Možné přístupy k terapii cystické fibrosy
Cystic fibrosis is a genetic disease caused by a mutation in the CFTR gene. This leads to an absence or a malfunction of CFTR chloride channel, which is also a crutial regulator of other ion channels. This thesis was aimed at gene therapy of cystic fibrosis using CFTR- mRNA gene transfer. To determi...
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| Format: | Dissertation |
| Language: | Czech |
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2018
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| Online Access: | http://www.nusl.cz/ntk/nusl-379350 |