Hart PS - Search Results

1

In vivo impact of a 4 bp deletion mutation in the DLX3 gene on bone development.

Choi SJ, Roodman GD, Feng JQ, Song IS, Amin K, Hart PS, Wright JT, Haruyama N, Hart TC. Choi SJ, et al. Among authors: hart ps, hart tc. Dev Biol. 2009 Jan 1;325(1):129-37. doi: 10.1016/j.ydbio.2008.10.014. Epub 2008 Oct 25. Dev Biol. 2009. PMID: 18996110 Free PMC article.

2

A 4 bp deletion mutation in DLX3 enhances osteoblastic differentiation and bone formation in vitro.

Choi SJ, Song IS, Ryu OH, Choi SW, Hart PS, Wu WW, Shen RF, Hart TC. Choi SJ, et al. Among authors: hart ps, hart tc. Bone. 2008 Jan;42(1):162-71. doi: 10.1016/j.bone.2007.08.047. Epub 2007 Sep 19. Bone. 2008. PMID: 17950683 Free PMC article.

3

Genetic studies of craniofacial anomalies: clinical implications and applications.

Hart TC, Hart PS. Hart TC, et al. Among authors: hart ps. Orthod Craniofac Res. 2009 Aug;12(3):212-20. doi: 10.1111/j.1601-6343.2009.01455.x. Orthod Craniofac Res. 2009. PMID: 19627523 Free PMC article. Review.

4

Disorders of human dentin.

Hart PS, Hart TC. Hart PS, et al. Among authors: hart tc. Cells Tissues Organs. 2007;186(1):70-7. doi: 10.1159/000102682. Cells Tissues Organs. 2007. PMID: 17627120 Free PMC article.

5

Invited commentary: The need for human genetics and genomics in dental school curricula.

Hart PS, Hart TC. Hart PS, et al. Among authors: hart tc. Mol Genet Genomic Med. 2016 Mar 17;4(2):123-5. doi: 10.1002/mgg3.216. eCollection 2016 Mar. Mol Genet Genomic Med. 2016. PMID: 27066512 Free PMC article. No abstract available.

6

Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature.

Hart PS, Michalec MD, Seow WK, Hart TC, Wright JT. Hart PS, et al. Among authors: hart tc. Arch Oral Biol. 2003 Aug;48(8):589-96. doi: 10.1016/s0003-9969(03)00114-6. Arch Oral Biol. 2003. PMID: 12828988

7

A nomenclature for X-linked amelogenesis imperfecta.

Hart PS, Hart TC, Simmer JP, Wright JT. Hart PS, et al. Among authors: hart tc. Arch Oral Biol. 2002 Apr;47(4):255-60. doi: 10.1016/s0003-9969(02)00005-5. Arch Oral Biol. 2002. PMID: 11922868 Review.

8

Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations.

Hart PS, Aldred MJ, Crawford PJ, Wright NJ, Hart TC, Wright JT. Hart PS, et al. Among authors: hart tc. Arch Oral Biol. 2002 Apr;47(4):261-5. doi: 10.1016/s0003-9969(02)00003-1. Arch Oral Biol. 2002. PMID: 11922869

9

Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfecta.

McKnight DA, Simmer JP, Hart PS, Hart TC, Fisher LW. McKnight DA, et al. Among authors: hart ps, hart tc. J Dent Res. 2008 Dec;87(12):1108-11. doi: 10.1177/154405910808701217. J Dent Res. 2008. PMID: 19029076 Free PMC article.

10

Two 3' polymorphisms in DLX5: g126427delTATC and g126249T-->C.

Hart PS, Michalec MD, Wright JT, Hart TC. Hart PS, et al. Among authors: hart tc. Hum Mutat. 2000 Nov;16(5):448. doi: 10.1002/1098-1004(200011)16:5<448::AID-HUMU22>3.0.CO;2-X. Hum Mutat. 2000. PMID: 11058915 No abstract available.

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