Zobrazeno 1 - 10
of 149
pro vyhledávání: '"Liang, Liang"'
Publikováno v:
Frontiers in Veterinary Science, Vol 11 (2024)
High temperature induces heat stress, adversely affecting the growth and lactation performance of cows. Research has shown the protective effect of taurine against hepatotoxicity both in vivo and in vitro. This study aimed to investigate the effect o
Externí odkaz:
https://doaj.org/article/7276643e57d9410ab2f77fe3ec79d01e
Publikováno v:
Frontiers in Public Health, Vol 12 (2024)
ObjectiveWith increasing rates of anxiety and depression during COVID-19, exercise treatment has drawn attention for its effects on COVID-19 patients with anxiety and depression. This study set out to assess the impact of exercise therapy on COVID-19
Externí odkaz:
https://doaj.org/article/58af1b40d9d64eb0b289b22364c49297
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
This report presents a case of Charcot–Marie–Tooth dominant intermediate D (CMTDID), a rare subtype of Charcot–Marie–Tooth disease, in a 52 years-old male patient. The patient exhibited mobility impairment, foot abnormalities (pes cavus), and
Externí odkaz:
https://doaj.org/article/0ad09017b23d43ecb1f81d0c1f7331c9
Autor:
Zhao-Jing Lin, Jie-Yi Long, Juan Li, Fang-Na Wang, Wei Chu, Lei Zhu, Ya-Li Li, Liang-Liang Fan
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
BackgroundCongenital cataracts stand as the primary cause of childhood blindness globally, characterized by clouding of the eye’s lens at birth or shortly thereafter. Previous investigations have unveiled that a variant in the V-MAF avian musculoap
Externí odkaz:
https://doaj.org/article/d6605ad43acb49169b49942d0e7a6508
Autor:
Guang-Zhao Cao, Liang-Liang Tian, Jing-Yi Hou, Yi Zhang, He Xu, Hong-Jun Yang, Jing-Jing Zhang
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2024)
Introduction: Diabetic ulcers have become one of the major complications of diabetes mellitus (DM) and are a leading cause of death and disabling disease. However, current therapies are not effective enough to meet clinical needs. A traditional Chine
Externí odkaz:
https://doaj.org/article/1314b7396aca4b24b6c608603a9c1143
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Prenatal diagnosis and genetic counseling play an important role in preventing and controlling birth defects. No reports were found of prenatal diagnosis of couples carrying both the thalassemia and deafness genes. In this study, we prese
Externí odkaz:
https://doaj.org/article/18f491a70d3c45a79a0dc166ae655f91
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Hereditary spastic paraplegia (HSP) is a progressive upper-motor neurodegenerative disease. Mutations in the WASHC5 gene are associated with autosomal dominant HSP, spastic paraplegia 8 (SPG8). However, due to the small number of reported
Externí odkaz:
https://doaj.org/article/55cc1d209ccd43ff8639f3b1e7ef910f
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Heterozygous mutations in the dehydrodolichol diphosphate synthase (DHDDS) gene are one of the causes generating developmental and epileptic encephalopathies. So far, only eleven mutations in the DHDDS gene have been identified. The mutat
Externí odkaz:
https://doaj.org/article/eb91288c84b6487ab96717e43fdeb2e8
Autor:
Chao-qiong Jin, Jing Zhao, Xiao-yun Ding, Liang-liang Yu, Guo-liang Ye, Xin-jian Zhu, Jian-wei Shen, Ye Yang, Bo Jin, Chun-li Zhang, Bin Lv
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
BackgroundEndoscopic submucosal dissection (ESD) for early gastric cancer (EGC) does not always lead to curative resection. Risk factors of lymph node metastasis (LNM)/local cancer residue after non-curative ESD for EGC have not been fully elucidated
Externí odkaz:
https://doaj.org/article/cbe17d3fbda943969387ce5555d2e531
Autor:
Lin Chen, Yin Xu, Ming-juan Fang, Yong-guang Shi, Jie Zhang, Liang-liang Zhang, Yu Wang, Yong-zhu Han, Ji-yuan Hu, Ren-min Yang, Xu-en Yu
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
Gerstmann-Sträussler-Scheinker syndrome (GSS) is a rare genetic prion disease caused by a mutation in the prion protein (PRNP) gene. It is typically characterized by progressive cerebellar ataxia and slowly progressive dementia. We present a case st
Externí odkaz:
https://doaj.org/article/1555b7b6dc994b57a9d660be871e0a3e