Yunting Lin
Overview
Explore the profile of Yunting Lin including associated specialties, affiliations and a list of published articles.
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54
Citations
313
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Recent Articles
1.
Zhou Z, Cai Y, Li X, Liu Z, Peng M, Lin Y, et al.
Front Neurol
. 2024 Aug;
15:1440883.
PMID: 39206282
Introduction: Nonketotic hyperglycinemia (NKH) is a rare, life-threatening genetic disorder. The patients usually show heterogeneous and nonspecific symptoms, resulting in diagnosis challenges using conventional approaches. Here, the clinical presentation and...
2.
Pan Z, Xu K, Huang G, Hu H, Yang H, Shen H, et al.
Adv Mater
. 2024 Jul;
36(38):e2407115.
PMID: 39081086
Small-interfering RNAs (siRNAs) offer promising prospects for treating pyroptosis-related autoimmune diseases. However, poor stability and off-target effects during in vivo transportation hinder their practical clinical applications. Precision delivery and adaptive...
3.
Lin Y, Song E, Jin H, Jin Y
Endocr Connect
. 2024 Jul;
13(9).
PMID: 39072509
Background: Reproductive hormones may be a risk factor for cardiovascular disease (CVD), but their influence is often underestimated. Obesity can exacerbate the progression of CVD. Arterial stiffness (AS) is correlated...
4.
Li S, Lin Y, Chen S, Zhang W, Chen Y, Lu X, et al.
Liver Int
. 2024 Jun;
44(9):2424-2433.
PMID: 38847512
Background And Aims: Few studies have focused on the outcomes of Wilson's disease (WD) diagnosed before age of 5 years. This study aimed to summarize the clinical features of early...
5.
Li T, Huang Y, Tao C, Yin X, Su X, Shao Y, et al.
Metab Brain Dis
. 2024 May;
39(5):753-762.
PMID: 38775997
Metachromatic leukodystrophy (MLD) is a rare hereditary neurodegenerative disease caused by deficiency of the lysosomal enzyme arylsulfatase A (ARSA). This study described the clinical and molecular characteristics of 24 Chinese...
6.
Su L, Sheng H, Li X, Cai Y, Mei H, Cheng J, et al.
Orphanet J Rare Dis
. 2024 May;
19(1):198.
PMID: 38750596
Background: Methylmalonic aciduria (MMA) is a group of rare genetic metabolic disorders resulting from defects in methylmalonyl coenzyme A mutase (MCM) or intracellular cobalamin (cbl) metabolism. MMA patients show diverse...
7.
Du R, Zhou C, Chen S, Li T, Lin Y, Xu A, et al.
Pediatr Nephrol
. 2024 Apr;
39(8):2377-2391.
PMID: 38589698
Background: Lowe syndrome is characterized by the presence of congenital cataracts, psychomotor retardation, and dysfunctional proximal renal tubules. This study presents a case of an atypical phenotype, investigates the genetic...
8.
Xu K, Yang H, Fang J, Qiu K, Shen H, Huang G, et al.
Bioact Mater
. 2024 Mar;
36:272-286.
PMID: 38496034
Nanoliposomes have a broad range of applications in the treatment of autoimmune inflammatory diseases because of their ability to considerably enhance drug transport. For their clinical application, nanoliposomes must be...
9.
Lin Y, Zhang Y, Ma J, Liu S, Liu Y, Yang C, et al.
Cleft Palate Craniofac J
. 2024 Feb;
:10556656241234575.
PMID: 38414442
Objective: Auriculocondylar syndrome (ARCND) is a set of rare craniofacial malformations characterized by variable micrognathia, ear malformations, and mandibular condyle hypoplasia, and other accompanying features with phenotypic complexity. ARCND2 caused...
10.
Jiang X, Shao Y, Liao Y, Zheng X, Peng M, Cai Y, et al.
Eur J Pharmacol
. 2024 Feb;
967:176379.
PMID: 38342361
Dopa and tetrahydrobiopterin (BH4) supplementation are recommended therapies for the dopa-responsive dystonia caused by GTP cyclohydrolase 1 (GCH1, also known as GTPCH) deficits. However, the efficacy and mechanisms of these...