Jinfan Zheng
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Explore the profile of Jinfan Zheng including associated specialties, affiliations and a list of published articles.
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11
Citations
106
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Recent Articles
1.
Kong W, Li C, Sun Z, Gao F, Zheng J, Jiang Y
Molecules
. 2023 Jul;
28(14).
PMID: 37513398
Heteroatom doping, particularly with nonmetallic atoms such as N, P, and S, has proven to be an effective strategy for modulating the fluorescent properties of carbon dots (CDs). However, there...
2.
Clinical and diagnostic features of anti-neurofascin-155 antibody-positive neuropathy in Han Chinese
Wang W, Liu C, Li W, Zhang D, Shan Y, Zheng J, et al.
Ann Clin Transl Neurol
. 2022 Mar;
9(5):695-706.
PMID: 35313093
Objective: To investigate the clinical features of Han Chinese patients with anti-neurofascin-155 (NF155) antibody-positive neuropathy. Methods: We screened 194 patients with peripheral neuropathy for NF155 antibodies using a cell-based assay...
3.
Liu F, Zhang Y, Liang Z, Sun Q, Liu H, Zhao J, et al.
Mol Psychiatry
. 2018 Apr;
23(7):1542-1554.
PMID: 29703946
Potassium channel Kv2.1 regulates potassium current in cortical neurons and potassium efflux is necessary for cell apoptosis. As a major component of delayed rectifier current potassium channels, Kv2.1 forms clusters...
4.
Zheng J, Liang Z, Hou Y, Liu F, Hu Y, Lin P, et al.
Clin Neurophysiol
. 2016 May;
127(6):2503-8.
PMID: 27178871
Background And Objective: Mutations in KCNJ18, which encodes the inwardly rectifying potassium channel Kir2.6, have rarely been reported in hypokalemic periodic paralysis. We describe the clinical phenotype of a novel...
5.
Ji K, Zheng J, Lv J, Xu J, Ji X, Luo Y, et al.
Free Radic Biol Med
. 2015 Apr;
84:161-170.
PMID: 25843656
Fibroblast growth factor 21 (FGF21) is a growth factor with pleiotropic effects on regulating lipid and glucose metabolism. Its expression is increased in skeletal muscle of mice and humans with...
6.
Shan J, Chen B, Lin P, Li D, Luo Y, Ji K, et al.
Neuromolecular Med
. 2014 Oct;
16(4):782-6.
PMID: 25283883
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant late-onset neuromuscular degenerative disease characterized by ptosis, dysphagia, and proximal muscle weakness. The genetic basis has been identified as an abnormal (GCN)...
7.
Cao L, Qiu X, Zheng J, Lin P, Wang S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
. 2014 Jun;
31(3):298-301.
PMID: 24928006
Objective: Mutations of presenilin 1 (PSEN1) gene are the most frequent cause for familial Alzheimers disease (AD). This study was set to explore potential mutation of PSEN1 gene in a...
8.
Ji K, Zheng J, Sun B, Liu F, Shan J, Li D, et al.
Neuromolecular Med
. 2013 Sep;
16(1):119-26.
PMID: 24062162
We report a case of 3-year-old boy who presented with Leigh syndrome but carried a mitochondrial G11778A mutation in the fourth subunit of the NADH dehydrogenase gene (MTND4). Additional to...
9.
Wen B, Li D, Shan J, Liu S, Li W, Zhao Y, et al.
Mol Genet Metab
. 2013 May;
109(2):154-60.
PMID: 23628458
Multiple acyl-coenzyme A dehydrogenation deficiency (MADD) has a wide range of phenotypic variation ranging from a neonatal lethal form to a mild late-onset form. Our previous data showed that in...
10.
Shan J, Wen B, Zhu J, Lin P, Zheng J, Yan C
Neurol Sci
. 2012 Aug;
34(4):561-3.
PMID: 22930366
Pantothenate kinase-associated neurodegeneration (PKAN) is an autosomal-recessive disorder characterized by neurodegeneration and iron accumulation in the brain. Classic and atypical PKAN are distinguished on the basis of age at onset...