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Yi-Dan Liu

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Articles 17
Citations 151
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Recent Articles
1.
Xu X, Liu Y
Zhongguo Yi Xue Ke Xue Yuan Xue Bao . 2024 Apr; 46(2):232-241. PMID: 38686720
DNA is susceptible to various factors and and experience different forms of damage,among which double-strand break(DSB)is a deleterious form.To maintain the stability of genetic information,organisms have developed multiple mechanisms to...
2.
Mu Z, Zhao Z, Yang S, Zhou L, Liu Y, Qian Z, et al.
Aging (Albany NY) . 2023 Aug; 15(16):8298-8314. PMID: 37610708
Diabetes is associated with higher prevalence of cognitive dysfunction, while the underlying mechanism is still elusive. In this study, we aim to explore the potential mechanism of diabetes-induced cognitive dysfunction...
3.
Liu Y, Tan D, Song D, Fan Y, Fu X, Ge L, et al.
Front Genet . 2023 Jun; 14:1170089. PMID: 37342771
, encoding protein O-mannose beta-1,2-N-acetylglucosaminyltransferase 1, is one of the genes responsible for dystroglycanopathy (DGP), which includes multiple phenotypes such as muscle-eye-brain disease (MEB), congenital muscular dystrophy with intellectual disability,...
4.
Wei C, Liu Y, Yang Y, Wu Y, Liu J, Chang X, et al.
Front Pediatr . 2023 May; 11:1160107. PMID: 37215601
The gene encodes tRNA nucleotidyltransferase 1, which catalyzes the addition of cytosine-cytosine-adenosine (CCA) to the ends of cytoplasmic and mitochondrial tRNAs. The most common clinical phenotype associated with is autosomal...
5.
Liu Y, Zhu Y, Shi Y, Liu X, Su W, Zhuo Y
Stem Cells Dev . 2023 Feb; 32(9-10):213-224. PMID: 36721381
Adult neural stem cells (NSCs) are restricted to the two neurogenic regions of the mammalian brain, where they self-renew and generate progenies of multiple lineages, including neurons, astrocytes, and oligodendrocytes....
6.
Ren Q, Sun R, Zheng K, Liu Y, Ruan X, Wang Y
Huan Jing Ke Xue . 2022 Jan; 43(2):995-1003. PMID: 35075873
The vegetable greenhouse soils in Yanglou Town, Ruzhou City, Henan Province were taken as the research object in the present study to explore the difference in soil physical and chemical...
7.
Liu Y, Huang S, Li M, Lek M, Song D, Tan D, et al.
Clin Genet . 2022 Jan; 101(4):448-453. PMID: 34988992
Retinol dehydrogenase 11 (RDH11) is an 11-cis-retinol dehydrogenase that has a well-characterized, albeit auxiliary role in the retinoid cycle. Diseases caused by mutations in the RDH11 gene are very rare,...
8.
Chen X, Song D, Jiang L, Tan D, Liu Y, Liu J, et al.
Front Genet . 2021 Aug; 12:692479. PMID: 34413876
Objective: Alpha-dystroglycanopathy (α-DGP) is a subtype of muscular dystrophy caused by defects in the posttranslational glycosylation of α-dystroglycan (α-DG). Our study aimed to summarize the clinical and genetic features of...
9.
Liu Y, Ma M, Hu X, Yan H, Zhang Y, Yang H, et al.
Front Neurol . 2020 Jul; 11:475. PMID: 32655475
Tuberous sclerosis complex (TSC) is a genetic disease characterized by seizures, mental deficiency, and abnormalities of the skin, brain, kidney, heart, and lungs. TSC is inherited in an autosomal dominant...
10.
Liu Y, Lin H, Li C, Sun G, Hu X, Ma M, et al.
Int J Neurosci . 2020 Jan; 130(11):1156-1160. PMID: 31944864
Sjögren-Larsson syndrome is a rare, autosomal, recessive neurocutaneous disorder caused by mutations in the gene, which encodes the fatty aldehyde dehydrogenase enzyme. Deficiency in fatty aldehyde dehydrogenase results in an...