@article{MTMT:34066112,
	title = {Transcriptional activity of the long control region in human papillomavirus type 33 intratype variants},
	url = {https://m2.mtmt.hu/api/publication/34066112},
	author = {Oraveczné Gyöngyösi, Eszter and László, Brigitta and Szalmás, Anita and Kónya, József and Veress, György},
	doi = {10.1186/s12985-023-02114-y},
	journal-iso = {VIROL J},
	journal = {VIROLOGY JOURNAL},
	volume = {20},
	unique-id = {34066112},
	issn = {1743-422X},
	year = {2023},
	eissn = {1743-422X}
}

@{MTMT:33131237,
	title = {A vírusok terjedése},
	url = {https://m2.mtmt.hu/api/publication/33131237},
	author = {Veress, György},
	booktitle = {Orvosi virológia},
	unique-id = {33131237},
	year = {2022},
	pages = {28-34}
}

@{MTMT:33131235,
	title = {A vírusok szaporodása},
	url = {https://m2.mtmt.hu/api/publication/33131235},
	author = {Veress, György},
	booktitle = {Orvosi virológia},
	unique-id = {33131235},
	year = {2022},
	pages = {19-27}
}

@{MTMT:33131230,
	title = {A vírusok taxonómiája},
	url = {https://m2.mtmt.hu/api/publication/33131230},
	author = {Veress, György},
	booktitle = {Orvosi virológia},
	unique-id = {33131230},
	year = {2022},
	pages = {10-18}
}

@{MTMT:33131208,
	title = {A vírusok kémiai összetétele és szerkezete},
	url = {https://m2.mtmt.hu/api/publication/33131208},
	author = {Veress, György},
	booktitle = {Orvosi virológia},
	unique-id = {33131208},
	year = {2022},
	pages = {3-9}
}

@article{MTMT:32061682,
	title = {Coordinated action of human papillomavirus type 16 E6 and E7 oncoproteins on competitive endogenous RNA (ceRNA) network members in primary human keratinocytes},
	url = {https://m2.mtmt.hu/api/publication/32061682},
	author = {László, Brigitta and Antal, László and Oraveczné Gyöngyösi, Eszter and Szalmás, Anita and Póliska, Szilárd and Veress, György and Kónya, József},
	doi = {10.1186/s12885-021-08361-y},
	journal-iso = {BMC CANCER},
	journal = {BMC CANCER},
	volume = {21},
	unique-id = {32061682},
	issn = {1471-2407},
	year = {2021},
	eissn = {1471-2407},
	orcid-numbers = {Antal, László/0000-0001-9831-1429}
}

@article{MTMT:31306115,
	title = {Orientation-dependent toxic effect of human papillomavirus type 33 long control region DNA in Escherichia coli cells},
	url = {https://m2.mtmt.hu/api/publication/31306115},
	author = {Oraveczné Gyöngyösi, Eszter and Szalmás, Anita and Kónya, József and Veress, György},
	doi = {10.1007/s11262-020-01754-4},
	journal-iso = {VIRUS GENES},
	journal = {VIRUS GENES},
	volume = {56},
	unique-id = {31306115},
	issn = {0920-8569},
	year = {2020},
	eissn = {1572-994X},
	pages = {298-305}
}

@CONFERENCE{MTMT:33542809,
	title = {Orientation-dependent toxic effect of human papillomavirus type 33 long control region DNA in Escherichia coli cells},
	url = {https://m2.mtmt.hu/api/publication/33542809},
	author = {Veress, György and Kónya, József and Oraveczné Gyöngyösi, Eszter},
	booktitle = {Acta Microbiologica et Immunologica Hungarica Volume 66 Supplement 1},
	unique-id = {33542809},
	year = {2019},
	pages = {109-110}
}

@CONFERENCE{MTMT:30648034,
	title = {PHYLOGENETIC ANALYSIS OF HUMAN PAPILLOMAVIRUS (HPV) 33 LONG CONTROL REGION (LCR)},
	url = {https://m2.mtmt.hu/api/publication/30648034},
	author = {Oraveczné Gyöngyösi, Eszter and Szalmás, Anita and László, Brigitta and Kónya, József and Veress, György},
	booktitle = {Abstracts of the 5th Central European Forum for Microbiology},
	unique-id = {30648034},
	abstract = {High-risk HPVs (HPV 16, 18, 31, 33, 45, 52, 58, etc.) are the etiological agents of cervix carcinoma.
		The LCR of the virus genome has a very important role in the regulation of the viral replication and
		transcription, and contains several transcription factor binding sites. The intratypic nucleotide
		variants of HPVs has different oncogenic potential, as we could see in the case of HPV 16, HPV 18
		and HPV 31, but this phenomenon has not been investigated in the case of other high-risk types, such
		as HPV 33. The goal of this study was to see the natural genetic variants of HPV 33 in Hungary, and
		to investigate the functional differences between the variants.
		Exfoliated cell samples were collected from the cervix of HPV 33 positive women with cytological
		and colposcopical abnormalities. After DNA isolation, HPV 33 LCR specific PCR was performed on
		the specimens and the PCR products were sequenced with the PCR primers. Multiple sequence
		alignment and phylogenetic analysis were carried out on the sequences. The sequences of our samples
		were compared to HPV 33 variants published in the literature. Several variants were identified from
		our samples with single nucleotide changes and a 79 bp deletion. According to the constructed
		phylogenetic tree, our variants belongs to the A lineage, A1 and A2 sublineages, which are the most
		frequent lineages in Europe. The nucleotide changes in the LCR can affect transcription factor
		binding sites and might result in altered transcriptional activity of the regulatory region. So, after cloning the HPV 33 variants into luciferase reporter plasmids, we are planning the functional analysis
		of the LCR with transient transfection experiments and luciferase tests.},
	year = {2017},
	pages = {24}
}

@article{MTMT:3065386,
	title = {Phylogenetic and functional analysis of sequence variation of human papillomavirus type 31 E6 and E7 oncoproteins},
	url = {https://m2.mtmt.hu/api/publication/3065386},
	author = {Ferenczi, Annamária and Oraveczné Gyöngyösi, Eszter and Szalmás, Anita and László, Brigitta and Kónya, József and Veress, György},
	doi = {10.1016/j.meegid.2016.05.020},
	journal-iso = {INFECT GENET EVOL},
	journal = {INFECTION GENETICS AND EVOLUTION},
	volume = {43},
	unique-id = {3065386},
	issn = {1567-1348},
	year = {2016},
	eissn = {1567-7257},
	pages = {94-100}
}