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Richard I. Whyte

Researcher at Beth Israel Deaconess Medical Center

Publications -  136
Citations -  8831

Richard I. Whyte is an academic researcher from Beth Israel Deaconess Medical Center. The author has contributed to research in topics: Lung cancer & Lung transplantation. The author has an hindex of 38, co-authored 132 publications receiving 8446 citations. Previous affiliations of Richard I. Whyte include Stanford University & Medical University of South Carolina.

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Diversity of gene expression in adenocarcinoma of the lung

TL;DR: Gene expression analysis promises to extend and refine standard pathologic analysis and make possible the subclassification of adenocarcinoma into subgroups that correlated with the degree of tumor differentiation as well as patient survival.
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Thin-section CT obtained at 10-mm increments versus limited three-level thin-section CT for idiopathic pulmonary fibrosis: correlation with pathologic scoring.

TL;DR: Limited thin-section CT reveals the pathologic changes associated with IPF as well as CT obtained at 10-mm increments as an added advantage of limited thin- section CT is that it exposes patients to less radiation.
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Idiopathic pulmonary fibrosis: predicting response to therapy and survival.

TL;DR: It is demonstrated that pretherapy pulmonary function, pathologic and radiographic parameters are different in individuals who respond to initial prednisone therapy and only HRCT imaging and pathologic fibrosis were able to reliably predict long-term survival in patients with biopsy-proven IPF.
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Interferon-gamma-inducible protein 10 (IP-10) is an angiostatic factor that inhibits human non-small cell lung cancer (NSCLC) tumorigenesis and spontaneous metastases.

TL;DR: The notion that tumor-derived IP-10 is an important endogenous angiostatic factor in NSCLC is supported, as a potent angiOSTatic factor that regulates non-small cell lung cancer-derived angiogenesis, tumor growth, and spontaneous metastasis.
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Inhibition of interleukin 8 attenuates angiogenesis in bronchogenic carcinoma.

TL;DR: These observations definitively establish IL-8 as a primary mediator of angiogenesis in bronchogenic carcinoma and offer a potential target for immunotherapies against solid malignancies.