1、

Methods: An immunohistochemical double staining technique was utilized in lingual, buccal tissue using UEA-1 in conjunction with a monoclonal antitype ⅳ collagen anti-body to observe the lymphatic capillaries and blood capillaries.

方法:利用荆豆凝集素及IV型胶原单克隆抗体分别标记内层细胞和基底膜,对舌、颊等组织进行免疫组化双重染色。

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2、

The salivary gland chromosomes of Anopheles anthropophagus Xu et Feng

嗜人按蚊的唾腺染色体

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3、

Study on the dyeing properties of Nomex aramid fibers

芳纶-Nomex染色性能探讨

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4、

The SCNs are located just above where your optic nerves at the base of the brain.

“超染色体交叉细胞核刚好位于大脑基部、眼神经汇合处之上的位置”.

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5、

The women prepared, spun and dyed the wool

女人们处理羊毛,纺羊毛并给羊毛染色。

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6、

The basic structure is divided into basal layer, alcohol-soluble pigmented resin layer-Layer and adhesive layer.

基本结构分基膜层 、 醇溶性染色树脂层、 镀铝层 和胶黏层.

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7、

Intervention study on the life style of patients with oligospermia or azoospermia

少精及无精症病人生活方式的干预研究特发性无精子症和严重少精子症患者Y染色体基因微缺失研究

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8、

Cytogenetic Investigation and Gene Analysis in Human Azoospermia and Oligozoospermia

人类无精子症及寡精子症之细胞染色体及基因分析

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9、

Chromosome aberration types and levels of sex hormones in 630 patients with azoospermia

630例无精子症患者染色体畸变及性激素水平

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10、

Azoic dyeing consists of reacting two components, neither of which itself is a dye, with one another inside the fiber to form an azo pigment.

不溶性偶氮娶嵯染色有两个反应组分组成,其中任何一个单独存在都不能称之为燃料,他们彼此在纤维中形成不溶性偶氮颜料。

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11、

Methods Immunohistochemistry was performed by using avidin biotin peroxidase complex procedure.

方法采用链霉素抗生物素蛋白生物素过氧化物酶免疫组化染色方法。

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12、

Methods: Avidin biotin complex immunoperoxidase staining for paraffin packed tissue.

方法:石蜡切片的ABC免疫组织化学染色法。

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13、

Methods: Seventy six specimens of various herniated disc tissue were immunostained with anti human IgG, using the avidin biotin peroxidase complex method.

方法:取76例不同类型突出腰椎间盘组织标本用生物素化羊抗人IgG抗体进行免疫组化染色。

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14、

Conclusion: LP is an autosomal recessive disease, and the mutation of pathogenic gene of LP is rare in Chinese people.

结论:LP是一种罕见的常染色体隐性遗传病,中国人群中其致病基因的突变频率很低;

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15、

Consanguineous marriage is often an important factor in autosomal recessive genetic disease, and inbreeding avoided can prevent this kind of disease.

近亲结婚往往是导致常染色体隐性遗传病的重要因素,避免近亲结婚可防止此类疾病的发生。

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16、

Rare autosomal recessive inheritance has also been described.

据报道很少一部分为常染色体隐性遗传型。

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17、

Result Two cases were definitely diagnosed, and this disease was autosomal recessive inherited disease.

结果2例病例得到准确诊断,本病为常染色体隐性遗传性疾病。

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18、

High-resolution Ultrasonography in the Assessment of Autosomal Recessive Polycystic Kidney Disease

高分辨率声呐部面仪高分辨超声在常染色体隐性遗传性多囊肾诊断中的价值

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19、

Mutation analysis of genes associated with autosomal recessive in early-onset parkinsonism

常染色体隐性遗传早发性帕金森综合征致病基因的突变分析

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20、

Clinical features of autosomal recessive juvenile Parkinson disease

常染色体隐性遗传性青少年型帕金森病的临床特征

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