Search Results - "Reid, Bryan M."

ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta by Wang, Shih-Kai, Choi, Murim, Richardson, Amelia S, Reid, Bryan M, Lin, Brent P, Wang, Susan J, Kim, Jung-Wook, Simmer, James P, Hu, Jan C-C

“…Integrins are cell-surface adhesion receptors that bind to extracellular matrices (ECM) and mediate cell-ECM interactions. Some integrins are known to play…”
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Hypomaturation amelogenesis imperfecta caused by a novel SLC24A4 mutation by Herzog, Curtis R, Reid, Bryan M., BS, Seymen, Figen, DDS, PhD, Koruyucu, Mine, DDS, PhD, Tuna, Elif Bahar, DDS, PhD, Simmer, James P., DDS, PhD, Hu, Jan C-C., BDS, PhD

“…In this case report of autosomal recessive pigmented hypomaturation amelogenesis imperfecta (AI), we identify a novel homozygous missense mutation (g.165151…”
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Ameloblast transcriptome changes from secretory to maturation stages by Simmer, James P, Richardson, Amelia S, Wang, Shih-Kai, Reid, Bryan M, Bai, Yongsheng, Hu, Yuanyuan, Hu, Jan C-C

“…The purpose of this study was to identify the major molecular components in the secretory and maturation stages of amelogenesis through transcriptome analyses…”
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Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds by Yang, Jie, Wang, Shih‐Kai, Choi, Murim, Reid, Bryan M., Hu, Yuanyuan, Lee, Yuan‐Ling, Herzog, Curtis R., Kim‐Berman, Hera, Lee, Moses, Benke, Paul J., Kent Lloyd, K. C., Simmer, James P., Hu, Jan C.‐C.

“…WNT10A is a signaling molecule involved in tooth development, and WNT10A defects are associated with tooth agenesis. We characterized Wnt10a null mice…”
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The dentin phosphoprotein repeat region and inherited defects of dentin by Yang, Jie, Kawasaki, Kazuhiko, Lee, Moses, Reid, Bryan M., Nunez, Stephanie M., Choi, Murim, Seymen, Figen, Koruyucu, Mine, Kasimoglu, Yelda, Estrella‐Yuson, Ninna, Lin, Brent P. J., Simmer, James P., Hu, Jan C.‐C.

“…Nonsyndromic dentin defects classified as type II dentin dysplasia and types II and III dentinogenesis imperfecta are caused by mutations in DSPP (dentin…”
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