Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Jian-Kang Li"'
Autor:
Zi-Tong Wang, Yu-ping Liu, Yi-Long Ma, Shuang-Yi Pan, Jian-Kang Li, Shao-Jun Shi, Zheng-Fang Wu, Zhi Li, Ya-Fang Shang, Zhao-Jun Wei
Publikováno v:
Heliyon, Vol 9, Iss 5, Pp e16226- (2023)
To evaluate the release and activity of Indian jujube phenolics in vivo, its peel and pulp were subjected to simulated digestions. The phenolics content and antioxidant activity of the digested samples were determined. The results showed that the tot
Externí odkaz:
https://doaj.org/article/5ff2e44661a446d5b608b9a370091a36
Autor:
Wei Li, Xiao-Sen Jiang, Dong-Ming Han, Jia-Yu Gao, Zheng-Tao Yang, Li Jiang, Qian Zhang, Sheng-Hai Zhang, Ya Gao, Ji-Hong Wu, Jian-Kang Li
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Purposes: We aimed to characterize the USH2A genotypic spectrum in a Chinese cohort and provide a detailed genetic profile for Chinese patients with USH2A-IRD.Methods: We designed a retrospective study wherein a total of 1,334 patients diagnosed with
Externí odkaz:
https://doaj.org/article/46e9588553ea46c58d0e25819407f491
Autor:
Feng-Juan Gao, Dan-Dan Wang, Jian-Kang Li, Fang-Yuan Hu, Ping Xu, Fang Chen, Yu-He Qi, Wei Liu, Wei Li, Sheng-Hai Zhang, Qing Chang, Ge-Zhi Xu, Ji-Hong Wu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background The retinoid isomerohydrolase RPE65 has received considerable attention worldwide since a successful clinical gene therapy was approved in 2017 as the first treatment for vision loss associated with RPE65-mediated inherited retina
Externí odkaz:
https://doaj.org/article/8758de29a81c4db8a9ca476c6c4960a9
Autor:
Fang-Yuan Hu, Feng-Juan Gao, Jian-kang Li, Ping Xu, Dan-Dan Wang, Sheng-Hai Zhang, Ji-Hong Wu
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-10 (2020)
Abstract Background Stargardt disease (STGD1) is a common recessive hereditary macular dystrophy in early adulthood or childhood, with an estimated prevalence of 1:8000 to 1:10,000. ABCA4 is the causative gene for STGD1. The current study aims at ide
Externí odkaz:
https://doaj.org/article/d2513c580e5d454786a9d2c49ca42548
Autor:
Feng-Juan Gao, Guo-Hong Tian, Fang-Yuan Hu, Dan-Dan Wang, Jian-Kang Li, Qing Chang, Fang Chen, Ge-Zhi Xu, Wei Liu, Ji-Hong Wu
Publikováno v:
BMC Ophthalmology, Vol 20, Iss 1, Pp 1-8 (2020)
Abstract Background To report the clinical and genetic findings from seven Chinese patients with choroideremia. Methods Five hundred seventy-eight patients with a clinically suspected diagnosis of retinitis pigmentosa (RP) underwent comprehensive oph
Externí odkaz:
https://doaj.org/article/fdb9e4a02fec4be4b2a418a1eeb84475
Autor:
Jian-Kang Li, Yu Chen, Bo-Lun Huang, Zhen-Zhao Tao, Xiao-Hang Luan, Xiao-Hui Sun, Tong-Jie Zhang, Vishal Gajjar
Publikováno v:
The Astronomical Journal, Vol 167, Iss 1, p 8 (2023)
In this paper, we propose a novel method for distinguishing extraterrestrial intelligence (ETI) signals from radio frequency interference (RFI) by leveraging polarization features. We exploit the sinusoidal variation of the linearly polarized compone
Externí odkaz:
https://doaj.org/article/6ec47b97f46c4db38b9d2b765d367ed7
Autor:
Zhen-Zhao Tao, Bo-Lun Huang, Xiao-Hang Luan, Jian-Kang Li, Hai-Chen Zhao, Hong-Feng Wang, Tong-Jie Zhang
Publikováno v:
The Astronomical Journal, Vol 166, Iss 5, p 190 (2023)
Search for extraterrestrial intelligence (SETI) has been mainly focused on nearby stars and their planets in recent years. Barnard’s star is the second closest star system to the Sun and the closest star in the Five-hundred-meter Aperture Spherical
Externí odkaz:
https://doaj.org/article/76138ed7141b4496b3aae8a9ed24a2b5
Autor:
Feng-Juan Gao, Fang-Yuan Hu, Ping Xu, Yu-He Qi, Jian-Kang Li, Yong-Jin Zhang, Fang Chen, Qing Chang, Fang Song, Si-Mai Shen, Ge-Zhi Xu, Ji-Hong Wu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-12 (2019)
Abstract Background Heimler syndrome (HS) is a rare hereditary systemic disorder, partial clinically overlapping with Usher syndrome. So far, our knowledge of HS is very limited, many cases are misdiagnosed or may not even be diagnosed at all. This s
Externí odkaz:
https://doaj.org/article/3ae7528d7f584d748109648bc37a583a
Autor:
Wei Li, Ning Qu, Jian-Kang Li, Yu-Xin Li, Dong-Ming Han, Yi-Xi Chen, Le Tian, Kang Shao, Wen Yang, Zhuo-Shi Wang, Xuan Chen, Xiao-Ying Jin, Zi-Wei Wang, Chen Liang, Wei-Ping Qian, Lu-Sheng Wang, Wei He
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
AimsTo characterize the genetic landscape and mutation spectrum of patients with corneal dystrophies (CDs) in a large Han ethnic Chinese Cohort with inherited eye diseases (IEDs).MethodsRetrospective study. A large IED cohort was recruited in this st
Externí odkaz:
https://doaj.org/article/1faa86177bab43d1bcd9f23e4979da52
Autor:
Jian-Kang Li, Li‐Li Li, Wei Li, Zi‐Wei Wang, Feng‐Juan Gao, Fang-Yuan Hu, Sheng‐Hai Zhang, Shou-Fang Qu, Jie Huang, Lu-Sheng Wang, Ji-Hong Wu, Fang Chen
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 7, Pp n/a-n/a (2020)
Abstract Background Age‐related cataracts (ARC) is the most common blinding eye disease worldwide, and its incidence tend to become younger. However, the relationship between genetic factors and mechanisms is not fully understood. The aim of the st
Externí odkaz:
https://doaj.org/article/5cee1cc2521841c28e4ccded37982c50