Zobrazeno 1 - 10
of 614
pro vyhledávání: '"GuiLin Li"'
Autor:
Jinfu Zhou, Guilin Li, Yinglin Zeng, Xiaolong Qiu, Peiran Zhao, Ting Huang, Xi Wang, Jinying Luo, Na Lin, Liangpu Xu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)
Abstract Background Primary carnitine deficiency (PCD) is a rare autosomal recessive fatty acid oxidation disorder caused by variants in SLC22A5, with its prevalence and SLC22A5 gene mutation spectrum varying across races and regions. This study aime
Externí odkaz:
https://doaj.org/article/ef41a74edb3e453691cd5ddcfb0451d9
Autor:
Yaochen Xie, Shuchen Gong, Lingkun Wang, Zhaoxu Yang, Chen Yang, Guilin Li, Huiyan Zha, Shuying Lv, Boneng Xiao, Xiaoyu Chen, Zhenning Di, Qiaojun He, Jincheng Wang, Qinjie Weng
Publikováno v:
BMC Complementary Medicine and Therapies, Vol 24, Iss 1, Pp 1-17 (2024)
Abstract Huanglian Jiedu Decoction (HJD) is a well-known Traditional Chinese Medicine formula that has been used for liver protection in thousands of years. However, the therapeutic effects and mechanisms of HJD in treating drug-induced liver injury
Externí odkaz:
https://doaj.org/article/fa17aa93cd094d6cba38a90d40d52a55
Publikováno v:
Journal of International Medical Research, Vol 52 (2024)
Vaginal atresia is a rare obstructive disease of the reproductive tract. It is characterized by the absence or underdevelopment of the vaginal canal and results in various clinical manifestations. Hysterectomy can physically and mentally burden young
Externí odkaz:
https://doaj.org/article/def886fc3ab84d58b1f75f0fc07541a1
Autor:
Jinfu Zhou, Yinglin Zeng, Jianping Tang, Shihong Chen, Guilin Li, Xiaolong Qiu, Peiran Zhao, Ting Huang, Jinying Luo, Na Lin, Liangpu Xu
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
IntroductionGlucose-6-phosphate dehydrogenase (G6PD) deficiency is a common X-linked hereditary disorder in southern China. However, the incidence rate of G6PD deficiency and the frequency of the most common G6PD gene variants vary widely. The purpos
Externí odkaz:
https://doaj.org/article/c36df7ec0d544eefbcb3f6a0f5cc1bfc
Publikováno v:
EXCLI Journal : Experimental and Clinical Sciences, Vol 23, Pp 364-383 (2024)
Osteosarcoma (OS) is a rare form of cancer and primary bone malignancy in children and adolescents. Current therapies include surgery, chemotherapy, and amputation. Therefore, a new therapeutic strategy is needed to dramatically change cancer treatme
Externí odkaz:
https://doaj.org/article/5f89bc0e8c324488bc8a5b714a0f0e5b
Publikováno v:
BMC Cancer, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Polymeric micelle systems for drug delivery, monitor and chemotherapy have gained significant attention, and reductive polymeric micelle systems have become particularly attractive due to their controlled release behavior without additional
Externí odkaz:
https://doaj.org/article/a193db0522da46f4a6b85967d97230f3
Autor:
Jinfu Zhou, Guilin Li, Lin Deng, Peiran Zhao, Yinglin Zeng, Xiaolong Qiu, Jinying Luo, Liangpu Xu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-7 (2023)
Abstract Background Glutaric acidemia type 1 (GA1) is a rare autosomal recessive inherited metabolic disorder caused by variants in the gene encoding the enzyme glutaryl-CoA dehydrogenase (GCDH). The estimated prevalence of GA1 and the mutational spe
Externí odkaz:
https://doaj.org/article/abaf0f2bfea244338e16c2c5e1c9ba0a
Publikováno v:
Cancer Medicine, Vol 12, Iss 5, Pp 5450-5460 (2023)
Abstract Purpose Reactive lymphocytes are substantial components of germinoma, which are believed to be related to the favorable prognosis of this intracranial tumor and better response to immunotherapy. However, the mechanisms managing the recruitme
Externí odkaz:
https://doaj.org/article/7f0d6118261549ccbc2b54f83f489c9b
Autor:
Guilin Li, Jingwei Li, Xinglong Zhi, Lisong Bian, Fan Yang, Hongqi Zhang, Jiaxing Yu, Jian Ren, Zhenlong Ji
Publikováno v:
Stroke and Vascular Neurology, Vol 8, Iss 4 (2023)
Objective Pial arteriovenous fistulas (PAVFs) are rare and mostly observed in children. However, the overall angioarchitecture, clinical features, treatments and long-term prognosis for pediatric patients remain unclear.Methods Clinical data of conse
Externí odkaz:
https://doaj.org/article/8851c1e5aa264b85a079f197fc469b51
Autor:
Xiaolong Qiu, Peiran Zhao, Jinying Luo, Guilin Li, Lin Deng, Yinglin Zeng, Liangpu Xu, Jinfu Zhou
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
The estimated prevalence of tetrahydrobiopterin deficiency (BH4D) and the mutational spectrum of the causal 6-pyruvoyl-tetrahydropterin synthase (PTS) gene vary widely according to race and region. This study assessed the prevalence and genetic chara
Externí odkaz:
https://doaj.org/article/805b4cb61dab410dab855099d5dbf981