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1 the majority of normal tissue obtained from reduction mammoplasty.
2 l human breast epithelial cells (HBECs) from reduction mammoplasty.
3 X-2 expression in a series of specimens from reduction mammoplasty, adenosis, ductal carcinoma in sit
4 stry in 17 normal breast tissue samples from reduction mammoplasties and in two independent tissue mi
6 s, including breast fibroblasts derived from reduction mammoplasty and tumor tissues, and human umbil
7 elial ducts within tumors and in tissue from reduction mammoplasties, and by epithelial-derived tumor
8 t cells separately purified from a set of 10 reduction mammoplasties by using a double antibody magne
9 n approach combining partial mastectomy with reduction mammoplasty could provide a safe oncologic pro
16 ved from a diseased tissue (e.g. MCF10A) and reduction mammoplasty of normal breast tissue (e.g. 184A
17 d either from breast cancer patients or from reduction mammoplasty operations expressed comparable es
18 assembled from 55 donors that had undergone reduction mammoplasties or risk reduction mastectomies.
20 ng human breast epithelial cells from either reduction mammoplasty or nonmalignant breast cell lines,
21 undergoing partial mastectomy and concurrent reduction mammoplasty performed at our institution from
22 consecutive simultaneous partial mastectomy/reduction mammoplasty procedures were performed in 79 pa
26 at varying degrees of risk (those undergoing reduction mammoplasties, those with atypical hyperplasti
27 ammary epithelial cells (HMEC) isolated from reduction mammoplasty tissue are proliferative for sever
28 mmary epithelial cells (HMECs) isolated from reduction mammoplasty tissue of seven individual donors.
29 lial cell (HMEC) culture model, derived from reduction mammoplasty tissue, and found that ectopic exp
30 ting functionally normal breast tissues from reduction mammoplasty tissues, in what we term the human
33 ly removed from 40 women undergoing elective reduction mammoplasty were extracted by a solid-phase pr