Validation of Tissue Microarray Technology in Breast Carcinoma
By R. Camp, L. Charette, David L. Rimm. Laboratory Investigation, 2000
843 citations recorded by the source corpus.
Subfields: Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/0241d1f1e1b49760652cfb774e7b49a581b86a1f
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In Molecular Biology
In Oncology
Citations in the corpus
- X-Tile (2004, result): “Because prior studies have shown that a single core adequately represents the staining pattern of an entire slide, all studies were done with a single sample of each tumor (7, 8).”
- Ki67 Index, HER2 Status, and Prognosis of Patients With Luminal B Breast Cancer (2009, neutral): “3/22 28/103 24/162 10-yr (95% CI) 5-y (95% CI) 57 (47-69) 64 (59-70) 79 (76-83)”
- Assessment of Ki67 in breast cancer: recommendations from the International Ki67 in Breast Cancer working group. (2011, background): “Once tissue is properly fixed and embedded in paraffin, antigenicity is well preserved, potentially for decades (41,42).”
- Expression of luminal and basal cytokeratins in human breast carcinoma (2004, methodology): “Breast cancer tissue microarrays were prepared as described previously [17–19].”
- Quantitative comparison of immunohistochemical staining measured by digital image analysis versus pathologist visual scoring (2012, background): “A limited number of tissue cores adequately represent protein expression in tumor specimens [15,16].”