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NMC Case Report Journal|August 17, 2022
Genetic Alteration May Proceed with a Histological Change in Glioblastoma: A Report from Initially Diagnosed as Nontumor Lesion CasesHayato Takeuchi, Yoshinobu Takahashi, Seisuke Tanigawa, et al.Asian Spine Journal|December 28, 2017
Generation of Induced Pluripotent Stem Cells and Neural Stem/Progenitor Cells from Newborns with Spina Bifida ApertaYohei Bamba, Masahiro Nonaka, Natsu Sasaki, et al.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 10, 2016
Pediatric thalamic glioma with H3F3A K27M mutation, which was detected before and after malignant transformation: a case reportKenichi Ishibashi, Takeshi Inoue, Hiroko Fukushima, et al.Plos One|October 8, 2016
Introduction of High Throughput Magnetic Resonance T2-Weighted Image Texture Analysis for WHO Grade 2 and 3 GliomasManabu Kinoshita, Mio Sakai, Hideyuki Arita, et al.Neuro-Oncology Advances|November 2, 2020
<i>TERT</i> promoter mutation associated with multifocal phenotype and poor prognosis in patients with <i>IDH</i> wild-type glioblastomaZensho Kikuchi, Ichiyo Shibahara, Tetsu Yamaki, et al.Cell Transplantation|August 31, 2017
In Vitro Screening of Exogenous Factors for Human Neural Stem/Progenitor Cell Proliferation Using Measurement of Total ATP Content in Viable CellsYonehiro Kanemura, Hideki Mori, Atsuyo Nakagawa, et al.Stem Cells Translational Medicine|March 20, 2019
Human Genomic Safe Harbors and the Suicide Gene-Based Safeguard System for iPSC-Based Cell TherapyYasuyoshi Kimura, Tomoko Shofuda, Yuichiro Higuchi, et al.Cell Transplantation|January 13, 2006
In vitro screening of exogenous factors for human neural stem/progenitor cell proliferation using measurement of total ATP content in viable cellsYonehiro Kanemura, Hideki Mori, Atsuyo Nakagawa, et al.Journal of Neurosurgery. Pediatrics|October 4, 2011
Prenatal molecular diagnosis of a severe type of L1 syndrome (X-linked hydrocephalus)Mami Yamasaki, Masahiro Nonaka, Nobuhiro Suzumori, et al.BMC Cancer|September 16, 2021
Infrequent RAS mutation is not associated with specific histological phenotype in gliomasYasuhide Makino, Yoshiki Arakawa, Ema Yoshioka, et al.Pageof 6