Zobrazeno 1 - 10
of 331
pro vyhledávání: '"Liwen, Wu"'
Publikováno v:
Complex & Intelligent Systems, Vol 11, Iss 1, Pp 1-15 (2024)
Abstract Due to the increasing sophistication of face forgery techniques, the images generated are becoming more and more realistic and difficult for human eyes to distinguish. These face forgery techniques can cause problems such as fraud and social
Externí odkaz:
https://doaj.org/article/2d5b748f6b924effb6a5cddacfadc652
Autor:
Amy D. Harper, Haluk Topaloglu, Eugenio Mercuri, Vasiliy Suslov, Liwen Wu, Cigdem Y. Ayanoglu, Michael Tansey, Michelle L. Previtera, Robert A. Crozier, Leslie Magnus, Paula R. Clemens
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Duchenne muscular dystrophy (DMD) is an X-linked recessive disease characterized by mutations in the dystrophin gene, causing motor and pulmonary function decline. Viltolarsen is indicated for patients with dystrophin gene mutations amenable
Externí odkaz:
https://doaj.org/article/9968d3b7d6514a56bdbd3bf8f3a6e367
Publikováno v:
IET Image Processing, Vol 18, Iss 10, Pp 2800-2815 (2024)
Abstract Image hiding is a task that hides secret images into cover images. The purposes of image hiding are to ensure the secret images are invisible to the human and the secret images can be recovered. The current state‐of‐the‐art steganograp
Externí odkaz:
https://doaj.org/article/2d99afd03be0498e9b79560255f99022
Autor:
Jiajia You, Li Liu, Xiongfeng Pan, Liwen Wu, Lihong Tan, Changci Zhou, Siwei Fang, Zhenghui Xiao, Jun Qiu
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
ObjectiveThe mechanisms driving the progression of infantile spasms are not well understood. We aimed to investigate the changes and correlations of the gut microbiota, the hypothalamus–pituitary–adrenal (HPA) axis hormones, and the inflammatory
Externí odkaz:
https://doaj.org/article/2360c12043704ef7b43e5eb3cbb296dc
Publikováno v:
Cell Death Discovery, Vol 10, Iss 1, Pp 1-12 (2024)
Abstract Mesial temporal lobe epilepsy (MTLE) is one of the most intractable epilepsies. Previously, we reported that mitochondrial DNA deletions were associated with epileptogenesis. While the underlying mechanism of mitochondrial DNA deletions duri
Externí odkaz:
https://doaj.org/article/adecc264356b42adb2e038adc5fbac16
Autor:
Jianchun Shao, Yujie Wang, Liwen Wu, Qingyin Zheng, Wenbo Zhu, Zhengbang Chen, Dianguang Zhang
Publikováno v:
Aquaculture Reports, Vol 40, Iss , Pp 102536- (2025)
An 8-week feeding trial was performed on Larimichthys crocea (initial body weight: 19.28 ± 1.85 g) to investigate the impact of replacing fish meal (FM) by chicken liver meal (CLM) on various aspects including growth performance, intestinal health a
Externí odkaz:
https://doaj.org/article/693204f65ca6437fb794418af47ca479
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract An increasing number of studies have focused on the role of NEDD4-2 in regulating neuronal excitability and the mechanism of epilepsy. However, the exact mechanism has not yet been elucidated. Here, we explored the roles of NEDD4-2 and the C
Externí odkaz:
https://doaj.org/article/59665e0b0acd44c8856ce7bf621c6c45
Autor:
Liwen Wu, Longze Zhang, Minglei Huang, Yan Wu, Sikan Jin, Yaqi Zhang, Xinyun Gan, Ting Yu, Guang Yu, Jidong Zhang, Xianyao Wang
Publikováno v:
Biomolecules, Vol 14, Iss 11, p 1353 (2024)
Autoimmune hepatitis (AIH) is an immune-mediated liver disease that currently faces limited treatment options. In its advanced stages, AIH can progress to liver fibrosis and cirrhosis. Recent research has increasingly focused on cell-free therapies,
Externí odkaz:
https://doaj.org/article/8892c7a0deb14f0393afb57086c67636
Publikováno v:
Frontiers in Neuroscience, Vol 18 (2024)
Alopecia intellectual disability syndromes 4 (APMR4) caused by Lanosterol synthase (LSS) gene variants is a very rare autosomal recessive neuroectodermal syndrome. It is characterized by congenital alopecia and variable degrees of intellectual disabi
Externí odkaz:
https://doaj.org/article/20f55496d7594a05bfff2630713bd0e3
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
IntroductionAnti-IgLON5 antibody-related encephalitis is a rare autoimmune disorder of the central nervous system, predominantly occurring in middle-aged elderly individuals, with paediatric cases being exceptionally rare. This study aims to enhance
Externí odkaz:
https://doaj.org/article/156b6e49b09d44d8854b0fa2c849c63f