角化

The ABC immunohistochemical method was performed to investigate the expression of EGFR in 32 cases of laryngeal keratosis tissue.

利用免疫组化ABC法检测32例喉角化症患者组织中EGFR的表达情况。

Clinical features also include hyperlinearity of the palms and soles, atopy and heat intolerance or keratosis pilaris.

临床特征还表现为手掌和脚掌的高度线性化，遗传性过敏症和不耐热性，或毛周角化。

Methods By immunohistochemical staining, the expression of p73, p53 and Ki67 was examined in 19 cases of seborrheic keratosis, 16 basal cell carcinoma, 11 Bowen's disease, 5 squamous cell carcinoma,as well as in 10 normal skin controls.

方法应用免疫组化方法检测19例脂溢性角化病、16例基底细胞癌、11例Bowen病、5例鳞状细胞癌及10例正常人皮肤p73、p53、Ki67的表达。

A portion of ductal cells and individual serous acinic cells of the minor salivary gland also expressed Fas not only in membranous but also in cytoplasmic pattern.

结果发现，在正常鼻咽粘膜表面及隐窝的假复层纤毛柱状上皮细胞胞膜、部分小涎腺的导管上皮和个别浆液性腺泡上皮细胞的胞膜和胞浆Fas阳性表达；鳞状化生上皮的表层细胞胞膜有Fas表达，但基底细胞未见Fas表达；浸润的淋巴细胞也不表达Fas.45.9%（17/37）的鼻咽非角化性癌Fas阳性，但只有不足10%的癌细胞胞膜微弱表达Fas。

COX-1 is mainly expressed constituently, catalyzing synthesized prostaglandins and participating in normal physiological processes of the kidneys, the gastrointestinal tract, platelets and other histological systems; while COX-2 is an inducible enzyme, expressed inductively under the action of stimulating factors, bacterial endotoxins, cytokines and growth factors, catalyzing synthesized PG monomer to participate in pathological molecular incidents such as regulating cell

COX-2在癌前病变组织如Barrett's综合征，肺不典型腺瘤增生，膀胱原位导管癌和光化性角化病中过度表达。

Germ-line mutations in the genes hTERT and hTR, encoding telomerase reverse transcriptase and telomerase RNA, respectively, cause autosomal dominant dyskeratosis congenita, a rare hereditary disorder associated with premature death from aplastic anemia and pulmonary fibrosis.

分别编码端粒末端转移酶反转录酶和端粒酶RNA的hTERT和hTR基因的种系突变导致常染色体显性先天性角化不良，它是一种罕见的因为再生障碍性贫血和肺纤维化而早亡的遗传性疾病。

Local examination revealed erythematous, scaling eyelid skin, keratinizing eyelid margin, and congestive conjunctiva in both eyes.

眼科局部检查发现病人双眼眼皮发红、皮肤呈角化落屑。眼睑周绿角质化及结膜充血。

Genetic studies have been performed on the hereditary diseases of disseminated superficial actinic porokeratosis, familial progressive hyperpigmentation and triphalangeal thumb-polysyndactyly syndrome by linkage analysis and sequencing.

本研究通过连锁分析和直接测序的方法，分别对播散性浅表性光化性汗孔角化症、家族性进行性色素过度沉着症和拇指三指节多指并指多掌骨畸形这三种疾病进行了遗传学分析。

Genetic studies have been performed on the hereditary diseases of disseminated superficial actinic porokeratosis, familial progressive hyperpigmentation and triphalangeal thumb-polysyndactyly syndrome by linkage analysis and sequencing.

中文摘要本研究通过连锁分析和直接测序的方法，分别对播散性浅表性光化性汗孔角化症、家族性进行性色素过度沉着症和拇指三指节多指并指多掌骨畸形这三种疾病进行了遗传学分析。

In a Mayo Clinic study of 78 patients with keratinizing squamous metaplasia of urinary bladder, a total of 42% of patients had concurrent or subsequent carcinoma of the bladder.

在梅欧医院{美}的研究中，78例膀胱角化性鳞状上皮化生病人中，有42％同时合并或以后发展成为膀胱癌。

And Pharaoh spoke to Joseph, saying, Your father and your brothers have come to you.

47：5 法老对约瑟说，你父亲和你弟兄们到你这里来了。

Additionally, the approximate flattening of surface strip using lines linking midpoints on perpendicular lines between geodesic curves and the unconditional extreme value method are discussed.

提出了用测地线方程、曲面上两点间短程线来计算膜结构曲面测地线的方法，同时，采用测地线间垂线的中点连线和用无约束极值法进行空间条状曲面近似展开的分析。