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001-es BibID:	BIBFORM024256
Első szerző:	Márton Ildikó (fogszakorvos)
Cím:	Distribution of interleukin-2 receptor alpha-chain and cells expressing major histocompatibility complex class II antigen in chronic human periapical lesions / I. J. Márton, B. Dezső, T. Radics, C. Kiss
Dátum:	1998
Megjegyzések:	In situ distribution of CD2+ T-lymphocytes, CD4+ and CD8+ T-cell subsets, CD14+ macrophages, interleukin-2 receptor alpha-chain (IL-2R alpha) and class II major histocompatibility complex antigen (major histocompatibility complex class II, HLA-DR) expressing cells were determined in 14 chronic human periapical granulomas by immunohistochemical method using monoclonal antibodies. CD2+ lymphocytes were rather evenly distributed within the classical granulation tissue and comprised 55% of the mononuclear cells. Macrophages were distributed all over the periapical area, but their proportion was much less than that of T lymphocytes. Both small, lymphocyte-like mononuclear cells and larger mononuclear cells resembling macrophages displayed mild to strong circumferential staining with the anti-HLA-DR antibody. The majority of lymphocytes expressed IL-2R alpha indicating the activated state of T cells within the lesion.
Tárgyszavak:	Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:	Oral Microbiology Immunology. - 13 : 4 (1998), p. 259-262. -
További szerzők:	Dezső Balázs (1951-) (pathológus) Radics Tünde (1963-) (egyetemi adjunktus, fogszakorvos) Kiss Csongor (1956-) (hematológus, onkológus)
Internet cím:	Intézményi repozitóriumban (DEA) tárolt változat Szerző által megadott URL DOI
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001-es BibID:	BIBFORM089017
035-os BibID:	(cikkazonosító)7742 (Scopus)85095421438 (WOS)000588974200001
Első szerző:	Szalóki Melinda (vegyész)
Cím:	Evaluation of the Effect of the Microscopic Glass Surface Protonation on the Hard Tissue Thin Section Preparation / Szalóki Melinda, Hegedűs Viktória, Fodor Tamás, Martos Renáta, Radics Tünde, Hegedűs Csaba, Dezső Balázs
Dátum:	2020
ISSN:	2076-3417
Megjegyzések:	In this study, a new procedure for mounting tissue blocks was described while cutting and grinding the section remains tightly bound to the inert glass surface both chemically and micro mechanically allowing good quality specimens for staining and microscopic analysis. The micromechanical interlocking was achieved by using of frosted glass, the chemical binding was made with 10-methacryloyloxydecyl dihydrogen phosphate monomer (10-MDP) containing bond material. The glass surface activation was achieved by nitric acid etching and the surface was characterized by zeta potential, X-ray photoelectron spectroscopy (XPS), and contact angle measurements. Cylindrical samples were prepared from epoxy embedding materials, cortical bovine bone, and dental titanium to investigate the shear bond strengths (SBS) to microscopic glass slide compared to a routinely used thermoplastic adhesive. Based on the experiments it was found that the micromechanical retention combined with MDP containing bond material improved the SBS data compared to the thermoplastic adhesive. The acid etched glass became positively charged that significantly increased the SBS data of bone and titanium compared with the uncharged version. Therefore, the thickness of the undecalcified bone section with metal can safely reduce to improve histological microscopic analysis.
Tárgyszavak:	Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban folyóiratcikk microscopic glass surface protonation nitric acid etching undecalcified thin bone section titanium implant 10-MDP adhesion
Megjelenés:	Applied Sciences-Basel. - 10 : 21 (2020), p. 1-21. -
További szerzők:	Hegedűs Viktória (1986-) (fogorvos) Fodor Tamás (1984-) (Ph.D hallgató) Martos Renáta (1975-) (fogszakorvos) Radics Tünde (1963-) (egyetemi adjunktus, fogszakorvos) Hegedűs Csaba (1953-) (fogszakorvos) Dezső Balázs (1951-) (pathológus)
Pályázati támogatás:	GINOP-2.3.2.-15-2016-00011 GINOP GINOP-2.3.2.-15-2016-00022 GINOP GINOP-2.3.2.-15-2016-00041 GINOP
Internet cím:	Szerző által megadott URL DOI Intézményi repozitóriumban (DEA) tárolt változat
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