Yüklüyor......
Human coagulation factor VIII domain-specific recombinant polypeptide expression
BACKGROUND: Hemophilia A is caused by heterogeneous mutations in F8. Coagulation factor VIII (FVIII), the product of F8, is composed of multiple domains designated A1-A2-B-A3-C1-C2. FVIII is known to interact with diverse proteins, and this characteristic may be important for hemostasis. However, li...
Kaydedildi:
| Yayımlandı: | Blood Res |
|---|---|
| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis
2015
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4486152/ https://ncbi.nlm.nih.gov/pubmed/26157780 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5045/br.2015.50.2.103 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|