Zobrazeno 1 - 10
of 631
pro vyhledávání: '"Shujie, Zhang"'
Autor:
Qiaoling Wei, Zhuoyao Gu, Weimin Tan, Hongyu Kong, Hao Fu, Qin Jiang, Wenjuan Zhuang, Shaochi Zhang, Lixia Feng, Yong Liu, Suyan Li, Bing Qin, Peirong Lu, Jiangyue Zhao, Zhigang Li, Songtao Yuan, Hong Yan, Shujie Zhang, Xiangjia Zhu, Jiaxu Hong, Chen Zhao, Bo Yan
Publikováno v:
Engineering, Vol 41, Iss , Pp 179-188 (2024)
In ophthalmology, the quality of fundus images is critical for accurate diagnosis, both in clinical practice and in artificial intelligence (AI)-assisted diagnostics. Despite the broad view provided by ultrawide-field (UWF) imaging, pseudocolor image
Externí odkaz:
https://doaj.org/article/3c3cbe574ce847ae87796d1ff7386f74
Autor:
Shujie Zhang, Haisong Qin, Qingming Wang, Yingfei Wang, Yanhui Liu, Qi Yang, Jingsi Luo, Zailong Qin, Xiang Ji, Lijuan Kan, Guoxing Geng, Jing Huang, Shengkai Wei, Qiuli Chen, Yiping Shen, Haiming Yuan, Baoling Lai
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-6 (2024)
Abstract Biallelic pathogenic variants in TARS2 lead to combined oxidative phosphorylation deficiency, subtype 21 (COXPD21, MIM #615918), which is a rare mitochondrial encephalomyopathy (ME) characterized by early-onset severe axial hypotonia, limb h
Externí odkaz:
https://doaj.org/article/8be34e77e1ac4cecbd08e2d7d860c3ed
Publikováno v:
Plant, Soil and Environment, Vol 70, Iss 10, Pp 632-643 (2024)
This study investigates the impact of various molecular weights (MWs) of fulvic acid (FA) on maize growth, grain yield, and nutrient uptake under different nitrogen levels (NLs). A 2 × 3 balanced design was employed, with high (0.2 g N/kg) and low (
Externí odkaz:
https://doaj.org/article/bb6c6ad8566c41a2a50fc95dc7be6d9c
Autor:
Qi Yang, Xunzhao Zhou, Sheng Yi, XiaoLing Li, Qiang Zhang, Shujie Zhang, Li Lin, Shang Yi, Biyan Chen, Zailong Qin, Jingsi Luo
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
IntroductionMutations in the protein WD repeat structural domain 26 (WDR26, MIM 617424) have been identified as the cause of autosomal dominant Skraban-Deardorff syndrome, a rare genetic disorder characterized by intellectual disability (ID), develop
Externí odkaz:
https://doaj.org/article/c20e17db125443eb98c7b4e20ec0d477
Publikováno v:
Journal of Ethnobiology and Ethnomedicine, Vol 20, Iss 1, Pp 1-34 (2024)
Abstract Background Homegardens are small-scale land use systems with significant implications for local livelihoods, biodiversity conservation, and sustainable development due to their diverse flora and fauna. Conducting homegarden surveys enables r
Externí odkaz:
https://doaj.org/article/8bba807515c54c96b913ccdea6955036
Publikováno v:
Frontiers in Public Health, Vol 12 (2024)
Background/objectiveWhile Physical Literacy has been highlighted as a determinant in health in recent study, there is a dearth of studies examining its effect on physical health, and there is a little in the way of empirical data linking Physical Lit
Externí odkaz:
https://doaj.org/article/2bc189e7ae0045bf831172d22bcbee7c
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
ObjectiveThis study revealed a core regulator and common upstream mechanisms for the multifaceted pathological processes of age-related macular degeneration (AMD) and provided proof-of-concept for this new therapeutic target.MethodsComprehensive gene
Externí odkaz:
https://doaj.org/article/8eadfabd31e84c48a7f42f1931eca149
Publikováno v:
Guoji laonian yixue zazhi, Vol 45, Iss 1, Pp 82-86 (2024)
Objective To investigate the expression of serum omentin-1 and oxidative stress parameters in elderly patients with type 2 diabetes mellitus(T2DM) complicated with osteoporosis. Methods A prospective study was conducted in 148 elderly patients with T
Externí odkaz:
https://doaj.org/article/87747d1e3beb439cab8254d5af1a903b
Publikováno v:
npj Urban Sustainability, Vol 4, Iss 1, Pp 1-11 (2024)
Abstract Family responsibility discrimination is a form of discrimination against men and women because of their caregiving responsibilities. Unlike prior studies that have predominantly focused on Western contexts, this study shifts attention to obs
Externí odkaz:
https://doaj.org/article/56c50a1b6ed64b3da4ce482f41606d86
Autor:
Qi Yang, Xunzhao Zhou, Yeying Ling, Qiang Zhang, Shang Yi, Qiuli Chen, Shujie Zhang, Zailong Qin, Jingsi Luo
Publikováno v:
Heliyon, Vol 10, Iss 6, Pp e27955- (2024)
Trichohepatoneurodevelopmental syndrome is an extremely uncommon autosomal recessive disorder resulting from variants in the CCDC47 gene, which encodes a Ca2+-binding endoplasmic reticulum (ER) transmembrane protein. To date, only four patients with
Externí odkaz:
https://doaj.org/article/a83d46d32c704998a1470d51eeacdb09