लोड हो रहा है...
Loss of HtrA1 serine protease induces synthetic modulation of aortic vascular smooth muscle cells
Homozygous mutations of human HTRA1 cause cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL). HtrA1(-/-) mice were examined for arterial abnormalities. Although their cerebral arteries were normal, the thoracic aorta was affected in HtrA1(-/-) mice....
में बचाया:
| में प्रकाशित: | PLoS One |
|---|---|
| मुख्य लेखकों: | , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Public Library of Science
2018
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5955505/ https://ncbi.nlm.nih.gov/pubmed/29768431 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0196628 |
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