sickle-cell信息详情
adj.镰状红细胞的
sickle cell───镰状细胞；[细胞]镰形红细胞；镰状细胞，镰刀形红细胞
sickle cell anemia───n.<美>镰状细胞血症；镰状细胞性贫血
sickle───adj.镰刀型的；n.镰刀；n.(Sickle)（美、加、英）茜克克丽（人名）；v.呈镰刀型
cell───n.(Cell)人名；(英)塞尔；n.细胞；电池；蜂房的巢室；单人小室；vi.住在牢房或小室中
adamantine sickle───金刚镰刀
sickle anemia───镰状贫血
cell stem cell───干细胞
sickle of leather───用皮革做的镰刀
effusion cell───[医]泻流室
Sickle-cell anaemia is passed on through a recessive gene.───镰状细胞贫血通过隐性基因遗传给后代。
Sickle-cell anaemia, caused by genes protect against malaria, is the most famous example.───例如，基因为抵抗疟疾而突变导致的镰刀状细胞贫血就是最好的例子。
It's only when you inherit the mutation from both parents that you get sickle-cell anemia.───只有当你同时遗传了父母双方的突变，你才会患上镰刀状细胞性贫血。
Or blood cells may be examined for signs of sickle-cell anemia, leukemia, or other disorders.───或检测血液细胞是否有镰状细胞性贫血，白血病或其他疾病的迹象。
People undergoing sickle cell crisis can experience extreme pain that is not always managed effectively.───人民经历镰状细胞性危机可以体验极度的痛苦也并不总是有效的管理。
This article describes an audit of pain management in sickle cell disease that was used to generate practice guidelines.───本文介绍了镰状细胞病疼痛的管理审计，这是用来生成实践准则。
Sickle-cell anaemia is a common genetic condition due to a haemoglobin disorder.───镰状细胞贫血是由血红蛋白异常引起的一种常见遗传病。
Such screening techniques and early intervention therapies have sharply lowered the mortality rate in children with sickle cell disease.───这样的筛选技术和早期介入性治疗显著降低了患镰形细胞贫血症儿童的死亡率。
Approximately 5% of the world's population are healthy carriers of a gene for sickle-cell disease or thalassaemia.───全世界近5%的健康人口携带有镰状细胞病或地中海贫血的基因。
Sickle-cell anaemia is passed on through a recessive gene.
Sickle-cell anemia is one of the most prevalent hereditary disorders with prominent morbidity and mortality.
Sickle-cell disease and severe forms of thalassaemia (thalassaemia major) can occur only when both parents are carriers of trait genes for the particular condition.
Variant hemoglobins (see sickle-cell anemia; hemoglobinopathy) can be used to trace past human migrations and to study genetic relationships among populations.
Sickle-cell disease is an inherited blood disorder in which the red blood cells change shape in a characteristic way.
Researchers discover how carriers of the sickle-cell anaemia gene are protected from malaria.
He then corrected the sickle-cell genetic defect and prodded the iPS cells to develop into the type of marrow stem cell that manufactures a mouse's blood cells.
Patients with sickle-cell disease should be screened for skin ulcerations or potential sources of osteomyelitis, which can cause seeding of the site of a prosthetic joint.
Haemoglobin disorders fall into two main categories: sickle-cell disease and thalassaemias.