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Page 1
Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies.
Ruangchan C, Ngamphiw C, Krasaesin A, Intarak N, Tongsima S, Kaewgahya M, Kawasaki K, Mahawong P, Paripurana K, Sookawat B, Jatooratthawichot P, Cox TC, Ohazama A, Ketudat Cairns JR, Porntaveetus T, Kantaputra P. Ruangchan C, et al. Among authors: cox tc. Int J Mol Sci. 2024 May 9;25(10):5179. doi: 10.3390/ijms25105179. Int J Mol Sci. 2024. PMID: 38791218 Free PMC article.
SERPINB3, Adult-Onset Immunodeficiency, and Generalized Pustular Psoriasis.
Kantaputra P, Daroontum T, Chuamanochan M, Chaowattanapanit S, Kiratikanon S, Choonhakarn C, Intachai W, Olsen B, Tongsima S, Ngamphiw C, Pontisso P, Cox TC, Ounjai P. Kantaputra P, et al. Among authors: cox tc. Genes (Basel). 2023 Jan 19;14(2):266. doi: 10.3390/genes14020266. Genes (Basel). 2023. PMID: 36833193 Free PMC article.
Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pain.
Kantaputra P, Daroontum T, Kitiyamas K, Piyakhunakorn P, Kawasaki K, Sathienkijkanchai A, Wasant P, Vatanavicharn N, Yasanga T, Kaewgahya M, Tongsima S, Cox TC, Arold ST, Ohazama A, Ngamphiw C. Kantaputra P, et al. Among authors: cox tc. Int J Mol Sci. 2024 Jun 8;25(12):6358. doi: 10.3390/ijms25126358. Int J Mol Sci. 2024. PMID: 38928066 Free PMC article.
Genetic Variants in the TBC1D2B Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis.
Kularbkaew T, Thongmak T, Sandeth P, Durward CS, Vittayakittipong P, Duke P, Iamaroon A, Kintarak S, Intachai W, Ngamphiw C, Tongsima S, Jatooratthawichot P, Cox TC, Ketudat Cairns JR, Kantaputra P. Kularbkaew T, et al. Among authors: cox tc. Int J Mol Sci. 2024 Aug 15;25(16):8867. doi: 10.3390/ijms25168867. Int J Mol Sci. 2024. PMID: 39201553 Free PMC article.
Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate.
Cox LL, Cox TC, Moreno Uribe LM, Zhu Y, Richter CT, Nidey N, Standley JM, Deng M, Blue E, Chong JX, Yang Y, Carstens RP, Anand D, Lachke SA, Smith JD, Dorschner MO, Bedell B, Kirk E, Hing AV, Venselaar H, Valencia-Ramirez LC, Bamshad MJ, Glass IA, Cooper JA, Haan E, Nickerson DA, van Bokhoven H, Zhou H, Krahn KN, Buckley MF, Murray JC, Lidral AC, Roscioli T. Cox LL, et al. Among authors: cox tc. Am J Hum Genet. 2018 Jun 7;102(6):1143-1157. doi: 10.1016/j.ajhg.2018.04.009. Epub 2018 May 24. Am J Hum Genet. 2018. PMID: 29805042 Free PMC article.
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans.
Cox TC, Lidral AC, McCoy JC, Liu H, Cox LL, Zhu Y, Anderson RD, Moreno Uribe LM, Anand D, Deng M, Richter CT, Nidey NL, Standley JM, Blue EE, Chong JX, Smith JD, Kirk EP, Venselaar H, Krahn KN, van Bokhoven H, Zhou H, Cornell RA, Glass IA, Bamshad MJ, Nickerson DA, Murray JC, Lachke SA, Thompson TB, Buckley MF, Roscioli T. Cox TC, et al. Among authors: cox ll. Hum Mutat. 2019 Oct;40(10):1813-1825. doi: 10.1002/humu.23793. Epub 2019 Jun 18. Hum Mutat. 2019. PMID: 31215115 Free PMC article.
236 results