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For: Maggi L, Mavroidis M, Psarras S, Capetanaki Y, Lattanzi G. Skeletal and Cardiac Muscle Disorders Caused by Mutations in Genes Encoding Intermediate Filament Proteins. Int J Mol Sci 2021;22:4256. [PMID: 33923914 DOI: 10.3390/ijms22084256] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
Number Citing Articles
1 Wang Y, Dobreva G. Epigenetics in LMNA-Related Cardiomyopathy. Cells 2023;12. [PMID: 36899919 DOI: 10.3390/cells12050783] [Reference Citation Analysis]
2 Qiu R, Wang S, Lin D, He Y, Huang S, Wu B, Li H, Wang M, Zheng F. Mice harboring a R133L heterozygous mutation in LMNA exhibited ectopic lipid accumulation, aging, and mitochondrial dysfunction in adipose tissue. FASEB J 2023;37:e22730. [PMID: 36583724 DOI: 10.1096/fj.202201252RR] [Reference Citation Analysis]
3 Onore ME, Savarese M, Picillo E, Passamano L, Nigro V, Politano L. Bi-Allelic DES Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac Function. Int J Mol Sci 2022;23. [PMID: 36555543 DOI: 10.3390/ijms232415906] [Reference Citation Analysis]
4 Brodehl A, Holler S, Gummert J, Milting H. The N-Terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic DES Mutations Affecting Filament Assembly. Cells 2022;11. [PMID: 36497166 DOI: 10.3390/cells11233906] [Reference Citation Analysis]
5 Krumbein M, Oberman F, Cinnamon Y, Golomb M, May D, Vainer G, Belzer V, Meir K, Fridman I, Haybaeck J, Poelzl G, Kehat I, Beeri R, Kessler S, Yisraeli JK. IGF2BP2 is Induced by Stress in the Heart and Mediates Dilated Cardiomyopathy.. [DOI: 10.1101/2022.11.03.515033] [Reference Citation Analysis]
6 Miyamoto H. 2020 Editor’s Choice Articles in the “Cell Nuclei: Function, Transport and Receptors” Section. Cells 2022;11:2625. [DOI: 10.3390/cells11172625] [Reference Citation Analysis]
7 Bariani R, Rigato I, Cason M, Marinas MB, Celeghin R, Pilichou K, Bauce B. Genetic Background and Clinical Features in Arrhythmogenic Left Ventricular Cardiomyopathy: A Systematic Review. J Clin Med 2022;11:4313. [PMID: 35893404 DOI: 10.3390/jcm11154313] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
8 Saez A, Gonzalez-Granado JM. Recent Advances in Intermediate Filaments-Volume 1. Int J Mol Sci 2022;23:5308. [PMID: 35628119 DOI: 10.3390/ijms23105308] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
9 Brodehl A, Hain C, Flottmann F, Ratnavadivel S, Gaertner A, Klauke B, Kalinowski J, Körperich H, Gummert J, Paluszkiewicz L, Deutsch MA, Milting H. The Desmin Mutation DES-c.735G>C Causes Severe Restrictive Cardiomyopathy by Inducing In-Frame Skipping of Exon-3. Biomedicines 2021;9:1400. [PMID: 34680517 DOI: 10.3390/biomedicines9101400] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
10 Gerull B, Brodehl A. Insights Into Genetics and Pathophysiology of Arrhythmogenic Cardiomyopathy. Curr Heart Fail Rep 2021. [PMID: 34478111 DOI: 10.1007/s11897-021-00532-z] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]