Zobrazeno 1 - 5
of 5
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...
Publikováno v:
Ophthalmic genetics. 41(6)
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
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