Found 2 results
Filters: Author is J.S. McDaniel  [Clear All Filters]
Y. Mu, Xu, Z., Contreras, C. I., McDaniel, J. S., Donly, K. J., and Chen, S., Phenotype characterization and sequence analysis of BMP2 and BMP4 variants in two Mexican families with oligodontia, vol. 11, pp. 4110-4120, 2012.
Aberg T, Wozney J and Thesleff I (1997). Expression patterns of bone morphogenetic proteins (Bmps) in the developing mouse tooth suggest roles in morphogenesis and cell differentiation. Dev. Dyn. 210: 383-396.<383::AID-AJA3>3.0.CO;2-C   Arte S, Nieminen P, Apajalahti S, Haavikko K, et al. (2001). Characteristics of incisor-premolar hypodontia in families. J. Dent. Res. 80: 1445-1450. PMid:11437217   Bei M, Kratochwil K and Maas RL (2000). BMP4 rescues a non-cell-autonomous function of Msx1 in tooth development. Development 127: 4711-4718. PMid:11023873   Capasso M, Ayala F, Russo R, Avvisati RA, et al. (2009). A predicted functional single-nucleotide polymorphism of bone morphogenetic protein-4 gene affects mRNA expression and shows a significant association with cutaneous melanoma in Southern Italian population. J. Cancer Res. Clin. Oncol. 135: 1799-1807. PMid:19557432   Chen S, Gluhak-Heinrich J, Martinez M, Li T, et al. (2008). Bone morphogenetic protein 2 mediates dentin sialophosphoprotein expression and odontoblast differentiation via NF-Y signaling. J. Biol. Chem. 283: 19359- 19370. PMid:18424784 PMCid:2443643   Choi JY, Shin CS, Hong YC and Kang D (2006). Single-nucleotide polymorphisms and haplotypes of bone morphogenetic protein genes and peripheral bone mineral density in young Korean men and women. Calcif. Tissue Int. 78: 203-211. PMid:16604289   Feng J, Yang G, Yuan G, Gluhak-Heinrich J, et al. (2011). Abnormalities in the enamel in bmp2-deficient mice. Cells Tissues Organs 194: 216-221. PMid:21597270 PMCid:3178081   Frazier-Bowers SA, Scott MR, Cavender A, Mensah J, et al. (2002). Mutational analysis of families affected with molar oligodontia. Connect. Tissue Res. 43: 296-300. PMid:12489173   Gabris K, Tarjan I, Csiki P, Konrad F, et al. (2001). Prevalence of congenital hypodontia in the permanent dentition and its treatment. Fogorv. Sz. 94: 137-140. PMid:11573454   Gerits A, Nieminen P, De MS and Carels C (2006). Exclusion of coding region mutations in MSX1, PAX9 and AXIN2 in eight patients with severe oligodontia phenotype. Orthod. Craniofac. Res. 9: 129-136. PMid:16918677   Gluhak-Heinrich J, Guo D, Yang W, Harris MA, et al. (2010). New roles and mechanism of action of BMP4 in postnatal tooth cytodifferentiation. Bone 46: 1533-1545. PMid:20206312 PMCid:2875306   Han D, Gong Y, Wu H, Zhang X, et al. (2008). Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis. Eur. J. Med. Genet. 51: 536-546. PMid:18657636   Kapadia H, Mues G and D'Souza R (2007). Genes affecting tooth morphogenesis. Orthod. Craniofac. Res. 10: 237-244. PMid:17973693   Kong H, Wang Y, Patel M, Mues G, et al. (2011). Regulation of bmp4 expression in odontogenic mesenchyme: from simple to complex. Cells Tissues Organs 194: 156-160. PMid:21546760 PMCid:3178073   Lammi L, Halonen K, Pirinen S, Thesleff I, et al. (2003). A missense mutation in PAX9 in a family with distinct phenotype of oligodontia. Eur. J. Hum. Genet. 11: 866-871. PMid:14571272   Lawson KA, Dunn NR, Roelen BA, Zeinstra LM, et al. (1999). Bmp4 is required for the generation of primordial germ cells in the mouse embryo. Genes Dev. 13: 424-436. PMid:10049358 PMCid:316469   Lin JY, Chen YJ, Huang YL, Tang GP, et al. (2008). Association of bone morphogenetic protein 4 gene polymorphisms with nonsyndromic cleft lip with or without cleft palate in Chinese children. DNA Cell Biol. 27: 601-605. PMid:18771417   Liu W, Dong X, Mai M, Seelan RS, et al. (2000). Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating beta-catenin/TCF signalling. Nat. Genet. 26: 146-147. PMid:11017067   Meng XL, Wang H, Yang H, Hai Y, et al. (2010). T allele at site 6007 of bone morphogenetic protein-4 gene increases genetic susceptibility to ossification of the posterior longitudinal ligament in male Chinese Han population. Chin. Med. J. 123: 2537-2542.   Nieminen P (2009). Genetic basis of tooth agenesis. J. Exp. Zool. B Mol. Dev. Evol. 312B: 320-342.   Nieminen P, Pekkanen M, Aberg T and Thesleff I (1998). A graphical www-database on gene expression in tooth. Eur. J. Oral Sci. 106: 7-11. PMid:9541196   Noor A, Windpassinger C, Vitcu I, Orlic M, et al. (2009). Oligodontia is caused by mutation in LTBP3, the gene encoding latent TGF-beta binding protein 3. Am. J. Hum. Genet. 84: 519-523. PMid:19344874 PMCid:2667979   Ramesh BL, Wilson SG, Dick IM, Islam FM, et al. (2005). Bone mass effects of a BMP4 gene polymorphism in postmenopausal women. Bone 36: 555-561. PMid:15777683   Scarel RM, Trevilatto PC, Di Hipólito O Jr, Camargo LE, et al. (2000). Absence of mutations in the homeodomain of the MSX1 gene in patients with hypodontia. Am. J. Med. Genet. 92: 346-349.<346::AID-AJMG10>3.0.CO;2-A   Schalk-van der Weide Y, Steen WH and Bosman F (1992). Distribution of missing teeth and tooth morphology in patients with oligodontia. ASDC J. Dent. Child. 59: 133-140. PMid:1583198   Schrauwen I, Thys M, Vanderstraeten K, Fransen E, et al. (2008). Association of bone morphogenetic proteins with otosclerosis. J. Bone Miner. Res. 23: 507-516. PMid:18021008 PMCid:2669162   Stockton DW, Das P, Goldenberg M, D'Souza RN, et al. (2000). Mutation of PAX9 is associated with oligodontia. Nat. Genet. 24: 18-19. PMid:10615120   Thesleff I (2003). Epithelial-mesenchymal signalling regulating tooth morphogenesis. J. Cell Sci. 116: 1647-1648. PMid:12665545   Thomadakis G, Ramoshebi LN, Crooks J, Rueger DC, et al. (1999). Immunolocalization of bone morphogenetic protein-2 and -3 and osteogenic protein-1 during murine tooth root morphogenesis and in other craniofacial structures. Eur. J. Oral Sci. 107: 368-377. PMid:10515202   Valdes AM, Hart DJ, Jones KA, Surdulescu G, et al. (2004). Association study of candidate genes for the prevalence and progression of knee osteoarthritis. Arthritis Rheum. 50: 2497-2507. PMid:15334463   Valdes AM, Van Oene M, Hart DJ, Surdulescu GL, et al. (2006). Reproducible genetic associations between candidate genes and clinical knee osteoarthritis in men and women. Arthritis Rheum. 54: 533-539. PMid:16453284   van den Boogaard MJ, Dorland M, Beemer FA and van Amstel HK (2000). MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans. Nat. Genet. 24: 342-343. PMid:10742093   Wang H, Liu D, Yang Z, Tian B, et al. (2008). Association of bone morphogenetic protein-2 gene polymorphisms with susceptibility to ossification of the posterior longitudinal ligament of the spine and its severity in Chinese patients. Eur. Spine J. 17: 956-964. PMid:18389292 PMCid:2443260   Zhang H and Bradley A (1996). Mice deficient for BMP2 are nonviable and have defects in amnion/chorion and cardiac development. Development 122: 2977-2986. PMid:8898212