Search Results - "Porntaveetus, T."

A novel PITX2 mutation in non‐syndromic orodental anomalies by Intarak, N, Theerapanon, T, Ittiwut, C, Suphapeetiporn, K, Porntaveetus, T, Shotelersuk, V

“…Objective To identify orodental characteristics and genetic aetiology of a family affected with non‐syndromic orodental anomalies. Subjects and Methods…”
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A novel de novo mutation substantiates KDF1 as a gene causing ectodermal dysplasia by Manaspon, C., Thaweesapphithak, S., Osathanon, T., Suphapeetiporn, K., Porntaveetus, T., Shotelersuk, V.

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A novel GJA1 mutation in oculodentodigital dysplasia with extensive loss of enamel by Porntaveetus, T, Srichomthong, C, Ohazama, A, Suphapeetiporn, K, Shotelersuk, V

“…Objective To characterize clinical features and identify genetic causes of a patient with oculodentodigital dysplasia (ODDD). Subjects and methods Clinical,…”
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Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia by Intarak, N., Theerapanon, T., Srijunbarl, A., Suphapeetiporn, K., Porntaveetus, T., Shotelersuk, V.

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Dental properties, ultrastructure, and pulp cells associated with a novel DSPP mutation by Porntaveetus, T, Osathanon, T, Nowwarote, N, Pavasant, P, Srichomthong, C, Suphapeetiporn, K, Shotelersuk, V

“…Objective To investigate physical characteristics and behaviours of dental pulp cells of teeth isolated from a dentinogenesis imperfecta (DGI) patient with a…”
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Excess NF-κB Induces Ectopic Odontogenesis in Embryonic Incisor Epithelium by Blackburn, J., Kawasaki, K., Porntaveetus, T., Kawasaki, M., Otsuka-Tanaka, Y., Miake, Y., Ota, M.S., Watanabe, M., Hishinuma, M., Nomoto, T., Oommen, S., Ghafoor, S., Harada, F., Nozawa-Inoue, K., Maeda, T., Peterková, R., Lesot, H., Inoue, J., Akiyama, T., Schmidt-Ullrich, R., Liu, B., Hu, Y., Page, A., Ramírez, Á., Sharpe, P.T., Ohazama, A.

“…Nuclear factor kappa B (NF-κB) signaling plays critical roles in many physiological and pathological processes, including regulating organogenesis…”
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Gene expression, micro‐CT and histomorphometrical analysis of sinus floor augmentation with biphasic calcium phosphate and deproteinized bovine bone mineral: A randomized controlled clinical trial by Arunjaroensuk, Sirida, Nampuksa, Katanchalee, Monmaturapoj, Naruporn, Thunyakitpisal, Pasutha, Porntaveetus, Thantrira, Mattheos, Nikos, Pimkhaokham, Atiphan

“…Aims The aim of this randomized controlled clinical trial was to compare the gene expression, micro‐CT, histomorphometrical analysis between biphasic calcium…”
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A novel de novo mutation substantiates KDF 1 as a gene causing ectodermal dysplasia by Manaspon, C., Thaweesapphithak, S., Osathanon, T., Suphapeetiporn, K., Porntaveetus, T., Shotelersuk, V.

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Cole‐Carpenter syndrome in a patient from Thailand by Porntaveetus, Thantrira, Theerapanon, Thanakorn, Srichomthong, Chalurmpon, Shotelersuk, Vorasuk

“…Cole‐Carpenter syndrome (CCS), commonly classified as a rare type of osteogenesis imperfecta, is a disorder with severe bone fragility, craniosynostosis, and…”
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A novel GJA 1 mutation in oculodentodigital dysplasia with extensive loss of enamel by Porntaveetus, T, Srichomthong, C, Ohazama, A, Suphapeetiporn, K, Shotelersuk, V

“…Objective To characterize clinical features and identify genetic causes of a patient with oculodentodigital dysplasia ( ODDD ). Subjects and methods Clinical,…”
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Lrp4 modulates extracellular integration of cell signaling pathways in development by Ohazama, Atsushi, Johnson, Eric B, Ota, Masato S, Choi, Hong Y, Choi, Hong J, Porntaveetus, Thantrira, Oommen, Shelly, Itoh, Nobuyuki, Eto, Kazuhiro, Gritli-Linde, Amel, Herz, Joachim, Sharpe, Paul T

“…The extent to which cell signaling is integrated outside the cell is not currently appreciated. We show that a member of the low-density receptor-related…”
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Wnt signaling in the murine diastema by Porntaveetus, Thantrira, Ohazama, Atsushi, Choi, Hong Y, Herz, Joachim, Sharpe, Paul T

“…The correct number and shape of teeth are critical factors for an aesthetic and functional dentition. Understanding the molecular mechanisms regulating tooth…”
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A novel de novo mutation substantiates KDF1 as a gene causing ectodermal dysplasia by Manaspon, C, Thaweesapphithak, S, Osathanon, T, Suphapeetiporn, K, Porntaveetus, T, Shotelersuk, V

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Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia by Intarak, N, Theerapanon, T, Srijunbarl, A, Suphapeetiporn, K, Porntaveetus, T, Shotelersuk, V

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