Neither paper indicated which form of leukodystrophy the men have there are about 40 known types of the largely genetic brain cell-damaging disorder or who diagnosed the brothers. 不管是媒体还是为兄弟俩诊断的人都没有指明他们患的是哪一类型的脑白质病变&可知的关于大脑细胞损伤性病变大约就有40种。
It is a love story about a man with a genetic disorder that causes him to time travel unpredictably, and about his wife, an artist. 这部电影讲述了一个由于遗传病而经常不可预知的在时间中穿梭的男子和他的艺术家妻子的爱情故事。
Molecular Genetic Studies of Major Mental Disorder Based on the Hypothesis of Abnormal Synaptic Plasticity 阻燃性增强热塑性塑料基于突触可塑性异常假说的重性精神障碍易感基因的分子遗传学研究
Traditionally, the genetic diagnosis of a mendelian disorder relied on the establishment of a clinical diagnosis followed by the sequencing of previously implicated genes. 通常上,孟德尔疾病的遗传诊断主要依靠临床诊断以及随后对疾病已知相关基因的测序。
If so, there could be a familial genetic disorder called fragile X, in which a certain portion of the X chromosome is abnormal. 如果有,那么你很可能有脆弱X基因的家族遗传病。也就是X基因的一部分是异常的。
Two of his grandchildren developed a rare genetic disorder, and one died. 他的两个孙儿得了一种罕见的遗传疾病,其中一个已经离开人世。
HEMOCHROMATOSIS-A genetic disorder involving increased absorption of iron by the gastrointestinal tract and deposition in the liver resulting ultimately in cirrhosis and liver failure. 血色沉着病&一种遗传性病症引起胃肠道吸收铁增多,沉积在肝脏,导致最终肝硬化或肝衰竭。
BERLIN ( Reuters)-A daily dose of aspirin can prevent cancer in people with a genetic disorder that increases their risk of developing the disease, scientists said on Monday. 柏林(路透社)&有研究者周一指出,有某些遗传病发病风险的人群每天服用阿司匹林能够起到预防的作用。
Human embryo preimplantation genetic diagnosis ( PGD) for sure can solve some problems who have genetic disorder or disease. 人类胚胎着床前遗传学诊断(PGD)能解决诸多有关遗传学异常或疾病的问题。
Background: Fibrodysplasia ossificans progressiva is a rare genetic disorder of ectopic skeletogenesis associated with dysregulation of bone morphogenetic protein ( BMP) signaling. 背景:进行性骨化性纤维发育不良是一种表现为异位骨化和BMP信号传导失调的少见的遗传性疾病。
Celiac disease is a genetic autoimmune disorder that damages the small intestine and interferes with absorption of nutrients from food. 乳糜泻是一种遗传性疾病,它能损害小肠功能,干扰食物中营养物质的吸收。
TSC is a genetic disorder that causes benign tumors to form in many different organs, primarily in the brain, eyes, heart, kidney, skin and lungs. TSC是一种遗传性疾病,导致良性肿瘤的形成,在许多不同的器官,主要是在脑部,眼睛,心脏,肾脏,皮肤和肺部。
In PGD, doctors examine embryo DNA for specific genetic signatures, usually in cases in which one or both parents have a genetic disorder or are known carriers. 在PGD中,医生要检查胚胎DNA中特异的遗传学标记,以防父母双方或一方有遗传性缺陷或者是不适于生育的疾病携带者。
Objective To explore the genetic etiology of obsessive-compulsive disorder ( OCD) and genetic association between OCD and tic disorder. 目的探讨强迫症的遗传病因学及强迫症与抽动障碍的遗传联系。
Reconstructing the face of a person who was in an accident, has suffered from cancer, or has a genetic disorder was once the subject of science fiction. 重塑因事故、罹患癌症或遗传疾病造成缺陷的面孔(一度成为科幻小说的主题)。
I have finally learned how to say, that I have a rare orphan genetic skin disorder named recessive dystrophic epidermolysis bullosa. 现在我终于学会解释自己的病了:这是一种罕见的遗传性皮肤病,叫隐性遗传营养不良型大疱性表皮松解症。
Likewise, in people with a genetic disorder such as sickle cell anemia, the new blood system would not have the sickle-cell mutation, eliminating the cause of disease. 同样的,对于遗传疾病(如镰状细胞性贫血)患者,新造血系统不再有镰状红细胞变异,因此消除了该疾病的病因。
Prenatal diagnosis of sex determination for sex-linked genetic disorder by using X-Y homologous gene 应用X-Y同源基因对性连锁遗传病进行产前性别诊断
Objective To investigate the possibility of prenatal diagnosis of the fetal suspected to be affected by anhidrotic ectodermal dysplasia ( EDA) in a family with X-linked EDA so as to provide a basis for prenatal diagnosis and genetic counseling of this disorder. 目的探讨对X连锁无汗性外胚叶发育不良(EDA)家系的EDA患胎进行产前诊断的可能性,为建立对该病的产前诊断及遗传咨询提供依据。
Objective: To investigate the association between Taq I Polymorphism of Dopamine Receptor D2 ( DRD2) and genetic susceptibility for stress disorder. 目的:对我国汉族SD患者的多巴胺受体D2基因(DRD2)TaqⅠ多态性进行检测,探讨其与SD的遗传易感性之间的关系。
A Study of the Genetic Factor and Mode of Genetic Transmission in Affective Disorder 情感性障碍遗传因素与遗传方式的研究
It will be suitable for clinical prenatal diagnosis of sex-linked genetic disorder by using PCR with x-y homologous primers. 结论:应用X-Y同源引物和SRY基因引物复合扩增,可用于临床上性连锁遗传病的产前性别诊断,方法可靠准确。
Schizophrenia: a genetic disorder of the synapse? Glutamatergic synapses might be the site of primary abnormalities 精神分裂症:是一种遗传性突触病吗?谷氨酸能突触可能是其主要病变部位
Conclusion Parental specific expression exists in the transmission of tic disorder, which gives evidence that genomic imprinting may be involved in the genetic mechanism of tic disorder. 结论抽动障碍的传递存在亲源特异性表达,抽动障碍病因学中可能存在遗传印迹机制。
The genetic disorder ataxia telangiectasia ( AT) is characterized by immunodeficiency, progressive cerebellar ataxia, gonadal abnormalities, radiosensitivity, and cancer predisposition. 基因缺陷所致共济失调-毛细血管扩张症(AT)表现为免疫缺陷、进行性共济失调、性腺发育异常、辐射敏感和易患癌症等。
Although follicular keratosis is a genetic disorder, it could have papilloma-tous proliferation and vegetation, resembling the infection of HP Vs. 毛囊角化病虽然是一种遗传性疾病,但其疣状增生以及皱襞部位的乳头瘤样增生却类似HPV感染的表现。
Ataxia Telangiectasia ( AT) as a genetic disorder results from single gene mutation, characterized by radiosensitivity, progressive nerve degeneration, immunodeficiency, premature aging and cancer predisposition. 共济失调性毛细血管扩张综合症(AT)是一种单基因突变引起的遗传性疾病,表现为高辐射敏感性、进行性神经退变、免疫缺陷、早衰及易患癌症等。
Genetic association between mood disorder and monoamine oxidase gene 情感性障碍与单胺氧化酶基因的遗传关联性分析