Japan (JP)

Sellar Region Atypical Teratoid/Rhabdoid Tumors (ATRT) in Adults Display DNA Methylation Profiles of the ATRT-MYC Subgroup (2018) Johann PD, Bens S, Oyen F, Wagener R, Giannini C, Perry A, Raisanen JM, et al. Journal article Dinuclear Iron(III) and Cobalt(III) Complexes Featuring a Biradical Bridge: Their Molecular Structures and Magnetic, Spectroscopic, and Redox Properties (2018) Mondal D, Majee MC, Kundu S, Mörtel M, Abbas G, Endo A, Khusniyarov M, Chaudhury M Journal article, Original article CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2018) Blok LS, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, et al. Journal article Pseudoexfoliation associated protective variant, rs7173049, reveals a novel regulatory region downstream of LOXL1 (2018) Berner D, Pasutto F, Hoja U, Zenkel M, Ozaki M, Williams S, Ramsay M, et al. Conference contribution Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation (2018) Teumer A, Chaker L, Groeneweg S, Li Y, Di Munno C, Barbieri C, Schultheiss UT, et al. Journal article UTX-mediated enhancer and chromatin remodeling suppresses myeloid leukemogenesis through noncatalytic inverse regulation of ETS and GATA programs (2018) Gozdecka M, Meduri E, Mazan M, Tzelepis K, Dudek M, Knights AJ, Pardo M, et al. Journal article Role of (-)-epigallocatechin gallate in the pharmacokinetic interaction between nadolol and green tea in healthy volunteers (2018) Abe O, Ono T, Sato H, Mueller F, Ogata H, Miura I, Shikama Y, et al. Journal article Optimization of a drug transporter probe cocktail: potential screening tool for transporter-mediated drug-drug interactions (2018) Stopfer P, Giessmann T, Hohl K, Hutzel S, Schmidt S, Gansser D, Ishiguro N, et al. Journal article De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder (2018) Gregor A, Sadleir LG, Asadollahi R, Azzarello-Burri S, Battaglia A, Ousager LB, Boonsawat P, et al. Journal article Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short stature (2018) Montalbano A, Juergensen L, Fukami M, Thiel C, Hauer N, Roeth R, Weiss B, et al. Journal article