Associated Papers
Unraveling the nexus of nesprin in dilated cardiomyopathy: From molecular insights to therapeutic prospects.
Qin Q et al.
Life Sciences, 2024
Nesprin-1: novel regulator of striated muscle nuclear positioning and mechanotransduction.
De Silva S et al.
Biochemical Society Transactions, 2023
Genotype-Phenotype Correlations in Human Diseases Caused by Mutations of LINC Complex-Associated Genes: A Systematic Review and Meta-Summary.
Storey EC et al.
Cells, 2022
36552829 (PubMed )
Supplement: cells-11-04065-s001.zip › Storey___Fuller_Supplementary_Materials_S2_Data_extraction.xlsx › ONM_proteins
Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis.
Zhou C et al.
Human Molecular Genetics, 2017
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