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Defective release of α granule and lysosome contents from platelets in mouse Hermansky-Pudlak syndrome models
Hermansky-Pudlak syndrome (HPS) is characterized by oculocutaneous albinism, bleeding diathesis, and other variable symptoms. The bleeding diathesis has been attributed to δ storage pool deficiency, reflecting the malformation of platelet dense granules. Here, we analyzed agonist-stimulated secretio...
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| Vydáno v: | Blood |
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| Hlavní autoři: | , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society of Hematology
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4351507/ https://ncbi.nlm.nih.gov/pubmed/25477496 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2014-07-586727 |
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