-
1
-
-
33646346351
-
Phenotypic variation in dentinogenesis imperfecta/dentin dysplasia linked to 4q21
-
Beattie, M.L., J.W. Kim, S.G. Gong, C.A. Murdock-Kinch, J.P Simmer, J.C. Hu (2006) Phenotypic variation in dentinogenesis imperfecta/dentin dysplasia linked to 4q21. J Dent Res 85: 329-333.
-
(2006)
J Dent Res
, vol.85
, pp. 329-333
-
-
Beattie, M.L.1
Kim, J.W.2
Gong, S.G.3
Murdock-Kinch, C.A.4
Simmer, J.P.5
Hu, J.C.6
-
2
-
-
11344257828
-
Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III
-
Dong, J., T. Gu, L. Jeffords, M. MacDougall (2005) Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III. Am J Med Genet A 132A: 305-309.
-
(2005)
Am J Med Genet A
, vol.132 A
, pp. 305-309
-
-
Dong, J.1
Gu, T.2
Jeffords, L.3
MacDougall, M.4
-
4
-
-
33749519573
-
Splicing site mutations in dentin sialophosphoprotein causing dentinogenesis imperfecta type II
-
Holappa, H., P. Nieminen, L. Tolva, P. Lukinmaa, S. Alaluusua (2006) Splicing site mutations in dentin sialophosphoprotein causing dentinogenesis imperfecta type II. Eur J Oral Sci 114: 381-384.
-
(2006)
Eur J Oral Sci
, vol.114
, pp. 381-384
-
-
Holappa, H.1
Nieminen, P.2
Tolva, L.3
Lukinmaa, P.4
Alaluusua, S.5
-
5
-
-
0019612201
-
The inorganic phase in dentinogenesis imperfecta
-
Kerebel, B., G. Daculsi, J. Menanteau, M. Kerebel (1981) The inorganic phase in dentinogenesis imperfecta. J Dent Res 60: 1655-1660.
-
(1981)
J Dent Res
, vol.60
, pp. 1655-1660
-
-
Kerebel, B.1
Daculsi, G.2
Menanteau, J.3
Kerebel, M.4
-
6
-
-
4344592119
-
A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II
-
Kim, J.W., S.H. Nam, K.T. Jang, S.H. Lee, C.C. Kim, S.H. Hahn, J.C. Hu, J.P. Simmer (2004) A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II. Hum Genet 115: 248-254.
-
(2004)
Hum Genet
, vol.115
, pp. 248-254
-
-
Kim, J.W.1
Nam, S.H.2
Jang, K.T.3
Lee, S.H.4
Kim, C.C.5
Hahn, S.H.6
Hu, J.C.7
Simmer, J.P.8
-
7
-
-
19944431252
-
Mutation hot spot in the DSPP gene causing dentinogenesis imperfecta type II
-
Kim, J.W, J.C. Hu, J.I. Lee, S.K. Moon, Y. J. Kim, K.T. Jang, S.H. Lee, C.C. Kim, S.H. Hahn, J.P. Simmer (2005) Mutation hot spot in the DSPP gene causing dentinogenesis imperfecta type II. Hum Genet 116: 186-191.
-
(2005)
Hum Genet
, vol.116
, pp. 186-191
-
-
Kim, J.W.1
Hu, J.C.2
Lee, J.I.3
Moon, S.K.4
Kim, Y.J.5
Jang, K.T.6
Lee, S.H.7
Kim, C.C.8
Hahn, S.H.9
Simmer, J.P.10
-
8
-
-
0035734938
-
Intrafibrilar mineral may be absent in dentinogenesis imperfecta type II (DI-II)
-
Kinney, J.H., J. Pople, C.H. Driessen, T.M. Breunig, G.W. Marshall, S.J. Marshall (2001) Intrafibrilar mineral may be absent in dentinogenesis imperfecta type II (DI-II). J Dent Res 80: 1555-1559.
-
(2001)
J Dent Res
, vol.80
, pp. 1555-1559
-
-
Kinney, J.H.1
Pople, J.2
Driessen, C.H.3
Breunig, T.M.4
Marshall, G.W.5
Marshall, S.J.6
-
9
-
-
0031021422
-
Dentin phosphoprotein and dentin sialoprotein are cleavage products expressed from a single transcript coded by a gene on human chromosome 4
-
MacDougall, M., D. Simmons, X. Luan, J. Nydegger, J. Feng, T.T. Gu (1997) Dentin phosphoprotein and dentin sialoprotein are cleavage products expressed from a single transcript coded by a gene on human chromosome 4. J Biol Chem 272: 835-842.
-
(1997)
J Biol Chem
, vol.272
, pp. 835-842
-
-
MacDougall, M.1
Simmons, D.2
Luan, X.3
Nydegger, J.4
Feng, J.5
Gu, T.T.6
-
10
-
-
33845258059
-
Molecular basis of human dentin diseases
-
MacDougall, M., J. Dong, A.C. Acevedo (2006) Molecular basis of human dentin diseases. Am J Med Genet 140: 2536-2546, 2006.
-
(2006)
Am J Med Genet
, vol.140
, pp. 2536-2546
-
-
MacDougall, M.1
Dong, J.2
Acevedo, A.C.3
-
11
-
-
0023808608
-
Dentinogenesis imperfecta in a six-generation family
-
Malmgren, B., M. Lundberg, S. Lindskog (1988) Dentinogenesis imperfecta in a six-generation family. Swed Dent J 12: 73-84.
-
(1988)
Swed Dent J
, vol.12
, pp. 73-84
-
-
Malmgren, B.1
Lundberg, M.2
Lindskog, S.3
-
12
-
-
2542434141
-
Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type II
-
Malmgren, B., S. Lindskog, A. Elgadi, S. Norgren (2004) Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type II. Hum Genet 114: 491-498.
-
(2004)
Hum Genet
, vol.114
, pp. 491-498
-
-
Malmgren, B.1
Lindskog, S.2
Elgadi, A.3
Norgren, S.4
-
13
-
-
0035070524
-
Novel COLIA1 mutation (G599C) associated with mild osteogenesis imperfecta and dentinogenesis imperfecta
-
Pallos, D., P.S. Hart, J.R. Cortelli, S. Vian, J.T. Wright, J. Korkko, D. Brunoni, T.C. Hart (2001) Novel COLIA1 mutation (G599C) associated with mild osteogenesis imperfecta and dentinogenesis imperfecta. Arch Oral Biol 46: 459-470.
-
(2001)
Arch Oral Biol
, vol.46
, pp. 459-470
-
-
Pallos, D.1
Hart, P.S.2
Cortelli, J.R.3
Vian, S.4
Wright, J.T.5
Korkko, J.6
Brunoni, D.7
Hart, T.C.8
-
14
-
-
0036796408
-
Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralization
-
Rajpar, M.H., M.J. Koch, R.M. Davies, K.T. Mellody, C.M. Kielty, M.J. Dixon (2002) Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralization. Hum Mol Genet 11: 2559-2565.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2559-2565
-
-
Rajpar, M.H.1
Koch, M.J.2
Davies, R.M.3
Mellody, K.T.4
Kielty, C.M.5
Dixon, M.J.6
-
15
-
-
0027535690
-
Heritable dentin defects: Nosology, pathology, and treatment
-
Ranta, H., P.L. Lukinmaa, J. Waltimo (1993) Heritable dentin defects: nosology, pathology, and treatment. Am J Med Genet 45: 193-200.
-
(1993)
Am J Med Genet
, vol.45
, pp. 193-200
-
-
Ranta, H.1
Lukinmaa, P.L.2
Waltimo, J.3
-
16
-
-
0015068926
-
Inherited defects in tooth structure
-
Rao, S., C.J. Witkop (1971) Inherited defects in tooth structure. Birth Defects 7: 153-184.
-
(1971)
Birth Defects
, vol.7
, pp. 153-184
-
-
Rao, S.1
Witkop, C.J.2
-
17
-
-
0015612856
-
A proposed classification for heritable human dentine defects with a description of a new entity
-
Shields, E.D., D. Bixler, A.M. El-Kafrawy (1973) A proposed classification for heritable human dentine defects with a description of a new entity. Arch Oral Biol 8: 543-553.
-
(1973)
Arch Oral Biol
, vol.8
, pp. 543-553
-
-
Shields, E.D.1
Bixler, D.2
El-Kafrawy, A.M.3
-
18
-
-
0042591182
-
Dentin sialophosphoprotein knockout mouse display widened predentin zone and develop defective dentin mineralization similar to human dentinogenesis imperfecta-III
-
Sreenath, T., T. Thyagarajan, B. Hall, G. Longenecker, R. D'Souza, S. Hong, T. Wright, M. MacDougall, J Sauk, A Kulkarni (2003) Dentin sialophosphoprotein knockout mouse display widened predentin zone and develop defective dentin mineralization similar to human dentinogenesis imperfecta-III. J Biol Chem 278: 24874-24880.
-
(2003)
J Biol Chem
, vol.278
, pp. 24874-24880
-
-
Sreenath, T.1
Thyagarajan, T.2
Hall, B.3
Longenecker, G.4
D'Souza, R.5
Hong, S.6
Wright, T.7
MacDougall, M.8
Sauk, J.9
Kulkarni, A.10
-
19
-
-
0013957063
-
Medical and dental findings in the Brandywine isolate
-
Witkop, C.J., C.J. MacLean, P.J. Schmidt, J.L. Henry (1966) Medical and dental findings in the Brandywine isolate. Ala J Med Sci 3: 382-403.
-
(1966)
Ala J Med Sci
, vol.3
, pp. 382-403
-
-
Witkop, C.J.1
MacLean, C.J.2
Schmidt, P.J.3
Henry, J.L.4
-
20
-
-
0016834265
-
Hereditary defects of dentine
-
Witkop, C.J. (1975) Hereditary defects of dentine. Dent Clin N Amer 19: 25-45.
-
(1975)
Dent Clin N Amer
, vol.19
, pp. 25-45
-
-
Witkop, C.J.1
-
21
-
-
0024117250
-
Amelogenesis imperfecta dentinogenesis imperfecta and dentin dysplasia revisited: Problems in classification
-
Witkop, C.J. (1989) Amelogenesis imperfecta dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification. J Oral Path 17: 547-553.
-
(1989)
J Oral Path
, vol.17
, pp. 547-553
-
-
Witkop, C.J.1
-
22
-
-
0035136682
-
Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP
-
Xiao, S., C. Yu, X. Chou, W. Yuan, Y. Wang, L. Bu, G. Fu, M. Qian, J. Yang, Y. Shi, L. Hu, B. Han, Z. Wang, W. Huang, J. Liu, Z. Chen, G. Zhao, X. Kong (2001) Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP. Nat Genet 27: 201-204.
-
(2001)
Nat Genet
, vol.27
, pp. 201-204
-
-
Xiao, S.1
Yu, C.2
Chou, X.3
Yuan, W.4
Wang, Y.5
Bu, L.6
Fu, G.7
Qian, M.8
Yang, J.9
Shi, Y.10
Hu, L.11
Han, B.12
Wang, Z.13
Huang, W.14
Liu, J.15
Chen, Z.16
Zhao, G.17
Kong, X.18
-
23
-
-
0035134329
-
DSPP mutation in dentinogenesis imperfecta Shields type II
-
Zhang, X., J. Zhao, C. Li, S. Gao, C. Qiu, P. Liu, G. Wu, B. Qiang, W.H.Y. Lo, Y. Shen (2001) DSPP mutation in dentinogenesis imperfecta Shields type II. Nat Genet 27: 151-152.
-
(2001)
Nat Genet
, vol.27
, pp. 151-152
-
-
Zhang, X.1
Zhao, J.2
Li, C.3
Gao, S.4
Qiu, C.5
Liu, P.6
Wu, G.7
Qiang, B.8
Lo, W.H.Y.9
Shen, Y.10
-
24
-
-
34848877727
-
A novel DSPP mutation is associated with type II dentinogenesis Imperfecta in a Chinese family
-
Zhang, G.X., L. Chen, J. Liu, Z. Zhao, E. Qu, X. Wang, W. Chang, C. Xu, Q.K. Wang, M. Lu (2007) A novel DSPP mutation is associated with type II dentinogenesis Imperfecta in a Chinese family. BMC Med Genet 8: 52.
-
(2007)
BMC Med Genet
, vol.8
, pp. 52
-
-
Zhang, G.X.1
Chen, L.2
Liu, J.3
Zhao, Z.4
Qu, E.5
Wang, X.6
Chang, W.7
Xu, C.8
Wang, Q.K.9
Lu, M.10
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