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Matthew J. Ravosa

Researcher at University of Notre Dame

Publications -  17
Citations -  305

Matthew J. Ravosa is an academic researcher from University of Notre Dame. The author has contributed to research in topics: Ovarian cancer & Masticatory force. The author has an hindex of 11, co-authored 17 publications receiving 248 citations.

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Get a Grip: Substrate Orientation and Digital Grasping Pressures in Strepsirrhines.

TL;DR: Functional variability across autopods, substrate and species that could underlie morphological variation within and across primates is observed and the complexity of arboreality should be considered when inferring locomotor modes in fossils.
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Ontogeny of Orbit Orientation in Primates.

TL;DR: The ontogeny of orbital convergence and frontation in 13 anthropoid and strepsirrhine species was characterized and interspecific variation in relative levels of frontation was linked to corresponding ontogenetic transpositions in encephalization that differed within both suborders.
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Ascites-induced compression alters the peritoneal microenvironment and promotes metastatic success in ovarian cancer.

TL;DR: A new role for ascites-induced compression is elucidated in promoting metastatic OvCa progression using a panel of in vitro, ex vivo and in vivo assays, and peritoneal collagen fibers adopted a more linear anisotropic alignment under compression, a collagen signature commonly correlated with enhanced invasion in solid tumors.
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Modeling the effect of ascites-induced compression on ovarian cancer multicellular aggregates.

TL;DR: Development of new in vitro model systems with which to evaluate cellular responses to compression enables experimental modeling of the intraperitoneal force environment of ovarian cancer patients with tense ascites.
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Integrin-linked kinase activity modulates the pro-metastatic behavior of ovarian cancer cells.

TL;DR: Results show that ILK is co-expressed in EOC with the pro-metastatic enzyme membrane type 1 matrix metalloproteinase (MT1-MMP) and catalyzed phosphorylation of the cytoplasmic tail of the proteinase and downregulation of ILK expression or activity reduced adhesion to and invasion of collagen gels and organotypic meso-mimetic cultures.