-
1
-
-
0037388133
-
Mineralized tissue and vertebrate evolution: The secretory calcium-binding phosphoprotein gene cluster
-
Kawasaki K, Weiss KM., Mineralized tissue and vertebrate evolution: the secretory calcium-binding phosphoprotein gene cluster. Proc Natl Acad Sci U S A. 2003; 100: 4060-5.
-
(2003)
Proc Natl Acad Sci U S A.
, vol.100
, pp. 4060-4065
-
-
Kawasaki, K.1
Weiss, K.M.2
-
2
-
-
0034332613
-
Novel consensus sequence for the Golgi apparatus casein kinase, revealed using proline-rich protein-1 (PRP1)-derived peptide substrates
-
Brunati AM, Marin O, Bisinella A, Salviati A, Pinna LA., Novel consensus sequence for the Golgi apparatus casein kinase, revealed using proline-rich protein-1 (PRP1)-derived peptide substrates. Biochem J. 2000; 351: 765-8.
-
(2000)
Biochem J.
, vol.351
, pp. 765-768
-
-
Brunati, A.M.1
Marin, O.2
Bisinella, A.3
Salviati, A.4
Pinna, L.A.5
-
3
-
-
84861658918
-
Secreted kinase phosphorylates extracellular proteins that regulate biomineralization
-
Tagliabracci VS, Engel JL, Wen J, Wiley SE, Worby CA, Kinch LN, Xiao J, Grishin NV, Dixon JE., Secreted kinase phosphorylates extracellular proteins that regulate biomineralization. Science. 2012; 336: 1150-3.
-
(2012)
Science.
, vol.336
, pp. 1150-1153
-
-
Tagliabracci, V.S.1
Engel, J.L.2
Wen, J.3
Wiley, S.E.4
Worby, C.A.5
Kinch, L.N.6
Xiao, J.7
Grishin, N.V.8
Dixon, J.E.9
-
4
-
-
35348873113
-
Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development
-
Simpson MA, Hsu R, Keir LS, Hao J, Sivapalan G, Ernst LM, Zackai EH, Al-Gazali LI, Hulskamp G, Kingston HM, Prescott TE, Ion A, Patton MA, Murday V, George A, Crosby AH., Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development. Am J Hum Genet. 2007; 81: 906-12.
-
(2007)
Am J Hum Genet.
, vol.81
, pp. 906-912
-
-
Simpson, M.A.1
Hsu, R.2
Keir, L.S.3
Hao, J.4
Sivapalan, G.5
Ernst, L.M.6
Zackai, E.H.7
Al-Gazali, L.I.8
Hulskamp, G.9
Kingston, H.M.10
Prescott, T.E.11
Ion, A.12
Patton, M.A.13
Murday, V.14
George, A.15
Crosby, A.H.16
-
5
-
-
33750454816
-
Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism
-
Feng JQ, Ward LM, Liu S, Lu Y, Xie Y, Yuan B, Yu X, Rauch F, Davis SI, Zhang S, Rios H, Drezner MK, Quarles LD, Bonewald LF, White KE., Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism. Nat Genet. 2006; 38: 1310-5.
-
(2006)
Nat Genet.
, vol.38
, pp. 1310-1315
-
-
Feng, J.Q.1
Ward, L.M.2
Liu, S.3
Lu, Y.4
Xie, Y.5
Yuan, B.6
Yu, X.7
Rauch, F.8
Davis, S.I.9
Zhang, S.10
Rios, H.11
Drezner, M.K.12
Quarles, L.D.13
Bonewald, L.F.14
White, K.E.15
-
6
-
-
84863698813
-
Inactivation of a novel FGF23 regulator, FAM20C, leads to hypophosphatemic rickets in mice
-
Wang X, Wang S, Li C, Gao T, Liu Y, Rangiani A, Sun Y, Hao J, George A, Lu Y, Groppe J, Yuan B, Feng JQ, Qin C., Inactivation of a novel FGF23 regulator, FAM20C, leads to hypophosphatemic rickets in mice. PLoS Genet. 2012; 8: e1002708.
-
(2012)
PLoS Genet.
, vol.8
-
-
Wang, X.1
Wang, S.2
Li, C.3
Gao, T.4
Liu, Y.5
Rangiani, A.6
Sun, Y.7
Hao, J.8
George, A.9
Lu, Y.10
Groppe, J.11
Yuan, B.12
Feng, J.Q.13
Qin, C.14
-
8
-
-
0033617953
-
The structural biology of the developing dental enamel matrix
-
Fincham AG, Moradian-Oldak J, Simmer JP., The structural biology of the developing dental enamel matrix. J Struct Biol. 1999; 126: 270-99.
-
(1999)
J Struct Biol.
, vol.126
, pp. 270-299
-
-
Fincham, A.G.1
Moradian-Oldak, J.2
Simmer, J.P.3
-
9
-
-
34247182737
-
Validation of amelogenesis imperfecta inferred from amelogenin evolution
-
Delgado S, Ishiyama M, Sire JY., Validation of amelogenesis imperfecta inferred from amelogenin evolution. J Dent Res. 2007; 86: 326-30.
-
(2007)
J Dent Res.
, vol.86
, pp. 326-330
-
-
Delgado, S.1
Ishiyama, M.2
Sire, J.Y.3
-
10
-
-
72449159548
-
Evolutionary analysis of mammalian enamelin, the largest enamel protein, supports a crucial role for the 32-kDa peptide and reveals selective adaptation in rodents and primates
-
Al-Hashimi N, Sire JY, Delgado S., Evolutionary analysis of mammalian enamelin, the largest enamel protein, supports a crucial role for the 32-kDa peptide and reveals selective adaptation in rodents and primates. J Mol Evol. 2009; 69: 635-56.
-
(2009)
J Mol Evol.
, vol.69
, pp. 635-656
-
-
Al-Hashimi, N.1
Sire, J.Y.2
Delgado, S.3
-
11
-
-
77953775520
-
Altered enamelin phosphorylation site causes amelogenesis imperfecta
-
Chan HC, Mai L, Oikonomopoulou A, Chan HL, Richardson AS, Wang SK, Simmer JP, Hu JC., Altered enamelin phosphorylation site causes amelogenesis imperfecta. J Dent Res. 2010; 89: 695-9.
-
(2010)
J Dent Res.
, vol.89
, pp. 695-699
-
-
Chan, H.C.1
Mai, L.2
Oikonomopoulou, A.3
Chan, H.L.4
Richardson, A.S.5
Wang, S.K.6
Simmer, J.P.7
Hu, J.C.8
-
12
-
-
0028222888
-
Isolation and characterization of a mouse amelogenin expressed in Escherichia coli
-
Simmer JP, Lau EC, Hu CC, Aoba T, Lacey M, Nelson D, Zeichner-David M, Snead ML, Slavkin HC, Fincham AG., Isolation and characterization of a mouse amelogenin expressed in Escherichia coli. Calcif Tissue Int. 1994; 54: 312-9.
-
(1994)
Calcif Tissue Int.
, vol.54
, pp. 312-319
-
-
Simmer, J.P.1
Lau, E.C.2
Hu, C.C.3
Aoba, T.4
Lacey, M.5
Nelson, D.6
Zeichner-David, M.7
Snead, M.L.8
Slavkin, H.C.9
Fincham, A.G.10
-
13
-
-
47249134998
-
Porcine dentin sialophosphoprotein: Length polymorphisms, glycosylation, phosphorylation, and stability
-
Yamakoshi Y, Lu Y, Hu JC, Kim JW, Iwata T, Kobayashi K, Nagano T, Yamakoshi F, Hu Y, Fukae M, Simmer JP., Porcine dentin sialophosphoprotein: length polymorphisms, glycosylation, phosphorylation, and stability. J Biol Chem. 2008; 283: 14835-44.
-
(2008)
J Biol Chem.
, vol.283
, pp. 14835-14844
-
-
Yamakoshi, Y.1
Lu, Y.2
Hu, J.C.3
Kim, J.W.4
Iwata, T.5
Kobayashi, K.6
Nagano, T.7
Yamakoshi, F.8
Hu, Y.9
Fukae, M.10
Simmer, J.P.11
-
14
-
-
0033278065
-
Characterization of recombinant pig enamelysin activity and cleavage of recombinant pig and mouse amelogenins
-
Ryu OH, Fincham AG, Hu CC, Zhang C, Qian Q, Bartlett JD, Simmer JP., Characterization of recombinant pig enamelysin activity and cleavage of recombinant pig and mouse amelogenins. J Dent Res. 1999; 78: 743-50.
-
(1999)
J Dent Res.
, vol.78
, pp. 743-750
-
-
Ryu, O.H.1
Fincham, A.G.2
Hu, C.C.3
Zhang, C.4
Qian, Q.5
Bartlett, J.D.6
Simmer, J.P.7
-
15
-
-
25444456098
-
FAM20: An evolutionarily conserved family of secreted proteins expressed in hematopoietic cells
-
Nalbant D, Youn H, Nalbant SI, Sharma S, Cobos E, Beale EG, Du Y, Williams SC., FAM20: an evolutionarily conserved family of secreted proteins expressed in hematopoietic cells. BMC Genomics. 2005; 6: 11.
-
(2005)
BMC Genomics.
, vol.6
, pp. 11
-
-
Nalbant, D.1
Youn, H.2
Nalbant, S.I.3
Sharma, S.4
Cobos, E.5
Beale, E.G.6
Du, Y.7
Williams, S.C.8
-
16
-
-
84865021971
-
The Raine syndrome protein FAM20C is a Golgi kinase that phosphorylates bio-mineralization proteins
-
Ishikawa HO, Xu A, Ogura E, Manning G, Irvine KD., The Raine syndrome protein FAM20C is a Golgi kinase that phosphorylates bio-mineralization proteins. PLoS One. 2012; 7: e42988.
-
(2012)
PLoS One.
, vol.7
-
-
Ishikawa, H.O.1
Xu, A.2
Ogura, E.3
Manning, G.4
Irvine, K.D.5
-
17
-
-
79955836955
-
Whole-exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome
-
O'Sullivan J, Bitu CC, Daly SB, Urquhart JE, Barron MJ, Bhaskar SS, Martelli-Júnior H, dos Santos Neto PE, Mansilla MA, Murray JC, Coletta RD, Black GC, Dixon MJ., Whole-exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome. Am J Hum Genet. 2011; 88: 616-20.
-
(2011)
Am J Hum Genet.
, vol.88
, pp. 616-620
-
-
O'Sullivan, J.1
Bitu, C.C.2
Daly, S.B.3
Urquhart, J.E.4
Barron, M.J.5
Bhaskar, S.S.6
Martelli-Júnior, H.7
Dos Santos Neto, P.E.8
Mansilla, M.A.9
Murray, J.C.10
Coletta, R.D.11
Black, G.C.12
Dixon, M.J.13
-
18
-
-
84874098001
-
FAM20A mutations can cause enamel-renal syndrome (ERS)
-
Wang SK, Aref P, Hu Y, Milkovich RN, Simmer JP, El-Khateeb M, Daggag H, Baqain ZH, Hu JC., FAM20A mutations can cause enamel-renal syndrome (ERS). PLoS Genet. 2013; 9: e1003302.
-
(2013)
PLoS Genet.
, vol.9
-
-
Wang, S.K.1
Aref, P.2
Hu, Y.3
Milkovich, R.N.4
Simmer, J.P.5
El-Khateeb, M.6
Daggag, H.7
Baqain, Z.H.8
Hu, J.C.9
-
19
-
-
84875969039
-
EXTL2, a member of EXT family of tumor suppressors, controls glycosaminoglycan biosynthesis in a xylose kinase-dependent manner
-
Nadanaka S, Zhou S, Kagiyama S, Shoji N, Sugahara K, Sugihara K, Asano M, Kitagawa H., EXTL2, a member of EXT family of tumor suppressors, controls glycosaminoglycan biosynthesis in a xylose kinase-dependent manner. J Biol Chem. 2013; 288: 9321-3.
-
(2013)
J Biol Chem.
, vol.288
, pp. 9321-9323
-
-
Nadanaka, S.1
Zhou, S.2
Kagiyama, S.3
Shoji, N.4
Sugahara, K.5
Sugihara, K.6
Asano, M.7
Kitagawa, H.8
-
20
-
-
0034283572
-
Purification of Golgi casein kinase from bovine milk
-
Duncan JS, Wilkinson MC, Burgoyne RD., Purification of Golgi casein kinase from bovine milk. Biochem J. 2000; 350 (Pt 2): 463-8.
-
(2000)
Biochem J.
, vol.350
, Issue.PART 2
, pp. 463-468
-
-
Duncan, J.S.1
Wilkinson, M.C.2
Burgoyne, R.D.3
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