Rchr
J-GLOBAL ID:201901002452283857   Update date: May. 21, 2020

LONG GUO

LONG GUO
Affiliation and department:
Research field  (1): Genomics
Research keywords  (5): scoliosis ,  Genetics ,  Sketetal dysplasia ,  cartilage ,  bone
Research theme for competitive and other funds  (1):
  • 2016 - 2018 Pathogenic analysis of idiopathic scoliosis using conditional knock-out mice of Gpr126
Papers (20):
  • Nao Otomo, Kazuki Takeda, Shunsuke Kawai, Ikuyo Kou, Long Guo, Mitsujiro Osawa, Cantas Alev, Noriaki Kawakami, Noriko Miyake, Naomichi Matsumoto, Yukuto Yasuhiko, Toshiaki Kotani, Teppei Suzuki, Koki Uno, Hideki Sudo, Satoshi Inami, Hiroshi Taneichi, Hideki Shigematsu, Kei Watanabe, Ikuho Yonezawa, Ryo Sugawara, Yuki Taniguchi, Shohei Minami, Kazuo Kaneko, Masaya Nakamura, Morio Matsumoto, Junya Toguchida, Kota Watanabe, Shiro Ikegawa. Bi-allelic loss of function variants of TBX6 causes a spectrum of malformation of spine and rib including congenital scoliosis and spondylocostal dysostosis. Journal of medical genetics. 2019. 56. 9. 622-628
  • Xue JY, Wang Z, Shinagawa S, Ohashi H, Otomo N, Elcioglu NH, Nakashima T, Nishimura G, Ikegawa S, Guo L. TNFRSF11A-Associated Dysosteosclerosis: A Report of the Second Case and Characterization of the Phenotypic Spectrum. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 2019. 34. 10. 1873-1879
  • Guo L, Bertola DR, Takanohashi A, Saito A, Segawa Y, Yokota T, Ishibashi S, Nishida Y, Yamamoto GL, Franco JFDS, Honjo RS, Kim CA, Musso CM, Timmons M, Pizzino A, Taft RJ, Lajoie B, Knight MA, Fischbeck KH, Singleton AB, Ferreira CR, Wang Z, Yan L, Garbern JY, Simsek-Kiper PO, Ohashi H, Robey PG, Boyde A, Matsumoto N, Miyake N, Spranger J, Schiffmann R, Vanderver A, Nishimura G, Passos-Bueno MRDS, Simons C, Ishikawa K, Ikegawa S. Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain Malformation. American journal of human genetics. 2019. 104. 5. 925-935
  • Otomo N, Mizumoto S, Lu HF, Takeda K, Campos-Xavier B, Mittaz-Crettol L, Guo L, Takikawa K, Nakamura M, Yamada S, Matsumoto M, Watanabe K, Ikegawa S. Identification of novel LFNG mutations in spondylocostal dysostosis. Journal of human genetics. 2019. 64. 3. 261-264
  • Guo L, Elcioglu NH, Karalar OK, Topkar MO, Wang Z, Sakamoto Y, Matsumoto N, Miyake N, Nishimura G, Ikegawa S. Dysosteosclerosis is also caused by TNFRSF11A mutation. Journal of human genetics. 2018. 63. 6. 769-774
more...
Books (1):
  • Zebrafish, Medaka, and Other Small Fishes - New Model Animals in Biology, Medicine, and Beyond
    Springer Nature Singapore 2019
Education (4):
  • 2011 - 2015 Kyoto University Medical school Regenerative medicine
  • 2010 - 2011 Kyoto University Medical school Regenerative medicine
  • 2007 - 2009 Xi'an Jiaotong University Medical school Surgery
  • 2002 - 2007 Xi'an Jiaotong University Medical school Clinical medicine
Work history (4):
  • 2019/01 - 現在 RIKEN Research Scientist
  • 2016/05 - 2018/12 RIKEN
  • 2015/04 - 2016/03 Kyoto University Research associate
  • 2011/04 - 2015/03 Kyoto University PhD student
Association Membership(s) (2):
JAPANESE SOCIETY FOR BONE AND MINERAL RESEARCH ,  THE JAPAN SOCIETY OF HUMAN GENETICS
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