Rchr
J-GLOBAL ID：202001016509342512
Update date: Aug. 06, 2024
WANG ZHENG
ワン ジェン | WANG ZHENG
Affiliation and department：
Job title：
研究員
Research field (3)：
Molecular biology
, Genetics
, Genomics
Research keywords (1)：
遺伝学 骨系統疾患 軟骨 骨 繊毛病
Research theme for competitive and other funds (3)：
- 2022 - 2025 運動器疾患のMulti disease GWAS 解析
- 2017 - 2019 Analysis on the pathogenesis of idiopathic scoliosis using Gpr126 conditional knock-out mice
- 2017 - 2019 Systematic sequence analysis for early onset skeletal dysplasia
Papers (28)：
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Zheng Wang, Mitsuhiro Kometani, Leonid Zeitlin, Yael Wilnai, Akira Kinoshita, Koh-ichiro Yoshiura, Hiroko Ninomiya, Takeshi Imamura, Long Guo, Jingyi Xue, et al. Heterozygous mutations in the straitjacket region of the latency-associated peptide domain of TGFB2 cause Camurati-Engelmann disease type II. Journal of Human Genetics. 2024
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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
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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
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Jing-Yi Xue, Giedre Grigelioniene, Zheng Wang, Gen Nishimura, Aritoshi Iida, Naomichi Matsumoto, Emma Tham, Noriko Miyake, Shiro Ikegawa, Long Guo. SLC4A2 Deficiency Causes a New Type of Osteopetrosis. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 2021. 37. 2. 226-235
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Jing-Yi Xue, Pelin O. Simsek-Kiper, Gulen Eda Utine, Li Yan, Zheng Wang, Ekim Z. Taskiran, Beren Karaosmanoglu, Gozde Imren, Rahsan Gocmen, Gen Nishimura, et al. Expanding the phenotypic spectrum of TNFRSF11A-associated dysosteosclerosis: a case with intracranial extramedullary hematopoiesis. Journal of Human Genetics. 2021. 66. 6. 607-611
ｍore...
Lectures and oral presentations (3)：
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New Discovery on the Basic Research of Camurati-Engelmann Disease
(第9回 Orthopedic Research Club 2019)
-
Identification of Disease Genes of Skeletal Dysplasia: Lessons from Skeletal Ciliopathy
(第8回 Orthopedic Research Club 2017)
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Identification of disease genes of skeletal dysplasia
(The 3rd Tsinghua-RIKEN Joint Symposium 2017)
Education (2)：
- 2003 - 2008 Peking Union Medical College, Tsinghua University Medical Genetics
- 1999 - 2003 Nanjing University
Work history (3)：
- 2016/10 - 現在 RIKEN RIKEN Center for Integrative Medical Sciences
- 2008/07 - 2016/09 Chinese Academy of Medical Sciences Institute of Basic Medical Sciences
- 2014/03 - 2016/03 RIKEN RIKEN Center for Integrative Medical Sciences Visiting scholar
Awards (1)：
- 2019/08 - 理化学研究所 桜舞賞・研究奨励賞 遺伝性骨疾患の新しい原因遺伝子の同定
Association Membership(s) (3)：
日本進化学会
, 日本骨代謝学会
, 日本人類遺伝学会
