Associated Papers
Nesprin-1: novel regulator of striated muscle nuclear positioning and mechanotransduction.
De Silva S et al.
Biochemical Society Transactions, 2023
Cell-Free DNA Sequencing Reveals Gene Variants in DNA Damage Repair Genes Associated with Prognosis of Prostate Cancer Patients.
Lieb V et al.
Cells, 2022
36429046 (PubMed )
Supplement: cells-11-03618-s001.zip › Suppl._files › Suppl._Table_S2_.xlsx › All
Cell-Free DNA Variant Sequencing Using Plasma and AR-V7 Testing of Circulating Tumor Cells in Prostate Cancer Patients.
Lieb V et al.
Cells, 2021
34831445 (PubMed )
Supplement: cells-10-03223-s001.zip › Suppl._Table_S1.xlsx › All
Nesprin-1/2: roles in nuclear envelope organisation, myogenesis and muscle disease.
Zhou C et al.
Biochemical Society Transactions, 2018
Identifying SYNE1 Ataxia With Novel Mutations in a Chinese Population.
Peng Y et al.
Frontiers in Neurology, 2018
30619065 (PubMed )
Supplement: Data_Sheet_1.PDF
Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis.
Zhou C et al.
Human Molecular Genetics, 2017
Homozygous SYNE1 mutation causes congenital onset of muscular weakness with distal arthrogryposis: a genotype-phenotype correlation.
Baumann M et al.
European Journal of Human Genetics : Ejhg, 2017
Select a paper to view details