Patients with platelet or dense -granule defects have bleeding problems. Although several proteins are known to be required for -granule development, less is known about -granule biogenesis. Our previ-ous work showed that the BEACH protein NBEAL2 and the Sec1/Munc18 protein VPS33B are required for-granule biogen-esis. Using a yeast two-hybrid screen, mass spectrometry, coimmunoprecipita-tion, and bioinformatics studies, we iden-tified VPS16B as a VPS33B-binding pro-tein. Immunoblotting confirmed VPS16B expression in various human tissues and cells including megakaryocytes and plate
Gray platelet syndrome (GPS) is an autosomal recessive bleeding disorder characterized by a lack of ...
NBEAL2 encodes a multidomain scaffolding protein with a putative role in granule ontogeny in human p...
International audienceGray platelet syndrome (GPS) is a rare recessive disorder caused by biallelic ...
Platelets are small, anucleate cells that fulfill a central role in hemostasis through their ability...
Platelets contain specialized granules that are required for platelet function in hemostasis. These ...
Platelet α-granules are central to the function of these cells in blood clotting and other physiolog...
Arthrogryposis, renal dysfunction, and cholestasis (ARC) syndrome is caused by deficiencies in the t...
VPS33B is a Sec1/Munc18 protein required for the biogenesis of α-granules in megakaryocytes, which g...
Platelets are small anucleate blood cells that co-ordinate blood clotting in response to vascular in...
Although platelets are small anucleate cell fragments, they are highly organized cells rich in diffe...
Platelets are small, abundant blood cells involved in many processes. Loss of function of Neurobeach...
Mutations in NBEAL2, the gene encoding the scaffolding protein Nbeal2 are causal of Gray Platelet Sy...
The Gray Platelet Syndrome (GPS) is a rare inherited bleeding disorder characterized by deficiency o...
Mutations in NBEAL2, the gene encoding the scaffolding protein Nbeal2, are causal of gray platelet s...
Gray platelet syndrome (GPS) is an autosomal recessive bleeding disorder characterized by a lack of ...
NBEAL2 encodes a multidomain scaffolding protein with a putative role in granule ontogeny in human p...
International audienceGray platelet syndrome (GPS) is a rare recessive disorder caused by biallelic ...
Platelets are small, anucleate cells that fulfill a central role in hemostasis through their ability...
Platelets contain specialized granules that are required for platelet function in hemostasis. These ...
Platelet α-granules are central to the function of these cells in blood clotting and other physiolog...
Arthrogryposis, renal dysfunction, and cholestasis (ARC) syndrome is caused by deficiencies in the t...
VPS33B is a Sec1/Munc18 protein required for the biogenesis of α-granules in megakaryocytes, which g...
Platelets are small anucleate blood cells that co-ordinate blood clotting in response to vascular in...
Although platelets are small anucleate cell fragments, they are highly organized cells rich in diffe...
Platelets are small, abundant blood cells involved in many processes. Loss of function of Neurobeach...
Mutations in NBEAL2, the gene encoding the scaffolding protein Nbeal2 are causal of Gray Platelet Sy...
The Gray Platelet Syndrome (GPS) is a rare inherited bleeding disorder characterized by deficiency o...
Mutations in NBEAL2, the gene encoding the scaffolding protein Nbeal2, are causal of gray platelet s...
Gray platelet syndrome (GPS) is an autosomal recessive bleeding disorder characterized by a lack of ...
NBEAL2 encodes a multidomain scaffolding protein with a putative role in granule ontogeny in human p...
International audienceGray platelet syndrome (GPS) is a rare recessive disorder caused by biallelic ...