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Publications

Toll-like receptor 4-mediated cytokine synthesis and post-stroke depressive symptoms. Korostynski M., Hoinkis D., Piechota M., Golda S., Pera J., Slowik A., Dziedzic T. Translational Psychiatry volume 11, Article number: 246, 2021 April 26.Beneficial Effect of IL-4 and SDF-1 on Myogenic Potential of Mouse and Human Adipose Tissue-Derived Stromal Cells. Archacka K., Bem J., Brzoska E., Czerwinska A., Grabowska I., Kasprzycka P., Hoinkis D., Siennicka K., Pojda Z., Bernas P., Binkowski R., Jastrzebska K., Kupiec A., Malesza M., Michalczewska E., Soszynska M., Ilach K., Streminska W., Ciemerych M. Cells 2020 Jun 17;9(6):1479.Opposite regulation of piRNAs, rRNAs and miRNAs in the blood after subarachnoid hemorrhage. Morga R., Borczyk M., Korostynski M., Piechota M., Hoinkis D., Golda S., Dziedzic T., Slowik A., Moskala M. & Pera J. Journal of Molecular Medicine, 2020 May 18.Underestimated Aspect of Mucopolysaccharidosis Pathogenesis: Global Changes in Cellular Processes Revealed by Transcriptomic Studies. Gaffke L., Pierzynowska K., Podlacha M., Hoinkis D., Rintz E., Brokowska J., Cyske Z., Wegrzyn G. Int J Mol Sci. 2020 Feb 11;21(4).Inflammatory Responses Induced by the Rupture of Intracranial Aneurysms Are Modulated by miRNAs. Korostynski M., Morga R., Piechota M., Hoinkis D., Golda S., Dziedzic T., Slowik A., Moskala M., Pera J. Mol Neurobiol. 2020 Feb;57(2):988-996.Genetic Signature of Acute Lymphoblastic Leukemia and Netherton Syndrome Co-incidence—First Report in the Literature. Skoczen S., Stepien K., Mlynarski W., Centkowski P., Kwiecinska K., Korostynski M., Piechota M., Wyrobek E., Moryl-Bujakowska A., Strojny W., Rej M., Kowalczyk J., Balwierz W. Front. Oncol., 17 January 2020.Systemic response to rupture of intracranial aneurysms involves expression of specific gene isoforms. Korostynski M., Piechota M., Morga R., Hoinkis D., Golda S., Zygmunt M., Dziedzic T., Moskala M., Slowik A., Pera J. J Transl Med. 2019 May 2;17(1):141.Genetic Profile and Clinical Implications of Hepatoblastoma and Neuroblastoma Coexistence in a Child. Skoczen S, Stepien K, Krzysztofik M, Luszawska T, Hnatko-Kolacz M, Korostynski M, Piechota M, Kolanek K, Wyrobek L, Wysocka K, GoreckI W, Balwierz W. Front. Oncol., 04 April 2019.Expression of alternatively spliced variants of the Dclk1 gene is regulated by psychotropic drugs. Zygmunt M, Hoinkis D, Hajto J, Piechota M, Skupień-Rabian B, Jankowska U, Kędracka-Krok S, Rodriguez Parkitna J, Korostynski M. BMC Neurosci. 2018 Sep 12;19(1):55.Whole-exome sequencing identifies novel pathogenic mutations and putative phenotype-influencing variants in Polish limb-girdle muscular dystrophy patients. Fichna JP., Macias A., Piechota M., Korostyński M., Potulska-Chromik A., Redowicz MJ., Zekanowski C. Hum Genomics. 2018, 12(1):34.A novel TPM2 gene splice-site mutation causes severe congenital myopathy with arthrogryposis and dysmorphic features. Mroczek M., Kabzińska D., Chrzanowska KH., Pronicki M., Kochański A. J Appl Genet. 2017, 58(2):199-203.The effect of a novel c.820C>T (Arg274Trp) mutation in the mitofusin 2 gene on fibroblast metabolism and clinical manifestation in a patient. Beręsewicz M., Boratyńska-Jasińska A., Charzewski Ł., Kawalec M., Kabzińska D., Kochański A., Krzyśko KA., Zabłocka B. PLoS One. 2017, 12(1):e0169999.