
Genetic Mechanism of Human Neutrophil Antigen 2 Deficiency …
2015年5月29日 · Human neutrophil antigen 2 (HNA-2) is coded by CD177 gene that involves in human myeloproliferative disorders. HNA-2 expression varies among humans and about …
Human neutrophil antigens: Nature, clinical significance and …
Human neutrophil antigens (HNAs) are a family of epitopes that are located on glycoproteins that are mostly expressed on human granulocytes. Antibodies that recognize these epitopes have …
Human neutrophil antigens: Nature, clinical significance and
Human neutrophil antigens (HNAs) are a family of epitopes that are located on glycoproteins that are mostly expressed on human granulocytes. Antibodies that recognize these epitopes have …
Molecular Genetics of the Human Neutrophil Antigens
2018年8月17日 · To date, five HNA systems are assigned, and during the last decades enormous efforts have been undertaken to identify the underlying genes and to characterize the …
Phenotyping and Genotyping of HNA: Prevalence, Risk of …
Antibodies to human neutrophil alloantigens (HNA) are involved in the pathophysiology of several clinical conditions including transfusion-related acute lung injury (TRALI), alloimmune and …
Genotyping of human neutrophil antigens (HNA) from whole …
2013年9月12日 · In this paper, we developed a bioinformatics tool for typing the HNA antigens from personal human whole-genome sequencing data. The NGS technology was evaluated for …
Molecular Genetics of the Human Neutrophil Antigens
The molecular basis of each of the five HNA antigen systems has been decoded during the past decades. This enables reliable molecular typing strategies, antibody detection and …
Antibodies directed against the neutrophil-specific Fcγ receptor IIIb (FcγRIIIb), which bears the HNA-1 antigens, are most frequently implicated in neonatal immune neutropenia and …
328 名健康壮族人进行hna-1~5 的基因分型和多态性研究, 调查了解汉族和壮族人群中hna-1~5 的基因频率多态性分布。 结 果在hna-1 系统,hna-1a 是汉族(0.6893)和壮族(0.7454)人群 …
SEPT9 gene sequencing analysis reveals recurrent mutations in ...
Hereditary neuralgic amyotrophy (HNA) is an autosomal dominant disorder that manifests as recurrent, episodic, painful brachial neuropathies. A gene for HNA maps to chromosome …
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