Zobrazeno 1 - 10
of 95
pro vyhledávání: '"Fang Fang Bi"'
Autor:
Kun Huang, Dan-Dan Wang, Wen-Bao Hu, Wei-Qian Zeng, Xia Xu, Qiu-Xiang Li, Fang-Fang Bi, Huan Yang, Jian Qiu
Publikováno v:
Journal of Translational Medicine, Vol 20, Iss 1, Pp 1-10 (2022)
Abstract Background Myotonic dystrophy type 1 (DM1), one of the most common forms of adult-onset muscular dystrophy, is caused by abnormally expanded CTG repeats in the 3′ untranslated region of the DMPK gene. The CUG repeats transcribed from the e
Externí odkaz:
https://doaj.org/article/9908958568a04201bf93ea59e4e0e755
Publikováno v:
PeerJ, Vol 11, p e15936 (2023)
Background An increasing number of observational studies have suggested an association between dental caries and Alzheimer’s disease (AD). The association between dental caries and Alzheimer’s disease may be mediated by confounders or reverse cau
Externí odkaz:
https://doaj.org/article/9b26464639fa4f9b99e777ba9b8b046b
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
BackgroundAmyotrophic lateral sclerosis (ALS) is a relentlessly progressive neurodegenerative disease affecting the motor neurons. Although much research has been conducted in this field, few bibliometric studies have been conducted. This study aimed
Externí odkaz:
https://doaj.org/article/844c9bafa5514911a57ba33fffcf70e5
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
BackgroundGlycogen storage disease (GSDs) is characterized by abnormally inherited glycogen metabolism. GSD IXd, which is caused by mutations in the PHKA1 gene, is an X-linked rare disease with mild myopathic symptoms. To date, only 13 patients with
Externí odkaz:
https://doaj.org/article/ad0820cdf35141c3ae8fa669a9cc76e3
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
ObjectivesMultiple sclerosis (MS) is a chronic inflammatory autoimmune and degenerative disorder of the central nervous system. Telomeres are protective structures located at the ends of linear chromosomes, and leukocyte telomere length (LTL) is clos
Externí odkaz:
https://doaj.org/article/dc5ad9c4aa714a2fb38239b91fc1949a
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/4b1ac5dcd17b4a488f1aa57554fe2e82
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Background: Congenital myopathy constitutes a heterogeneous group of orphan diseases that are mainly classified on the basis of muscle biopsy findings. This study aims to estimate the prevalence of congenital myopathy through a systematic review and
Externí odkaz:
https://doaj.org/article/1b98123c5c4948f4a6722c39c969b3e9
Publikováno v:
Current Neuropharmacology. 21:1594-1605
Background: Congenital myasthenic syndromes (CMS) refer to a series of inherited disorders caused by defects in various proteins. Mutation in the collagen-like tail subunit of asymmetric acetylcholinesterase (COLQ) is the second-most common cause of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe88e8457abde6792d0c7a1eb82377d2
https://doi.org/10.2174/1570159x21666230126145652
https://doi.org/10.2174/1570159x21666230126145652
Publikováno v:
Cancer Medicine, Vol 8, Iss 2, Pp 656-668 (2019)
Abstract Breast cancer 1 (BRCA1) and autophagy both play a significant role in drug resistance. However, little is known about the dynamic cross talk between BRCA1 and autophagy in the regulation of drug sensitivity. Here, we investigated the drug re
Externí odkaz:
https://doaj.org/article/a7788ebfd5424895bdc4ee10d76c5679
Publikováno v:
Epileptic Disorders. 25:150-159
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72f9f4f32921045e8108982ff5f7e00b
https://doi.org/10.1002/epd2.20001
https://doi.org/10.1002/epd2.20001