Chromatin changes induced by nuclear lamina in embryonic stem cell
The Hutchinson-Gilford progeria syndrome (HGPS) is a rare genetic disorder caused by a mutation in the LMNA gene, which leads to the premature ageing of affected children. This mutation triggers the production of progerin, a truncated form of the lamin A protein. Progerin has recently been shown to...
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| Format: | Final Year Project |
| Language: | English |
| Published: |
2016
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| Online Access: | http://hdl.handle.net/10356/67170 |
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| Institution: | Nanyang Technological University |
| Language: | English |