Dentin defects caused by a Dspp−1 frameshift mutation are associated with the activation of autophagy von Liang, Tian, Smith, Charles E., Hu, Yuanyuan, Zhang, Hong, Zhang, Chuhua, Xu, Qian, Lu, Yongbo, Qi, Ling, Hu, Jan C.-C., Simmer, James P.

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Hypomaturation Enamel Defects in Klk4 Knockout/LacZ Knockin Mice von Simmer, James P., Hu, Yuanyuan, Lertlam, Rangsiyakorn, Yamakoshi, Yasuo, Hu, Jan C.-C.

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FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome von Wang, Shih‐Kai, Zhang, Hong, Wang, Yin‐Lin, Lin, Hung‐Ying, Seymen, Figen, Koruyucu, Mine, Wright, J. Timothy, Kim, Jung‐Wook, Simmer, James P., Hu, Jan C.‐C.

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FAM20A mutations can cause enamel-renal syndrome (ERS) von Wang, Shih-Kai, Aref, Parissa, Hu, Yuanyuan, Milkovich, Rachel N, Simmer, James P, El-Khateeb, Mohammad, Daggag, Hinda, Baqain, Zaid H, Hu, Jan C-C

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Enamelin is critical for ameloblast integrity and enamel ultrastructure formation von Hu, Jan C-C, Hu, Yuanyuan, Lu, Yuhe, Smith, Charles E, Lertlam, Rangsiyakorn, Wright, John Timothy, Suggs, Cynthia, McKee, Marc D, Beniash, Elia, Kabir, M Enamul, Simmer, James P

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AMELX Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis Imperfecta von Wang, Shih-Kai, Zhang, Hong, Lin, Hua-Chieh, Wang, Yin-Lin, Lin, Shu-Chun, Seymen, Figen, Koruyucu, Mine, Simmer, James P, Hu, Jan C-C

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The dynamics of TGF-β in dental pulp, odontoblasts and dentin von Niwa, Takahiko, Yamakoshi, Yasuo, Yamazaki, Hajime, Karakida, Takeo, Chiba, Risako, Hu, Jan C.-C., Nagano, Takatoshi, Yamamoto, Ryuji, Simmer, James P., Margolis, Henry C., Gomi, Kazuhiro

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Mutations in RELT cause autosomal recessive amelogenesis imperfecta von Kim, Jung‐Wook, Zhang, Hong, Seymen, Figen, Koruyucu, Mine, Hu, Yuanyuan, Kang, Jenny, Kim, Youn J., Ikeda, Atsushi, Kasimoglu, Yelda, Bayram, Merve, Zhang, Chuhua, Kawasaki, Kazuhiko, Bartlett, John D., Saunders, Thomas L., Simmer, James P., Hu, Jan C‐C.

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Functions of KLK4 and MMP-20 in dental enamel formation von Lu, Yuhe, Papagerakis, Petros, Yamakoshi, Yasuo, Hu, Jan C.-C., Bartlett, John D., Simmer, James P.

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Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta von Parry, David A., Smith, Claire E.L., El-Sayed, Walid, Poulter, James A., Shore, Roger C., Logan, Clare V., Mogi, Chihiro, Sato, Koichi, Okajima, Fumikazu, Harada, Akihiro, Zhang, Hong, Koruyucu, Mine, Seymen, Figen, Hu, Jan C.-C., Simmer, James P., Ahmed, Mushtaq, Jafri, Hussain, Johnson, Colin A., Inglehearn, Chris F., Mighell, Alan J.

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Phenotypic variability in LAMA3‐associated amelogenesis imperfecta von Wang, Shih‐Kai, Zhang, Hong, Wang, Yin‐Lin, Seymen, Figen, Koruyucu, Mine, Simmer, James P., Hu, Jan C.‐C.

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Novel homozygous KREMEN1 mutation causes ectodermal dysplasia von Lee, Yejin, Zhang, Hong, Seymen, Figen, Koruyucu, Mine, Kasimoglu, Yelda, Lee, Zang Hee, Hu, Jan C.‐C., Simmer, James P., Kim, Jung‐Wook

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Mouse Dspp frameshift model of human dentinogenesis imperfecta von Liang, Tian, Hu, Yuanyuan, Zhang, Hong, Xu, Qian, Smith, Charles E., Zhang, Chuhua, Kim, Jung-Wook, Wang, Shih-Kai, Saunders, Thomas L., Lu, Yongbo, Hu, Jan C.-C., Simmer, James P.

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PAX9 mutations and genetic synergism in familial tooth agenesis von Chu, Kuan‐Yu, Wang, Yin‐Lin, Chen, Jung‐Tsu, Lin, Chia‐Hui, Yao, Chung‐Chen Jane, Chen, Yi‐Jane, Chen, Huan‐Wen, Simmer, James P., Hu, Jan C.‐C., Wang, Shih‐Kai

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Enamel Defects and Ameloblast-specific Expression in Enam Knock-out/lacZ Knock-in Mice von Hu, Jan C.-C., Hu, Yuanyuan, Smith, Charles E., McKee, Marc D., Wright, J. Timothy, Yamakoshi, Yasuo, Papagerakis, Petros, Hunter, Graeme K., Feng, Jerry Q., Yamakoshi, Fumiko, Simmer, James P.

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Quantitative analysis of the core 2D arrangement and distribution of enamel rods in cross‐sections of mandibular mouse incisors von Smith, Charles E., Hu, Yuanyuan, Hu, Jan C‐C., Simmer, James P.

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Evolution of Klk4 and enamel maturation in eutherians von Kawasaki, Kazuhiko, Hu, Jan C.-C., Simmer, James P.

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FAM83H Mutations in Families with Autosomal-Dominant Hypocalcified Amelogenesis Imperfecta von Kim, Jung-Wook, Lee, Sook-Kyung, Lee, Zang Hee, Park, Joo-Cheol, Lee, Kyung-Eun, Lee, Myoung-Hwa, Park, Jong-Tae, Seo, Byoung-Moo, Hu, Jan C.-C., Simmer, James P.

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ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta von 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

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Enamel defects in Acp4R110C/R110C mice and human ACP4 mutations von Liang, Tian, Wang, Shih-Kai, Smith, Charles, Zhang, Hong, Hu, Yuanyuan, Seymen, Figen, Koruyucu, Mine, Kasimoglu, Yelda, Kim, Jung-Wook, Zhang, Chuhua, Saunders, Thomas L., Simmer, James P., Hu, Jan C.-C.

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