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Saul Suster

Researcher at Medical College of Wisconsin

Publications -  484
Citations -  19658

Saul Suster is an academic researcher from Medical College of Wisconsin. The author has contributed to research in topics: Carcinoma & Thymic carcinoma. The author has an hindex of 66, co-authored 470 publications receiving 18256 citations. Previous affiliations of Saul Suster include University of Alabama at Birmingham & University of Alabama.

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The role of microRNA genes in papillary thyroid carcinoma

TL;DR: It is concluded that up-regulation of several miRs and regulation of KIT are involved in PTC pathogenesis, and that sequence changes in genes targeted by miRNAs can contribute to their regulation.
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The pathologic classification of neuroendocrine tumors: a review of nomenclature, grading, and staging systems.

TL;DR: Issues in the pathologic assessment of NETs that are common among primaries of different sites are examined and the distinction of well-differentiated from poorly differentiated NETs and the significance of proliferative rate in prognostic assessment are examined.
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Thymic carcinoma. A clinicopathologic study of 60 cases.

TL;DR: The morphologic features of the tumors in patients with thymic carcinoma correlated well with their clinical behavior; histologic type constituted the most reliable and important predictor of prognosis.
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Down-regulation of Micro-RNA-1 (miR-1) in Lung Cancer SUPPRESSION OF TUMORIGENIC PROPERTY OF LUNG CANCER CELLS AND THEIR SENSITIZATION TO DOXORUBICIN-INDUCED APOPTOSIS BY miR-1

TL;DR: It is reported that micro-RNA-1 (miR-1), abundant in the cardiac and smooth muscles, is expressed in the lung and is down-regulated in human primary lung cancer tissues and cell lines and has potential therapeutic application against lung cancers.
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Cytokeratin 20 immunoreactivity distinguishes Merkel cell (primary cutaneous neuroendocrine) carcinomas and salivary gland small cell carcinomas from small cell carcinomas of various sites.

TL;DR: The frequent CK20 positivity observed in salivary gland small cell carcinomas in this series suggests that at least some of them may be more closely related biologically to Merkel cell carcinoma than to pulmonary-type smallcell carcinoma, which may explain why they are far less clinically aggressive than other small cell cancers.