Associated Papers
Genetics and cancer-related Laminopathies: Involvement of Lamins and Lamin-Chromatin Interactions.
Desgrouas C et al.
Sub-cellular Biochemistry, 2025
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 › Lamins
The ChinaMAP analytics of deep whole genome sequences in 10,588 individuals.
Cao Y et al.
Cell Research, 2020
32355288 (PubMed )
Supplement: 41422_2020_322_MOESM14_ESM.xlsx › S7
ZMPSTE24 Is Associated with Elevated Inflammation and Progerin mRNA.
Messner M et al.
Cells, 2020
Molecular and Mechanobiological Pathways Related to the Physiopathology of FPLD2.
Varlet AA et al.
Cells, 2020
Unraveling LMNA Mutations in Metabolic Syndrome: Cellular Phenotype and Clinical Pitfalls.
Desgrouas C et al.
Cells, 2020
LMNA Sequences of 60,706 Unrelated Individuals Reveal 132 Novel Missense Variants in A-Type Lamins and Suggest a Link between Variant p.G602S and Type 2 Diabetes.
Florwick A et al.
Frontiers in Genetics, 2017
Lamin A tail modification by SUMO1 is disrupted by familial partial lipodystrophy-causing mutations.
Simon DN et al.
Molecular Biology of the Cell, 2013
High prevalence of laminopathies among patients with metabolic syndrome.
Dutour A et al.
Human Molecular Genetics, 2011
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