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Pathology International|April 5, 2003
Non-functional adrenocortical adenoma with extensive degenerationYouhei Masugi, Kaori Kameyama, Motohiko Aiba, et al.
The Journal of Cell Biology|December 2, 2021
Live imaging of transcription sites using an elongating RNA polymerase II-specific probeSatoshi Uchino, Yuma Ito, Yuko Sato, et al.
Surgery Today|November 4, 2010
Primary leiomyosarcoma of the breast treated by partial resection of the breast including nipple and areola: report of a caseTakako Kamio, Masako Nishizawa, Kei Aoyama, et al.
Journal of Surgical Oncology|April 29, 2021
High prevalence of pulmonary embolism prior to cancer therapies in patients with ovarian and endometrial cancers detected by contrast-enhanced CT using D-dimer as an indexYuji Habu, Akira Mitsuhashi, Shinsuke Hanawa, et al.
Oncology Reports|June 18, 2015
Telomere shortening in breast cancer correlates with the pathological features of tumor progressionMakoto Kammori, Yoshiyuki Sugishita, Takahiro Okamoto, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|February 5, 2003
Gliofibrous nodule in the cerebello-medullary fissureKazunari Yoshida, Kenji Hiraga, Hisatsugu Ishimori, et al.
The American Journal of Gastroenterology|July 24, 2002
Characterization of structures with T-lymphocyte aggregates in ileal villi of Crohn's diseaseMakoto Naganuma, Mamoru Watanabe, Takanori Kanai, et al.
Journal of Zoo and Wildlife Medicine : Official Publication of the American Association of Zoo Veterinarians|April 1, 2017
ANESTHETIC MANAGEMENT OF AN INDO-PACIFIC BOTTLENOSE DOLPHIN (TURSIOPS ADUNCUS) REQUIRING SURGICAL DEBRIDEMENT OF A TAIL ABSCESSJun Tamura, Makio Yanagisawa, Yusuke Endo, et al.
Bioscience Trends|October 25, 2016
Polyphosphate-induced matrix metalloproteinase-13 is required for osteoblast-like cell differentiation in human adipose tissue derived mesenchymal stem cellsNobuaki Ozeki, Makio Mogi, Naoko Hase, et al.
Journal of Human Genetics|October 21, 2003
Different attenuated phenotypes of GM2 gangliosidosis variant B in Japanese patients with HEXA mutations at codon 499, and five novel mutations responsible for infantile acute formAkemi Tanaka, Lan Thi Ngcok Hoang, Yasuaki Nishi, et al.
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