Ranhui Duan
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Explore the profile of Ranhui Duan including associated specialties, affiliations and a list of published articles.
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62
Citations
1832
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Recent Articles
1.
Li G, Huang Y, Han W, Wei L, Huang H, Zhu Y, et al.
Cell Death Dis
. 2024 Jul;
15(7):544.
PMID: 39085203
UFMylation is a highly conserved ubiquitin-like post-translational modification that catalyzes the covalent linkage of UFM1 to its target proteins. This modification plays a critical role in the maintenance of endoplasmic...
2.
Xue J, Zhu Y, Pan Y, Huang H, Wei L, Peng Y, et al.
J Mol Diagn
. 2024 Jul;
26(10):897-905.
PMID: 39032823
Fragile X syndrome is the leading genetic cause of intellectual disability and autism spectrum disorders. Female premutation carriers exhibit no obvious symptoms during reproductive age, but the premutation allele can...
3.
Cheng J, Wang Z, Tang M, Zhang W, Li G, Tan S, et al.
Proc Natl Acad Sci U S A
. 2024 Mar;
121(12):e2315707121.
PMID: 38489388
KCTD10 belongs to the KCTD (potassiumchannel tetramerization domain) family, many members of which are associated with neuropsychiatric disorders. However, the biological function underlying the association with brain disorders remains to...
4.
Zhu Y, Li J, Pan Y, Huang W, Xi H, Duan R
J Community Genet
. 2024 Jan;
15(2):177-185.
PMID: 38277068
Fragile X syndrome is the most common inherited cause of intellectual disability. Considering China's low prevalence, distinct healthcare system, middle-income economic status, and unique culture, China cannot simply replicate the...
5.
Kuang H, Li Y, Wang Y, Shi M, Duan R, Xiao Q, et al.
Cell Rep
. 2023 Nov;
42(12):113445.
PMID: 37980560
The INTS11 endonuclease is crucial in modulating gene expression and has only recently been linked to human neurodevelopmental disorders (NDDs). However, how INTS11 participates in human development and disease remains...
6.
Liu Q, Chen J, Xue J, Zhou X, Tian Y, Xiao Q, et al.
Eur J Neurol
. 2023 Nov;
31(2):e16145.
PMID: 37975799
Background And Purpose: The role of GGC repeat expansions within NOTCH2NLC in Parkinson's disease (PD) and the substantia nigra (SN) dopaminergic neuron remains unclear. Here, we profile the NOTCH2NLC GGC...
7.
Tian Y, Hou X, Cao W, Zhou L, Jiao B, Zhang S, et al.
J Peripher Nerv Syst
. 2023 Sep;
28(4):629-641.
PMID: 37749855
Background And Aims: Neuronal intranuclear inclusion disease (NIID) is a rare progressive neurodegenerative disorder mainly caused by abnormally expanded GGC repeats within the NOTCH2NLC gene. Most patients with NIID show...
8.
Chen J, Zhao Y, Zhou X, Xue J, Xiao Q, Pan H, et al.
Front Aging Neurosci
. 2023 Aug;
15:1234027.
PMID: 37583466
Objective: There is controversial evidence that premutation or "gray zone" (GZ) allele (small CGG expansion, 45-54 repeats) was associated with Parkinson's disease (PD). We aimed to explore further the association...
9.
Zhou L, Tian Y, Zhang S, Jiao B, Liao X, Zhou Y, et al.
Front Neurol
. 2023 Jun;
14:1168904.
PMID: 37388545
Background: This study aimed to investigate the features of autonomic dysfunction (AutD) in a large cohort of patients with neuronal intranuclear inclusion disease (NIID). Methods: A total of 122 patients...
10.
Wang M, Yang H, Lin Z, Li X, Liu L, Huang S, et al.
J Neurol
. 2023 Jun;
270(10):4959-4967.
PMID: 37365282
With complicated conditions and a large number of potentially causative genes, the diagnosis of a patient with complex inherited peripheral neuropathies (IPNs) is challenging. To provide an overview of the...