Huntington's disease
英
美 [ˈhʌntɪŋtənz dɪˈziːz]
n. 亨廷顿舞蹈病
双语例句
- Their research suggests a possible means by which huntington's disease functions.
研究也表明了亨廷顿疾病发病的一个可能途径。 - When this transportation system goes awry in the parts of the brain affected in huntington's disease, motor skills, cognitie skills and een speech can be affected.
这种转运系统出现错误并累及到亨廷顿疾病患者的脑部，使其运动能力，认知能力甚至言语受损。 - Modern molecular genetics revealed that Huntington's disease is caused by a mutation in the gene coding for the protein Huntingtin.
现代分子遗传学研究发现，亨廷顿氏病是由编码亨廷顿蛋白质的基因突变引起的。 - Consider the role of acetylcholine in learning and memory formation and relate it to the deficits observed in Alzheimer's and Huntington's disease.
思考乙醯胆碱在学习和记忆形成所扮演的脚色并将它运用在思考阿尔滋海默症和亨丁顿舞蹈症中所观察到的不足。 - Huntington's disease is one of a number of degenerative diseases marked by clumps of malformed protein in brain cells.
亨廷顿病是一种大量的脑细胞内蛋白变质为特征的一大类疾病中的一种。 - One particularly bad gene leads to Huntington's disease, which progressively destroys key nerve cells.
一个坏基因可以导致遗传性慢性舞蹈病的发生，此病能逐渐破坏人体中关键性的神经细胞。 - Some genes are all-or-nothing predictors of certain traits, such as Huntington's disease, Bishop says.
一些基因要不全能、要不不能预测确定的特性，像亨廷顿氏舞蹈病，Bishop说。 - Huntington's disease and Parkinson's disease are related movement disorders that have seemingly opposing symptoms.
汉丁顿症以及帕金森氏症两者为相关但表面上却有相反病徵的的运动障碍。 - Study of the Rat Model of Huntington's Disease Induced by 3-Nitropropionic Acid
三硝基丙酸诱导大鼠亨廷顿氏病模型的改进研究 - Some characteristics are inherited this way ( more or less), and they tend to be the ones that textbooks focus on: for example eye colour, colour-blindness, Huntington's disease.
一些特性是按这种方式遗传（或多或少），并且他们成为了课本的焦点：举个例子，眼睛的颜色、色盲、亨廷顿氏舞蹈病。 - If the drugs can stimulate autophagy effectively over long-term periods in human brains, then they may have the potential to help delay the onset of Huntington's disease.
如果这些药物能够在人脑内长时间有效地刺激细胞自噬作用，那么他们或许具有抑制亨延顿舞蹈综合征发生的能力。 - Huntington's disease is one of a number of degenerative diseases marked by build up of a malformed proteins in brain cells, mainly in the basal ganglia and the cerebral cortex.
亨延顿舞蹈综合征是许多以畸形蛋白在脑细胞内聚积为特征的退行性疾病中的一类，畸形蛋白主要在基底神经节和大脑皮层堆积。 - Huntington's disease: is a disorder passed down through families in which nerve cells in the brain waste away, or degenerate.
亨廷顿病（舞蹈病）是一种家族遗传病，缘于大脑中的神经元衰弱或退化造成的失调紊乱。 - Only later did she begin to display the symptoms of Huntington's Disease, an inherited brain disorder that produces horrific delusions and uncontrolled movements.
在此之后，她才开始显示出亨廷顿病的症状，这是一种会导致恐怖错觉和行动失控的遗传性脑疾。 - "We know the genetics of Huntington's disease and can predict the majority of people at risk," says Professor Rubinsztein.
“我们知道亨延顿舞蹈综合征的遗传学特征，能预测大多数这类人的风险性，”Rubinsztein教授说。 - Impaired function of pancreatic β cells in the R6/ 2 transgenic mouse model of Huntington's disease
R6/2型亨廷顿病转基因小鼠胰岛β细胞功能损伤 - However, there are currently no treatments available that slow the neurodegeneration in people with Huntington's disease.
然而，现在临床上还没有可用的减缓亨延顿舞蹈综合征神经退行性变的方法。 - Mayo Clinic researchers have discovered a protein interaction that may explain how the deadly Huntington's disease affects the brain.
Mayo研究人员发现一种蛋白相互作用机制，该机制有可能解释致命性的Huntington's病如何影响大脑。 - The gene responsible for Huntington's disease was discovered in1993, but there is still no cure.
导致Huntington疾病的基因在1993年已经被发现，但到现在都还没有治愈的方法。 - These images are from an70 year old woman who has a clinical diagnosis of Huntington's disease.
这些影像摄自一位70岁女性，临床诊断有亨廷顿舞蹈病。 - Huntington's disease: a survey of the pedigree of 4 families
Huntington舞蹈病&附4个家谱调查 - Molecular analysis of huntington's disease with expanded CAG trinucleotide repeat in Chinese
中国人亨廷顿病CAG三核苷酸重复的分子分析 - Molecular Diagnosis of Huntington's Disease: an analysis of two large families
亨廷顿病的基因诊断及家系分析 - Research progress in molecular pathology of Huntington's disease
亨廷顿舞蹈病的分子病理研究进展 - The role of the striatum in rule application: The model of Huntington's disease at early stage
纹状体在语法应用中的作用：亨廷顿病早期模型 - Executive dysfunction in early stages of Huntington's disease is associated with striatal and insular atrophy: A neuropsychological and voxel-based morphometric study
早期亨廷顿病患者的执行能力障碍与纹状体和岛叶萎缩相关：一项神经心理学和基于体素的形态测量学研究 - Compared with Huntington's disease ( HD), the content of NF subunits was increased in AD brain gray matter and the increased level of NF-H and NF-M were mainly in abnormal hyperphosphorylated form.
与亨廷顿氏病患者相比，AD患者大脑灰质非水溶性级分三种NF亚基的含量均升高，且升高的NF-H和NF-M主要表现为异常过度磷酸化形式。 - Preclinical Huntington's disease: Compensatory brain responses during learning
亨廷顿病的临床前期：学习期间大脑的代偿性反应 - Incidence and mutation rates of Huntington's disease in Spain: Experience of 9 years of direct genetic testing
西班牙亨廷顿病的发病率和突变率：一项基于9年直接基因检测的结果 - Role of hypokinesia and bradykinesia in gait disturbances in Huntington's disease: A biomechanical study
运动功能减退和运动徐缓在亨廷顿病患者步态障碍中的作用：一项生物力学研究