ALAS2基因的可遗传突变是人类X连锁铁粒幼细胞性贫血的原因。
Heritable mutations of ALAS2 gene are responsible for the human X-linked sideroblastic anemia.
对于镰状细胞性贫血。
目的：探讨巨幼细胞性贫血（MA）形态学上的分型。
Objective: To investigate the morphotyping of megaloblastic anemia (MA).
羟基脲是一种抗肿瘤药，也可以用来治疗镰状细胞性贫血。
A cancer drug called hydroxyurea (Droxia, Hydrea) also is used to treat sickle cell anemia.
目的探讨老年人巨幼细胞性贫血的病因，临床特点及治疗效果。
Objective To study the etiology, clinical manifestations and therapeutic effects of megaloblastic anemia in elder.
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。
Or blood cells may be examined for signs of sickle-cell anemia, leukemia, or other disorders.
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。
It's only when you inherit the mutation from both parents that you get sickle-cell anemia.
镰状细胞性贫血是最流行的遗传性疾病之一，具有很高的发病率和死亡率。
Sickle-cell anemia is one of the most prevalent hereditary disorders with prominent morbidity and mortality.
镰状细胞性贫血和亨庭顿综合症就是这样的疾病，单个变异起了很大的作用。
Examples of so-called SNP diseases are sickle-cell anemia and Huntington's disease, where a single variant or mutation has a dramatic effect.
目的分析近年来无锡地区巨幼红细胞性贫血(mga)患者的常见病因及临床意义。
OBJECTIVE To investigate the clinical significance and common causes of megaloblastic anemia (MGA) in Wuxi district.
人的重大遗传性血红蛋白病：例如地中海贫血和镰状细胞性贫血，没有在其它动物中发现。
Hemoglobinopathies such as thalassemias and sickle cell anemia, important genetic diseases of people, have not been seen in other animals.
如西非人以及他们的后代易患一种叫做镰状细胞性贫血的疾病，这种病在西非之外几乎都没人听说过。
West Africans, and people of West African descent, are susceptible to a disease called sickle-cell anaemia that is virtually unknown elsewhere.
巨幼细胞贫血（大细胞性贫血）中多叶核嗜中性粒细胞，有8叶，而不是正常的3到4叶。
Here is a hypersegmented neutrophil that is present with megaloblastic anemias. There are 8 lobes instead of the usual 3 or 4.
最近的实验发现，用该方法制造的新组织可以缓解帕金森病小鼠和链状细胞性贫血小鼠症状。
More recent experiments have shown that fresh tissue derived in this manner can alleviate the symptoms of Parkinson's disease and sickle-cell anemia in mouse models.
儿童中风的危险因素包括心脏病、镰状细胞性贫血、血凝固障碍、血管畸形和水痘、HIV和其它的病毒感染。
Risk factors for stroke in children include heart disease, sickle-cell anemia, some blood-clotting disorders, vascular malformations, and viral infections, such as varicella, HIV and others.
美国患adpkd的人数超过囊性纤维化、肌营养不良、血友病、唐氏综合症、镰刀细胞性贫血数种疾病加起来的患者。
In the U. S., the number of individuals affected by ADPKD is greater than the number affected by cystic fibrosis, muscular dystrophy, hemophilia, Down's syndrome, and sickle cell anemia combined.
(营养性)巨幼细胞性贫血(维生素缺乏性贫血)为了制造足量、健康的红细胞，除了铁以外，身体还需要叶酸和维生素b12等原料。
Vitamin deficiency anemias. In addition to iron, your body needs folate and vitamin B-12 to produce sufficient Numbers of healthy red blood cells.
英国生化学家AnthonyAllison在20世纪50年代观察到非洲人携带单拷贝的基因突变引起的镰状细胞性贫血保护了他们受到疟疾的侵扰。
In the 1950s Anthony Allison, a British biochemist, observed that Africans who carry a single copy of the genetic mutation that causes sickle-cell anaemia are protected against malaria.
不过，CRISPR这种基因编辑技术可是货真价实的。它有可能在未来的某一天治愈细胞性贫血等与基因相关的疾病，种出更好的庄稼，或者带来大量可供移植的器官。
But CRISPR is very real, with the potential, one day, to cure genetically-linked diseases like sickle cell anemia, produce better crops, and create a huge supply of organs for transplant.
在急性失血性贫血中有红细胞丢失，但通常是循环血量减少导致死亡，而不是红细胞数量损失。
In acute blood loss anemia, RBC are lost, but mortality is usually related to loss of circulating volume, rather than to loss of RBC.
糖酵解的关键酶——丙酮酸激酶，如果它有遗传缺陷，就导致会atp缺乏、红细胞寿命缩短和溶血性贫血。
Inherited deficiency of pyruvate kinase, a key glycolytic enzyme, causes ATP deficiency, which leads to reduced RBC life span and hemolytic anemia.
例如免疫介导的溶血性贫血，产生了对抗自身红细胞的抗体。
For example, in immune-mediated hemolytic anemia, antibodies are produced against the host's own RBC.
一些慢性病理状态癌症、肾衰竭、肝衰竭等病症会造成红细胞缺乏，进而引发慢性病性贫血。
Chronic conditions. For example, if you have cancer, kidney or liver failure, or another chronic condition, you may be at risk of what's called anemia of chronic disease.
当发生血管内溶血性贫血，更多红细胞在血液循环(血红蛋白血症)被破坏以至于超出肝球蛋白质的结合能力。
In intravascular hemolytic anemia, more RBC are destroyed in the circulation (hemoglobinemia) than can be bound to haptoglobin.
当发生血管内溶血性贫血，更多红细胞在血液循环(血红蛋白血症)被破坏以至于超出肝球蛋白质的结合能力。
In intravascular hemolytic anemia, more RBC are destroyed in the circulation (hemoglobinemia) than can be bound to haptoglobin.
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