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CACNA1S mutation-associated dental anomalies: A calcium channelopathy.
Kantaputra P, Butali A, Eliason S, Chalkley C, Nakornchai S, Bongkochwilawan C, Kawasaki K, Kumchiang A, Ngamphiw C, Tongsima S, Ketudat Cairns JR, Olsen B, Intachai W, Ohazama A, Tucker AS, Amendt BA. Kantaputra P, et al. Oral Dis. 2024 Apr;30(3):1350-1359. doi: 10.1111/odi.14551. Epub 2023 Mar 13. Oral Dis. 2024. PMID: 36825457 Free PMC article.
Dentinogenesis imperfecta-associated syndromes.
Kantaputra PN. Kantaputra PN. Am J Med Genet. 2001 Nov 15;104(1):75-8. doi: 10.1002/ajmg.10031. Am J Med Genet. 2001. PMID: 11746032 Review. No abstract available.
The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32.
Fujimoto M, Kantaputra PN, Ikegawa S, Fukushima Y, Sonta S, Matsuo M, Ishida T, Matsumoto T, Kondo S, Tomita H, Deng HX, D'urso M, Rinaldi MM, Ventruto V, Takagi T, Nakamura Y, Niikawa N. Fujimoto M, et al. Among authors: kantaputra pn. J Hum Genet. 1998;43(1):32-6. doi: 10.1007/s100380050033. J Hum Genet. 1998. PMID: 9609995
Clinical Spectrum and Tumour Risk Analysis in Patients with Beckwith-Wiedemann Syndrome Due to CDKN1C Pathogenic Variants.
Cardoso LCA, Parra A, Gil CR, Arias P, Gallego N, Romanelli V, Kantaputra PN, Lima L, Llerena Júnior JC, Arberas C, Guillén-Navarro E, Nevado J, Spanish OverGrowth Registry Initiative, Tenorio-Castano J, Lapunzina P. Cardoso LCA, et al. Among authors: kantaputra pn. Cancers (Basel). 2022 Aug 5;14(15):3807. doi: 10.3390/cancers14153807. Cancers (Basel). 2022. PMID: 35954470 Free PMC article.
DeltaNp63 knockdown mice: A mouse model for AEC syndrome.
Koster MI, Marinari B, Payne AS, Kantaputra PN, Costanzo A, Roop DR. Koster MI, et al. Am J Med Genet A. 2009 Sep;149A(9):1942-7. doi: 10.1002/ajmg.a.32794. Am J Med Genet A. 2009. PMID: 19681108 Free PMC article.
119 results