Heritable mutations of ALAS2 gene are responsible for the human X-linked sideroblastic anemia.
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。
Within minutes of being inhaled into the lungs cigarette smoke causes genetic mutations linked to lung cancer, according to a new study in the Chemical Research in Toxicology.
最近的一项毒理学化学研究显示，几分钟之内，将香烟烟雾大量吸入肺部，香烟烟雾则产生与肺癌有关的基因突变。
Mitochondrial DNA mutations are linked to a growing list of human diseases including neurodegenerative diseases, diabetes, cancer and infertility.
线粒体dNA突变与越来越多的人类疾病有关，其中包括神经退行性疾病、糖尿病、癌症及不育症。
The overarching cause of autism is still unknown, and cases have been linked to about 100 mutations, some inherited and some developing spontaneously.
导致自闭症的主要原因尚未确定，研究发现自闭症病例与100种基因变异有关，其中一些可以遗传，一些则是自然发生。
The Duke test examines the genes of HIV strains for mutations at certain positions that are known to be linked to drug resistance.
杜克试验在和抗药相关的当前已知位点检测HIV株的基因突变。
The TB test, called a line probe assay, costs less than $8 and detects mutations in bacterial DNA linked to drug resistance.
这种TB检测方法称为多列探针检测法，用不到8美元即可检出与耐药性相关的细菌DNA突变。
Resistance to Bt toxins in some insects is linked with mutations that disrupt a toxin-binding cadherin protein.
一些抗苏云金杆菌毒素的昆虫的抗性是和毒素结合钙粘蛋白的断裂相关。
A major question in the field of many chronic diseases has been whether the risk of developing a disease is more closely linked to common or rare mutations.
许多慢性病的主要问题在于发病风险与普通突变密切相关还是与罕见突变密切相关。
The absence of ALAS2 leads to maturation arrest of primitive erythroid cells. Heritable mutations of ALAS2 gene are responsible for the human X-linked sideroblastic anemia (XLSA).
ALAS2的缺失能导致红细胞发育的停滞，ALAS2基因的遗传性突变能引起X-连锁的成高铁红细胞贫血（XLSA）。
Objective to detect mutations of the RP2 gene in two Chinese families with X linked retinitis pigmentosa (XLRP).
目的检测引起2个家系产生X连锁视网膜色素变性的RP2基因突变。
Objective To analyze the ABCD1 gene mutations in 5 cases of X-linked adrenoleukodystrophy (X-ALD) patients and 2 cases of their mothers.
目的对5例x -连锁肾上腺脑白质营养不良(X -ALD)患儿及其中2例的母亲进行ABCD 1基因突变分析。
Kelly Frazer, a genomicist at the University of California, San Diego, says the new studies help explain why many common mutations linked to diseases are located so far from any gene.
加州大学圣地亚哥分校基因学家Kelly Frazer说这些新的研究有助于解释与疾病相关的普通变异为何离任何基因都那么远。
Mutations in the Leucine-rich repeat kinase 2 are the major cause of genetically-linked late onset Parkinson's affecting a high proportion of individuals with Parkinson's in certain populations.
在激酶2中出现富含亮氨酸的突变，是基因相关的迟发型阿尔茨海默病的主要原因，在特定人群中影响大部分的阿尔茨海默病患者。
Mutations in the Leucine-rich repeat kinase 2 are the major cause of genetically-linked late onset Parkinson's affecting a high proportion of individuals with Parkinson's in certain populations.
在激酶2中出现富含亮氨酸的突变，是基因相关的迟发型阿尔茨海默病的主要原因，在特定人群中影响大部分的阿尔茨海默病患者。
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