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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.
Proteomics|May 5, 2019
Phosphoproteome Profiling of Isogenic Cancer Cell-Derived Exosome Reveals HSP90 as a Potential Marker for Human CholangiocarcinomaChurat Weeraphan, Amornrat Phongdara, Parunya Chaiyawat, et al.
International Journal of Oncology|June 1, 2017
Secretomic profiling of cells from hollow fiber bioreactor reveals PSMA3 as a potential cholangiocarcinoma biomarkerChris Verathamjamras, Churat Weeraphan, Daranee Chokchaichamnankit, et al.
Biomedicines|August 27, 2021
HMP-S7 Is a Novel Anti-Leukemic Peptide Discovered from Human MilkWararat Chiangjong, Jirawan Panachan, Thitinee Vanichapol, et al.
Journal of Molecular Biology|March 1, 2008
Structural insights into rice BGlu1 beta-glucosidase oligosaccharide hydrolysis and transglycosylationWatchalee Chuenchor, Salila Pengthaisong, Robert C Robinson, et al.
Oncology Letters|May 12, 2020
Identification of potential cervical cancer serum biomarkers in Thai patientsSiriporn Keeratichamroen, Pantipa Subhasitanont, Daranee Chokchaichamnankit, et al.
ACS Applied Materials & Interfaces|July 13, 2016
Penetration of Oxidized Carbon Nanospheres through Lipid Bilayer Membrane: Comparison to Graphene Oxide and Oxidized Carbon Nanotubes, and Effects of pH and Membrane CompositionJiraporn Seemork, Titiporn Sansureerungsikul, Kamonluck Sathornsantikun, et al.
Molecular Genetics and Metabolism|June 15, 2012
Clinical and molecular findings in Thai patients with isolated methylmalonic acidemiaNithiwat Vatanavicharn, Voraratt Champattanachai, Somporn Liammongkolkul, et al.
British Journal of Haematology|April 13, 2024
Proteomic profiling of circulating β-thalassaemia/haemoglobin E extra-cellular vesicles reveals that association with immunoglobulin induces membrane vesiculationKunwadee Phongpao, Nuttanan Pholngam, Daranee Chokchaichamnankit, et al.
BMC Medical Genetics|September 13, 2019
Clinical course, mutations and its functional characteristics of infantile-onset Pompe disease in ThailandLukana Ngiwsara, Duangrurdee Wattanasirichaigoon, Thipwimol Tim-Aroon, et al.
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