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Plos One|September 17, 2020
Clinical factors affecting evoked magnetic fields in patients with Parkinson's diseaseRyoji Naganuma, Ichiro Yabe, Megumi Takeuchi, et al.
Gan to Kagaku Ryoho. Cancer & Chemotherapy|July 18, 2008
[A case of primary breast cancer who responded remarkably to the neoadjuvant chemotherapy with the combination of docetaxel and cyclophosphamide]Hiroshi Yoshibayashi, Hiroshi Ishiguro, Masahiro Takada, et al.
Glycobiology|February 17, 2018
Variant in human POFUT1 reduces enzymatic activity and likely causes a recessive microcephaly, global developmental delay with cardiac and vascular featuresHideyuki Takeuchi, Derek Wong, Michael Schneider, et al.
International Journal of Clinical Oncology|October 29, 2015
A retrospective analysis on the utility and complications of upper arm ports in 433 cases at a single instituteYukiko Mori, Satoshi Nagayama, Jun-Ichiro Kawamura, et al.
Developmental Biology|June 15, 2016
Genetic and biochemical evidence that gastrulation defects in Pofut2 mutants result from defects in ADAMTS9 secretionBrian A Benz, Sumeda Nandadasa, Megumi Takeuchi, et al.
Molecular Therapy. Nucleic Acids|August 31, 2023
Disease modeling and gene correction of LGMDR21 iPSCs elucidates the role of POGLUT1 in skeletal muscle maintenance, regeneration, and the satellite cell nicheJose L Ortiz-Vitali, Jianbo Wu, Nasa Xu, et al.
The Journal of Rheumatology|September 1, 2004
Immunogenetic features in 120 Japanese patients with idiopathic inflammatory myopathyTakefumi Furuya, Masayuki Hakoda, Naoyuki Tsuchiya, et al.
International Cancer Conference Journal|June 1, 2019
Granulocyte-colony-stimulating factor-producing metaplastic carcinoma of the breast with significant elevation of serum interleukin-17 and vascular endothelial growth factor levelsYukiko Fukui, Masahiro Kawashima, Kosuke Kawaguchi, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|February 15, 2022
O-fucosylation of thrombospondin type 1 repeats is essential for ECM remodeling and signaling during bone developmentSanjiv Neupane, Steven J Berardinelli, Daniel C Cameron, et al.
Human Molecular Genetics|October 11, 2019
ADAMTS9 and ADAMTS20 are differentially affected by loss of B3GLCT in mouse model of Peters plus syndromeBernadette C Holdener, Christopher J Percival, Richard C Grady, et al.
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