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Sharona Even-Ram

Researcher at Hebrew University of Jerusalem

Publications -  26
Citations -  4172

Sharona Even-Ram is an academic researcher from Hebrew University of Jerusalem. The author has contributed to research in topics: Receptor & Embryonic stem cell. The author has an hindex of 19, co-authored 26 publications receiving 3975 citations. Previous affiliations of Sharona Even-Ram include National Institutes of Health.

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Cell migration in 3D matrix.

TL;DR: Analysis of the different modes of migration of cells in matrices provides new insights, but also raises some debates about the mechanisms and regulation of cell migration in three-dimensional matrices.
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A Rac switch regulates random versus directionally persistent cell migration.

TL;DR: Total Rac1 activity can provide a regulatory switch between patterns of cell migration by a mechanism distinct from chemotaxis, and be used to determine whether cell patterns of migration are intrinsically random or directionally persistent.
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Myosin IIA regulates cell motility and actomyosin–microtubule crosstalk

TL;DR: It is concluded that myosin IIA negatively regulates cell migration and it is suggested that it maintains a balance between the actomyosin and microtubules systems by regulating microtubule dynamics.
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Directed Differentiation of Human Embryonic Stem Cells into Functional Retinal Pigment Epithelium Cells

TL;DR: It is demonstrated that nicotinamide promotes the differentiation of hESCs to neural and subsequently to RPE fate and factors from the TGF-beta superfamily, which presumably pattern RPE development during embryogenesis, further direct RPE differentiation.
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Thrombin receptor overexpression in malignant and physiological invasion processes

TL;DR: Thrombin receptor, a member of the protease-activated receptor family, is preferentially expressed in highly metastatic human breast carcinomas cell lines and breast carcinoma biopsy specimens and introduction of thrombin receptors antisense cDNA considerably inhibited the invasion of metastatic breast carcin cancer cells in culture through a reconstituted basement membrane.