着色

Xeroderma pigmentosum is a rare medical condition whereby individuals are unable to have direct contact with the sunlight and other sources of ultraviolet rays.

干是一种罕见的着色个人身体状况而无法直接接触阳光和其它紫外线的来源。

Objective To study the association between polymorphism of DNA repair gene xeroderma pigmentosum GAsp1104His and the risks of developing laryngeal and hypopharyngeal carcinomas.

目的研究DNA修复基因着色性干皮病G组基因Asp1104His多态性与喉癌和喉咽癌风险的相关性。

Keep Necessary Receipts Receipts which come from the purchase of necessary items for the individual with xeroderma pigmentosum should be saved for tax reasons.

保持必要的收益，收益则来自购买必要的物品，让个人与着色性干皮病，应节省税收原因。

Obtain Handicapped Parking Decal Should it be necessary for the individual with xeroderma pigmentosum to travel in the car, it is extremely important that the individual and their family have a handicapped parking sticker for the vehicle.

获得残障停车标记，如果有必要对个别着色性干皮病旅行小轿车这是极为重要的个人和他们的家庭有残障停车贴的车。

Several critical genes (so-called core factors) participate in NER process, and deficient in these proteins may result in therecessive syndrome xeroderma pigmentosum.

很多重要的蛋白参与了 NER 过程，其中有一些蛋白的先天缺陷可以导致着色性干皮病表型。

At present, the foreign reports show that Freck1e is the followed trait of some diseases such as xeroderma pigmeniosa, incontineniia pigmenti and PJS syndrome.

目前，国外对本病的相关报道均认为该病为其它疾病的伴随性状如着色性干皮病、色素失禁症、PJS综合症等，其遗传方式不明。

Objective To investigate the relationship of excision repair cross-complementing 1(ERCC1), xeroderma pigmentosum group D, and breast cancer susceptibility gene 1(BRCA1) polymorphisms with the efficacy of platinum-based chemotherapy for treatment of the patients with advanced non-small cell lung cancer.

目的 探讨核苷酸切除修复系统的3个重要基因切除修复交叉互补基因1(ERCC1)、着色性干皮病基因D和乳腺癌易感基因1(BRCA1)的单核苷酸多态性与晚期非小细胞肺癌患者铂类药物化疗效果的相关性。

A number of nucleic acid repair genes such as excision repair cross-complementing gene 1(ERCC1) and human xeroderma pigmentosum gene D(XPD/ERCC2),the level descent may be susceptible factors to one or certain kinds of tumors; but if these genes′ level are higher,the ability to repair damage and chemotherapy-induced genetic damage will be enhanced,it may be resistance to chemotherapeutic drugs.

一些核酸修复基因，如切除修复交叉互补基因1(ERCC1)及人类着色性干皮病基因D(XPD/ERCC2)的水平下降，可能会成为某种或某几种肿瘤的易感因素；但如果此种基因的水平较高，修复损伤的能力提高，对化疗药物所致基因损伤的修复能力也就增强了，那么可能对化疗药物产生耐药现象。

Study on clinical character and genetic model of Dyschromatosis Symmetrical Hereditaria and Freckle Pigmentary inherited disease, which occupies a part of population in genodermatosis, is disease of monogenic inheritance. The genes of some diseases have been identified, such as Xeroderma, incontinentia pigmentation and PJS syndromes.

色素性遗传性疾病在遗传性皮肤病中占有不小的比重，这类疾病大都属单基因遗传病，而且有些疾病的遗传基因已经被找到，如着色性干皮病、色素失禁症、PJS综合症等。

Results Following up lasted 3 month to 2 years, the amount of tear increased, the symptom of corneal xerosis decreased, the using of artificial tear substitutes decreased and the stain of fluorosin decreased.

结果 泪道栓塞术后观察3月至2年，眼干患者泪液量增加，眼干症状减轻，人工泪液使用减少，角膜荧光染色着色减少。2例1个泪道栓丢失，1例1个泪道栓滑人泪道，1例治疗后出现泪溢。

Now, however, all children continue in "comprehensive" schools, and the eleven-plus determines which courses of study the child will follow.

然而现在，所有的孩子都要在综合学校继续学习，所以这次考试只是决定他们将要学习哪些课程。

Cultivatable land , and led to a general recognition that development must not be carried at the cost of agriculture .

城区的迅速扩大在很多情况下侵占了宝贵的可耕地，使人们普遍认识到发展不能以牺牲农业为代价。