P. Mrówka

发表

Cytotoxic Potential of Bioactive Compounds from Aspergillus flavus, an Endophytic Fungus Isolated from Cynodon dactylon, against Breast Cancer: Experimental and Computational Approach

Arjun Kumar Kalimuthu, J. Pijanowska, P. Maszczyk, 2022, Molecules.

PPARγ ligands increase antileukemic activity of second- and third-generation tyrosine kinase inhibitors in chronic myeloid leukemia cells

T. Stokłosa, E. Głodkowska-Mrówka, I. Seferyńska, 2016, Blood Cancer Journal.

Effect of substrate stiffness on the osteogenic differentiation of bone marrow stem cells and bone‐derived cells

Jacek Przybylski, J. Przybylski, Malgorzata Witkowska‐Zimny, 2013, Cell biology international.

α2β1 integrin-mediated mechanical signals during osteodifferentiation of stem cells from the Wharton's jelly of the umbilical cord.

E. Wróbel, P. Mrówka, Małgorzata Witkowska-Zimny, 2015, Folia histochemica et cytobiologica.

Studies on enzymatic degradation of multifunctional composite consisting of chitosan microspheres and shape memory polyurethane matrix

W. Świȩszkowski, M. Bil, P. Mrówka, 2020 .

Moisture-cured silicone-urethanes-candidate materials for tissue engineering: a biocompatibility study in vitro.

J. Kozakiewicz, J. Przybylski, M. Lewandowska-Szumieł, 2010, Journal of biomedical materials research. Part A.

PPARγ Agonists in Combination Cancer Therapies.

E. Głodkowska-Mrówka, P. Mrówka, 2019, Current cancer drug targets.

Structure guided design and synthesis of furyl thiazolidinedione derivatives as inhibitors of GLUT 1 and GLUT 4, and evaluation of their anti-leukemic potential.

C. V. Iancu, F. Meyer‐Almes, J. Choe, 2020, European journal of medicinal chemistry.

Differential expression of BIRC family genes in chronic myeloid leukaemia – BIRC3 and BIRC8 as potential new candidates to identify disease progression

T. Stokłosa, E. Głodkowska-Mrówka, I. Seferyńska, 2014, British journal of haematology.

Statins in prevention and therapy of cancer

P. Mrówka, E. Głodkowska, Eliza Głodkowska, 2008 .

Pioglitazone, a Ppar-gamma Ligand, Exerts Cytostatic/cytotoxic Effects against Cancer Cells, That Do Not Result from Inhibition of Proteasome

D. Nowis, J. Gołąb, M. Makowski, 2008 .

Inhibition of cyclooxygenase-2 indirectly potentiates antitumor effects of photodynamic therapy in mice.

P. Mróz, D. Nowis, J. Gołąb, 2003, Clinical cancer research : an official journal of the American Association for Cancer Research.

Dynamic Changes in the Ability to Release Neutrophil ExtraCellular Traps in the Course of Childhood Acute Leukemias

E. Głodkowska-Mrówka, U. Demkow, O. Ciepiela, 2021, International journal of molecular sciences.

Proteasome inhibition potentiates antitumor effects of photodynamic therapy in mice through induction of endoplasmic reticulum stress and unfolded protein response.

Michael R Hamblin, P. Agostinis, P. Mróz, 2009, Cancer research.

Integrin αv signaling influences phenotype and maturation of primary human osteoblasts on alumina surface

E. Głodkowska-Mrówka, E. Wróbel, P. Mrowka, 2014 .

Statins Impair Antitumor Effects of Rituximab by Inducing Conformational Changes of CD20

P. Parren, M. Lekka, D. Nowis, 2008, PLoS medicine.

Statins inhibit ABCB1 and ABCG2 drug transporter activity in chronic myeloid leukemia cells and potentiate antileukemic effects of imatinib.

P. Włodarski, T. Stokłosa, E. Głodkowska-Mrówka, 2014, Experimental hematology.

Discovery of novel N-substituted thiazolidinediones (TZDs) as HDAC8 inhibitors: in-silico studies, synthesis, and biological evaluation.

F. Meyer‐Almes, J. Choe, R. Aguilera, 2020, Bioorganic chemistry.

Discovery of 5-naphthylidene-2,4-thiazolidinedione derivatives as selective HDAC8 inhibitors and evaluation of their cytotoxic effects in leukemic cell lines.

F. Meyer‐Almes, Kalpana Tilekar, N. Upadhyay, 2019, Bioorganic chemistry.

Design and in vitro evaluation of electrospun shape memory polyurethanes for self-fitting tissue engineering grafts and drug delivery systems.

E. Głodkowska-Mrówka, A. Manda-Handzlik, M. Bil, 2020, Materials science & engineering. C, Materials for biological applications.

Heme oxygenase-1 protects tumor cells against photodynamic therapy-mediated cytotoxicity

D. Nowis, J. Gołąb, G. Wilczynski, 2006, Oncogene.

Ciglitazone, an agonist of peroxisome proliferator-activated receptor gamma, exerts potentiated cytostatic/cytotoxic effects against tumor cells when combined with lovastatin.

D. Nowis, J. Gołąb, T. Stokłosa, 2008, International journal of oncology.

[Selected, biochemical markers of hypoxia].

J. Przybylski, P. Kwasiborski, P. Kowalczyk, 2012, Przeglad lekarski.

Quantitative phase imaging supported by Raman micro-spectroscopy for identifying and quantifying changes in myeloid cells treated with proteasome inhibitor

M. Kujawińska, W. Krauze, M. Baczewska, 2023, BiOS.

l-Ornithine-N5-monooxygenase (PvdA) Substrate Analogue Inhibitors for Pseudomonas aeruginosa Infections Treatment: Drug Repurposing Computational Studies

J. C. Rosy, S. Murugesan, P. Maszczyk, 2022, Biomolecules.

Permuted 2,4-thiazolidinedione (TZD) analogs as GLUT inhibitors and their in-vitro evaluation in leukemic cells.

C. V. Iancu, F. Meyer‐Almes, J. Choe, 2020, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Multifunctional composite combining chitosan microspheres for drug delivery embedded in shape memory polyester-urethane matrix

W. Świȩszkowski, D. Kołbuk, M. Bil, 2021 .

Pioglitazone, a PPAR-gamma ligand, exerts cytostatic/cytotoxic effects against cancer cells, that do not result from inhibition of proteasome.

D. Nowis, J. Gołąb, I. Młynarczuk-Biały, 2008, Acta biochimica Polonica.

Pioglitazone, a Ppar-gamma Ligand, Exerts Cytostatic/cytotoxic Effects against Cancer Cells, That Do Not Result from Inhibition of Proteasome

D. Nowis, J. Gołąb, M. Makowski, 2022 .

α2β1 integrin-mediated mechanical signals during osteodifferentiation of stem cells from the Wharton's jelly of the umbilical cord.

E. Wróbel, P. Mrówka, Małgorzata Witkowska-Zimny, 2015, Folia histochemica et cytobiologica.