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Paul J. van Diest

Researcher at Utrecht University

Publications -  514
Citations -  22750

Paul J. van Diest is an academic researcher from Utrecht University. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 70, co-authored 459 publications receiving 18892 citations. Previous affiliations of Paul J. van Diest include University Medical Center Utrecht & VU University Medical Center.

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Alcohol based tissue fixation as an alternative for formaldehyde: influence on immunohistochemistry

TL;DR: Omission of pepsin pretreatment seems to be important to retain proper morphology of immunostained tissues preserved in alcohol based fixatives when switching to less toxic and non-carcinogenic alcohol-based fixatives like RCL2, no major changes in the daily routine of immunohistochemistry are anticipated.
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Whole slide images as a platform for initial diagnostics in histopathology in a medium-sized routine laboratory

TL;DR: The gradual integration of WSI into routine pathology diagnostics in a medium-sized routine pathology laboratory and the implemented adjustments to the workflow are described to encourage the wide adaptation in routine diagnostics.
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Fallopian tube intraluminal tumor spread from noninvasive precursor lesions: a novel metastatic route in early pelvic carcinogenesis.

TL;DR: It is shown that intraluminal shedding of tumor cells in the fallopian tubes from serous carcinoma cases are common and a likely route of abdominal spread, and warrant a reconsideration of the malignant potential of STICs and indicate that intralsized shedding could be a risk factor for early intraperitoneal metastasis.
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Loss of p120‐catenin induces metastatic progression of breast cancer by inducing anoikis resistance and augmenting growth factor receptor signaling

TL;DR: It is shown that somatic loss of p120-catenin (p120) in a conditional mouse model of noninvasive mammary carcinoma results in formation of stromal-dense tumors that resemble human metaplastic breast cancer and metastasize to lungs and lymph nodes.
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Mutation profiling of key cancer genes in primary breast cancers and their distant metastases

TL;DR: Somatic genetic alterations in ER-negative breast cancer metastases may be distinct from those of their primary tumors, suggesting that for treatment-decision making, genetic analyses of DNA obtained from the metastatic lesion rather than from the primary tumor should be considered.