Yunting Lin
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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
11.
Xu T, Yu X, Xu K, Lin Y, Wang J, Pan Z, et al.
Stem Cell Res Ther
. 2024 Jan;
15(1):18.
PMID: 38229196
Background: Extracellular vesicles (EVs) derived from mesenchymal stromal cells (MSCs) offer promising prospects for stimulating cartilage regeneration. The different formation mechanisms suggest that exosomes and ectosomes possess different biological functions....
12.
Jiang M, Peng M, Lu Z, Shao Y, Liu Z, Li X, et al.
J Pediatr Endocrinol Metab
. 2023 Nov;
36(12):1154-1160.
PMID: 37939726
Objectives: To find biochemical and molecular markers can assist in identifying serious liver damage of neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) patients. Methods: 138 patients under 13 days...
13.
Lu Z, Zhang W, Mao X, Li D, Chen X, Liu L, et al.
Clin Genet
. 2023 Oct;
105(2):209-213.
PMID: 37867468
Marbach-Rustad progeroid syndrome is an extremely rare disease caused by a heterozygous variant in the LEMD2 gene. To date, only two patients and one LEMD2 pathogenic variant have been reported...
14.
Ma J, Zhang Y, Ding X, Liang Z, Yang C, Deng Z, et al.
Calcif Tissue Int
. 2023 Jun;
113(3):266-275.
PMID: 37278761
Rare genetic skeletal disorders (GSDs) remain the major problem in orthopedics and result in significant morbidity in patients, but the causes are highly diverse. Precise molecular diagnosis will benefit management...
15.
Lin Y, Chen X, Xie B, Guan Z, Chen X, Li X, et al.
Front Genet
. 2023 Apr;
14:1085210.
PMID: 37025457
Wiedemann-Steiner syndrome (WSS) is a rare autosomal dominant disorder caused by deleterious heterozygous variants of the gene. This study aims to describe the phenotypic and genotypic features of Chinese WSS...
16.
Su X, Lin Y, Liu L, Mei H, Xu A, Zeng C, et al.
J Pediatr Endocrinol Metab
. 2022 Nov;
36(1):74-80.
PMID: 36433712
Objectives: Congenital generalized lipodystrophy (CGL) is a group of rare autosomal inherited diseases characterized by a widespread loss of adipose tissue. The main purpose of this study was to evaluate...
17.
Lin Y, Guan Z, Mei H, Zhang W, Zhou Z, Su L, et al.
Front Pediatr
. 2022 Nov;
10:1007219.
PMID: 36405822
Purpose: Vitamin D-dependent rickets type 1A (VDDR1A) is a rare autosomal recessive disorder caused by deficiency of the gene. This study aims to investigate the phenotypic and genotypic features of...
18.
Lin Y, Chen X, Liang C, Li D, Liu L, Li X
Eur J Ophthalmol
. 2022 Oct;
33(5):NP1-NP4.
PMID: 36262071
Background: gene is known to cause autosomal dominant congenital cataract. Here we report a novel compound heterozygous variant of gene in two siblings that mimics an autosomal recessive trait. Patients...
19.
Xu T, Lin Y, Yu X, Jiang G, Wang J, Xu K, et al.
Am J Sports Med
. 2022 Jul;
50(10):2740-2752.
PMID: 35867349
Background: Extracellular vesicles derived from mesenchymal stem cells (MSC-EVs) have gained momentum as a treatment for tendinopathy. Multiple studies have demonstrated significant differences in cargo composition between the 2 subtypes...
20.
Lin Y, Zhang W, Li D, Chen X, Lu Z, Li X, et al.
Clin Genet
. 2022 Jun;
102(3):246-247.
PMID: 35754111
A. The family pedigree. B. Whole exome sequencing of the proband-parent trio revealed c.611_612dupTG(p.M205*) variant of FITM2 gene as suspicious variant. C. Sanger sequencing confirmed that c.611_612dupTG(p.M205*) variant of FITM2...