Ruth Lininger to Loss of Heterozygosity
This is a "connection" page, showing publications Ruth Lininger has written about Loss of Heterozygosity.
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Lininger RA, Zhuang Z, Man Y, Park WS, Emmert-Buck M, Tavassoli FA. Loss of heterozygosity is detected at chromosomes 1p35-36 (NB), 3p25 (VHL), 16p13 (TSC2/PKD1), and 17p13 (TP53) in microdissected apocrine carcinomas of the breast. Mod Pathol. 1999 Dec; 12(12):1083-9.
Score: 0.174
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Lininger RA, Fujii H, Man YG, Gabrielson E, Tavassoli FA. Comparison of loss heterozygosity in primary and recurrent ductal carcinoma in situ of the breast. Mod Pathol. 1998 Dec; 11(12):1151-9.
Score: 0.163
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Lininger RA, Park WS, Man YG, Pham T, MacGrogan G, Zhuang Z, Tavassoli FA. LOH at 16p13 is a novel chromosomal alteration detected in benign and malignant microdissected papillary neoplasms of the breast. Hum Pathol. 1998 Oct; 29(10):1113-8.
Score: 0.161
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Man YG, Magrane GG, Lininger RA, Shen T, Kuhls E, Bratthauer GL. Morphologically similar epithelial and stromal cells in primary bilateral breast tumors display different genetic profiles: implications for treatment. Appl Immunohistochem Mol Morphol. 2004 Dec; 12(4):305-14.
Score: 0.062