There's a good model of Huntington's disease in sheep.
绵羊可能会患上亨廷顿舞蹈症。
单词 | Huntington Disease |
释义 |
Huntington Disease
原声例句
科学60秒 2018年3月合集 There's a good model of Huntington's disease in sheep. 绵羊可能会患上亨廷顿舞蹈症。 Osmosis-遗传 In people with Huntington disease, this repeat goes on for 36 or more times in a row. 而对于HD患者,该段重复序列拷贝达到36次以上。 生物学基础入门 For example, genetic testing may be used to confirm a diagnosis of cystic fibrosis or Huntington's disease. 例如,基因检测可用于确认囊性纤维化或亨廷顿病的诊断。 VOA Special 2017年11月合集 Scientists aim to use the sheep as models to study disorders of the brain, such as Huntington's disease. 科学家旨在以绵羊为模型来研究脑紊乱疾病,如享廷顿病。 Osmosis-遗传 This phenomenon is called anticipation, which means that Huntington disease families often show earlier symptom onset with each generation. HD家族中连续后代中有发病提前倾向,称为早现现象。 Osmosis-遗传 Huntington disease is an autosomal dominant genetic disorder, which means that one affected copy of a gene is enough to cause disease. HD是一种常染色体显性遗传病,意味着可以代代相传。 Osmosis-遗传 CAG codes for the amino acid glutamine, so people with Huntington disease patients will have 36 or more glutamines in a row in the huntingtin protein. 因为CAG序列对应的是谷氨酰胺(氨基酸),所以在HD患者体内,huntingtin蛋白质上会有36个以上连续的谷氨酰胺。 Osmosis-遗传 This increased dopamine helps explain why neuroleptics, which are dopamine receptor antagonists, and tetrabenazine which depletes dopamine, are used to treat chorea in patients with Huntington disease. 多巴胺水平的增高解释了为什么神经抑制剂-多巴胺受体拮抗剂和丁苯那嗪(中枢多巴胺耗竭剂)被用来治疗亨廷顿病患者的舞蹈症。 TED演讲(视频版) 2020年4月合集 This explains why a mutation like the one that causes Huntington's disease, another degenerative neurological disorder, hasn't been eliminated by natural selection. 这就解释了为什么像导致亨廷顿病(另一种退行性神经系统疾病) 的突变还没有被自然选择消除。 Osmosis-精神心理 Individuals with these disorders all suffer from tics, which are quick, nonrhythmic movements or vocalizations that happen over and over, and are not caused by some other disorder like Huntington's disease or substance abuse. 上述三种疾病的患者都有抽动症状,即快速、无规律的动作或发声;这种持续存在的抽动并不是其他疾病的并发症,纵然亨廷顿病、药物滥用等也会导致类似抽动的症状。 经济学人 Science and technology Being able to change larger pieces of the genome, as is the case with prime editing, makes it possible to treat diseases where errors stretch over a long distance, like Huntington's disease. 能够改变基因组的较大片段(就像主要编辑的情况一样)可以治疗错误延伸到很远距离的疾病,比如亨廷顿氏病。
中文百科
亨丁顿舞蹈症 Huntington's disease(重定向自Huntington Disease)
![]() ![]() ![]() ![]() 亨丁顿舞蹈症(英语:Huntington's disease,缩写:HD),又译亨廷顿舞蹈症、杭丁顿舞蹈症等,是一种遗传性神经退行性疾病,起因于第4对染色体CAG串行异常大量重复,病发时会无法控制四肢,就像手舞足蹈一样,并伴随着智能减退,最后因吞咽、呼吸困难等原因而死亡。该疾病由美国医学家乔治·亨丁顿于1872年发现,因而得名。这种病在欧美的出现率比在亚洲高,但香港也有不少病例。该疾病的症状通常于同一家庭的成员间遗传,原则上可猜测子代的发病与否。最初的症状常常是一些情绪或认知上细微的问题。患者普遍缺乏协调性、步态不稳等症状。随着病情的进展,不协调、不平稳的肢体动作变得更加明显可见,并且会伴随心理和行为能力的下降。患者的体能会逐渐恶化,最后导致运动协调困难,而心理能力普遍下降至阿兹海默症的程度。肺炎、心脏疾病、跌倒的物理损伤等并发症,使发病后的寿命约只剩下15年。症状可以开始于任一年龄,但通常于40岁左右发病。约6%的病例为21岁之前发生运动不能刚性综合症,这类患者症状发展较快、并略有不同。此种变种症状被列为青少年亨丁顿舞蹈症、或 Westphal 变种亨丁顿舞蹈症。
英语百科
Huntington's disease 亨丁顿舞蹈症(重定向自Huntington Disease)
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Huntington's disease (HD) is a neurodegenerative genetic disorder that affects muscle coordination and leads to mental decline and behavioral symptoms. Symptoms of the disease can vary between individuals and affected members of the same family, but usually progress predictably. The earliest symptoms are often subtle problems with mood or cognition. A general lack of coordination and an unsteady gait often follow. As the disease advances, uncoordinated, jerky body movements become more apparent, along with a decline in mental abilities and behavioral symptoms. Physical abilities gradually worsen until coordinated movement becomes difficult. Mental abilities generally decline into dementia. Complications such as pneumonia, heart disease, and physical injury from falls reduce life expectancy to around twenty years from the point at which symptoms begin. Physical symptoms can begin at any age from infancy to old age, but usually begin between 35 and 44 years of age. The disease may develop earlier in life in each successive generation. About 6% of cases start before the age of 21 years with an akinetic-rigid syndrome; they progress faster and vary slightly. The variant is classified as juvenile, akinetic-rigid, or Westphal variant HD. |
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