| [1] |
Nalbant D, Youn H, Nalbant SI, et al.FAM20: an evolutionarily conserved family of secreted proteins expressed in hematopoietic cells[J].[J].BMC Genomics, 2005, 6(1):11-21
|
| [2] |
Cui J, Xiao J, Tagliabracci VS, et al.A secretory kinase complex regulates extracellular protein phosphorylation[J][J].Elife, 2015, 1(4):e06120-e06130
|
| [3] |
Jaureguiberry G,De la Dure-Molla M, Parry D, Quentric M, Himmerkus, N, Koike T. et al..Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations[J][J].Nephron Physiol., 2012, 122(1-2):1-6
|
| [4] |
Ooya K, Nalbandian J, Noikura T.Autosomal recessive rough hypoplastic amelogenesis imperfecta: a case report with clinical,light microscopic,radiographic,and electron microscopic observations[J][J].Oral surgery, oral medicine, oral pathology, 1988, 65(4):449-458
|
| [5] |
Martelli-Júnior H, Bonan P R F, dos Santos L A N, et al.Case reports of a new syndrome associating gingival fibromatosis and dental abnormalities in a consanguineous family[J][J].Journal of periodontology, 2008, 79(7):1287-1296
|
| [6] |
Muriel de la Dure-Molla M, Quentric M, Yamaguti P M, et al.Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations[J][J].Orphanet journal of rare diseases, 2014, 9(1):84-90
|
| [7] |
Piranit Nik Kantaputra, Chotika Bongkochwilawan, Mark Lubinsky, et al.Periodontal disease and FAM20A mutations[J] [J]. Journal of Human Genetics, 2017, 62(7):679-686
|
| [8] |
James O’Sullivan, Carolina C, Bitu, Sarah B. Daly, et al..Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome[J][J].The American Journal of Human Genet, 2011, 88(5):616-620
|
| [9] |
Wang X, Wang S, Li C, et al.Inactivation of a novel FGF23 regulator,FAM20C,leads to hypophosphatemic rickets in mice[J][J].PLoS Genet, 2012, 8(5):e1002708-E1002710
|
| [10] |
Wang X, Wang S, Lu Y, et al.FAM20C plays an essential role in the formation of murine teeth[J] [J].J Biol Chem, 2012, 287(43):35934-35942
|
| [11] |
Simpson MA, Hsu R, Keir LS, et al.Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development[J][J].Am J Hum Genet, 2007, 81(5):906-912
|
| [12] |
Ababneh FK, AlSwaid A, Youssef T, et al.Hereditary deletion of the entire FAM20C gene in a patient with Raine syndrome[J] [J]. Am J Med Genet A , 2013, 161A(12):3155-3160
|
| [13] |
Takeyari S, Yamamoto T, Kinoshita Y, et al.Hypophosphatemic osteomalacia and bone sclerosis caused by a novel homozygous mutation of the FAM20C gene in an elderly man with a mild variant of Raine syndrome[J] [J].Bone, 2014, 67(oct):56-62
|
| [14] |
Simpson MA, Scheuerle A, Hurst J, et al.Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia[J][J].Clin Genet, 2009, 75(3):271-276
|
| [15] |
Li-Li Li, Pei-Hong Liu, Xiao-Hua Xie，et al.Loss of epithelial FAM20A in mice causes amelogenesis imperfecta, tooth eruption delay and gingival overgrowth[J][J].International Journal of Oral Science , 2016, 8(2):98-109
|
| [16] |
Weinberg MA, Bral M.Laboratory animal models in periodontology[J][J].J Clin Periodontol, 1999, 26(6):335-340
|
| [17] |
Qiao B, Gopalan V, Chen Z, et al.Epithelial-mesenchymal transition and mesenchymal-epithelial transition are essential for the acquisition of stem cell properties in hTERT-immortalised oral epithelial cells[J][J].Biol Cell, 2012, 104(8):476-489
|
