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Dysfunction of complement receptors CR3 (CD11b/18) and CR4 (CD11c/18) in preeclampsia: a genetic and functional study
OBJECTIVE: To study genetic variants and their function within genes coding for complement receptors in preeclampsia. DESIGN: A case-control study. SETTING: Preeclampsia is a common vascular disease of pregnancy. The clearance of placenta-derived material is one of the functions of the complement sy...
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| Vydáno v: | BJOG |
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| Hlavní autoři: | , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8255276/ https://ncbi.nlm.nih.gov/pubmed/33539617 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/1471-0528.16660 |
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