角化过度

This is a light of hereditary skin diseases, the cause is hyperkeratosis around the hair follicles, the formation of hair follicles in line with the small papules.

这是一种轻型的遗传性皮肤病，病因是毛囊周围过度角化，形成与毛囊一致的小丘疹。

As a result of squamous cell hyperplasia and hyperkeratosis and a certain special-shaped, and long-term不愈can be transformed into squamous cell carcinoma.

由于鳞状上皮的过度增生和过度角化并有一定异型性，长期不愈可转变为鳞状细胞癌。

False-negative results （ n = 1 ） were caused by extreme hyperkeratosis, and false positive （ n = 4 ） were cases with scarring or inflammation.

特异性为86.7％。假阴性结果（1例）是由重度的上皮过度角化所致；黏膜的炎症充血和瘢痕易于产生假阳性结果（4例）。

Hyperkeratosis or parakeratosis on an otherwise negative Papsmear is not a marker for significant CIN and may be related toinfection or trauma with inflammation, such as from use of a diaphragm .

在其他的巴氏涂片阴性的片子上的过度角化或角化不全，这种情况可能与感染相关，也可能与感染合并血肿相关，，如使用隔膜。

Follicular hyperkeratosis and focal minimal perifollicular erythema were found at the hairline.

尚未落发的毛孔周围则主要有过度角化伴随局部些微变红的变化。

Dysplasias may also involve the vulvar epithelium, seen here at the right with overlying hyperkeratosis (producing an area of leukoplakia ), with more normal keratinizing squamous epithelium at the left.

不典型性增生可累及外阴上皮，右侧为表层的过度角化，左侧为萎缩的角化的鳞状上皮。

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。

Hyperkeratotic Porokeratosis of Mibelli in a Patient with Hepatocellular Cell Carcinoma, Hepatitis B and Recurrent Hypoglycemia

篇名 在肝细胞癌，B型肝炎和反覆性低血糖病人身上的过度角化米贝利汗孔角化症

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。

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。