Add to ORKGPlatelets are small anucleate blood cells that co-ordinate blood clotting in response to vascular injury. In additional to their hemostatic role, platelets are involved in a diverse range of physiological and pathological processes. Platelets contain abundant secretory vesicles associated with their functions, which are generally classed as α-granules, δ-granules and lysosomes. These vesicles originate in megakaryocytes (MK), hematopoietic cells that produce platelets in the bone marrow. The inherited bleeding disorder Gray Platelet Syndrome (GPS) is characterized by platelet α-granule deficiency arising from loss of function of neurobeachin-like 2 (NBEAL2). The goal of my study was to investigate the roles and functions of NBEAL2 in MKs an...
Mutations in the human NBEAL2 gene cause gray platelet syndrome (GPS), a bleeding diathesis characte...
The Gray Platelet Syndrome (GPS) is a rare inherited bleeding disorder characterized by deficiency o...
The Gray Platelet Syndrome (GPS) is a rare inherited bleeding disorder characterized by deficiency o...
Platelets are small, abundant blood cells involved in many processes. Loss of function of Neurobeach...
Platelets are small, abundant blood cells involved in many processes. Loss of function of Neurobeach...
NBEAL2 encodes a multidomain scaffolding protein with a putative role in granule ontogeny in human p...
Mutations in NBEAL2, the gene encoding the scaffolding protein Nbeal2, are causal of gray platelet s...
Mutations in NBEAL2, the gene encoding the scaffolding protein Nbeal2, are causal of gray platelet s...
Mutations in the human NBEAL2 gene cause gray platelet syndrome (GPS), a bleeding diathesis characte...
Mutations in the human NBEAL2 gene cause gray platelet syndrome (GPS), a bleeding diathesis characte...
Mutations in the human NBEAL2 gene cause gray platelet syndrome (GPS), a bleeding diathesis characte...
Mutations in the human NBEAL2 gene cause gray platelet syndrome (GPS), a bleeding diathesis characte...
Mutations in the human NBEAL2 gene cause gray platelet syndrome (GPS), a bleeding diathesis characte...
Mutations in NBEAL2, the gene encoding the scaffolding protein Nbeal2 are causal of Gray Platelet Sy...
Gray platelet syndrome (GPS) is a rare disorder primarily characterised by the absence of α-granules...
Mutations in the human NBEAL2 gene cause gray platelet syndrome (GPS), a bleeding diathesis characte...
The Gray Platelet Syndrome (GPS) is a rare inherited bleeding disorder characterized by deficiency o...
The Gray Platelet Syndrome (GPS) is a rare inherited bleeding disorder characterized by deficiency o...
Platelets are small, abundant blood cells involved in many processes. Loss of function of Neurobeach...
Platelets are small, abundant blood cells involved in many processes. Loss of function of Neurobeach...
NBEAL2 encodes a multidomain scaffolding protein with a putative role in granule ontogeny in human p...
Mutations in NBEAL2, the gene encoding the scaffolding protein Nbeal2, are causal of gray platelet s...
Mutations in NBEAL2, the gene encoding the scaffolding protein Nbeal2, are causal of gray platelet s...
Mutations in the human NBEAL2 gene cause gray platelet syndrome (GPS), a bleeding diathesis characte...
Mutations in the human NBEAL2 gene cause gray platelet syndrome (GPS), a bleeding diathesis characte...
Mutations in the human NBEAL2 gene cause gray platelet syndrome (GPS), a bleeding diathesis characte...
Mutations in the human NBEAL2 gene cause gray platelet syndrome (GPS), a bleeding diathesis characte...
Mutations in the human NBEAL2 gene cause gray platelet syndrome (GPS), a bleeding diathesis characte...
Mutations in NBEAL2, the gene encoding the scaffolding protein Nbeal2 are causal of Gray Platelet Sy...
Gray platelet syndrome (GPS) is a rare disorder primarily characterised by the absence of α-granules...
Mutations in the human NBEAL2 gene cause gray platelet syndrome (GPS), a bleeding diathesis characte...
The Gray Platelet Syndrome (GPS) is a rare inherited bleeding disorder characterized by deficiency o...
The Gray Platelet Syndrome (GPS) is a rare inherited bleeding disorder characterized by deficiency o...