Andras Jeney
Affiliations: | Semmelweis Egyetem, Hungary |
Area:
Molecular Biology, Oncology, Cell BiologyGoogle:
"Andras Jeney"Children
Sign in to add traineeIstvan Babo | grad student | 2005 | Semmelweis Egyetem |
Revekka Harisi | grad student | 2005 | Semmelweis Egyetem |
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Publications
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Petővári G, Dankó T, Tőkés AM, et al. (2020) In Situ Metabolic Characterisation of Breast Cancer and Its Potential Impact on Therapy. Cancers. 12 |
Petővári G, Dankó T, Krencz I, et al. (2019) Inhibition of Metabolic Shift can Decrease Therapy Resistance in Human High-Grade Glioma Cells. Pathology Oncology Research : Por |
Petővári G, Hujber Z, Krencz I, et al. (2018) Targeting cellular metabolism using rapamycin and/or doxycycline enhances anti-tumour effects in human glioma cells. Cancer Cell International. 18: 211 |
Krencz I, Sebestyen A, Papay J, et al. (2018) In situ analysis of mTORC1/2 and cellular metabolism-related proteins in human Lymphangioleiomyomatosis. Human Pathology |
Sebestyén A, Hujber Z, Petővári G, et al. (2018) Substrate oxidation differences in human glioma cells and their potential clinical significance Biochimica Et Biophysica Acta (Bba) - Bioenergetics. 1859: e104 |
Hujber Z, Petővári G, Szoboszlai N, et al. (2017) Rapamycin (mTORC1 inhibitor) reduces the production of lactate and 2-hydroxyglutarate oncometabolites in IDH1 mutant fibrosarcoma cells. Journal of Experimental & Clinical Cancer Research : Cr. 36: 74 |
Jeney A, Hujber Z, Szoboszlai N, et al. (2016) Characterisation of bioenergetic pathways and related regulators by multiple assays in human tumour cells. Cancer Cell International. 16: 4 |
Harisi R, Jeney A. (2015) Extracellular matrix as target for antitumor therapy. Oncotargets and Therapy. 8: 1387-98 |
Péterfia B, Füle T, Baghy K, et al. (2012) Syndecan-1 enhances proliferation, migration and metastasis of HT-1080 cells in cooperation with syndecan-2. Plos One. 7: e39474 |
Harisi R, Szekely G, Jeney A. (2011) Molecular targets in antimetastatic therapy of gastrointestinal tumors Zeitschrift FüR Gastroenterologie. 49 |