Nbeal2 interacts with Dock7, Sec16a, and Vac14

Mutations in NBEAL2, the gene encoding the scaffolding protein Nbeal2, are causal of gray platelet syndrome (GPS), a rare recessive bleeding disorder characterized by platelets lacking α-granules and progressive marrow fibrosis. We present here the interactome of Nbeal2 with additional validation by...

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Bibliografiske detaljer
Udgivet i:Blood
Main Authors: Mayer, Louisa, Jasztal, Maria, Pardo, Mercedes, Aguera de Haro, Salvadora, Collins, Janine, Bariana, Tadbir K., Smethurst, Peter A., Grassi, Luigi, Petersen, Romina, Nurden, Paquita, Favier, Rémi, Yu, Lu, Meacham, Stuart, Astle, William J., Choudhary, Jyoti, Yue, Wyatt W., Ouwehand, Willem H., Guerrero, Jose A.
Format: Artigo
Sprog:Inglês
Udgivet: American Society of Hematology 2018
Fag:
Platelets and Thrombopoiesis
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5877783/
https://ncbi.nlm.nih.gov/pubmed/29187380
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2017-08-800359
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