Pages that link to "Q46576200"
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The following pages link to Obliteration of cardiomyocyte nuclear architecture in a patient with LMNA gene mutation. (Q46576200):
Displaying 11 items.
- Breaching the nuclear envelope in development and disease (Q26823239) (← links)
- Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption (Q37603454) (← links)
- Genetic cardiomyopathies. Lessons learned from humans, mice, and zebrafish (Q38024282) (← links)
- Nesprin-1 mutations in human and murine cardiomyopathy (Q39599077) (← links)
- The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins (Q44326037) (← links)
- Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathies. (Q46138874) (← links)
- Bypassing Border Control: Nuclear Envelope Rupture in Disease. (Q48165276) (← links)
- Biomechanical defects and rescue of cardiomyocytes expressing pathologic nuclear lamins (Q50061903) (← links)
- Mitochondria in the Nuclei of Rat Myocardial Cells (Q90398636) (← links)
- High glucose induces phosphorylation and oxidation of mitochondrial proteins in renal tubular cells: A proteomics approach (Q91555257) (← links)
- Assessment of fibroblast nuclear morphology aids interpretation of LMNA variants (Q93017338) (← links)