2016 - 2018 Pathogenic analysis of idiopathic scoliosis using conditional knock-out mice of Gpr126
論文 (39件)：
Long Guo, Smrithi Salian, Jing-Yi Xue, Nicola Rath, Justine Rousseau, Hyunyun Kim, Sophie Ehresmann, Shahida Moosa, Norio Nakagawa, Hiroshi Kuroda, et al. Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans. American journal of human genetics. 2023. 110. 7. 1068-1085
Masahiro Nakajima, Masaru Koido, Long Guo, Chikashi Terao, Shiro Ikegawa. A novel CCDC91 isoform associated with ossification of the posterior longitudinal ligament of the spine works as a non-coding RNA to regulate osteogenic genes. The American Journal of Human Genetics. 2023
Yoshiro Yonezawa, Long Guo, Hisaya Kakinuma, Nao Otomo, Soichiro Yoshino, Kazuki Takeda, Masahiro Nakajima, Toshiyuki Shiraki, Yoji Ogura, Yohei Takahashi, et al. Identification of a functional susceptibility variant for adolescent idiopathic scoliosis that upregulates EGR1-mediated UNCX expression. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 2022. 38. 1. 144-153
Toshiyuki Itai, Zheng Wang, Gen Nishimura, Hirofumi Ohashi, Long Guo, Yasuhiro Wakano, Takahiro Sugiura, Hiromi Hayakawa, Mayumi Okada, Takashi Saisu, et al. De novo heterozygous variants in KIF5B cause kyphomelic dysplasia. Clinical genetics. 2022. 102. 1. 3-11
Long Guo, Aritoshi Iida, Gandham SriLakshmi Bhavani, Kalpana Gowrishankar, Zheng Wang, Jing-yi Xue, Juan Wang, Noriko Miyake, Naomichi Matsumoto, Takanori Hasegawa, et al. Deficiency of TMEM53 causes a previously unknown sclerosing bone disorder by dysregulation of BMP-SMAD signaling. Nature Communications. 2021. 12. 1. 2046-2046
Guo Long, Hiroshi Yamashita, Tetsushi Sakuma, Ikuyo Kou, Aki Takimoto, Takashi Yamamoto, Taiji Adachi, Yuji Hiraki, Shiro Ikegawa, Chisa Shukunami. Increased and decreased expression of the ladybird homeobox 1 cause scoliosis in zebrafish. 第4回ゲノム編集研究会(2014.10.6-7. 広島). 2014
郭 龍, 山下 寛, 黄 郁代, 滝本 晶, 安達泰治, 開 祐司, 池川 志郎, 宿南 知佐. Increased expression of the ladybird homeobox 1 (lbx1) cause scoliosis in zebrafish mimicking human adolescent idiopathic scoliosis and congenital scoliosis. 第61回日本生化学会近畿支部例会(2014.5.17. 京都). 2014
Bo Qu, Jinlu Ma, Long Guo, Haohua Wang, Lv Yi. Mig-7 overexpression correlates with hepatocellular carcinoma metastasis through induction of vasculogenic mimicry. JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS. 2009. 209. 3. S52-S52
Identification of TMEM53, a nuclear membrane protein, as the disease gene for a novel type of skeletal dysplasia and a gate keeper of BMP-SMAD signaling at nuclear pore
(4th RIKEN IMS-Stanford ISCBRM Joint Symposium 2020)
