School personnel information

写真b

Fujiwara Makoto


Date of Birth

1977.05

Keyword

osteocytes, sclerostin

Mail Address

Mail Address

Laboratory Phone number

+81-6-6879-3932

Laboratory Fax number

+81-6-6879-3939

Gender

Male

Organization 【 display / non-display

  • 2015.04.01 - 2017.03.31, Course for Oral Sciences, Graduate School of Dentistry, Assistant Professor

  • 2019.03.16 - , Course for Oral Sciences, Graduate School of Dentistry, Assistant Professor

  • 2015.04.01 - , Division of Medicine, Graduate School of Medicine

Education 【 display / non-display

Osaka University Faculty of Medicine  Graduated 2003.03
Osaka University Graduate School, Division of Medical Sciences  Unfinished 2015.03

Research topics 【 display / non-display

  • Embryonic medicine and pediatrics-related

  • Embryonic medicine and pediatrics-related

 

Academic Papers 【 display / non-display

  • The mitophagy receptor Bcl-2-like protein 13 stimulates adipogenesis by regulating mitochondrial oxidative phosphorylation and apoptosis in mice, Makoto Fujiwara, Journal of Biological Chemistry,23 12683-12694, 2019.08, Papers

  • Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta, Ohata Y, Takeyari S, Nakano Y, Kitaoka T, Nakayama H, Bizaoui V, Yamamoto K, Miyata K, Yamamoto K, Fujiwara M, Kubota T, Michigami T, Yamamoto K, Yamamoto T, Namba N, Ebina K, Yoshikawa H, Ozono K, Osteoporos Int., 2019.08, Papers

  • Adult hypophosphatasia with compound heterozygous p.Phe327Leu missense and c.1559delT frameshift mutations in tissue-nonspecific alkaline phosphatase gene: a case report, Kazunori Fukushima, Journal of Medical Case Reports,24, 2019.04, Papers

  • Metreleptin treatment for congenital generalized lipodystrophy type 4 (CGL4): a case report, Takeyari S, Takakuwa S, Miyata K, Yamamoto K, Nakayama H, Ohata Y, Fujiwara M, Kitaoka T, Kubota T, Namba N, Sakai N, Ozono K, Clin Pediatr Endocrinol.,28(1) 1-7, 2019.02, Papers

  • Functional analysis of monocarboxylate transporter 8 mutations in Japanese Allan-Herndon-Dudley syndrome patients, Islam MSIslam M. S, Namba N, Ohata Y, Fujiwara M, Nakano C, Takeyari S, Miyata K, Nakano Y, Yamamoto K, Nakayama H, Kitaoka T, Kubota T, Ozono K, Endocrine Journal,28 19-29, 2019.01, Papers

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