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The purpose of this study was to investigate the gelatinolytic activity in human pulp cells stimulated with various pharmacological agents.
The aim of this study was to evaluate the expression of estrogen receptor (ER -α in human pulp tissuER -α
In this study, black-pigmented bacteria induced not only t-PA but also PAI-1 gene expression in human pulp and osteoblastic cells.
The aim of this study was to investigate the effects of dentin bonding agents on the expression of COX-2 in human pulp cells.
However, the mechanisms and signal transduction pathways involved in the production of MMPs in human pulp cells are not fully understood.
The supernatants of Porphyromonas endodontalis, Porphyromonas gingivalis, and Prevotella intermedia were used to evaluate tissue-type plasminogen activator (t-PA) and type 1 plasminogen activator inhibitor (PAI-1) gene expression in human pulp and osteoblastic cells.
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This study examined the effect of nitric oxide (NO) on interleukin-8 (IL-8) production and the involvement of mitogen-activated protein kinase (MAPK) and nuclear factor-kappa B (NF-κB) signaling pathways in primary cultured human pulp cells.
We have chosen to use 3 mM HEMA according to previous studies by Falconi et al. [ 43], in which 3 mM HEMA has been demonstrated to be responsible for a reduction of cell viability lower than 50%%, and by Kurata [ 16], which shows a drastic anti-proliferative effect of 1 mM HEMA followed by a further increase at 3 and 5 mM in fibroblasts derived from human pulp.
The objective of this study was to examine the effects of fluoride on human pulp cells in vitro.
Osteopontin, which has previously been detected in JDM deposits [ 8], was found in several other forms of pathological calcification: human pulp stones [ 49], urinary stones [ 50], human atherosclerotic lesions [ 51], and dental calculus [ 52].
Because the lack of specific surface markers has hindered the isolation and subsequent biochemical characterization of dental pulp stem cells, this study sought to determine the existence of SP cells and the expression of ABCG2 in human dental pulp and evaluate whether such SP cells had features associated with stem cells.
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