Double fluorescence in situ hybridization with D N A probes specific for the (peri)centromeric regions of chromosomes 3, 7, 9, I I, 12, 18, and X was performed on fresh isolated nuclei and frozen tissue sections prepared from 2 nodular hyperplasias, 2 adenomas, and 7 papillary carcinomas of the thyr
Numeric chromosome aberrations in prostate cancer detected by in situ hybridization
โ Scribed by Ryosuke Nemoto; Isao Nakamura; Katsuo Uchida; Masaoki Harada
- Publisher
- Springer
- Year
- 1998
- Tongue
- English
- Weight
- 763 KB
- Volume
- 3
- Category
- Article
- ISSN
- 1341-9625
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
A loss of chromosome-9 material is one of the most frequent genomic aberrations known in bladder cancer. In order to better understand the role of chromosome-9 losses in bladder cancer, I25 formalin-fixed and 37 unfixed bladder tumors were examined using fluorescence in situ hybridization (FISH). A
We investigated the feasibility of automated counting of in situ hybridization signals (ISH) in interphase cells isolated from paraffin embedded prostate tissue. In total, 34 specimens from 7 patients with prostate cancer were stained with probes specific for the centromeric regions of chromosomes Y
At least 50 per cent of all first-trimester spontaneous abortions are cytogenetically abnormal, including trisomy, monosomy X, triploidy, tetraploidy and structural chromosome anomalies. Traditionally, the detection of aneuploidy in fetal tissues is performed by tissue sampling, cell culturing, meta