 Bisphenol A-Glycidyl Methacrylate
"Bisphenol A-Glycidyl Methacrylate" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The reaction product of bisphenol A and glycidyl methacrylate that undergoes polymerization when exposed to ultraviolet light or mixed with a catalyst. It is used as a bond implant material and as the resin component of dental sealants and composite restorative materials.
| Descriptor ID |
D017438
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| MeSH Number(s) |
D02.241.081.069.600.150 D02.455.426.559.389.657.100 D05.750.716.822.308.200 D25.339.816.500.200 D25.720.716.822.308.200 J01.637.051.339.816.500.200 J01.637.051.720.716.822.308.200
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| Concept/Terms |
Bisphenol A-Glycidyl Methacrylate- Bisphenol A-Glycidyl Methacrylate
- Bisphenol A Glycidyl Methacrylate
- Methacrylate, Bisphenol A-Glycidyl
- Bis(Phenol A-Glycydyl Methacrylate)
- Bis-GMA
- Bis GMA
- Bis(Phenol A-Glycidyl Methacrylate)
Bisphenol A-Glycidyl Methacrylate Homopolymer- Bisphenol A-Glycidyl Methacrylate Homopolymer
- Bisphenol A Glycidyl Methacrylate Homopolymer
- Bis(Phenol A-Glycidyl Methacrylate), Homopolymer
- Poly(Bis-GMA)
- Bis-GMA Resin
- Bis GMA Resin
- Bis-GMA Resins
- Resin, Bis-GMA
- Resins, Bis-GMA
- Bisphenol A-Glycidyl Methacrylate Polymer
- Bisphenol A Glycidyl Methacrylate Polymer
- 2-Propenoic acid, 2-methyl-, (1-methylethylidene)bis(4,1-phenyleneoxy(2-hydroxy-3,1-propanediyl)) ester, homopolymer
- Bis-GMA Polymer
- Bis GMA Polymer
- Bis-GMA Polymers
- Polymer, Bis-GMA
- Polymers, Bis-GMA
Concise Enamel Bond- Concise Enamel Bond
- Bond, Concise Enamel
- Enamel Bond, Concise
- Concise Enamel Bond System
Concise Resin- Concise Resin
- Concise Resins
- Resin, Concise
- Resins, Concise
- Concise Composite Resin
- Composite Resin, Concise
- Composite Resins, Concise
- Concise Composite Resins
- Resin, Concise Composite
- Resins, Concise Composite
Conclude Resin- Conclude Resin
- Resin, Conclude
- Conclude Composite Resin
- Composite Resin, Conclude
- Resin, Conclude Composite
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Below are MeSH descriptors whose meaning is more general than "Bisphenol A-Glycidyl Methacrylate".
- Chemicals and Drugs [D]
- Organic Chemicals [D02]
- Carboxylic Acids [D02.241]
- Acids, Acyclic [D02.241.081]
- Acrylates [D02.241.081.069]
- Methacrylates [D02.241.081.069.600]
- Bisphenol A-Glycidyl Methacrylate [D02.241.081.069.600.150]
- Hydrocarbons [D02.455]
- Hydrocarbons, Cyclic [D02.455.426]
- Hydrocarbons, Aromatic [D02.455.426.559]
- Benzene Derivatives [D02.455.426.559.389]
- Phenols [D02.455.426.559.389.657]
- Bisphenol A-Glycidyl Methacrylate [D02.455.426.559.389.657.100]
- Macromolecular Substances [D05]
- Polymers [D05.750]
- Plastics [D05.750.716]
- Resins, Synthetic [D05.750.716.822]
- Composite Resins [D05.750.716.822.308]
- Bisphenol A-Glycidyl Methacrylate [D05.750.716.822.308.200]
- Biomedical and Dental Materials [D25]
- Dental Materials [D25.339]
- Resins, Synthetic [D25.339.816]
- Composite Resins [D25.339.816.500]
- Bisphenol A-Glycidyl Methacrylate [D25.339.816.500.200]
- Polymers [D25.720]
- Plastics [D25.720.716]
- Resins, Synthetic [D25.720.716.822]
- Composite Resins [D25.720.716.822.308]
- Bisphenol A-Glycidyl Methacrylate [D25.720.716.822.308.200]
- Technology, Industry, Agriculture [J]
- Technology, Industry, and Agriculture [J01]
- Manufactured Materials [J01.637]
- Biomedical and Dental Materials [J01.637.051]
- Dental Materials [J01.637.051.339]
- Resins, Synthetic [J01.637.051.339.816]
- Composite Resins [J01.637.051.339.816.500]
- Bisphenol A-Glycidyl Methacrylate [J01.637.051.339.816.500.200]
- Polymers [J01.637.051.720]
- Plastics [J01.637.051.720.716]
- Resins, Synthetic [J01.637.051.720.716.822]
- Composite Resins [J01.637.051.720.716.822.308]
- Bisphenol A-Glycidyl Methacrylate [J01.637.051.720.716.822.308.200]
Below are MeSH descriptors whose meaning is more specific than "Bisphenol A-Glycidyl Methacrylate".
This graph shows the total number of publications written about "Bisphenol A-Glycidyl Methacrylate" by people in this website by year, and whether "Bisphenol A-Glycidyl Methacrylate" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
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| 1997 | 1 | 0 | 1 | | 1999 | 1 | 0 | 1 | | 2000 | 0 | 2 | 2 | | 2001 | 1 | 3 | 4 | | 2002 | 0 | 1 | 1 | | 2003 | 0 | 1 | 1 | | 2004 | 0 | 2 | 2 | | 2005 | 1 | 4 | 5 | | 2007 | 1 | 0 | 1 | | 2008 | 2 | 2 | 4 | | 2009 | 2 | 0 | 2 | | 2010 | 0 | 3 | 3 | | 2011 | 0 | 1 | 1 | | 2012 | 0 | 1 | 1 | | 2014 | 0 | 1 | 1 | | 2015 | 1 | 2 | 3 | | 2017 | 0 | 1 | 1 | | 2019 | 0 | 1 | 1 | | 2021 | 0 | 3 | 3 |
To return to the timeline, click here.
Below are the most recent publications written about "Bisphenol A-Glycidyl Methacrylate" by people in Profiles.
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Mori DI, Powell A, Kehe GM, Schurr MJ, Nair DP, Puranik CP. Acrylated Hydroxyazobenzene Copolymers in Composite-Resin Matrix Inhibits Streptococcus mutans Biofilms In Vitro. Pediatr Dent. 2021 Nov 15; 43(6):484-491.
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Wang X, Gao G, Song HB, Zhang X, Stansbury JW, Bowman CN. Evaluation of a photo-initiated copper(I)-catalyzed azide-alkyne cycloaddition polymer network with improved water stability and high mechanical performance as an ester-free dental restorative. Dent Mater. 2021 10; 37(10):1592-1600.
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Rad IY, Lewis S, Barros MD, Kipper M, Stansbury JW. Suppression of hydrolytic degradation in labile polymer networks via integrated styrenic nanogels. Dent Mater. 2021 08; 37(8):1295-1306.
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Fronza BM, Lewis S, Shah PK, Barros MD, Giannini M, Stansbury JW. Modification of filler surface treatment of composite resins using alternative silanes and functional nanogels. Dent Mater. 2019 06; 35(6):928-936.
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Song HB, Wang X, Patton JR, Stansbury JW, Bowman CN. Kinetics and mechanics of photo-polymerized triazole-containing thermosetting composites via the copper(I)-catalyzed azide-alkyne cycloaddition. Dent Mater. 2017 06; 33(6):621-629.
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Randolph LD, Steinhaus J, M?ginger B, Gallez B, Stansbury J, Palin WM, Leloup G, Leprince JG. Photopolymerization of highly filled dimethacrylate-based composites using Type I or Type II photoinitiators and varying co-monomer ratios. Dent Mater. 2016 Feb; 32(2):136-48.
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Podg?rski M, Becka E, Claudino M, Flores A, Shah PK, Stansbury JW, Bowman CN. Ester-free thiol-ene dental restoratives--Part A: Resin development. Dent Mater. 2015 Nov; 31(11):1255-62.
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Forman DL, McLeod RR, Shah PK, Stansbury JW. Evaporation of low-volatility components in polymeric dental resins. Dent Mater. 2015 Sep; 31(9):1090-9.
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Feitosa VP, Sauro S, Ogliari FA, Stansbury JW, Carpenter GH, Watson TF, Sinhoreti MA, Correr AB. The role of spacer carbon chain in acidic functional monomers on the physicochemical properties of self-etch dental adhesives. J Dent. 2014 May; 42(5):565-74.
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Park HY, Kloxin CJ, Fordney MF, Bowman CN. Stress relaxation of trithiocarbonate-dimethacrylate-based dental composites. Dent Mater. 2012 Aug; 28(8):888-93.
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