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The present study evaluates the biological relevance of several LPCs using a well characterized rodent malaria model.
Here we demonstrate, using a well characterized Drosophila melanogaster malignant tumour model3,4, that non-cell-autonomous autophagy is induced both in the tumour microenvironment and systemically in distant tissues.
This was achieved by comparing breakdown diagrams of protonated leucine enkephalin obtained using the new cell with those obtained using a well characterized cell.
The antigens were cloned in Escherichia coli, expressed, and purified before testing in an antibody detection ELISA test, using a well characterized panel of 18 and 48 sera from Map infected and uninfected cattle, respectively.
Our aim was to characterize the effects of preeclampsia on fetal programming of adult growth and metabolic function, and evaluate the role of preventive pravastatin therapy, using a well characterized murine model.
Using a well characterized model system for breast cancer, we define here the molecular and cellular consequences of adriamycin treatment in breast tumor cells.
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The five LBD and two NRR antibodies were characterized for their effect on Jag2-induced Notch signaling, using a well-characterized NIH 3T3 cell line expressing Jag-2 [51]–[52].
We synthesized a thin film composite membrane using a well-characterized porous support membrane.
Using a well-characterized hiPSC line (hCD34iPSC16 16, we induced the formation of myeloid cell forming complexes (MCFCs) from embryoid bodies (EBs) in small-scale suspension culture on an orbital shaker (Supplementary Fig. 1a and 1b).
Using a well-characterized model of acute excitotoxic brain injury in neonatal rats, experiments were designed to evaluate whether monocyte chemoattractant protein-1 plays a role in the progression of tissue damage.
The purpose of this study was to evaluate the association between unexplained stillbirth (SB) and single-nucleotide polymorphisms (SNPs) in genes involved in placental function using a well-characterized cohort.
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