Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Sermporn Thaweesapphithak"'
Autor:
Sermporn Thaweesapphithak, Kittipat Termteerapornpimol, Siriwong Wongsirisuwan, Soranun Chantarangsu, Thantrira Porntaveetus
Publikováno v:
Journal of Translational Medicine, Vol 22, Iss 1, Pp 1-16 (2024)
Abstract Cleidocranial Dysplasia (CCD) is a rare genetic disorder characterized by skeletal abnormalities and dental anomalies, primarily caused by variants in the RUNX2 gene. Understanding the spectrum of RUNX2 variants and their effects on CCD phen
Externí odkaz:
https://doaj.org/article/96ddd449bbb34dd6ae60a8decaa89c51
Autor:
Sermporn Thaweesapphithak, Thanakorn Theerapanon, Khanti Rattanapornsompong, Narin Intarak, Pimsiri Kanpittaya, Vorapat Trachoo, Thantrira Porntaveetus, Vorasuk Shotelersuk
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract Cleidocranial dysplasia (CCD) is a genetic disorder caused by mutations in the RUNX2 gene, affecting bone and teeth development. Previous studies focused on mutations in the RUNX2 RHD domain, with limited investigation of mutations in the C-
Externí odkaz:
https://doaj.org/article/6b656ab253bd4330b9bcd2f1dbdbe7c0
Autor:
Sermporn THAWEESAPPHITHAK, Jirawat SAENGSIN, Wuttichart KAMOLVISIT, Thanakorn THEERAPANON, Thantrira PORNTAVEETUS, Vorasuk SHOTELERSUK
Publikováno v:
Journal of Applied Oral Science, Vol 30 (2022)
Abstract Cleidocranial dysplasia (CCD) is a skeletal disorder affecting cranial sutures, teeth, and clavicles, and is associated with the RUNX2 mutations. Although numerous patients have been described, a direct genotype–phenotype correlation for R
Externí odkaz:
https://doaj.org/article/94ff1210b8194d24841ea53d063b5519
Autor:
Sermporn Thaweesapphithak, Chairat Tantrawatpan, Pakpoom Kheolamai, Duangrat Tantikanlayaporn, Sittiruk Roytrakul, Sirikul Manochantr
Publikováno v:
Stem Cell Research & Therapy, Vol 10, Iss 1, Pp 1-18 (2019)
Abstract Background Mesenchymal stromal cells (MSCs) are considered potential candidates that hold great promise in the treatment of immune-related diseases. For therapeutic applications, it is necessary to isolate and expand MSCs with procedures com
Externí odkaz:
https://doaj.org/article/d3e1abfc9d1a42d3a7b1702a9d41e774
Autor:
Charinya Kanchanasevee, Kanokwan Sriwattanapong, Thanakorn Theerapanon, Sermporn Thaweesapphithak, Wanna Chetruengchai, Thantrira Porntaveetus, Vorasuk Shotelersuk
Publikováno v:
Frontiers in Physiology, Vol 11 (2020)
Tooth agenesis is one of the most common orodental anomalies that demonstrate phenotypic and genotypic heterogeneity with a prevalence of 2.5%–7%. Mutations in WNT10A have been proposed to be the most common cause of nonsyndromic tooth agenesis (NS
Externí odkaz:
https://doaj.org/article/600c105645e542e68d5636be6bb1c888
Autor:
Narin Intarak, Oadcharawadee Nutchoey, Anucharte Srijunbarl, Vorasuk Shotelersuk, Thanakorn Theerapanon, Thantrira Porntaveetus, Lawan Boonprakong, Sermporn Thaweesapphithak
Publikováno v:
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology. 131:694-701
Objective Dentinogenesis imperfecta (DI) requires dental treatment. This study investigated the characteristics of DI teeth associated with osteogenesis imperfecta (OI) and COL1A2 mutations. Study Design Whole exome and Sanger sequencing were perform
Autor:
Rakkierti Garuyakich, Kanokwan Sriwattanapong, Issree Nitayavardhana, Thanakorn Theerapanon, Chureerat Phokaew, Thantrira Porntaveetus, Vorasuk Shotelersuk, Pintu-on Chantarawaratit, Sermporn Thaweesapphithak
Publikováno v:
Oral diseasesREFERENCES. 28(3)
Objectives Autosomal-dominant hypocalcified amelogenesis imperfecta (ADHCAI) shows phenotypic heterogeneity. Our aim was to characterise the ADHCAI phenotypes, tooth properties and genotypes. Methods Three unrelated ADHCAI probands and seven addition
Autor:
Pintu-on Chantarawaratit, Rakkierti Garuyakich, Sermporn Thaweesapphithak, Chureerat Phokaew, Thantrira Porntaveetus, Vorasuk Shotelersuk, Kanokwan Sriwattanapong, Thanakorn Theerapanon, Issree Nitayavardhana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d42d9487b3cee5a82503ed93381fff14
https://doi.org/10.1111/odi.13780/v2/response1
https://doi.org/10.1111/odi.13780/v2/response1
Autor:
Vorasuk Shotelersuk, Wanna Chetruengchai, Kanokwan Sriwattanapong, Thanakorn Theerapanon, Thantrira Porntaveetus, Charinya Kanchanasevee, Sermporn Thaweesapphithak
Publikováno v:
Frontiers in Physiology, Vol 11 (2020)
Tooth agenesis is one of the most common orodental anomalies that demonstrate phenotypic and genotypic heterogeneity with a prevalence of 2.5%–7%. Mutations in WNT10A have been proposed to be the most common cause of nonsyndromic tooth agenesis (NS
Autor:
Narin Intarak, Vorasuk Shotelersuk, Thantrira Porntaveetus, Thanakorn Theerapanon, Kanya Suphapeetiporn, Sermporn Thaweesapphithak
Publikováno v:
Molecular genetics and genomics : MGG. 294(3)
The latent transforming growth factor-beta-binding protein 3 (LTBP3), encoding extracellular matrix proteins, plays a role in skeletal formation. Mutations in LTBP3 have been associated with various types of skeletal dysplasia. We aimed to characteri