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The Journal of Medical Investigation : JMI|September 29, 2017
Construction of a combinatorial pipeline using two somatic variant calling methods for whole exome sequence data of gastric cancerTomohiro Kohmoto, Kiyoshi Masuda, Takuya Naruto, et al.The Journal of Obstetrics and Gynaecology Research|August 27, 2009
Soluble tumor necrosis factor receptor-I in preterm infants with chorioamnionitisMiho Sato, Shigeru Nishimaki, Hiromi An, et al.Journal of Virology|March 6, 2015
Clinical Control of HIV-1 by Cytotoxic T Cells Specific for Multiple Conserved EpitopesHayato Murakoshi, Tomohiro Akahoshi, Madoka Koyanagi, et al.Journal of Human Genetics|October 16, 2024
Two-hit mutation causes Wilms tumor in an individual with FBXW7-related neurodevelopmental syndromeYoko Saito, Dai Keino, Yukiko Kuroda, et al.The Journal of Rheumatology|January 18, 2011
Association of IRF5 polymorphisms with susceptibility to macrophage activation syndrome in patients with juvenile idiopathic arthritisMasakatsu Yanagimachi, Takuya Naruto, Takako Miyamae, et al.American Journal of Obstetrics and Gynecology|November 18, 2004
Interleukin-6, interleukin-8, and soluble tumor necrosis factor receptor-I in the cord blood as predictors of chronic lung disease in premature infantsHiromi An, Shigeru Nishimaki, Makiko Ohyama, et al.Stem Cell Research & Therapy|April 16, 2024
Monoallelic KRAS (G13C) mutation triggers dysregulated expansion in induced pluripotent stem cell-derived hematopoietic progenitor cellsHuan-Ting Lin, Masatoshi Takagi, Kenji Kubara, et al.Human Cell|September 14, 2023
A short-term three dimensional culture-based drug sensitivity test is feasible for malignant bone tumorsHiroaki Goto, Takashi Ohtsu, Mieko Ito, et al.Clinical Transplantation|December 25, 2009
Influence of CYP3A5 and ABCB1 gene polymorphisms on calcineurin inhibitor-related neurotoxicity after hematopoietic stem cell transplantationMasakatsu Yanagimachi, Takuya Naruto, Reo Tanoshima, et al.Human Genome Variation|August 10, 2017
The first Japanese patient with mandibular hypoplasia, deafness, progeroid features and lipodystrophy diagnosed via POLD1 mutation detectionAsami Okada, Tomohiro Kohmoto, Takuya Naruto, et al.Pageof 11