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Atsuo Nakayama

Nagoya University

65

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1065

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Novel MSX1 frameshift mutation in a Japanese family with nonsyndromic oligodontia.

2021 Human genome variation
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Reduction in miR-219 expression underlies cellular pathogenesis of oligodendrocytes in a mouse model of Krabbe disease.

2021 Brain Pathology
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Impaired social facilitation on voluntary exercise of BALB/cCrSlc mice, a proposed as an autism spectrum disorder model.

2020 Neuroscience Research
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Identification of nuclear localization signals in the human homeoprotein MSX1

2018 Biochemistry and Cell Biology
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An aberrant splice acceptor site due to a novel intronic nucleotide substitution in MSX1 gene is the cause of congenital tooth agenesis in a Japanese family.

2015 PLOS ONE
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Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patient

2015 Mutagenesis
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Characterization of novel MSX1 mutations identified in Japanese patients with nonsyndromic tooth agenesis.

2014 PLOS ONE
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DDX6 post-transcriptionally down-regulates miR-143/145 expression through host gene NCR143/145 in cancer cells

2013 Biochimica et Biophysica Acta
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A novel mutation in the C-terminal region of RUNX2/CBFA1 distal to the DNA-binding runt domain in a Japanese patient with cleidocranial dysplasia

2011 International Journal of Oral and Maxillofacial Surgery
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Inhibition of deacetylase activity of Hdac6 causes antidepressant-like behavior in mice

2011 Neuroscience Research
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