The impact of altered lamin B1 levels on nuclear lamina structure and function in aging and human diseases
Author:
Funder
National Research Foundation of Korea
Ministry of Science, ICT and Future Planning
Publisher
Elsevier BV
Subject
Cell Biology
Reference54 articles.
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2. A large genomic deletion leads to enhancer adoption by the lamin B1 gene: a second path to autosomal dominant adult-onset demyelinating leukodystrophy (ADLD);Giorgio;Hum Mol Genet,2015
3. Sequencing of the reannotated LMNB2 gene reveals novel mutations in patients with acquired partial lipodystrophy;Hegele;Am J Hum Genet,2006
4. Lamin B1 duplications cause autosomal dominant leukodystrophy;Padiath;Nat Genet,2006
5. Deficiencies in lamin B1 and lamin B2 cause neurodevelopmental defects and distinct nuclear shape abnormalities in neurons;Coffinier;Mol Biol Cell,2011
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