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Pediatrics International : Official Journal of the Japan Pediatric Society|June 7, 2016
Mitochondrial respiratory chain complex IV deficiency complicated with chronic intestinal pseudo-obstruction in a neonateYuya Hashimura, Ichiro Morioka, Chieko Hisamatsu, et al.
Human Reproduction (Oxford, England)|April 23, 2021
An axonemal alteration in apical endometria of human adenomyosisKhaleque N Khan, Akira Fujishita, Takashi Suematsu, et al.
Acta Neuropathologica|April 30, 2024
Viral entry and translation in brain endothelia provoke influenza-associated encephalopathyShihoko Kimura-Ohba, Mieko Kitamura, Yusuke Tsukamoto, et al.
Histochemistry and Cell Biology|April 26, 2016
HEK293 cells express dystrophin Dp71 with nucleus-specific localization of Dp71abAtsushi Nishida, Sato Yasuno, Atsuko Takeuchi, et al.
Frontiers in Oncology|September 7, 2021
A 14-Marker Multiplexed Imaging Panel for Prognostic Biomarkers and Tumor Heterogeneity in Head and Neck Squamous Cell CarcinomaJunichi Mitsuda, Takahiro Tsujikawa, Kanako Yoshimura, et al.
Experimental Animals|July 10, 2015
Oncogenic Lmo3 cooperates with Hen2 to induce hydrocephalus in miceEriko Isogai, Kazuhiro Okumura, Megumi Saito, et al.
Pathology International|October 20, 2020
Mantle cell lymphoma with EBV-positive Hodgkin and Reed-Sternberg-like cells in a patient after autologous PBSCT: Phenotypically distinct but genetically related tumorsRisa Kanai, Aya Miyagawa-Hayashino, Yukiko Shishido-Hara, et al.
Biochemical and Biophysical Research Communications|March 12, 2008
Ionizing radiation downregulates ASPM, a gene responsible for microcephaly in humansAkira Fujimori, Takeshi Yaoi, Hiroshi Ogi, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|January 10, 2024
Neonatal uterine bleeding: Risk factors and its association with endometriosis-related symptoms later in lifeKanae Ogawa, Khaleque N Khan, Haruo Kuroboshi, et al.
Brain Pathology (Zurich, Switzerland)|August 1, 2023
Altered properties of amyloidogenic prion protein in genetic Creutzfeldt-Jakob disease with PRNP V180I mutation in response to pentosan polysulfateMasahiro Shijo, Motoi Yoshimura, Tsuyoshi Omae, et al.
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