Gene mutations are alterations in the DNA code.

因突变是指DNA 密码的改变。

Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum.

XPF轻微突变导致致癌倾向综合征着色性干皮病。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的因突变,进一步开展因诊断和因治疗奠定础。

Technique of mutation breeding in gladiola was studied by meansof electron beam.

用电子束辐射唐菖蒲种球，研究唐菖蒲的诱变育种。

We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.

研究遗传性白内障致病因，实验动物模型是一个非常好的方式。

Abstract： Technique of mutation breeding in gladiola was studied by means of electron beam.

摘 要： 用电子束辐射唐菖蒲种球，研究唐菖蒲的诱变育种。

Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.

结果先证者表因外显子6区13389G缺失,引起移码突变。

JianYang Tangelo,a new citrus hybrid cultivar,originated from a bud mutation of a tangelo cultivar introduced from abroad.

建阳橘柚是从国外引进的橘柚品种中通过芽变选育成的杂柑类新品种。

Methods Morulae of four mutation hairless mice and one cataract mouse were transplanted into uterus using embryonic transfer method.

方法利用胚胎移植技术对四种突变无毛小鼠和一种白内障小鼠的桑葚胚进行子宫内移植。

CodonCode Aligner is a program for sequence assembly, contig editing, and mutation detection, available for Windows and Mac OS X.

DNA测序trace图编辑、突变分析、contig编辑、序列拼接软件。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因ELN突变引起管的疾病，但没有认知的异常，这些资料暗示了激1半合性因在视觉空间建构认知障碍中的作用。

At least some of the mutations responsible for this loss of vision differed between the 29 populations of cavefish known to exist.

目前存的29种洞穴鱼，其眼盲亦与这些突变有关，但是其因突变的位置并不相同。

This indicats that gamma ray irradiation can increase the frequency of mutations and produces special types of flower in Godetia grandiflora breeding.

花色变异主要是颜色变浅，甚至变白色。花瓣变异可由原来的单瓣变重瓣花。

Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).

结果23个杂合子突变中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突变分别22个(96%)、20个(87%)和23个(100%)。

The mutation potential of ethephon was by investigated the micronucleus test of bone marrow polychromatophilic erythroblasts (PCE) cells and sperm shape abnormality test in mice.

摘要测定乙烯利对人体健康的影响，采用小鼠骨髓细胞微核试验和小鼠精子畸形试验分别检测了乙烯利对小鼠体细胞和生殖细胞的致突变性。

CONCLUSION: Base pair substitution mutation and frame shift mutation were caused by folpet in Ames test.And DNA breakage in human PMNC might be induced by folpet.

灭菌丹可引起鼠伤寒沙门氏菌碱置换和移码突变，并可能损伤人外周淋巴细胞DNA的完整性。

Allelotype analysis was done at five short tandem repeat markers (D17S855, D17S1322, D17S1323, D17S1326, and D17S1327) in or adjacent to BRCA1 on the recurrent mutation carriers.

对发携带有相同突变的个体选取5个与BRCA1因连锁的标记（D17S855、D17S1322、D17S1323、D17S1326和D17S1327）进行单倍型分析。

Recent studies indicate an increased frequency of mutations in the gene encoding glucocerebrosidase (GBA), a deficiency of which causes Gaucher's disease, among patients with Parkinson's disease.

最近的研究表明，在帕金森患者的脑苷脂（GBA）因编码中突变频率增加。脑苷脂的缺乏可导致高歇氏病。

A mutant, TS-N-121 was obtained by mutation and plate screening from a parent strain Mycobacterium fortuitum MF2 , which could transform sterol into androstanedione as the main product.

从雄甾二酮的转化产生菌偶发分枝杆菌MF2出发,经紫外诱变结合平板筛选,获得一株主要转化生产睾酮的突变株TS-N-121。

Liver function tests and hepatitis B virus (HBV) DNA (Versant 3.0) were assessed bimonthly, whereas adefovir-related mutations were searched by INNO-LiPA assay at baseline and at yearly intervals.

我们评估了阿德-拉米联合治疗能否克服这种风险。