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Geraldine S. Pinkus

Researcher at Brigham and Women's Hospital

Publications -  286
Citations -  29136

Geraldine S. Pinkus is an academic researcher from Brigham and Women's Hospital. The author has contributed to research in topics: Lymphoma & Immunoperoxidase. The author has an hindex of 84, co-authored 278 publications receiving 27112 citations. Previous affiliations of Geraldine S. Pinkus include University of Texas MD Anderson Cancer Center & Montreal General Hospital.

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Programmed Death Ligand 1 Is Expressed by Non–Hodgkin Lymphomas and Inhibits the Activity of Tumor-Associated T Cells

TL;DR: PD-L1 may thwart effective antitumor immune responses and represents an attractive target for lymphoma immunotherapy in establishing cell lines from an aggressive PD-L 1+ mature B-cell lymphoma.
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Epithelial membrane antigen--a diagnostic discriminant in surgical pathology: immunohistochemical profile in epithelial, mesenchymal, and hematopoietic neoplasms using paraffin sections and monoclonal antibodies.

TL;DR: Based on the observations in this large series of neoplasms, EMA is an excellent marker of epithelial differentiation, appears to be highly reliable for discriminating between poorly differentiated carcinomas and malignant lymphomas, and is especially helpful in characterizing small cell anaplastic carcinomas.
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Diagnostic Relevance of Clonal Cytogenetic Aberrations in Malignant Soft-Tissue Tumors

TL;DR: Cytogenetic analyses reveal clonal chromosome aberrations in virtually all malignant soft-tissue tumors, particularly in small round-cell tumors in children.
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Immunohistochemistry of a gross cystic disease fluid protein (GCDFP-15) of the breast. A marker of apocrine epithelium and breast carcinomas with apocrine features.

TL;DR: This report is the first to characterize GCDFP-15 as a specific tissue marker of apocrine epithelium as a pathologic secretion from breast composed of several glycoproteins, including a unique 15,000-dalton monomer protein, GCD FP-15.
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Immunohistochemical localization of keratin in normal human tissues.

TL;DR: The ability to identify keratin proteins within fixed, embedded tissue (including those known to lack tonofilament bundles) may prove useful in the study of tissue histogenesis and carcinogenesis, and in the pathologic assessment of poorly differentiated malignant neoplasms and tumors of controversial cellular origin.