Zobrazeno 1 - 10
of 527
pro vyhledávání: '"Fen Lu"'
Autor:
Xiaomei Tang, Fen Lu, Ziwen Xiao, Yue Wang, Guoqing Hu, Kexin Cai, Ruichang Yin, Wei Song, Luoluo Xie, Guoling Guo, Wenming Wang, Lun Liu, Li Liu, Zhenfeng Ye, Wei Heng, Xianping Guo, Dongsheng Wang, Bing Jia
Publikováno v:
BMC Plant Biology, Vol 24, Iss 1, Pp 1-14 (2024)
Abstract Background Anthracnose, mainly caused by Colletotrichum fructicola, leads to severe losses in pear production. However, there is limited information available regarding the molecular response to anthracnose in pears. Results In this study, t
Externí odkaz:
https://doaj.org/article/ac3cb942e7e149588b4a029ad6a061c1
Autor:
Ya-ling Zhang, Yuan Qu, Huan-huan Song, Guo Cheng, Fen Lu, Ting-ting Cui, Ye Gong, Xiao-li Ding, Yang Yang, Qian Zhang, Lu-ting Yang, Ya-ping Yan
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 178, Iss , Pp 117188- (2024)
Multiple sclerosis (MS) is an autoimmune-mediated chronic inflammatory demyelinating disease of the central nervous system (CNS) that poses significant treatment challenges. Currently, it is believed that inflammatory and neuroprotective reactive ast
Externí odkaz:
https://doaj.org/article/774ff8927f4d4e9686a7811b52e0dcbe
Publikováno v:
Frontiers in Microbiology, Vol 15 (2024)
BackgroundPear black spot (PBS) is caused by Alternaria alternata and causes severe damage worldwide. It is particularly important to screen for synergistic fungicide combinations to address issues associated with the low efficacy of biocontrol agent
Externí odkaz:
https://doaj.org/article/039b21b4bd1e43ecbcb8f2414bcf1806
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Background Charcot-Marie-Tooth disease (CMT) is a group of single-gene hereditary diseases of peripheral nerve with high clinical variability and genetic heterogeneity. The typical clinical manifestations include progressive muscle weakness
Externí odkaz:
https://doaj.org/article/7fc473ee92e543898fa219242b0dfb4c
Autor:
Chunli Wang, Wei Zhou, Luyan Zhang, Luhan Fu, Wei Shi, Yan Qing, Fen Lu, Jian Tang, Xiucheng Gao, Aihua Zhang, Zhanjun Jia, Yue Zhang, Xiaoke Zhao, Bixia Zheng
Publikováno v:
BMC Genomics, Vol 24, Iss 1, Pp 1-14 (2023)
Abstract Objectives Microcephaly is caused by reduced brain volume and most usually associated with a variety of neurodevelopmental disorders (NDDs). To provide an overview of the diagnostic yield of whole exome sequencing (WES) and promote novel can
Externí odkaz:
https://doaj.org/article/83a6a1e2d9c0428db512058938725f42
Publikováno v:
中西医结合护理, Vol 8, Iss 10, Pp 135-138 (2022)
Based on the literature review and analysis, this article elaborated the research background, the current situation and results of Traditional Chinese Medicine in the treatment of periodontitis, so as to explore the application prospect of TCM in the
Externí odkaz:
https://doaj.org/article/198723f178be4ece94ec2973b811d841
Publikováno v:
Frontiers in Ecology and Evolution, Vol 11 (2023)
IntroductionImproving the development efficiency of human–earth systems is a practical requirement for achieving high-quality regional development.MethodsThe article designs a data envelopment analysis (DEA) model under the constraints of coordinat
Externí odkaz:
https://doaj.org/article/d1e8a3e5627d4a58b0eaf545fb383a71
Autor:
Xiang-Ming Hu, Wen-Ting Wei, De-Yi Huang, Cai-Di Lin, Fen Lu, Xiao-Ming Li, Huo-Sheng Liao, Zhi-Hong Yu, Xiao-Ping Weng, Shi-Bin Wang, Cai-Lan Hou, Fu-Jun Jia
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 17, Iss 1, Pp 1-7 (2022)
Abstract Background The current study aimed to investigate the sleep quality of patients after valve replacement surgery due to infective endocarditis and identify risk factors for disturbed sleep post hospitalisation. Methods Eighty patients were as
Externí odkaz:
https://doaj.org/article/24f955be72a84718a4287a72604320b1
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Biallelic TENM3 variants were recently reported to cause non-syndromic microphthalmia with coloboma-9 (MCOPCB9) and microphthalmia and/or coloboma with developmental delay (MCOPS15). To date, only eight syndromic and non-syndromic microphthalmia case
Externí odkaz:
https://doaj.org/article/e443c6bd6421464c91aab57e6a45fa1e
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-5 (2021)
Abstract Background The Raynaud-Claes type of X-linked syndromic mental retardation (MRXSRC) is a very rare condition, by intellectual disability ranged from borderline to profound, impaired language development, brain abnormalities, facial dysmorphi
Externí odkaz:
https://doaj.org/article/3af77ba6c366490ba77318f002dc3fb8