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219 related items for PubMed ID: 16998816
1. Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test. Juriloff DM, Harris MJ, McMahon AP, Carroll TJ, Lidral AC. Birth Defects Res A Clin Mol Teratol; 2006 Aug; 76(8):574-9. PubMed ID: 16998816 [Abstract] [Full Text] [Related]
2. The clf2 gene has an epigenetic role in the multifactorial etiology of cleft lip and palate in the A/WySn mouse strain. Plamondon JA, Harris MJ, Mager DL, Gagnier L, Juriloff DM. Birth Defects Res A Clin Mol Teratol; 2011 Aug; 91(8):716-27. PubMed ID: 21384535 [Abstract] [Full Text] [Related]
3. Investigations of the genomic region that contains the clf1 mutation, a causal gene in multifactorial cleft lip and palate in mice. Juriloff DM, Harris MJ, Dewell SL, Brown CJ, Mager DL, Gagnier L, Mah DG. Birth Defects Res A Clin Mol Teratol; 2005 Feb; 73(2):103-13. PubMed ID: 15690355 [Abstract] [Full Text] [Related]
4. Epigenetic mechanism causes Wnt9b deficiency and nonsyndromic cleft lip and palate in the A/WySn mouse strain. Juriloff DM, Harris MJ, Mager DL, Gagnier L. Birth Defects Res A Clin Mol Teratol; 2014 Oct; 100(10):772-88. PubMed ID: 25257647 [Abstract] [Full Text] [Related]
5. A digenic cause of cleft lip in A-strain mice and definition of candidate genes for the two loci. Juriloff DM, Harris MJ, Dewell SL. Birth Defects Res A Clin Mol Teratol; 2004 Aug; 70(8):509-18. PubMed ID: 15329828 [Abstract] [Full Text] [Related]
6. Genetic analysis of the construction of the AEJ.A congenic strain indicates that nonsyndromic CL(P) in the mouse is caused by two loci with epistatic interaction. Juriloff DM. J Craniofac Genet Dev Biol; 1995 Aug; 15(1):1-12. PubMed ID: 7601909 [Abstract] [Full Text] [Related]
7. The major locus for multifactorial nonsyndromic cleft lip maps to mouse chromosome 11. Juriloff DM, Mah DG. Mamm Genome; 1995 Feb; 6(2):63-9. PubMed ID: 7767007 [Abstract] [Full Text] [Related]
8. Unravelling the complex genetics of cleft lip in the mouse model. Juriloff DM, Harris MJ, Brown CJ. Mamm Genome; 2001 Jun; 12(6):426-35. PubMed ID: 11353389 [Abstract] [Full Text] [Related]
9. Mouse genetic models of cleft lip with or without cleft palate. Juriloff DM, Harris MJ. Birth Defects Res A Clin Mol Teratol; 2008 Feb; 82(2):63-77. PubMed ID: 18181213 [Abstract] [Full Text] [Related]
10. Nonlinear gene expression-phenotype relationships contribute to variation and clefting in the A/WySn mouse. Green RM, Leach CL, Diewert VM, Aponte JD, Schmidt EJ, Cheverud JM, Roseman CC, Young NM, Marcucio RS, Hallgrimsson B. Dev Dyn; 2019 Dec; 248(12):1232-1242. PubMed ID: 31469941 [Abstract] [Full Text] [Related]
11. Studies with Wnt genes and nonsyndromic cleft lip and palate. Menezes R, Letra A, Kim AH, Küchler EC, Day A, Tannure PN, Gomes da Motta L, Paiva KB, Granjeiro JM, Vieira AR. Birth Defects Res A Clin Mol Teratol; 2010 Nov; 88(11):995-1000. PubMed ID: 20890934 [Abstract] [Full Text] [Related]
12. Association of WNT9B Gene Polymorphisms With Nonsyndromic Cleft Lip With or Without Cleft Palate in Brazilian Nuclear Families. Fontoura C, Silva RM, Granjeiro JM, Letra A. Cleft Palate Craniofac J; 2015 Jan; 52(1):44-8. PubMed ID: 24437584 [Abstract] [Full Text] [Related]
13. Expression of Wnt9b and activation of canonical Wnt signaling during midfacial morphogenesis in mice. Lan Y, Ryan RC, Zhang Z, Bullard SA, Bush JO, Maltby KM, Lidral AC, Jiang R. Dev Dyn; 2006 May; 235(5):1448-54. PubMed ID: 16496313 [Abstract] [Full Text] [Related]
14. Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate. Chiquet BT, Blanton SH, Burt A, Ma D, Stal S, Mulliken JB, Hecht JT. Hum Mol Genet; 2008 Jul 15; 17(14):2212-8. PubMed ID: 18413325 [Abstract] [Full Text] [Related]
15. Major gene determination of liability to spontaneous cleft lip in the mouse. Biddle FG, Fraser FC. J Craniofac Genet Dev Biol Suppl; 1986 Jul 15; 2():67-88. PubMed ID: 3491126 [Abstract] [Full Text] [Related]
16. Phenotypic and molecular analyses of A/WySn mice. Gong SG. Cleft Palate Craniofac J; 2001 Sep 15; 38(5):486-91. PubMed ID: 11522170 [Abstract] [Full Text] [Related]
17. Phenotypic variability and craniofacial dysmorphology: increased shape variance in a mouse model for cleft lip. Parsons TE, Kristensen E, Hornung L, Diewert VM, Boyd SK, German RZ, Hallgrímsson B. J Anat; 2008 Feb 15; 212(2):135-43. PubMed ID: 18093101 [Abstract] [Full Text] [Related]
18. A comparative study of development during primary palate formation in A/WySn, C57BL/6, and their F1 crosses. Ciriani D, Diewert VM. J Craniofac Genet Dev Biol; 1986 Feb 15; 6(4):369-77. PubMed ID: 3793861 [Abstract] [Full Text] [Related]
19. Accumulation of rare coding variants in genes implicated in risk of human cleft lip with or without cleft palate. Marini NJ, Asrani K, Yang W, Rine J, Shaw GM. Am J Med Genet A; 2019 Jul 15; 179(7):1260-1269. PubMed ID: 31063268 [Abstract] [Full Text] [Related]
20. Mutation analysis of the MSX1 gene exons and intron in patients with nonsyndromic cleft lip and palate. Lace B, Vasiljeva I, Dundure I, Barkane B, Akota I, Krumina A. Stomatologija; 2006 Jul 15; 8(1):21-4. PubMed ID: 16687911 [Abstract] [Full Text] [Related] Page: [Next] [New Search]