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ABSTRACT One of the greatest achievements of humankind in science is the near completion of the draft of the Human Genome Project in 2001. Information gained from this draft is now used to develop new molecular biological techniques used by oral health professionals. Although dental caries are considered to be an infectious disease, there are some genetic determinants for both the microorganisms and the host that causes susceptibility to dental decays. Studies including the monozygotic and dizygotic twins pioneered the genetic studies in understanding the genetic nature of tooth decays. As the outcomes of human genome project are started to be applied in the oral medicine, many researchers studied genes and their protein products that may contribute to tooth decay. The studied genes include HLA genes, AMELX, CDI4, vitamin D receptor genes and genes that code for saliva components. Although some researchers correlate some polymorphisms and dental caries in small study groups, molecular markers that indicate increased risk or protection against dental caries have not been identified. Clinicians will hold more effective and preventive therapies whenever genetic factors contributing to carries risk and protection factors are identified.
Related ArticlesThe Role and Impact of SNPs in Pharmacogenomics and Personalized Medicine.Laing, Rachel E.; Hess, Patricia; Yingjie Shen; Jian Wang; Hu, Sean X.//Current Drug Metabolism;Jun2011, Vol. 12 Issue 5, p460

No abstract available.

Pulpal responses to cavity preparation in aged rat molars.Kawagishi, Eriko; Nakakura-Ohshima, Kuniko; Nomura, Shuichi; Ohshima, Hayato//Cell & Tissue Research;Sep2006, Vol. 326 Issue 1, p111

The dentin-pulp complex is capable of repair after tooth injuries including dental procedures. However, few data are available concerning aged changes in pulpal reactions to such injuries. The present study aimed to clarify the capability of defense in aged pulp by investigating the responses of...

Association of Dental Caries with HLA Class II Allele in Brazilian Adolescents.Valarini, N.; Maciel, S.M.; Moura, S.K.; Poli-Frederico, R.C.//Caries Research;2012, Vol. 46 Issue 6, p530

The purpose of this study was to evaluate the association between the frequencies of DR and DQ HLA class II alleles and the prevalence of dental caries in Brazilian adolescents. The study sample consisted of 164 adolescents aged 15- 19 years. For the assessment of caries experience the DMFT...

Immunobiology.Middleton, P.G.; Cullup, H.; Dickinson, A.M.; Norden, J.; Jackson, G.H.; Taylor, P.R.A.; Cavet, J.//Bone Marrow Transplantation;8/15/2002, Vol. 30 Issue 4, p223

Investigates the role of polymorphism of the vitamin D receptor (VDR) gene in human leukocyte antigen-matched sibling bone marrow transplantation for polymorphisms previously associated with human disease pathology. Allele frequencies and haplotypes; Association of patient genotype with...

Enrichment of vitamin D response elements in RA-associated loci supports a role for vitamin D in the pathogenesis of RA.Yarwood, A; Martin, P; Bowes, J; Lunt, M; Worthington, J; Barton, A; Eyre, S//Genes & Immunity;Jul2013, Vol. 14 Issue 5, p325

The aim of this study was to explore the role of vitamin D in rheumatoid arthritis (RA) pathogenesis by investigating the enrichment of vitamin D response elements (VDREs) in confirmed RA susceptibility loci and testing variants associated with vitamin D levels for association with RA....

Candidate Genes Implicated in Type 1 Diabetes Susceptibility.Aribi, Mourad//Current Diabetes Reviews;2008, Vol. 4 Issue 2, p110

Type 1 diabetes (T1D) is an autoimmune disease resulting from pancreatic beta-cells destruction, often appearing on a genetic ground susceptibility under the influence of one or more environmental factors. Multiplex families studies, using genetic markers allowed the identification of various...

Genome-wide pathway analysis of a genome-wide association study on multiple sclerosis.Song, Gwan; Choi, Sung; Ji, Jong; Lee, Young//Molecular Biology Reports;Mar2013, Vol. 40 Issue 3, p2557

The aims of this study were to identify candidate single nucleotide polymorphisms (SNPs) and mechanisms of multiple sclerosis (MS) and to generate SNP to gene to pathway hypotheses. A MS genome-wide association study (GWAS) dataset that included 505,763 SNPs in 500 cases and 500 controls of...

Full Genotyping of a Highly Polymorphic Human Gene Trait by Time-Resolved Fluorescence Resonance Energy Transfer.Totè, Edoardo; Lamperti, Marco; Bondani, Maria; Salerno, Domenico; Cassina, Valeria; Nardo, Luca//PLoS ONE;Sep2014, Vol. 9 Issue 9, p1

The ability of detecting the subtle variations occurring, among different individuals, within specific DNA sequences encompassed in highly polymorphic genes discloses new applications in genomics and diagnostics. DQB1 is a gene of the HLA-II DQ locus of the Human Leukocyte Antigens (HLA) system....

Immunohistochemical Localization of HLA-DR-positive Cells in Unerupted and Erupted Normal and Carious Human Teeth.Yoshiba, N.; Yoshiba, K.; Nakamura, H.; Iwaku, M.; Ozawa, H.//Journal of Dental Research;Aug1996, Vol. 75 Issue 8, p1585

Class II major histocompatibility complex (MHC) antigen-expressing cells are generally associated with the early phase of the immune response. We have studied the distribution of class II-expressing cells in developing, normal, and carious human teeth to clarify when human pulp acquires an...


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