박사

Genetic analysis of non-syndromic familial multiple supernumerary premolars

배두환 2018년
논문상세정보
' Genetic analysis of non-syndromic familial multiple supernumerary premolars' 의 주제별 논문영향력
논문영향력 선정 방법
논문영향력 요약
주제
  • Non-syndromic supernumerary tooth
  • PDGFRB
  • targeted exome sequencing
  • 비증후군성 다수 과잉치
동일주제 총논문수 논문피인용 총횟수 주제별 논문영향력의 평균
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' Genetic analysis of non-syndromic familial multiple supernumerary premolars' 의 참고문헌

  • Wang K, Li M, Hakonarson H: ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res 38(16): e164-e164, 2010.
  • Ulucan H, Gul D, Sapp JC, Cockerham J, Johnston JJ, Biesecker LG: Extending the spectrum of Ellis van Creveld syndrome: a large family with a mild mutation in the EVC gene. BMC Med Genet 9: 92, 2008.
  • Rajab LD, Hamdan MA: Supernumerary teeth: review of the literature and a survey of 152 cases. Int J Paediatr Dent 12(4): 244-254, 2002.
  • O'Connell M, Burrows NP, van Vlijmen-Willems MJ, Clark SM, Schalkwijk J: Tenascin-X deficiency and Ehlers-Danlos syndrome: a case report and review of the literature. Br J Dermatol 163(6): 1340-1345, 2010.
  • Nanci A: Development of the tooth and its supporting tissues. In: Ten Cate's Oral Histology-Pageburst on VitalSource: Development, Structure, and Function 7th ed. Nanci A, ed. Elsevier Health Sciences. 2007. p. 79-107.
  • McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, Kernytsky A, et al.: The Genome Analysis Toolkit: A MapReduce framework for analyzing nextgeneration DNA sequencing data. Genome Res 20(9): 1297-1303, 2010.
  • Mazzeu JF, Pardono E, Vianna-Morgante AM, Richieri-Costa A, Ae Kim C, Brunoni D, et al.: Clinical characterization of autosomal dominant and recessive variants of Robinow syndrome. Am J Med Genet A 143(4): 320-325, 2007.
  • Manrique Mora MC, Bolanos Carmona MV, Briones Lujan MT: Molarization and development of multiple supernumerary teeth in the premolar region. J Dent Child (Chic) 71(2): 171-174, 2004.
  • Maas SM, Shaw AC, Bikker H, Ludecke HJ, van der Tuin K, Badura-Stronka M, et al.: Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome. Eur J Med Genet 58(5): 279-292, 2015.
  • Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, et al.: The Sequence Alignment/Map format and SAMtools. Bioinformatics 25(16): 2078-2079, 2009.
  • Li H, Durbin R: Fast and accurate long-read alignment with Burrows–Wheeler transform. Bioinformatics 26(5): 589-595, 2010.
  • Li FF, Liu Z, Yan P, Shao X, Deng X, Sam C, et al.: Identification of a novel mutation associated with familial adenomatous polyposis and colorectal cancer. Int J Mol Med 36(4): 1046-1056, 2015.
  • Klinghoffer RA, Mueting-Nelsen PF, Faerman A, Shani M, Soriano P: The two PDGF receptors maintain conserved signaling in vivo despite divergent embryological functions. Mol Cell 7(2): 343-354, 2001.
  • Khambete N, Kumar R: Genetics and presence of non-syndromic supernumerary teeth: A mystery case report and review of literature. Contemp Clin Dent 3(4): 499- 502, 2012.
  • Kaya GS, Yapici G, Omezli MM, Dayi E: Non-syndromic supernumerary premolars. Medicina Oral Patolog a Oral y Cirugia Bucal 16(4): e522-e525, 2011.
  • Jugessur A, Farlie PG, Kilpatrick N: The genetics of isolated orofacial clefts: from genotypes to subphenotypes. Oral Dis 15(7): 437-453, 2009.
  • Hong N, Chen YH, Xie C, Xu BS, Huang H, Li X, et al.: Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing. J Zhejiang Univ Sci B 15(8): 727-734, 2014.
  • Hellstrom M, Kalen M, Lindahl P, Abramsson A, Betsholtz C: Role of PDGF-B and PDGFR-beta in recruitment of vascular smooth muscle cells and pericytes during embryonic blood vessel formation in the mouse. Development 126(14): 3047-3055, 1999.
  • Galluccio G, Castellano M, La Monaca C: Genetic basis of non-syndromic anomalies of human tooth number. Arch Oral Biol 57(7): 918-930, 2012.
  • Dummett CO, JR, Thikkurissy S: Anomalies of the developing dentition. In: Pediatric dentistry: infancy through adolescence 5th ed. Casamassimo PS, Fields HW, Jr, McTigue DJ, Nowak A, eds. Elsevier Health Sciences. 2013.
  • Bufalino A, Parana ba LMR, Gouv a AF, Gueiros LA, Martelli-J nior H, Junior JJ, et al.: Cleidocranial dysplasia: oral features and genetic analysis of 11 patients. Oral Dis 18(2): 184-190, 2012.
  • Bsoul S, Terezhalmy G, Abboud H, Woodruff K, Abboud SL: PDGF BB and bFGF stimulate DNA synthesis and upregulate CSF-1 and MCP-1 gene expression in dental follicle cells. Arch Oral Biol 48(6): 459-465, 2003.
  • Aggarwal VR, Sloan P, Horner K, Macfarlane TV, Clancy T, Evans G, et al.: Dentoosseous changes as diagnostic markers in familial adenomatous polyposis families. Oral Dis 9(1): 29-33, 2003.