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The β2-M transcript expression levels have a positive correlation with Bcl-2 transcript expression levels (P = 0.011).> The paraffin-embedded sections from the 164 patients' specimens with breast cancer and the 123 patients with benign breast tumors were immunohistochemically stained using β2-M, ER, PR, HER-2, p53 and Ki67 antibodies.
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Hence, we randomly selected a control group (surgical resection specimens diagnosed with breast cancer), from the same observation interval (see Materials and Methods for details).
Indeed, it has been demonstrated, with the use of gross analysis of human breast cancer specimens compared with breast cancer cell lines, that the tumors expressed sets of genes in common not only with these cell lines but also with cells of hematopoietic lineage and stromal origin [ 1].
Indeed, it has been demonstrated using gross analysis of human breast cancer specimens compared with breast cancer cell lines that the tumours expressed sets of genes in common not only with these cell lines but also with cells of hematopoietic lineage and stromal origin (Perou et al, 2000).
For instance, a comparison between the LC50 values of 135 previously treated breast cancer specimens with 33 untreated breast cancer specimens indicated a trend toward greater sensitivity in the previously treated specimens.
Primary breast tumor specimens with matching normal breast tissue samples were obtained from Fu Jen Catholic University, and Cardinal Tien Hospital, Taiwan, after surgical removal of the tumor according to the IRB approved protocol.
The aim of the present study was to provide data on the accuracy of US- guided CNB and frozen section analysis comparing histological diagnoses made on frozen section specimens of the CNB with those made on paraffin sections of CNB and definitive results of tumorectomy specimens in patients with breast lesions.
Single-cell photoacoustic microscopy can perform high-throughput measurements of intratumoral metabolic heterogeneity in specimens from patients with breast cancer.
Four apparently normal breast tissue specimens from patients with breast cancer were also included in the analyses.
Data and specimens from women with breast cancer and healthy controls were obtained from the Data Bank and Biorepository (DBBR) at Roswell Park Cancer Institute (RPCI).
Therefore, we tested the PSA RT-PCR assay on blood specimens from women with breast cancer.
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