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DIGITAL.CSIC
Dataset . 2023 . Peer-reviewed
Data sources: DIGITAL.CSIC
DIGITAL.CSIC
Dataset . 2022
License: CC BY
Data sources: Datacite
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Supplementary Materials Peptides against Low Density Lipoprotein (LDL) Aggregation Inhibit Intracellular Cholesteryl Ester Loading and Proliferation of Pancreatic Tumor Cells

Authors: Benitez-Amaro, Aleyda; Martínez-Bosch, Neus; Manero-Rupérez, Noemí; Claudi, Lene; La Chica Lhoëst, Maria Teresa; Soler, Marta; Ros-Blanco, Lia; +2 Authors

Supplementary Materials Peptides against Low Density Lipoprotein (LDL) Aggregation Inhibit Intracellular Cholesteryl Ester Loading and Proliferation of Pancreatic Tumor Cells

Abstract

Figure S1: Effect of peptides DP3 and IP321 on the intracellular CE/FC ratio induced by nLDLs and AgLDLs in RWP-1 and Capan-1 cells, Figure S2: Time-course effects of nLDLs and AgLDLs on intracellular CE/FC ratio in PANC-1 cells, Figure S3: Optical microscopy of PANC-1 cells exposed to nLDL, and AgLDL ± DP3/IP321 peptides, Figure S4: Flow Cytometric analysis of cell proliferation and viability of PANC-1 cell cultures stained with PI, Figure S5: Uncropped blot for main Figure 1, Figure S6: Uncropped blots for main Figure 2, Figure S7: Uncropped blot for main Figure 4B, Figure S8: Uncropped blot for main Figure 5A, Figure S9: Uncropped blots for Figure S1, Figure S10: Uncropped blots for Figure S2, Figure S11: Flow cytometry dot plots for Figure 6C and Figure S4, Table S1: Raw data for Figure 4A, File S1: Flow Cytometry Analysis, raw data PANC-1 cell concentration (counts/mL) shown in Figure 6C, Figures S4 and S11.

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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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