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Archives of Oral Biology|August 12, 2022
Mutations in LRP6 highlight the role of WNT signaling in oral exostoses and dental anomaliesPiranit Kantaputra, Peeranat Jatooratthawichot, Kanoknart Chintakanon, et al.
Archives of Oral Biology|September 25, 2020
Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2Piranit Nik Kantaputra, Prapai Dejkhamron, Sissades Tongsima, et al.
Genes|February 25, 2023
SERPINB3, Adult-Onset Immunodeficiency, and Generalized Pustular PsoriasisPiranit Kantaputra, Teerada Daroontum, Mati Chuamanochan, et al.
Biology|February 25, 2023
Rare Variants in LRP4 Are Associated with Mesiodens, Root Maldevelopment, and Oral Exostoses in HumansPiranit Nik Kantaputra, Peeranat Jatooratthawichot, Ploy Adisornkanj, et al.
Plos Neglected Tropical Diseases|June 29, 2010
Structural optimization and de novo design of dengue virus entry inhibitory peptidesJoshua M Costin, Ekachai Jenwitheesuk, Shee-Mei Lok, et al.
The Journal of Dermatology|August 14, 2021
SERPINA1, generalized pustular psoriasis, and adult-onset immunodeficiencyPiranit Kantaputra, Suteeraporn Chaowattanapanit, Salin Kiratikanon, et al.
Diagnostics (Basel, Switzerland)|April 13, 2023
Heterozygous Variants in FREM2 Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and OdontomasPiranit Nik Kantaputra, Kanich Tripuwabhrut, Robert P Anthonappa, et al.
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