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Wolfgang Weninger

Researcher at Medical University of Vienna

Publications -  362
Citations -  25279

Wolfgang Weninger is an academic researcher from Medical University of Vienna. The author has contributed to research in topics: Cytotoxic T cell & Immune system. The author has an hindex of 72, co-authored 325 publications receiving 21882 citations. Previous affiliations of Wolfgang Weninger include University of Pennsylvania & Royal Prince Alfred Hospital.

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Matrix Crosslinking Forces Tumor Progression by Enhancing Integrin Signaling

TL;DR: Reduction of lysyl oxidase-mediated collagen crosslinking prevented MMTV-Neu-induced fibrosis, decreased focal adhesions and PI3K activity, impeded malignancy, and lowered tumor incidence, and data show how collagenCrosslinking can modulate tissue fibrosis and stiffness to force focal adhesion, growth factor signaling and breast malignancies.
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Selective imprinting of gut-homing T cells by Peyer's patch dendritic cells

TL;DR: It is established that Peyer's patch dendritic cells imprint gut-homing specificity on T cells, and thus license effector/memory cells to access anatomical sites most likely to contain their cognate antigen.
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Angiosarcomas Express Mixed Endothelial Phenotypes of Blood and Lymphatic Capillaries: Podoplanin as a Specific Marker for Lymphatic Endothelium

TL;DR: In this article, a light and electron microscopic immunohistochemistry (EMI) was used to detect podoplanin, a ∼38kd membrane glycoprotein of podocytes, specifically expressed in the endothelium of lymphatic capillaries, but not in the blood vasculature.
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High-throughput discovery of novel developmental phenotypes

Mary E. Dickinson, +85 more
- 22 Sep 2016 - 
TL;DR: It is shown that human disease genes are enriched for essential genes, thus providing a dataset that facilitates the prioritization and validation of mutations identified in clinical sequencing efforts and reveals that incomplete penetrance and variable expressivity are common even on a defined genetic background.
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Asymmetric T lymphocyte division in the initiation of adaptive immune responses.

TL;DR: It is shown that a dividing T lymphocyte initially responding to a microbe exhibits unequal partitioning of proteins that mediate signaling, cell fate specification, and asymmetric cell division, suggesting a mechanism by which a single lymphocyte can apportion diverse cell fates necessary for adaptive immunity.