Shih-Kai Wang

发表

ENAM mutations and digenic inheritance

Jung‐Wook Kim, F. Seymen, J. Simmer, 2019, Molecular genetics & genomic medicine.

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

J. Simmer, S. Núñez, A. S. Richardson, 2015, Molecular genetics & genomic medicine.

Tooth Development: Learn from "The Normal" and "The Abnormal".

Shih-Kai Wang, 2014 .

Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families.

Jung‐Wook Kim, J. Simmer, Karen A Uston, 2011, European journal of oral sciences.

Root anomalies and dentin dysplasia in autosomal recessive hyperphosphatemic familial tumoral calcinosis (HFTC).

Murim Choi, F. Visioli, A. R. Vieira, 2015, Oral surgery, oral medicine, oral pathology and oral radiology.

Potential contribution of neural crest cells to dental enamel formation.

Y. Mishina, Y. Komatsu, Shih-Kai Wang, 2011, Biochemical and biophysical research communications.

Fam83h null mice support a neomorphic mechanism for human ADHCAI

Murim Choi, Jung‐Wook Kim, Yuan-Ling Lee, 2015, Molecular genetics & genomic medicine.

Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds

Murim Choi, Yuan-Ling Lee, K. C. Kent Lloyd, 2014, Molecular genetics & genomic medicine.

Novel PAX9 and COL1A2 Missense Mutations Causing Tooth Agenesis and OI/DGI without Skeletal Abnormalities

J. Simmer, J. Hu, Shih-Kai Wang, 2012, PloS one.

Synergistic Mutations of LRP6 and WNT10A in Familial Tooth Agenesis

Yin-Lin Wang, Yi-Ping Wang, J. Simmer, 2021, Journal of personalized medicine.

The Modified Shields Classification and 12 Families with Defined DSPP Mutations

Yuan-Ling Lee, Kevin Y. Lee, F. Seymen, 2022, Genes.

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

Murim Choi, Jung‐Wook Kim, J. Simmer, 2014, Human molecular genetics.

The Enamel Phenotype in Homozygous Fam83h Truncation Mice

Jung‐Wook Kim, J. Simmer, Yuanyuan Hu, 2019, Molecular genetics & genomic medicine.

AMBN mutations causing hypoplastic amelogenesis imperfecta and Ambn knockout‐NLS‐lacZ knockin mice exhibiting failed amelogenesis and Ambn tissue‐specificity

Jung‐Wook Kim, J. Simmer, A. S. Richardson, 2019, Molecular genetics & genomic medicine.

A Genetic Model for the Secretory Stage of Dental Enamel Formation.

Jung‐Wook Kim, Y. Yamakoshi, J. Simmer, 2021, Journal of structural biology.

Ameloblast transcriptome changes from secretory to maturation stages

Yongsheng Bai, J. Simmer, A. S. Richardson, 2014, Connective tissue research.

FAM20A Mutations Can Cause Enamel-Renal Syndrome (ERS)

Z. Baqain, J. Simmer, H. Daggag, 2013, PLoS genetics.

Transcriptome analysis of gingival tissues of enamel-renal syndrome.

Yi-Ping Wang, J. Simmer, Wenjie Zhong, 2019, Journal of periodontal research.

Mouse Dspp frameshift model of human dentinogenesis imperfecta

Jung‐Wook Kim, J. Simmer, T. Saunders, 2021, Scientific Reports.

Enamel defects in Acp4R110C/R110C mice and human ACP4 mutations

F. Seymen, J. Simmer, T. Saunders, 2022, Scientific Reports.

Dental malformations associated with biallelic MMP20 mutations

Jung‐Wook Kim, Yin-Lin Wang, B. Foster, 2020, Molecular genetics & genomic medicine.

Secreted protein kinases?

J. Simmer, Shih-Kai Wang, Andrew C Samann, 2013, Trends in biochemical sciences.

FAM20C Functions Intracellularly Within Both Ameloblasts and Odontoblasts In Vivo

J. Simmer, J. Hu, Shih-Kai Wang, 2013, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

FAM20A Mutations Associated with Enamel Renal Syndrome

M. Yeganeh, J. Simmer, J. Hu, 2014, Journal of dental research.

Novel KLK4 and MMP20 Mutations Discovered by Whole-exome Sequencing

F. Seymen, J. Simmer, J. D. Bartlett, 2013, Journal of dental research.

FAM20A Mutations Associated with Enamel Renal Syndrome

J. Simmer, S. Dugan, J. Roggenbuck, 2014, Journal of dental research.

Altered Enamelin Phosphorylation Site Causes Amelogenesis Imperfecta

J. Simmer, A. S. Richardson, J. Hu, 2010, Journal of dental research.