Zobrazeno 1 - 10
of 191
pro vyhledávání: '"HuiFang Yan"'
Publikováno v:
Frontiers in Plant Science, Vol 15 (2024)
Seed vigor is an important trait closely related to improved seed quality and long-term germplasm conservation, and it gradually decreases during storage, which has become a major concern for agriculture. However, the underlying regulatory mechanisms
Externí odkaz:
https://doaj.org/article/d35a060ce62d4065aae35c7d18cdead9
Publikováno v:
Agriculture, Vol 14, Iss 8, p 1305 (2024)
Legumes are important grains and forages, providing high-quality proteins, vitamins, and micronutrients to humans and animals. Medicago truncatula is a close relative of alfalfa (Medicago sativa). Caffeic acid O-methyltransferase (COMT), a key gene t
Externí odkaz:
https://doaj.org/article/3c5ebec07782499290070207d4475563
Publikováno v:
Plants, Vol 13, Iss 15, p 2061 (2024)
Seed physical dormancy (hard-seededness) is an interesting ecological phenomenon and important agronomic trait. The loss of seed coat impermeability/hard-seededness is a key target trait during the domestication of leguminous crops which allows seeds
Externí odkaz:
https://doaj.org/article/008fa81765c046988bf9ca98152653f1
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 13, p 7244 (2024)
Low temperature is the most common abiotic factor that usually occurs during the seed germination of alfalfa (Medicago sativa L.). However, the potential regulatory mechanisms involved in alfalfa seed germination under low temperature stress are stil
Externí odkaz:
https://doaj.org/article/c5a1596557274049a6ab6bf93d4b5057
Publikováno v:
PeerJ, Vol 12, p e16250 (2024)
Brassinosteroids (BRs) play many pivotal roles in plant growth and development, especially in cell elongation and vascular development. Although its biosynthetic and signal transduction pathway have been well characterized in model plants, their biol
Externí odkaz:
https://doaj.org/article/ab8b0869523a4b85b7a36aaa39341214
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
BackgroundThe diffuse large B-cell lymphoma (DLBCL) has the highest incidence of all lymphomas worldwide. To investigate the functions of lymphocyte activation gene 3 (LAG-3) and programmed cell death 1 (PD-1) in tissues and peripheral blood of patie
Externí odkaz:
https://doaj.org/article/2c376e8e8f5f4591a877f413b83479dc
Publikováno v:
Frontiers in Plant Science, Vol 14 (2023)
Globally, the species of Amanita are key components of ectomycorrhizal ecosystems. Some of them are widely known as poisonous or edible fungi. Although many new Amanita species from China have been described, the species diversity of Yanshan Mountain
Externí odkaz:
https://doaj.org/article/89ecbec28053443ebf29d3c9cd759e22
Autor:
Ruoyu Duan, Haoran Ji, Huifang Yan, Junyu Wang, Yu Zhang, Qian Zhang, Dongxiao Li, Binbin Cao, Qiang Gu, Ye Wu, Yuwu Jiang, Ming Li, Jingmin Wang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background The natural history and genotype–phenotype correlation of Pelizaeus–Merzbacher disease (PMD) of Chinese patients has been rarely reported. Method Patients who met the criteria for PMD were enrolled in our study. Genomic analys
Externí odkaz:
https://doaj.org/article/038f81a8bfc34ca3984b5e5d724bc500
Autor:
Yu Zhang, Hui Yan, Jieyu Liu, Huifang Yan, Yinan Ma, Cuijie Wei, Zhaoxia Wang, Hui Xiong, Xingzhi Chang
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-13 (2022)
Abstract Background Congenital myopathies are a group of rare neuromuscular diseases characterized by specific histopathological features. The relationship between the pathologies and the genetic causes is complex, and the prevalence of myopathy-caus
Externí odkaz:
https://doaj.org/article/18c61635d4ab41f2b8a8be123fbb3018
Autor:
Jinhong Zhang, Yan Lu, Xiaoyu Tian, Xinyi Men, Yange Zhang, Huifang Yan, Fan Yang, Zuozhen Yang, Xiuxia Wang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 10, Pp n/a-n/a (2022)
Abstract Background Global developmental delay (GDD) has a heterogeneous clinical profile among patients, accounting for approximately 1%–3% of cases in children. An increasing number of gene defects have been demonstrated to be associated with GDD
Externí odkaz:
https://doaj.org/article/c3d7c2a1028d4b12803d01cf75f36ad3