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Items: 5

1.
Novel KLK4 and MMP20 Mutations Discovered by Whole-exome Sequencing
S.-K. Wang, Y. Hu, J.P. Simmer, F. Seymen, N.M.R.P. Estrella, S. Pal, B.M. Reid, M. Yildirim, M. Bayram, J.D. Bartlett, J.C.-C. Hu
J Dent Res. 2013 Mar; 92(3): 266–271. doi: 10.1177/0022034513475626
PMCID:
PMC3576998
AbstractArticlePDF–496K
2.
Amelogenesis Imperfecta: Genotype-Phenotype Studies in 71 Families
J. Timothy Wright, Melody Torain, Kimberly Long, Kim Seow, Peter Crawford, Michael J. Aldred, P. Suzanne Hart, Tom C. Hart
Cells Tissues Organs. 2011 Aug; 194(2-4): 279–283. Published online 2011 May 19. doi: 10.1159/000324339
PMCID:
PMC3178091
AbstractArticlePDF–140K
3.
Hypomaturation Enamel Defects in Klk4 Knockout/LacZ Knockin Mice
James P. Simmer, Yuanyuan Hu, Rangsiyakorn Lertlam, Yasuo Yamakoshi, Jan C.-C. Hu
J Biol Chem. 2009 Jul 10; 284(28): 19110–19121. Published online 2009 May 6. doi: 10.1074/jbc.M109.013623
PMCID:
PMC2707199
AbstractArticlePDF–3.7M
4.
Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta
P Hart, T Hart, M Michalec, O Ryu, D Simmons, S Hong, J Wright
J Med Genet. 2004 Jul; 41(7): 545–549. doi: 10.1136/jmg.2003.017657
PMCID:
PMC1735847
SummaryPDF–1.1M
5.
Molecular cloning and characterization of prostase, an androgen-regulated serine protease with prostate-restricted expression
Peter S. Nelson, Lu Gan, Camari Ferguson, Patrick Moss, Richard Gelinas, Leroy Hood, Kai Wang
Proc Natl Acad Sci U S A. 1999 Mar 16; 96(6): 3114–3119. doi: 10.1073/pnas.96.6.3114
PMCID:
PMC15904
AbstractArticlePDF–239K

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