@article{MTMT:34732273,
	title = {Az oktatás és az egészségmagatartás relatív jelentősége az egészség és a jóllét szempontjából},
	url = {https://m2.mtmt.hu/api/publication/34732273},
	author = {Dürgő, Hajnalka},
	doi = {10.58701/mej.14960},
	journal-iso = {MEJ},
	journal = {MULTIDISZCIPLINÁRIS EGÉSZSÉG ÉS JÓLLÉT},
	volume = {2},
	unique-id = {34732273},
	year = {2024},
	eissn = {2939-8150},
	pages = {36-40}
}

@article{MTMT:34690439,
	title = {Az infravörös távérzékelés újszerű használata: lakóházak födémszigetelésének településszintű vizsgálata},
	url = {https://m2.mtmt.hu/api/publication/34690439},
	author = {Dürgő, Hajnalka and Szalma, Elemér Imre},
	journal-iso = {MAGYAR ENERGETIKA},
	journal = {MAGYAR ENERGETIKA},
	volume = {30},
	unique-id = {34690439},
	issn = {1216-8599},
	year = {2023},
	pages = {2-10}
}

@{MTMT:34192018,
	title = {A Technika Tanszék története Szegeden: múlt, jelen és jövő},
	url = {https://m2.mtmt.hu/api/publication/34192018},
	author = {Benkő, Zsolt István and Dudás, Tünde and Dürgő, Hajnalka},
	booktitle = {150 éve a pedagógusképzésért – Neveléstudományi konferencia},
	unique-id = {34192018},
	year = {2023},
	pages = {115-116}
}

@{MTMT:34191784,
	title = {A technika oktatásának evolúciója},
	url = {https://m2.mtmt.hu/api/publication/34191784},
	author = {Benkő, Zsolt István and Dudás, Tünde and Dürgő, Hajnalka},
	booktitle = {150 éve a pedagógusképzésért – Neveléstudományi konferencia},
	unique-id = {34191784},
	year = {2023},
	pages = {113-114}
}

@book{MTMT:33297549,
	title = {Ember és technika},
	url = {https://m2.mtmt.hu/api/publication/33297549},
	isbn = {9786155946813},
	author = {Dudás, Tünde and Dürgő, Hajnalka and Benkő, Zsolt István},
	publisher = {JGYF Kiadó; JGYTF Kiadó},
	unique-id = {33297549},
	keywords = {technika},
	year = {2022}
}

@inproceedings{MTMT:32541004,
	title = {Combining UAV-based zone spraying and VRA technology to achieve a 50% chemical decrease for EU's Green Deal},
	url = {https://m2.mtmt.hu/api/publication/32541004},
	author = {Szalma, Elemér and Dürgő, Hajnalka},
	booktitle = {Proceedings of the 27th International Symposium on Analytical and Environmental Problems},
	unique-id = {32541004},
	year = {2021},
	pages = {314-318}
}

@mastersthesis{MTMT:2994140,
	title = {Gümő-specifikus NCR peptidek azonosítása, vad és mutáns Medicago truncatula gyökérgümők összehasonlító fehérjeanalízise, és az NCR247 lehetséges bakteriális interakciós partnereinek felderítése},
	url = {https://m2.mtmt.hu/api/publication/2994140},
	author = {Dürgő, Hajnalka},
	doi = {10.14232/phd.2547},
	publisher = {SZTE},
	unique-id = {2994140},
	year = {2015}
}

@article{MTMT:2891431,
	title = {Identification of nodule-specific cysteine-rich plant peptides in endosymbiotic bacteria},
	url = {https://m2.mtmt.hu/api/publication/2891431},
	author = {Dürgő, Hajnalka and Klement, Éva and Hunyadi-Gulyás Éva, Csilla and Szűcs, Attila and Kereszt, Attila and Medzihradszky F., Katalin and Kondorosi, Éva},
	doi = {10.1002/pmic.201400385},
	journal-iso = {PROTEOMICS},
	journal = {PROTEOMICS},
	volume = {15},
	unique-id = {2891431},
	issn = {1615-9853},
	abstract = {The symbiosis of Medicago truncatula with Sinorhizobium meliloti or Sinorhizobium medicae soil bacteria results in the formation of root nodules where bacteria inside the plant cells are irreversibly converted to polyploid, nondividing nitrogen-fixing bacteroids. Bacteroid differentiation is host-controlled and the plant effectors are symbiosis-specific secreted plant peptides. In the M. truncatula genome there are more than 600 symbiotic peptide genes including 500 small genes coding for nodule-specific cysteine-rich (NCR) peptides. While NCR transcripts represent >5% of the nodule transcriptome, the existence of only eight NCR peptides has been demonstrated so far. The predicted NCRs are secreted peptides targeted to the endosymbionts. Correspondingly, all the eight detected peptides were present in the bacteroids. Here, we report on large-scale detection of NCR peptides from nodules and from isolated, semipurified endosymbionts at various stages of their differentiation. In total 138 NCRs were detected in the bacteroids; 38 were cationic while the majority was anionic. The presence of early NCRs in nitrogen-fixing bacteroids indicates their high stability, and their long-term maintenance suggests persisting biological roles in the bacteroids. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.},
	keywords = {MS; symbiosis; Medicago truncatula; Bacteroid; Plant proteomics; NCR-peptides},
	year = {2015},
	eissn = {1615-9861},
	pages = {2291-2295},
	orcid-numbers = {Szűcs, Attila/0000-0003-2803-7123; Kondorosi, Éva/0000-0002-4065-8515}
}

@article{MTMT:2583121,
	title = {Medicago truncatula symbiotic peptide NCR247 contributes to bacteroid differentiation through multiple mechanisms},
	url = {https://m2.mtmt.hu/api/publication/2583121},
	author = {Farkas, Attila and Maróti, Gergely and Dürgő, Hajnalka and Györgypál, Zoltán and Lima, Rui and Medzihradszky F., Katalin and Kereszt, Attila and Mergaert, P and Kondorosi, Éva},
	doi = {10.1073/pnas.1404169111},
	journal-iso = {P NATL ACAD SCI USA},
	journal = {PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA},
	volume = {111},
	unique-id = {2583121},
	issn = {0027-8424},
	abstract = {Symbiosis between rhizobia soil bacteria and legume plants results in the formation of root nodules where plant cells are fully packed with nitrogen fixing bacteria. In the host cells, the bacteria adapt to the intracellular environment and gain the ability for nitrogen fixation. Depending on the host plants, the symbiotic fate of bacteria can be either reversible or irreversible. In Medicago and related legume species, the bacteria undergo a host-directed multistep differentiation process culminating in the formation of elongated and branched polyploid bacteria with definitive loss of cell division ability. The plant factors are nodule-specific symbiotic peptides. Approximately 600 of them are nodule-specific cysteine-rich (NCR) peptides produced in the rhizobium-infected plant cells. NCRs are targeted to the endosymbionts, and concerted action of different sets of peptides governs different stages of endosymbiont maturation, whereas the symbiotic function of individual NCRs is unknown. This study focused on NCR247, a cationic peptide exhibiting in vitro antimicrobial activities. We show that NCR247 acts in those nodule cells where bacterial cell division is arrested and cell elongation begins. NCR247 penetrates the bacteria and forms complexes with many bacterial proteins. Interaction with FtsZ required for septum formation is one of the host interventions for inhibiting bacterial cell division. Complex formation with the ribosomal proteins affects translation and contributes to altered proteome and physiology of the endosymbiont. Binding to the chaperone GroEL amplifies the NCR247-modulated biological processes. We show that GroEL1 of Sinorhizobium meliloti is required for efficient infection, terminal differentiation, and nitrogen fixation.},
	year = {2014},
	eissn = {1091-6490},
	pages = {5183-5188},
	orcid-numbers = {Maróti, Gergely/0000-0002-3705-0461; Kondorosi, Éva/0000-0002-4065-8515}
}

@article{MTMT:2042472,
	title = {The guanine-quadruplex structure in the human c-myc gene's promoter is converted into B-DNA form by the human poly(ADP-ribose)polymerase-1},
	url = {https://m2.mtmt.hu/api/publication/2042472},
	author = {Fekete, Anna and Kenesi, E and Hunyadi-Gulyás Éva, Csilla and Dürgő, Hajnalka and Berko, B and Dunai, Zsuzsanna and Bauer, Pál},
	doi = {10.1371/journal.pone.0042690},
	journal-iso = {PLOS ONE},
	journal = {PLOS ONE},
	volume = {7},
	unique-id = {2042472},
	issn = {1932-6203},
	abstract = {The important regulatory role of the guanine-quadruplex (GQ) structure, present in the nuclease hypersensitive element (NHE) III 1 region of the human c-myc (h c-myc) gene's promoter, in the regulation of the transcription of that gene has been documented. Here we present evidences, that the human nuclear poly(ADP-ribose)polymerase-1 (h PARP-1) protein participates in the regulation of the h c-myc gene expression through its interaction with this GQ structure, characterized by binding assays, fluorescence energy transfer (FRET) experiments and by affinity pull-down experiments in vitro, and by chromatin immunoprecipitation (ChIP)-qPCR analysis and h c-myc-promoter-luciferase reporter determinations in vivo. We surmise that h PARP-1 binds to the GQ structure and participates in the conversion of that structure into the transcriptionally more active B-DNA form. The first Zn-finger structure present in h PARP-1 participates in this interaction. PARP-1 might be a new member of the group of proteins participating in the regulation of transcription through their interactions with GQ structures present in the promoters of different genes. © 2012 Fekete et al.},
	year = {2012},
	eissn = {1932-6203},
	orcid-numbers = {Bauer, Pál/0000-0001-5648-9368}
}