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The use of mouse models to investigate shear bond strength in amelogenesis imperfecta
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نویسنده
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pugach m.k. ,ozer f. ,li y. ,sheth k. ,beasley r. ,resnick a. ,daneshmehr l. ,kulkarni a.b. ,bartlett j.d. ,gibson c.w. ,lindemeyer r.g.
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منبع
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journal of dental research - 2011 - دوره : 90 - شماره : 11 - صفحه:1352 -1357
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چکیده
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Patients with amelogenesis imperfecta (ai) have defective enamel; therefore,bonded restorations of patients with ai have variable success rates. to distinguish which cases of ai may have good clinical outcomes with bonded materials,we evaluated etching characteristics and bond strength of enamel in mouse models,comparing wild-type (wt) with those having mutations in amelogenin (amelx) and matrix metalloproteinase-20 (mmp20),which mimic 2 forms of human ai. etched enamel surfaces were compared for roughness by scanning electron microscopy (sem) images. bonding was compared through shear bond strength (sbs) studies with 2 different systems (etch-and-rinse and self-etch). etched enamel surfaces of incisors from amelx knock-out (amelxko) mice appeared randomly organized and non-uniform compared with wt. etching of mmp20ko surfaces left little enamel,and the etching pattern was indistinguishable from unetched surfaces. sbs results were significantly different when amelxko and mmp20ko enamel surfaces were compared. a significant increase in sbs was measured for all samples when the self-etch system was compared with the etch-and-rinse system. we have developed a novel system for testing shear bond strength of mouse incisors with ai variants,and analysis of these data may have important clinical implications for the treatment of patients with ai. © 2011 international & american associations for dental research.
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کلیدواژه
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acid-etching; amelogenesis imperfecta; amelogenin; enamel; matrix metalloproteinase-20; shear bond strength
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آدرس
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department of anatomy and cell biology,university of pennsylvania,school of dental medicine,philadelphia,pa 19104, United States, department of preventive and restorative sciences,university of pennsylvania,school of dental medicine,philadelphia,pa 19104, United States, department of anatomy and cell biology,university of pennsylvania,school of dental medicine,philadelphia,pa 19104, United States, department of anatomy and cell biology,university of pennsylvania,school of dental medicine,philadelphia,pa 19104, United States, department of anatomy and cell biology,university of pennsylvania,school of dental medicine,philadelphia,pa 19104, United States, department of anatomy and cell biology,university of pennsylvania,school of dental medicine,philadelphia,pa 19104, United States, department of preventive and restorative sciences,university of pennsylvania,school of dental medicine,philadelphia,pa 19104, United States, functional genomics section,laboratory of cell and developmental biology,national institute of dental and craniofacial research,nih,bethesda,md 20892, United States, forsyth institute,department of developmental biology,harvard school of dental medicine,cambridge,ma 02142, United States, department of anatomy and cell biology,university of pennsylvania,school of dental medicine,philadelphia,pa 19104, United States, division of pediatric dentistry,university of pennsylvania,school of dental medicine,240 s. 40th street,philadelphia,pa 19104-6030, United States
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Authors
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