Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger–Huët anomaly)

2002/07/15 by Katrin Hoffmann, Christine K. Dreger, Christine Karin Dreger +16 · 3 citations
Biochemistry, Genetics and Molecular Biology · #Genomics and Chromatin Dynamics #Nuclear Structure and Function #RNA Research and Splicing

paper · doi:10.1038/ng925

crossref issued 2002/07/15 · crossref published 2002/07/15 · crossref published-online 2002/07/15 · openalex publication_date 2002/07/15 · crossref created 2002/07/28 · crossref published-print 2002/08/01 · crossref deposited 2023/05/18 · openalex created_date 2025/10/10 · crossref indexed 2026/07/08 · openalex updated_date 2026/07/29

Citations

• Characterization of a second highly conserved B-type lamin present in cells previously thought to contain only a single B-type lamin

Cited by

• Autosomal Recessive HEM/Greenberg Skeletal Dysplasia Is Caused by 3β-Hydroxysterol Δ14-Reductase Deficiency Due to Mutations in the Lamin B Receptor Gene
• The end adjusts the means: Heterochromatin remodelling during terminal cell differentiation
• Laminopathy [wikipedia]