Katalóg evidencie publikačnej činnosti PU

ID záznamu:	112907
Kategória:	ADM
Autor:	Grejtáková Daniela (60%)
Autor:	Dojčáková Dana (5%)
Autor:	Boroňová Iveta (5%)
Autor:	Kyjovská L. (5%)
Autor:	Hubcejová Jaroslava (5%)
Autor:	Gregušiak Fecenková Michaela (5%)
Autor:	Zigová Michaela (5%)
Autor:	Priganc M. (5%)
Autor:	Bernasovská Jarmila (5%)
Názov:	WNT10A variants in relation to nonsyndromic hypodontia in eastern Slovak population [print, elektronický dokument]
Zdroj:	Journal of Genetics [print, elektronický dokument]
Lokácia:	Roč. 97, č. 5. - New Delhi, (2018), s. 1169-1177
ISSN:	0022-1333. - ISSN 0973-7731
Ohlas:	[1] 2021. ZENG, Y., BAUGH, E., AKYALCIN, S. et al. Functional effects of WNT10A rare variants associated with tooth agenesis. In Journal of dental research, ISSN 0022-0345; 1544-0591. 2021, vol. 100, no. 3, s. 302-309. WOS:000620669200011;SCOPUS.
Ohlas:	[3] 2020. XINYA, D.U., XIAOYU, L.I., CUN, X.I.E. et al. Detection of MSX1 gene mutations in patients with congenital tooth loss in Van der Woude syndrome. In Journal of prevention and treatment for stomatological diseases [online], ISSN 2097-0234. 2020 [cit. 2022-02-08], vol. 28, no. 1, s. 51. Dostupný na internete <http://www.kqjbfz.com/CN/10.12016/j.issn.2096-1456.2020.01.008>
Ohlas:	[3] 2019. BRÉZULIER, D., SOREL, O. Préconisations lors de la fermeture des espaces d’agénésie d’incisives latérales maxillaires : Revue systématique de la littérature=Recommendations for space closure therapy in maxillary lateral incisor agenesis cases: systematic review of literature. In Revue d'orthopédie dento-faciale [online], ISSN 2110-543X. 2019 [cit. 2022-03-21], vol. 53, no. 2, s. 147-156. Dostupný na internete <https://odf.edpsciences.org/articles/odf/abs/2019/02/odf2019532p147/odf2019532p147.html>
Ohlas:	[1] 2022. SAID, N.M., YASSIN, F., ELKREEM, E.A. Wnt10a missense gene polymorphism association with obesity risk: List of literature and a case-control study with Roc analysis for serum β-catenin level in Egypt. In Gene reports, ISSN 2452-0144. 2022, vol. 27, art. no. 101496. SCOPUS.
Ohlas:	[1] 2022. ZHANG, Z., PAN, X., CHEN, M. et al. Wnt signalling in oral and maxillofacial diseases. In Cell biology international, ISSN 1065-6995. 2022, roč. 46, č. 1, s. 34-45. SCOPUS;WOS:000712995500001.
Ohlas:	[1] 2023. FAN, L., MA, L., ZHU, G.R. et al. A genome-wide association study of premolar agenesis in a Chinese population. In Oral diseases, ISSN 1354-523X. 2023, roč. 29, č. 3, s. 1102-1114. WOS:000732053700001; SCOPUS.
Ohlas:	[1] 2023. REN, J.B., ZHAO, Y., YUAN, Y.Y. et al. Novel PAX9 compound heterozygous variants in a Chinese family with non- syndromic oligodontia and genotype- phenotype analysis of PAX9 variants. In Journal of applied oral science, ISSN 1678-7757. 2023, roč. 31, art. no. e20220403. WOS:000962155500001; SCOPUS.
Ohlas:	[1] 2023. WAN SAIMI, W.N.W., AHMAD, A.H., ISMAIL, K. et al. A scoping review: gene mutations of nonsyndromic hypodontia and its prevalence in gender and type of teeth. In Journal oh health and translational medicine, ISSN 1823-7339. 2023, šp. č. 1, s. 283-290. SCOPUS.
Ohlas:	[1] 2023. SONG, Y., SONG, F., XIAO, X. et al. Expression levels of WNT signaling pathway genes during early tooth development. In Organogenesis, ISSN 1547-6278. 2023, roč. 19, č. 1, art. no. 2212583. SCOPUS; WOS:000989126000001.
Oblasť výskumu:	130