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Elisheva Smith

Researcher at University of Southern California

Publications -  27
Citations -  1311

Elisheva Smith is an academic researcher from University of Southern California. The author has contributed to research in topics: Osteoblast & Tobamovirus. The author has an hindex of 16, co-authored 23 publications receiving 1060 citations. Previous affiliations of Elisheva Smith include University of Massachusetts Amherst.

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Glucocorticoids Inhibit the Transcriptional Activity of LEF/TCF in Differentiating Osteoblasts in a Glycogen Synthase Kinase-3β-dependent and -independent Manner

TL;DR: It is shown that DEX inhibition of the differentiation-related cell cycle is associated with a decrease in β-catenin levels and inhibition of LEF/TCF-mediated transcription, and cross-talk between the PI3K/Akt and Wnt signaling pathways is suggested.
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A New Israeli Tobamovirus Isolate Infects Tomato Plants Harboring Tm-22 Resistance Genes

TL;DR: In samples collected from commercial cultivars across Israel, a single virus was found that caused the disease and the complete genome sequence of the new Israeli tobamovirus showed high sequence identity to the Jordanian isolate of tomato brown rugose fruit virus.
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Glucocorticoids Inhibit Developmental Stage-specific Osteoblast Cell Cycle DISSOCIATION OF CYCLIN A-CYCLIN-DEPENDENT KINASE 2 FROM E2F4-p130 COMPLEXES

TL;DR: In this paper, glucocorticoids induce premature attenuation of the osteoblast cell cycle, possibly contributing to the osteoporosis induced by these drugs in vivo, but not earlier stages, results in reduction of cyclin A and CDK2 levels with a parallel decrease in the associated kinase activity.
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Bone morphogenetic protein-2 restores mineralization in glucocorticoid-inhibited MC3T3-E1 osteoblast cultures.

TL;DR: The anti‐glucocorticoid potential of BMP‐2 in osteoblasts was tested in MC3T3‐E1 cells using dexamethasone (1 μM) and rhB MP‐2 (10 or 100 ng/ml).
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Gene expression profiling of glucocorticoid-inhibited osteoblasts

TL;DR: Microarray-based gene expression analysis of GC-arrested MC3T3-E1 cultures reveals novel gene targets whose regulation by GCs in osteoblasts may shed light on and provide new therapeutic approaches to osteoporosis.