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Items: 1 to 20 of 83

1.

Abrogation of epithelial BMP2 and BMP4 causes Amelogenesis Imperfecta by reducing MMP20 and KLK4 expression.

Xie X, Liu C, Zhang H, Jani PH, Lu Y, Wang X, Zhang B, Qin C.

Sci Rep. 2016 May 5;6:25364. doi: 10.1038/srep25364.

2.

MMP20, KLK4, and MMP20/KLK4 double null mice define roles for matrix proteases during dental enamel formation.

Hu Y, Smith CE, Richardson AS, Bartlett JD, Hu JC, Simmer JP.

Mol Genet Genomic Med. 2015 Dec 20;4(2):178-96. doi: 10.1002/mgg3.194. eCollection 2016 Mar.

3.

Matrix metalloproteinase-20 mediates dental enamel biomineralization by preventing protein occlusion inside apatite crystals.

Prajapati S, Tao J, Ruan Q, De Yoreo JJ, Moradian-Oldak J.

Biomaterials. 2016 Jan;75:260-70. doi: 10.1016/j.biomaterials.2015.10.031. Epub 2015 Oct 22.

PMID:
26513418
4.

A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement.

Prasad MK, Geoffroy V, Vicaire S, Jost B, Dumas M, Le Gras S, Switala M, Gasse B, Laugel-Haushalter V, Paschaki M, Leheup B, Droz D, Dalstein A, Loing A, Grollemund B, Muller-Bolla M, Lopez-Cazaux S, Minoux M, Jung S, Obry F, Vogt V, Davideau JL, Davit-Beal T, Kaiser AS, Moog U, Richard B, Morrier JJ, Duprez JP, Odent S, Bailleul-Forestier I, Rousset MM, Merametdijan L, Toutain A, Joseph C, Giuliano F, Dahlet JC, Courval A, El Alloussi M, Laouina S, Soskin S, Guffon N, Dieux A, Doray B, Feierabend S, Ginglinger E, Fournier B, de la Dure Molla M, Alembik Y, Tardieu C, Clauss F, Berdal A, Stoetzel C, Manière MC, Dollfus H, Bloch-Zupan A.

J Med Genet. 2016 Feb;53(2):98-110. doi: 10.1136/jmedgenet-2015-103302. Epub 2015 Oct 26.

5.

Critical roles for WDR72 in calcium transport and matrix protein removal during enamel maturation.

Wang SK, Hu Y, Yang J, Smith CE, Nunez SM, Richardson AS, Pal S, Samann AC, Hu JC, Simmer JP.

Mol Genet Genomic Med. 2015 Jul;3(4):302-19. doi: 10.1002/mgg3.143. Epub 2015 Mar 29.

6.

Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report.

Cherkaoui Jaouad I, El Alloussi M, Chafai El Alaoui S, Laarabi FZ, Lyahyai J, Sefiani A.

BMC Oral Health. 2015 Jan 30;15:14. doi: 10.1186/1472-6831-15-14.

7.

Bmp2 deletion causes an amelogenesis imperfecta phenotype via regulating enamel gene expression.

Guo F, Feng J, Wang F, Li W, Gao Q, Chen Z, Shoff L, Donly KJ, Gluhak-Heinrich J, Chun YH, Harris SE, MacDougall M, Chen S.

J Cell Physiol. 2015 Aug;230(8):1871-82. doi: 10.1002/jcp.24915.

8.

Hypomaturation amelogenesis imperfecta caused by a novel SLC24A4 mutation.

Herzog CR, Reid BM, Seymen F, Koruyucu M, Tuna EB, Simmer JP, Hu JC.

Oral Surg Oral Med Oral Pathol Oral Radiol. 2015 Feb;119(2):e77-81. doi: 10.1016/j.oooo.2014.09.003. Epub 2014 Sep 16.

9.

Novel ITGB6 mutation in autosomal recessive amelogenesis imperfecta.

Seymen F, Lee KE, Koruyucu M, Gencay K, Bayram M, Tuna EB, Lee ZH, Kim JW.

Oral Dis. 2015 May;21(4):456-61. doi: 10.1111/odi.12303. Epub 2015 Jan 19.

10.

ENAM mutations with incomplete penetrance.

Seymen F, Lee KE, Koruyucu M, Gencay K, Bayram M, Tuna EB, Lee ZH, Kim JW.

J Dent Res. 2014 Oct;93(10):988-92. doi: 10.1177/0022034514548222. Epub 2014 Aug 20.

11.

Alteration of conserved alternative splicing in AMELX causes enamel defects.

Cho ES, Kim KJ, Lee KE, Lee EJ, Yun CY, Lee MJ, Shin TJ, Hyun HK, Kim YJ, Lee SH, Jung HS, Lee ZH, Kim JW.

J Dent Res. 2014 Oct;93(10):980-7. doi: 10.1177/0022034514547272. Epub 2014 Aug 12.

12.

Kallikrein-related peptidase-4 (KLK4): role in enamel formation and revelations from ablated mice.

Bartlett JD, Simmer JP.

Front Physiol. 2014 Jul 4;5:240. doi: 10.3389/fphys.2014.00240. eCollection 2014. Review.

13.

WDR72 models of structure and function: a stage-specific regulator of enamel mineralization.

Katsura KA, Horst JA, Chandra D, Le TQ, Nakano Y, Zhang Y, Horst OV, Zhu L, Le MH, DenBesten PK.

Matrix Biol. 2014 Sep;38:48-58. doi: 10.1016/j.matbio.2014.06.005. Epub 2014 Jul 4.

14.

Deletion of ameloblastin exon 6 is associated with amelogenesis imperfecta.

Poulter JA, Murillo G, Brookes SJ, Smith CE, Parry DA, Silva S, Kirkham J, Inglehearn CF, Mighell AJ.

Hum Mol Genet. 2014 Oct 15;23(20):5317-24. doi: 10.1093/hmg/ddu247. Epub 2014 May 23.

15.

Mouse genetic background influences the dental phenotype.

Li Y, Konicki WS, Wright JT, Suggs C, Xue H, Kuehl MA, Kulkarni AB, Gibson CW.

Cells Tissues Organs. 2013;198(6):448-56. doi: 10.1159/000360157. Epub 2014 Apr 8.

16.

Matrix metalloproteinase-20 over-expression is detrimental to enamel development: a Mus musculus model.

Shin M, Hu Y, Tye CE, Guan X, Deagle CC, Antone JV, Smith CE, Simmer JP, Bartlett JD.

PLoS One. 2014 Jan 23;9(1):e86774. doi: 10.1371/journal.pone.0086774. eCollection 2014.

17.

A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfecta.

Poulter JA, Brookes SJ, Shore RC, Smith CE, Abi Farraj L, Kirkham J, Inglehearn CF, Mighell AJ.

Hum Mol Genet. 2014 Apr 15;23(8):2189-97. doi: 10.1093/hmg/ddt616. Epub 2013 Dec 6.

18.

Dental enamel development: proteinases and their enamel matrix substrates.

Bartlett JD.

ISRN Dent. 2013 Sep 16;2013:684607. doi: 10.1155/2013/684607. Review.

19.

MMP20 modulates cadherin expression in ameloblasts as enamel develops.

Guan X, Bartlett JD.

J Dent Res. 2013 Dec;92(12):1123-8. doi: 10.1177/0022034513506581. Epub 2013 Sep 25.

20.

Genes expressed in dental enamel development are associated with molar-incisor hypomineralization.

Jeremias F, Koruyucu M, Küchler EC, Bayram M, Tuna EB, Deeley K, Pierri RA, Souza JF, Fragelli CM, Paschoal MA, Gencay K, Seymen F, Caminaga RM, dos Santos-Pinto L, Vieira AR.

Arch Oral Biol. 2013 Oct;58(10):1434-42. doi: 10.1016/j.archoralbio.2013.05.005. Epub 2013 Jun 19.

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