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Human cell-based artificial antigen-presenting cells for cancer immunotherapy

Immunological reviews, 2014-01, Vol.257 (1), p.191-209

2014

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Multidrug resistance (MDR) reversers: High activity and efficacy in a series of asymmetrical N,N-bis(alkanol)amine aryl esters

European journal of medicinal chemistry, 2014-11, Vol.87, p.398-412

2014

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Augmentation of iNOS expression in myeloid progenitor cells expedites neutrophil differentiation

Journal of leukocyte biology, 2019-08, Vol.106 (2), p.397-412

2019

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Stromal cell-mediated inhibition of erythropoiesis can be attenuated by Sotatercept (ACE-011), an activin receptor type II ligand trap

Experimental hematology, 2013-02, Vol.41 (2), p.155-166.e17

2013

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Killing of xenogenous and virally infected homogenous target cells by shrimp lymphocyte-like haemocytes

Fish & shellfish immunology, 2024-10, Vol.153, p.109873, Article 109873

2024

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Fabrication of a cell-recognition/electron-transfer/cross-linker, peptide-immobilized electrode for the sensing of K562 cells

Analytica chimica acta, 2020-06, Vol.1116, p.53-61

2020

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Sonodynamic therapy induces the interplay between apoptosis and autophagy in K562 cells through ROS

The international journal of biochemistry & cell biology, 2015-03, Vol.60, p.82-92

2015

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Functional analysis of repositioned anilide derivatives as anticancer compounds

Journal of the Indian Chemical Society, 2022-01, Vol.99 (1), p.100276, Article 100276

2022

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Graphene oxide/poly-L-lysine assembled layer for adhesion and electrochemical impedance detection of leukemia K562 cancer cells

Biosensors & bioelectronics, 2013-04, Vol.42, p.112-118

2013

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Can image analysis provide evidence that lysosomal sequestration mediates daunorubicin resistance?

Chemico-biological interactions, 2020-08, Vol.327, p.109138-109138, Article 109138

2020

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High-level embryonic globin production with efficient erythroid differentiation from a K562 erythroleukemia cell line

Experimental hematology, 2018-06, Vol.62, p.7-16.e1

2018

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Selective and sensitive detection of chronic myeloid leukemia using fluorogenic DNAzyme probes

Analytica chimica acta, 2020-08, Vol.1123, p.28-35

2020

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Design and synthesis of new potent N,N-bis(arylalkyl)piperazine derivatives as multidrug resistance (MDR) reversing agents

European journal of medicinal chemistry, 2018-03, Vol.147, p.7-20

2018

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Design, synthesis and biological evaluation of stereo- and regioisomers of amino aryl esters as multidrug resistance (MDR) reversers

European journal of medicinal chemistry, 2019-11, Vol.182, p.111655-111655, Article 111655

2019

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Mechanical phenotyping of K562 cells by the Micropipette Aspiration Technique allows identifying mechanical changes induced by drugs

Scientific reports, 2018-01, Vol.8 (1), p.1219-14, Article 1219

2018

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Hemin accumulation and identification of a heme‐binding protein clan in K562 cells by proteomic and computational analysis

Journal of cellular physiology, 2022-02, Vol.237 (2), p.1315-1340

2022

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Design and synthesis of aminoester heterodimers containing flavone or chromone moieties as modulators of P-glycoprotein-based multidrug resistance (MDR)

Bioorganic & medicinal chemistry, 2018-01, Vol.26 (1), p.50-64

2018

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Antitumor Activity and Mechanism of Action of the Antimicrobial Peptide AMP-17 on Human Leukemia K562 Cells

Molecules (Basel, Switzerland), 2022-11, Vol.27 (22), p.8109

2022

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Clioquinol inhibits the proteasome and displays preclinical activity in leukemia and myeloma

Leukemia, 2009-03, Vol.23 (3), p.585-590

2009

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Biocompatible Conductive Architecture of Carbon Nanofiber-Doped Chitosan Prepared with Controllable Electrodeposition for Cytosensing

Analytical chemistry (Washington), 2007-06, Vol.79 (12), p.4442-4447

2007

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Global DNA hypomethylation, rather than reactive oxygen species (ROS), a potential facilitator of cadmium-stimulated K562 cell proliferation

Toxicology letters, 2008-06, Vol.179 (1), p.43-47

2008

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Impact of P-glycoprotein on intracellular drug concentration in peripheral blood mononuclear cells and K562 cells

Drug metabolism and pharmacokinetics, 2023-04, Vol.49, p.100487-100487, Article 100487

2023

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Tumor necrosis factor‑related apoptosis‑inducing ligand is a novel transcriptional target of runt‑related transcription factor 1

International journal of oncology, 2022-01, Vol.60 (1), p.1, Article 6

2022

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Lipid raft-associated protein sorting in exosomes

Blood, 2003-12, Vol.102 (13), p.4336-4344

2003

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N-alkanol-N-cyclohexanol amine aryl esters: Multidrug resistance (MDR) reversing agents with high potency and efficacy

European journal of medicinal chemistry, 2017-02, Vol.127, p.586-598

2017

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Human cell-based artificial antigen-presenting cells for cancer immunotherapy

Multidrug resistance (MDR) reversers: High activity and efficacy in a series of asymmetrical N,N-bis(alkanol)amine aryl esters

Augmentation of iNOS expression in myeloid progenitor cells expedites neutrophil differentiation

Stromal cell-mediated inhibition of erythropoiesis can be attenuated by Sotatercept (ACE-011), an activin receptor type II ligand trap

Killing of xenogenous and virally infected homogenous target cells by shrimp lymphocyte-like haemocytes

Fabrication of a cell-recognition/electron-transfer/cross-linker, peptide-immobilized electrode for the sensing of K562 cells

Sonodynamic therapy induces the interplay between apoptosis and autophagy in K562 cells through ROS

Functional analysis of repositioned anilide derivatives as anticancer compounds

Graphene oxide/poly-L-lysine assembled layer for adhesion and electrochemical impedance detection of leukemia K562 cancer cells

Can image analysis provide evidence that lysosomal sequestration mediates daunorubicin resistance?

High-level embryonic globin production with efficient erythroid differentiation from a K562 erythroleukemia cell line

Selective and sensitive detection of chronic myeloid leukemia using fluorogenic DNAzyme probes

Design and synthesis of new potent N,N-bis(arylalkyl)piperazine derivatives as multidrug resistance (MDR) reversing agents

Design, synthesis and biological evaluation of stereo- and regioisomers of amino aryl esters as multidrug resistance (MDR) reversers

Mechanical phenotyping of K562 cells by the Micropipette Aspiration Technique allows identifying mechanical changes induced by drugs

Hemin accumulation and identification of a heme‐binding protein clan in K562 cells by proteomic and computational analysis

Design and synthesis of aminoester heterodimers containing flavone or chromone moieties as modulators of P-glycoprotein-based multidrug resistance (MDR)

Antitumor Activity and Mechanism of Action of the Antimicrobial Peptide AMP-17 on Human Leukemia K562 Cells

Clioquinol inhibits the proteasome and displays preclinical activity in leukemia and myeloma

Biocompatible Conductive Architecture of Carbon Nanofiber-Doped Chitosan Prepared with Controllable Electrodeposition for Cytosensing

Global DNA hypomethylation, rather than reactive oxygen species (ROS), a potential facilitator of cadmium-stimulated K562 cell proliferation

Impact of P-glycoprotein on intracellular drug concentration in peripheral blood mononuclear cells and K562 cells

Tumor necrosis factor‑related apoptosis‑inducing ligand is a novel transcriptional target of runt‑related transcription factor 1

Lipid raft-associated protein sorting in exosomes

N-alkanol-N-cyclohexanol amine aryl esters: Multidrug resistance (MDR) reversing agents with high potency and efficacy

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