Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria
Lamin A is a component of the nuclear lamina mutated in a group of human inherited disorders known as laminopathies. Among laminopathies, progeroid syndromes and lipodystrophies feature accumulation of prelamin A, the precursor protein which, in normal cells, undergoes a multi-step processing to yie...
שמור ב:
| Principais autores: | , , , , , , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
PAGEPress Publications
2009-03-01
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| סדרה: | European Journal of Histochemistry |
| גישה מקוונת: | http://ejh.pagepress.org/index.php/ejh/article/view/1232 |
| תגים: |
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