The effect of 12-O-tetradecanoylphorbol-13-acetate on Sertoli cell morphology and cytoskeletal organization: an in vitro study by means of cryo-SEM and fluorescent techniques

2002 ◽  
Vol 94 (2) ◽  
pp. 117-125 ◽  
Author(s):  
Evridiki Panagopoulou ◽  
Mirsini Kouloukoussa ◽  
Irene Voloudaki-Baltatzi ◽  
Christos Kittas ◽  
Evangelos Marinos
1985 ◽  
Vol 132 (2) ◽  
pp. 729-734 ◽  
Author(s):  
M. Benahmed ◽  
C. Grenot ◽  
E. Tabone ◽  
P. Sanchez ◽  
A.M. Morera

2016 ◽  
Vol 14 (6) ◽  
pp. 5325-5333 ◽  
Author(s):  
Yanfeng Zhu ◽  
Hua Xu ◽  
Min Li ◽  
Zhibin Gao ◽  
Jie Huang ◽  
...  

2007 ◽  
Vol 83A (1) ◽  
pp. 178-183 ◽  
Author(s):  
Cristina Morelli ◽  
Giovanni Barbanti-Brodano ◽  
Alessandra Ciannilli ◽  
Katia Campioni ◽  
Stefano Boriani ◽  
...  

Endocrinology ◽  
2014 ◽  
Vol 156 (2) ◽  
pp. 680-693 ◽  
Author(s):  
Elizabeth I. Tang ◽  
Ka-Wai Mok ◽  
Will M. Lee ◽  
C. Yan Cheng

1984 ◽  
Vol 438 (1 Hormonal Cont) ◽  
pp. 684-687 ◽  
Author(s):  
M. BENAHMED ◽  
J. REVENTOS ◽  
E. TABONE ◽  
J. M. SAEZ

2015 ◽  
Vol 238 (2) ◽  
pp. S282
Author(s):  
B. Egbowon ◽  
W. Harris ◽  
G. Arnott ◽  
C. LloydMills ◽  
A. Hargreaves

Materials ◽  
2021 ◽  
Vol 14 (9) ◽  
pp. 2442
Author(s):  
Małgorzata Fischer ◽  
Anna Mertas ◽  
Zenon Paweł Czuba ◽  
Małgorzata Skucha-Nowak

Microinvasive dentistry is based on the treatment of early carious lesions with the use of dental infiltrants. The commercially available Icon dental infiltrant does not contain any bacteriostatic component. An experimental preparation enriched with the missing component was synthesised. The aim of this study was to evaluate the cytotoxicity of the experimental preparation. Mouse fibroblasts of the L-929 lineage were used for the in vitro study. Cell morphology and viability were assessed. In the cytotoxicity analysis, it was shown that the experimental preparation (42.8 ± 10.3) after 24 h at two-fold dilution showed similar cytotoxicity to Icon (42.7 ± 8.8) (p > 0.05), while at four-fold dilution experimental preparation (46.7 ± 3.1), it was less toxic than Icon (34.2 ± 3.1) (p < 0.05). The experimental preparation has the potential to provide an alternative to the Icon commercial preparation. Further research is needed to evaluate the cytotoxicity of the experimental preparation over a longer period of time.


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