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European Journal of Histochemistry : EJH|February 3, 2012
Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeriaV Cenni, C Capanni, M Columbaro, et al.
Neuromuscular Disorders : NMD|June 29, 2010
Prevalent cardiac phenotype resulting in heart transplantation in a novel LMNA gene duplicationL Volpi, G Ricci, C Passino, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|November 3, 2001
Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblastsP Sabatelli, P Bonaldo, G Lattanzi, et al.
European Journal of Histochemistry : EJH|September 27, 2018
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeriaS Dominici, V Fiori, M Magnani, et al.
European Journal of Histochemistry : EJH|April 9, 2009
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeriaS Dominici, V Fiori, M Magnani, et al.
Journal of Medical Genetics|September 23, 2008
Site-dependent differences in both prelamin A and adipogenic genes in subcutaneous adipose tissue of patients with type 2 familial partial lipodystrophyD Araújo-Vilar, G Lattanzi, B González-Méndez, et al.
The Journal of Physiology|June 23, 2015
ClC-1 mutations in myotonia congenita patients: insights into molecular gating mechanisms and genotype-phenotype correlationP Imbrici, L Maggi, G F Mangiatordi, et al.
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