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NBEAL2 Gene - GeneCards | NBEL2 Protein | NBEL2 Antibody
NBEAL2 Gene - GeneCards | NBEL2 Protein | NBEL2 Antibody

Spontaneous 8bp Deletion in Nbeal2 Recapitulates the Gray Platelet Syndrome  in Mice | PLOS ONE
Spontaneous 8bp Deletion in Nbeal2 Recapitulates the Gray Platelet Syndrome in Mice | PLOS ONE

NBEAL2 CRISPR Knockout and Activation Products (m) | SCBT - Santa Cruz  Biotechnology
NBEAL2 CRISPR Knockout and Activation Products (m) | SCBT - Santa Cruz Biotechnology

American Journal of Hematology | Blood Research Journal | Wiley Online  Library
American Journal of Hematology | Blood Research Journal | Wiley Online Library

Correlation between platelet phenotype and NBEAL2 genotype in patients with  congenital thrombocytopenia and α-granule deficiency | Haematologica
Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and α-granule deficiency | Haematologica

Deficiency in platelet alpha granules. Nbeal2 gps/gps platelets appear... |  Download Scientific Diagram
Deficiency in platelet alpha granules. Nbeal2 gps/gps platelets appear... | Download Scientific Diagram

NBEAL2's partners in activated T cells a Immunoblotting of NBEAL2 in T... |  Download Scientific Diagram
NBEAL2's partners in activated T cells a Immunoblotting of NBEAL2 in T... | Download Scientific Diagram

Neutrophil specific granule and NETosis defects in gray platelet syndrome.  - Abstract - Europe PMC
Neutrophil specific granule and NETosis defects in gray platelet syndrome. - Abstract - Europe PMC

NBEAL2 Gene - GeneCards | NBEL2 Protein | NBEL2 Antibody
NBEAL2 Gene - GeneCards | NBEL2 Protein | NBEL2 Antibody

Mutation analysis of NBEAL2 in Family 4. (A) Pedigree of the family... |  Download Scientific Diagram
Mutation analysis of NBEAL2 in Family 4. (A) Pedigree of the family... | Download Scientific Diagram

NBEAL2 (Neurobeachin-Like 2) Is Required for Retention of Cargo Proteins by  α-Granules During Their Production by Megakaryocytes | Arteriosclerosis,  Thrombosis, and Vascular Biology
NBEAL2 (Neurobeachin-Like 2) Is Required for Retention of Cargo Proteins by α-Granules During Their Production by Megakaryocytes | Arteriosclerosis, Thrombosis, and Vascular Biology

NBEAL2 (Neurobeachin-Like 2) Is Required for Retention of Cargo Proteins by  α-Granules During Their Production by Megakaryocytes | Arteriosclerosis,  Thrombosis, and Vascular Biology
NBEAL2 (Neurobeachin-Like 2) Is Required for Retention of Cargo Proteins by α-Granules During Their Production by Megakaryocytes | Arteriosclerosis, Thrombosis, and Vascular Biology

NBEAL2 deficiency in humans leads to low CTLA-4 expression in activated  conventional T cells | Nature Communications
NBEAL2 deficiency in humans leads to low CTLA-4 expression in activated conventional T cells | Nature Communications

NBEAL2 (Neurobeachin-Like 2) Is Required for Retention of Cargo Proteins by  α-Granules During Their Production by Megakaryocytes | Arteriosclerosis,  Thrombosis, and Vascular Biology
NBEAL2 (Neurobeachin-Like 2) Is Required for Retention of Cargo Proteins by α-Granules During Their Production by Megakaryocytes | Arteriosclerosis, Thrombosis, and Vascular Biology

NBEAL2 (Neurobeachin-Like 2) Is Required for Retention of Cargo Proteins by  α-Granules During Their Production by Megakaryocytes | Arteriosclerosis,  Thrombosis, and Vascular Biology
NBEAL2 (Neurobeachin-Like 2) Is Required for Retention of Cargo Proteins by α-Granules During Their Production by Megakaryocytes | Arteriosclerosis, Thrombosis, and Vascular Biology

Neurobeachin-like protein 2 NBEAL2 Antibody
Neurobeachin-like protein 2 NBEAL2 Antibody

NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis  of platelet α-granules | Nature Genetics
NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granules | Nature Genetics

Neutrophil specific granule and NETosis defects in gray platelet syndrome -  ScienceDirect
Neutrophil specific granule and NETosis defects in gray platelet syndrome - ScienceDirect

ARC Journals on X: "The Role of Genetic Mutations in Gene NBEAL2 in Gray  Platelet Syndrome -By Shahin Asadi Read More : https://t.co/5H5H9MOLKf ARC  Journal of Hematology Submit Paper at:editor_ajh@arcjournals.org About  Journal :
ARC Journals on X: "The Role of Genetic Mutations in Gene NBEAL2 in Gray Platelet Syndrome -By Shahin Asadi Read More : https://t.co/5H5H9MOLKf ARC Journal of Hematology Submit Paper at:editor_ajh@arcjournals.org About Journal :

NBEAL2 (Neurobeachin-Like 2) Is Required for Retention of Cargo Proteins by  α-Granules During Their Production by Megakaryocytes | Arteriosclerosis,  Thrombosis, and Vascular Biology
NBEAL2 (Neurobeachin-Like 2) Is Required for Retention of Cargo Proteins by α-Granules During Their Production by Megakaryocytes | Arteriosclerosis, Thrombosis, and Vascular Biology

NBEAL2 Gene - GeneCards | NBEL2 Protein | NBEL2 Antibody
NBEAL2 Gene - GeneCards | NBEL2 Protein | NBEL2 Antibody

Aaron Goodman - “Papa Heme” on X: "Grey Platelet Syndrome Mutation in NBEAL2  gene Platelets can't form alpha granules thus they appear grey! Large  platelets Bleeding With time marrow becomes fibrotic.  https://t.co/RqbFG0y4D9" /
Aaron Goodman - “Papa Heme” on X: "Grey Platelet Syndrome Mutation in NBEAL2 gene Platelets can't form alpha granules thus they appear grey! Large platelets Bleeding With time marrow becomes fibrotic. https://t.co/RqbFG0y4D9" /

Full article: A novel nonsense NBEAL2 gene mutation causing severe bleeding  in a patient with gray platelet syndrome
Full article: A novel nonsense NBEAL2 gene mutation causing severe bleeding in a patient with gray platelet syndrome

Mutations in Neurobeachin-like 2 do not impact Weibel-Palade body  biogenesis and von Willebrand factor secretion in gray platelet syndrome  Endothelial Colony Forming Cells - ScienceDirect
Mutations in Neurobeachin-like 2 do not impact Weibel-Palade body biogenesis and von Willebrand factor secretion in gray platelet syndrome Endothelial Colony Forming Cells - ScienceDirect

Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome  | Nature Genetics
Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome | Nature Genetics