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NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granulesGray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3pVPS33B regulates protein sorting into and maturation of α-granule progenitor organelles in mouse megakaryocytesZinc finger protein, Hzf, is required for megakaryocyte development and hemostasisAbnormal megakaryocyte development and platelet function in Nbeal2(-/-) miceThe α-granule proteome: novel proteins in normal and ghost granules in gray platelet syndrome.Current Strategies in Diagnosis of Inherited Storage Pool DefectsHomozygosity mapping with SNP arrays confirms 3p21 as a recessive locus for gray platelet syndrome and narrows the interval significantlyAbnormal proplatelet formation and emperipolesis in cultured human megakaryocytes from gray platelet syndrome patientsDefective alpha-granule production in megakaryocytes from gray platelet syndrome: ultrastructural studies of bone marrow cells and megakaryocytes growing in culture from blood precursors.Dissection of autophagy in human platelets.Gray platelet syndrome. Dissociation between abnormal sorting in megakaryocyte alpha-granules and normal sorting in Weibel-Palade bodies of endothelial cells.Platelets of the Wistar Furth rat have reduced levels of alpha-granule proteins. An animal model resembling gray platelet syndrome.Gray platelet syndrome. Demonstration of alpha granule membranes that can fuse with the cell surface.Decreased content and surface expression of alpha-granule membrane protein GMP-140 in one of two types of platelet alpha delta storage pool deficiency.Super-resolution microscopy as a potential approach to diagnosis of platelet granule disorders.The VPS33B-binding protein VPS16B is required in megakaryocyte and platelet α-granule biogenesis.Biochemical studies of two patients with the gray platelet syndrome. Selective deficiency of platelet alpha granulesThe activity and subcellular distribution of the peroxisomal enzyme acyl-CoA oxidase in human blood platelets.Development of giant granules in platelets during prolonged storage.The organization of microtubules and microtubule coils in giant platelet disorders.The surface-connected canalicular system of blood platelets--a fenestrated membrane system.Functional platelets after storage in vitro for 15--21 days.
P2860
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P2860
description
1979 nî lūn-bûn
@nan
1979年の論文
@ja
1979年論文
@yue
1979年論文
@zh-hant
1979年論文
@zh-hk
1979年論文
@zh-mo
1979年論文
@zh-tw
1979年论文
@wuu
1979年论文
@zh
1979年论文
@zh-cn
name
Ultrastructural studies of the gray platelet syndrome
@ast
Ultrastructural studies of the gray platelet syndrome
@en
type
label
Ultrastructural studies of the gray platelet syndrome
@ast
Ultrastructural studies of the gray platelet syndrome
@en
prefLabel
Ultrastructural studies of the gray platelet syndrome
@ast
Ultrastructural studies of the gray platelet syndrome
@en
P2860
P1476
Ultrastructural studies of the gray platelet syndrome
@en
P2093
P2860
P304
P407
P577
1979-05-01T00:00:00Z