. States CBTRotU 2010 Hinsdale, IL: Central Brain Tumor Registry of the United States ( http://www cbtrus org/2010-NPCR-SEER/CBTRUS-WEBREPORT-Final-3-2-10 pdf )[Accessed June 24, 2011]

2. Glioblastoma survival in the United States before and during the temozolomide era;Johnson;J Neurooncol,2012

3. Glioblastoma survival in the United States improved after Food and Drug Administration approval of bevacizumab: a population-based analysis;Johnson;Cancer,2013

4. Malignant gliomas in adults;Wen;N Engl J Med,2008

5. G-Cimp status prediction of glioblastoma samples using mRNA expression data;Baysan;PloS ONE,2012

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