Association of MSX1 799G>T variant with nonsyndromic cleft lip/palate in South Indian adolescent patients

International Journal of Paediatric Dentistry

Volumn 22, Issue 3, 2012, Pages 228-231

  Singh, Varun P ^a   Ramu, Dinesh ^b  

^a B P KOIRALA INSTITUTE OF HEALTH SCIENCES   (Nepal)

^b DAPM RV Dental College and Hospital   (India)

Author keywords

[No Author keywords available]

Indexed keywords

GUANINE; MSX1 PROTEIN, HUMAN; THYMINE; TRANSCRIPTION FACTOR MSX1;

ADOLESCENT; ARTICLE; BASE PAIRING; CHROMOSOME MAP; CLEFT LIP; CLEFT PALATE; DNA SEQUENCE; GENETIC MARKER; GENETIC VARIABILITY; GENETICS; HUMAN; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

ADOLESCENT; BASE PAIRING; CHROMOSOME MAPPING; CLEFT LIP; CLEFT PALATE; GENETIC MARKERS; GENETIC VARIATION; GUANINE; HUMANS; MSX1 TRANSCRIPTION FACTOR; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; SEQUENCE ANALYSIS, DNA; THYMINE;

EID: 84859145246     PISSN: 09607439     EISSN: 1365263X     Source Type: Journal    
DOI: 10.1111/j.1365-263X.2011.01184.x     Document Type: Article

References (15)

1. Morkuniene A, Steponaviciute D, Ambrozaityte L, Utkus A, Linkeviciane L, Kucinskas V. TGFA, TGFB3, GABRB3, RARA and BCL3 loci associated with nonsyndromic orofacial clefts? A Lithuanian study. Biologija 2007; 18: 1-6.
2. Wong FK, Hagg U. An update on the aetiology of orofacial clefts. Hong Kong Med J 2004; 10: 331-336.
3. Lace B, Vasijeva I, Dundure I, Barkane I, Akota I, Krumina A. Mutation analysis of the MSX1 gene exons and intron in patients a nonsyndromic cleft lip and palate. Stomatologija 2006; 8: 21-24.
4. Tongkobpetch S, Siriwan P, Shotelersuk V. MSX1 mutations contribute to non syndromic cleft lip in a Thai population. J Hum Genet 2006; 51: 671-676.
5. Mitchell L, Beaty TH, Lidral AC et al. Guidelines for the design and analysis of studies on nonsyndromic cleft lip and cleft palate in humans: summary report from a workshop of the international consortium for oral clefts Genetics. Cleft Palate Craniofac J 2002; 39: 274-278.
6. Khoury MJ, Flanders WD. Nontraditional epidemiologic approaches in the analysis of gene-environment interaction: case-control studies with no controls! Am J Epidemiol 1996; 144: 207-213.
7. Chang H, Yen S, Kim RE. Genetic analysis of the mammalian transforming growth factor- Beta superfamily. Endocr Rev 2002; 23: 787-823.
8. Suzuki Y, Jezewski P, Machida J et al. In a Vietnamese population, MSX1 variants contribute to cleft lip and palate. Genet Med 2004; 6: 117-125.
9. Satakata I, Maas R. MSX1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nat Genet 1994; 6: 348-356.
10. Kaartinen V. Abnormal lung development and cleft palate in mice lacking TGF-Beta 3 indicates defects of epithelial-mesenchymal interaction. Nat Genet 1995; 11: 415-421.
11. Shapira Y, Lubit E, Kuftinec M, Stom D. Hypodontia in children with various types of clefts. Angle Orthod 2000; 709: 16-21.
12. Lidral AC, Romitti PA, Basart AM et al. Association of MSX1 and TGFB3 with nonsyndromic clefting in humans. Am J Hum Genet 1998; 63: 557-568.
13. Suazo J, Santos MJ, Carreno H, Jara L, Blanco R. Linkage disequilibrium between MSX1 and nonsyndromic cleft lip/palate in the Chilean population. J Dent Res 2004; 83: 782-785.
14. Lidral AC, Romitti PA, Basart AM. Studies of the candidate genes TGFB2, MSX1, TGFA and TGFB3 in the etiology of cleft lip and palate in the Philippines. Cleft Palate Craniofa J 1997; 34: 557-568.
15. Jagomägi T, Nikopensius T, Krjutskov K et al. MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate. Eur J Oral Sci 2010; 118: 213-220.