Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Xinhe Fang"'
Autor:
Xinhe Fang, Meijiao Ma, Weining Rong, Yuan-Yuan Lian, Xueli Wu, Yongying Gao, Hui-Ping Li, Xunlun Sheng
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
IntroductionJoubert syndrome a rare genetic disorder, is characterized by abnormalities in the development of the central nervous system with “molar signs” on magnetic resonance imaging of the brain and accompanied by cerebellar vermis hypoplasia
Externí odkaz:
https://doaj.org/article/bb116e5c0a39438db92e56935ef602e8
Publikováno v:
Ophthalmic Genetics. 41:591-598
Background: Achromatopsia (ACHM) is an inherited retinal disease affecting the cone cell function. To date, six pathogenic genes of ACHM have been identified. However, the diagnostic and therapeuti...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::178c8952db2f43de897f4685d7e01a2c
https://doi.org/10.1080/13816810.2020.1802762
https://doi.org/10.1080/13816810.2020.1802762
Publikováno v:
Ophthalmic genetics. 41(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ec3d58f266045b81ca56eda9a60a5fb0
https://pubmed.ncbi.nlm.nih.gov/32787476
https://pubmed.ncbi.nlm.nih.gov/32787476
Autor:
Sheng-Yuan Liu, J. X. Ge, Xinhe Fang, Chao Zhang, Yuefang Wu, Tie Liu, Jinhua He, Bing-Gang Ju, Sheng-Li Qin, Mengyao Tang, Kee-Tae Kim
Publikováno v:
The Astrophysical Journal. 887:243
To deepen our understanding of the chemical properties of the Planck Galactic Cold Clump (PGCC) G168.72-15.48, we performed observations of nine molecular species, namely, \ce{c-C3H}, \ce{H2CO}, \ce{HC5N}, \ce{HC7N}, \ce{SO}, \ce{CCH}, \ce{N2H+}, \ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::142bd758ec962c044de4ebf7a1f8990a
https://doi.org/10.3847/1538-4357/ab5447
https://doi.org/10.3847/1538-4357/ab5447
Autor:
Mengyao Tang, J. X. Ge, Sheng-Li Qin, Tie Liu, Yuefang Wu, Kee-Tae Kim, Sheng-Yuan Liu, Chao Zhang, J. H. He, Bing-Gang Ju, Xinhe Fang
Publikováno v:
Astrophysical Journal; 12/20/2019, Vol. 887 Issue 2, p1-1, 1p
Autor:
Yuan, Shiqin1 (AUTHOR), Qi, Rui1,2 (AUTHOR), Fang, Xinhe1 (AUTHOR), Wang, Xiaoguang1 (AUTHOR), Zhou, Liang1 (AUTHOR), Sheng, Xunlun1 (AUTHOR) shengxunlun@163.com
Publikováno v:
Ophthalmic Genetics. Dec2020, Vol. 41 Issue 6, p591-598. 8p.