Publications
Found 14 results
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“Complete mitochondrial genome of the Liuyang black goat and its phylogenetic relationship with other Caprinae”, vol. 15, p. -, 2016.
, “Complete mitochondrial genome of the Liuyang black goat and its phylogenetic relationship with other Caprinae”, vol. 15, p. -, 2016.
, “Investigating the association between XRCC1 gene polymorphisms and susceptibility to gastric cancer”, vol. 15, p. -, 2016.
, “Investigating the association between XRCC1 gene polymorphisms and susceptibility to gastric cancer”, vol. 15, p. -, 2016.
, , , “Clinical value of ultrasound-guided percutaneous biopsy of pulmonary lesions”, vol. 14, pp. 3784-3790, 2015.
, “Cloprostenol and pregnant mare serum gonadotropin promote estrus synchronization, uterine development, and follicle-stimulating hormone receptor expression in mice”, vol. 14, pp. 7184-7195, 2015.
, “Identification and characterization of the duck enteritis virus (DEV) US2 gene”, vol. 14, pp. 13779-13790, 2015.
, “Reproductive outcome of a case with familial balanced translocation t(3;6): implications for genetic counseling”, vol. 14, pp. 2809-2815, 2015.
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“Mutational analysis of AXIN2, MSX1, and PAX9 in two Mexican oligodontia families”, vol. 12, pp. 4446-4458, 2013.
, “Phenotype characterization and sequence analysis of BMP2 and BMP4 variants in two Mexican families with oligodontia”, vol. 11, pp. 4110-4120, 2012.
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Bei M, Kratochwil K and Maas RL (2000). BMP4 rescues a non-cell-autonomous function of Msx1 in tooth development. Development 127: 4711-4718.
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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.
http://dx.doi.org/10.1007/s00432-009-0628-y
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.
http://dx.doi.org/10.1074/jbc.M709492200
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.
http://dx.doi.org/10.1007/s00223-005-0139-z
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.
http://dx.doi.org/10.1159/000324644
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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.
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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.
http://dx.doi.org/10.1111/j.1601-6343.2006.00367.x
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.
http://dx.doi.org/10.1016/j.bone.2010.02.024
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.
http://dx.doi.org/10.1016/j.ejmg.2008.06.002
PMid:18657636
Kapadia H, Mues G and D'Souza R (2007). Genes affecting tooth morphogenesis. Orthod. Craniofac. Res. 10: 237-244.
http://dx.doi.org/10.1111/j.1601-6343.2007.00407.x
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.
http://dx.doi.org/10.1159/000324747
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.
http://dx.doi.org/10.1038/sj.ejhg.5201060
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.
http://dx.doi.org/10.1101/gad.13.4.424
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.
http://dx.doi.org/10.1089/dna.2008.0777
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.
http://dx.doi.org/10.1038/79859
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.
http://dx.doi.org/10.1016/j.ajhg.2009.03.007
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.
http://dx.doi.org/10.1016/j.bone.2004.12.005
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.
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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.
http://dx.doi.org/10.1359/jbmr.071112
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.
http://dx.doi.org/10.1038/71634
PMid:10615120
Thesleff I (2003). Epithelial-mesenchymal signalling regulating tooth morphogenesis. J. Cell Sci. 116: 1647-1648.
http://dx.doi.org/10.1242/jcs.00410
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.
http://dx.doi.org/10.1046/j.0909-8836.1999.eos107508.x
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.
http://dx.doi.org/10.1002/art.20443
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.
http://dx.doi.org/10.1002/art.21621
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.
http://dx.doi.org/10.1038/74155
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.
http://dx.doi.org/10.1007/s00586-008-0651-8
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