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Studies of genes in the FGF signaling pathway and oral clefts with or without dental anomalies.

作者信息

Menezes Renato, Letra Ariadne, Ruff Joe, Granjeiro Jose M, Vieira Alexandre R

机构信息

Department of Oral Biology, School of Dental Medicine, University of Pittsburgh 15261, USA.

出版信息

Am J Med Genet A. 2008 Jun 15;146A(12):1614-7. doi: 10.1002/ajmg.a.32341.

DOI:10.1002/ajmg.a.32341
PMID:18478591
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2643017/
Abstract
摘要

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Studies of genes in the FGF signaling pathway and oral clefts with or without dental anomalies.成纤维细胞生长因子（FGF）信号通路中的基因与伴有或不伴有牙齿异常的口腔裂隙的研究。
Am J Med Genet A. 2008 Jun 15;146A(12):1614-7. doi: 10.1002/ajmg.a.32341.
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本文引用的文献

1
A simple and cost-effective protocol for DNA isolation from buccal epithelial cells.一种从颊上皮细胞中分离DNA的简单且经济高效的方法。
Braz Dent J. 2007;18(2):148-52. doi: 10.1590/s0103-64402007000200012.
2
Defining subphenotypes for oral clefts based on dental development.基于牙齿发育定义口腔裂隙的亚表型。
J Dent Res. 2007 Oct;86(10):986-91. doi: 10.1177/154405910708601013.
3
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.一项全基因组关联研究确定了FGFR2基因中的等位基因与散发性绝经后乳腺癌风险相关。
Nat Genet. 2007 Jul;39(7):870-4. doi: 10.1038/ng2075. Epub 2007 May 27.
4
Genome-wide association study identifies novel breast cancer susceptibility loci.全基因组关联研究确定了新的乳腺癌易感基因座。
Nature. 2007 Jun 28;447(7148):1087-93. doi: 10.1038/nature05887.
5
Impaired FGF signaling contributes to cleft lip and palate.成纤维细胞生长因子（FGF）信号传导受损会导致唇腭裂。
Proc Natl Acad Sci U S A. 2007 Mar 13;104(11):4512-7. doi: 10.1073/pnas.0607956104. Epub 2007 Mar 6.
6
Epidemiology of Hoffmeister's "genetically determined predisposition to disturbed development of the dentition" in patients with cleft lip and palate.唇腭裂患者中霍夫迈斯特氏“牙列发育紊乱的遗传易感性”的流行病学研究
Cleft Palate Craniofac J. 2006 Jul;43(4):457-65. doi: 10.1597/04-156.1.
7
FGF signalling in craniofacial development and developmental disorders.成纤维细胞生长因子信号在颅面发育及发育障碍中的作用
Oral Dis. 2006 Mar;12(2):102-11. doi: 10.1111/j.1601-0825.2005.01176.x.
8
Taking it to the max: the genetic and developmental mechanisms coordinating midfacial morphogenesis and dysmorphology.发挥到极致：协调面中部形态发生和畸形的遗传与发育机制。
Clin Genet. 2004 Mar;65(3):163-76. doi: 10.1111/j.0009-9163.2004.00225.x.
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Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.FGFR1功能丧失性突变导致常染色体显性遗传性卡尔曼综合征。
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