The impact of molecular genetics on oral health paradigms

Critical Reviews in Oral Biology and Medicine

Volumn 11, Issue 1, 2000, Pages 26-56

  Hart, T C ^a,b   Marazita, M L ^b   Wright, J T ^c  

^a WAKE FOREST SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF PITTSBURGH   (United States)

^c UNIVERSITY OF NORTH CAROLINA   (United States)

Author keywords

Complex disease traits; Human Genome Project; Mendelian disease traits; Molecular genetics; Oral medicine

Indexed keywords

CHROMOSOMAL LOCALIZATION; CLEFT LIP; CLEFT PALATE; CRANIOFACIAL SYNOSTOSIS; DISEASE ASSOCIATION; GENETIC DISORDER; HEALTH CARE; HUMAN; MEDICAL GENETICS; MOLECULAR GENETICS; MOUTH CARCINOMA; PERIODONTAL DISEASE; PRIORITY JOURNAL; PROPHYLAXIS; REVIEW; STOMATOLOGY;

EID: 0033967927     PISSN: 10454411     EISSN: None     Source Type: Journal    
DOI: 10.1177/10454411000110010201     Document Type: Review

References (46)

1. Aberdam D, Aguzzi A, Baudoin C, Galliano M-F, Ortonne J-P, Meneguzzi G (1994). Developmental expression of nicein adhesionprotein (laminin-5) subunits suggests multiple morphogenic roles. Cell Adhes Commun 2:115-129.
2. Aldred MJ, Crawford PJM (1995). Amelogenesis imperfecta towards a new classification. Oral Dis 1:2-5.
3. Aldred M, Crawford P, Roberts E, Gillespie C, Thomas N, Fenton I, et al. (1992a). Genetic heterogeneity in X-linked amelogenesis imperfecta. Genomics 14:567-573.
4. Aldred MJ, Crawford PJM, Roberts E, Thomas NST (1992b). Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1). Hum Genet 90:413-416.
5. Anderson DC, Schmalstieg FC, Finegold MJ, Hughes BJ, Rothlein R, Miller LJ, et al. (1985). The severe and moderate phenotypes of heritable Mac-1, LFA-1 deficiency: their quantitative definition and relation to leukocyte dysfunction and clinical features. J Infect Dis 152:668-689.
6. Anonymous (1994). Examinations for oral cancer - United States, 1992. Morbid Mortal Weekly Rept 43:198-200.
7. Aplin HM, Hirst KL, Crosby AH. Dixon MJ (1995). Mapping of the human dentin matrix phosphoprotein gene (DMP1) to the dentinogenesis imperfecta type II critical region at chromosome 4q21. Genomics 30:347-349.
8. Ardinger HH, Buetow KH, Bell GI, Bardach J, VanDemark DR, Murray JC (1989). Association of genetic variation of the transforming growth factor alpha gene with cleft lip and palate. Am J Hum Genet 45:348-353.
9. Atula S, Auvinen E, Grenman R, Syrjanen S (1997). Human papillomavirus and Epstein-Barr virus in epithelial carcinomas of the head and neck region. Anticancer Res 17:4427-4433.
10. Axelsson P, Paulander J, Lindhe J (1998). Relationship between smoking and dental status in 35-, 50-, 65-, and 75-year-old individuals. J Clin Periodontol 25:297-305.
11. Backman B, Holm A (1986). Amelogenesis imperfecta: prevalence and incidence in a northern Swedish county. Community Dent Oral Epidemiol 14:43-47.
12. Backman B, Holmgren G (1988). Amelogenesis imperfecta: a genetic study. Hum Hered 38:189-206.
13. Backman B, Forsman K, Lind L, Westermark E, Holmgren G (1995). One gene for autosomal dominant amelogenesis imperfecta (ADAI) is localized to chromosome 4q (abstract). Connect Tissue Res 32:314.
14. Ball SP, Cook PJ, Mars M, Buckton KE (1982). Linkage between dentinogenesis imperfecta and Gc. Ann Hum Genet 46:35-40.
15. Bartlett JD, Simmer JP, Xue J, Margolis HC, Moreno EC (1996). Molecular cloning and mRNA tissue distribution of a novel matrix metalloproteinase isolated from porcine enamel organ. Gene 183:123-128.
16. Beck JD, Koch GG, Rozier RG, Tudor GE (1990). Prevalence and risk indicators for periodontal attachment loss in a population of older community-dwelling blacks and whites. J Periodontol 61:521-528.
17. Beiraghi S, Foroud T, Diouhy S, Bixler D, Conneally PM, Delozier-Blanchet D, et al. (1994). Possible location of a major gene for cleft lip and palate to 4q. Clin Genet 46:255-256.
18. Bell J (1998). The new genetics: the new genetics in clinical practice. Br Med J 316:618-620.
19. Blanton SH, Crowder E, Malcolm S, Winter R, Gasser DL, Stal S, et al. (1996). Exclusion of linkage between cleft lip with or without cleft palate and markers on chromosomes 4 and 6. Am J Hum Genet 58:239-241.
20. Bongers V, Braakhuis BJ, Tobi H, Lubsen H, Snow GB (1996). The relation between cancer incidence among relatives and the occurrence of multiple primary carcinomas following head and neck cancer. Cancer Epidemiol Biomark Prev 5:595-598.
21. Bozzo L, de Almedia OP, Scully C, Aldred MI (1994). Hereditary gingival fibromatosis. Report of an extensive four-generation pedigree. Oral Surg Oral Med Oral Pathol 78:452-454.
22. Brennan JA, Mao L, Hruban RH, Boyle JO, Eby YJ, Koch WM, et al. (1995a). Molecular assessment of histopathological staging in squamous-cell carcinoma of the head and neck. N Engl J Med 332:429-435.
23. Brennan JA, Boyle JO, Koch WM, Goodman SN, Hruban RH, Eby YJ, et al. (1995b). Association between cigarette smoking and mutation of the p53 gene in squamous-cell carcinoma of the head and neck. N Engl J Med 332:712-717.
24. Bruckner RJ, Rickles NH, Porter DR (1962). Hypophosphatasia with premature shedding of teeth and aplasia of cementum. Oral Surg 15:1351-1369.
25. Byers PH (1994). Ehlers-Danlos syndrome: recent advances and current understanding of the clinical and genetic heterogeneity. J Invest Dermatol 103:47-52.
26. Byers PH, Chessler SD, Starman BJ, Willing MC, Wallis GA, Kadler K, et al. (1992). Molecular basis of osteogenesis imperfecta. In: The chemistry and biology of mineralized tissues. Amsterdam: Elsevier Science Publ., pp. 427-432.
27. Califano J, van der Riet P, Westra W, Nawroz H, Clayman G, Piantadosi S, et al. (1996). Genetic progression model for head and neck cancer: implications for field cancerization. Cancer Res 56:2488-2492.
28. Carinci F, Pezzetti F, Scapoli L, Padula E, Baciliero U, Curioni C, et al. (1995). Nonsyndromic cleft lip and palate: evidence of linkage to a microsatellite marker on 6p23. Am J Hum Genet 56:337-339.
29. Carter CO (1976). Genetics of common single malformations. Br Med Bull 32:21-26.
30. Carter CO, Evans K, Coffey R, Roberts JAF, Buck A, Roberts MJ (1982). A three generation family study of cleft lip with or without cleft palate. J Med Genet 19:246-261.
31. Chenevix-Trench G, Jones J, Green A, Duffy DL, Martin N (1992). Cleft lip with or without cleft palate: associations with transforming growth factor-alpha and retinoic acid receptor loci. Am J Hum Genet 51:1377-1385.
32. Christensen K, Schmidt MM, Vaeth M, Olsen J (1995). Absence of an environmental effect on the recurrence of facial-cleft defects. N Engl J Med 333:161-164.
33. Christersson LA, Grossi SG, Dunford RG, Machtei EE, Genco RJ (1992). Dental plaque and calculus: risk indicators for their formation. J Dent Res 71:1425-1430.
34. Chung CS, Bixler D, Watanabe T, Koguchi H, Fogh-Andersen P (1986). Segregation analysis of cleft lip with or without cleft palate: a comparison of Danish and Japanese data. Am J Hum Genet 39:603-611.
35. Cloos J, Spitz MR, Schantz SR Hsu TC, Zhang ZF, Tobi H, et al. (1996). Genetic susceptibility to head and neck squamous cell carcinoma. J Natl Cancer Inst 88:530-535.
36. Cohen MM Jr (1986). Craniosynostosis: diagnosis, evaluation, and management. New York: Raven Press, pp. 413-590.
37. Cohen MM Jr (1993a). Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis. Am J Med Genet 45:300-307.
38. Cohen MM Jr (1993b). Sutural biology and the correlates of craniosynostosis. Am J Med Genet 47:581-616.
39. Collier PM, Sauk JJ, Rosenbloom J, Yuan ZA, Gibson CW (1997). An amelogenin gene defect associated with human X-linked amelogenesis imperfecta. Arch Oral Biol 42:235-242.
40. Collins FS, Patrinos A, Jordan E, Chakravarti A, Gesteland R, Walters L (1998). New goals for the U.S. human genome project: 1998-2003. Science 282:682-689.
41. Conry JP, Messer LB, Boraas JC, Aeppli DP, Bouchard TJ Jr (1993). Dental caries and treatment characteristics in human twins reared apart. Arch Oral Biol 38:937-943.
42. Crawford PJM, Aldred MJ (1990). Amelogenesis imperfecta with taurodontism and the tricho-dento-osseous syndrome: separate conditions or a spectrum of disease? Clin Genet 38:44-50.
43. Crosby AH, Scherpbier-Heddema T, Wijmenga C, Altherr MR, Murray JC, Buetow KH. et al. (1995). Genetic mapping of the dentinogenesis imperfecta type II locus. Am J Hum Genet 57:832-839.
44. Daly AK, Cholerston S, Gregory W, Idle JR (1993). Metabolic polymorphisms. Pharmacol Ther 57:129-160.
45. Day GL, Blot WJ, Austin DF, Bernstein L, Greenberg RS, Preston-Martin S (1993). Racial differences in risk of oral and pharyngeal cancer: alcohol, tobacco, and other determinants. J Natl Cancer Inst 85:465-473.
46. Dean JA, Hartsfield JK Jr, Wright JT, Casada JC, Hart TC (1997). Genetic linkage of dentin dysplasia Type II to chromosome 4q13. J Craniofac Genet Dev Biol 17:172-177.