Wang G - Search Results

1

Development of differential diagnostic models for distinguishing between limb-girdle muscular dystrophy and idiopathic inflammatory myopathy.

Wang G, Fu L, Zhang L, Shao K, Hou Y, Dai T, Lin P, Yan C, Zhao B. Wang G, et al. Arthritis Res Ther. 2024 Dec 19;26(1):215. doi: 10.1186/s13075-024-03458-8. Arthritis Res Ther. 2024. PMID: 39695751 Free PMC article.

2

Novel compound heterozygous mutations in the TTN gene: elongation and truncation variants causing limb-girdle muscular dystrophy type 2J in a Han Chinese family.

Wang G, Lv X, Xu L, Zhang R, Yan C, Lin P. Wang G, et al. Neurol Sci. 2022 May;43(5):3427-3433. doi: 10.1007/s10072-022-05979-z. Epub 2022 Mar 3. Neurol Sci. 2022. PMID: 35239051

3

[Analysis of clinical features and genetic variants in three Chinese pedigrees affected with Limb girdle muscular dystrophy type 2I].

Wang G, Xu L, Zhao D, Yan C, Lin P. Wang G, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Nov 10;39(11):1205-1210. doi: 10.3760/cma.j.cn511374-20220107-00016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 36317204 Chinese.

4

A female carrier of spinal and bulbar muscular atrophy diagnosed with DNAJB6-related distal myopathy.

Xu L, Geng H, Lv X, Wang G, Yan C, Zhang D, Lin P. Xu L, et al. Among authors: wang g. J Hum Genet. 2022 Jul;67(7):441-444. doi: 10.1038/s10038-022-01022-3. Epub 2022 Feb 15. J Hum Genet. 2022. PMID: 35165376

5

Somatic and germinal mosaicism in a Han Chinese family with laminopathies.

Wang G, Hou Y, Lv X, Yan C, Lin P. Wang G, et al. Eur J Hum Genet. 2023 Sep;31(9):1073-1077. doi: 10.1038/s41431-022-01266-9. Epub 2022 Dec 16. Eur J Hum Genet. 2023. PMID: 36526864 Free PMC article.

6

Aberrant mRNA processing caused by splicing mutations in TTN-related neuromuscular disorders.

Wang G, Wu W, Lv X, Yan C, Lin P. Wang G, et al. J Hum Genet. 2023 Nov;68(11):777-782. doi: 10.1038/s10038-023-01182-w. Epub 2023 Jul 5. J Hum Genet. 2023. PMID: 37407718

7

Expanding the spectrum of HSPB8-related myopathy: a novel mutation causing atypical pediatric-onset axial and limb-girdle involvement with autophagy abnormalities and molecular dynamics studies.

Yang G, Lv X, Yang M, Feng Y, Wang G, Yan C, Lin P. Yang G, et al. Among authors: wang g. J Hum Genet. 2024 Nov 15. doi: 10.1038/s10038-024-01305-x. Online ahead of print. J Hum Genet. 2024. PMID: 39548192

8

Tcap Deficiency in Zebrafish Leads to ROS Production and Mitophagy, and Idebenone Improves its Phenotypes.

Lv X, Zhang R, Xu L, Wang G, Yan C, Lin P. Lv X, et al. Among authors: wang g. Front Cell Dev Biol. 2022 Mar 15;10:836464. doi: 10.3389/fcell.2022.836464. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 35372370 Free PMC article.

9

[Research progress on the pathogenesis and intervention of statins-associated muscle symptoms].

Wang GY, Lin PF, Yan CZ. Wang GY, et al. Zhonghua Nei Ke Za Zhi. 2022 Aug 1;61(8):953-958. doi: 10.3760/cma.j.cn112138-20210914-00642. Zhonghua Nei Ke Za Zhi. 2022. PMID: 35922224 Chinese.

10

Exon skipping caused by splicing mutation in TNNT1 nemaline myopathy.

Wang G, Zhao D, Yan C, Lin P. Wang G, et al. J Hum Genet. 2023 Feb;68(2):97-101. doi: 10.1038/s10038-022-01096-z. Epub 2022 Nov 29. J Hum Genet. 2023. PMID: 36446828

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