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cells
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  上皮细胞
    Adrenomedullin Modulation of Retinal Pigment Epithelial Cells and the Intracellular Signal Transduction Pathways
    肾上腺髓质素调节视网膜色素上皮细胞及细胞内信号传导通路的研究
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    HSP70 and HSP27 Expression in Lens Epithelial Cells in Contusion Eyes of Rat Model and Modulated by Thermotolerance or Quercetin
    钝挫性眼外伤动物模型中晶状体上皮细胞热休克蛋白的表达及其调节
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    Effects of PKB and Its Regulator Elements-FGF,PTEN on the Proliferation of Lens Epithelial Cells
    PKB及其调节因子FGF、PTEN在晶状体上皮细胞增殖中的作用
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    In Vitro Study of DNA Damage and the Related Anti-stress Reaction Induced by Acute Exposure of Microwave from Mobile Phone on Cultured Human Lens Epithelial Cells
    急性手机微波辐射对人晶状体上皮细胞DNA的损伤作用及细胞抗损伤反应的实验研究
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    Low Concentration of H_2O_2 Promoted-Cell Adhesion and Migration in Cultured Rabbit Corneal Epithelial Cells
    低浓度H_2O_2促进兔角膜培养上皮细胞黏附及移行的离体实验研究
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  “cells”译为未确定词的双语例句
    The Differentiation of Bone Marrow Mesenchymal Stem Cells into Retina in Rat Eye and the Trherapeutical Effect on Severe Injured Retina
    骨髓间充质干细胞分化为视网膜结构及其在重度视网膜损伤中的治疗作用
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    Neuroprotective Effect of Nipradilol on Retinal Ganglion Cells
    Nipradilol对视网膜神经节细胞保护作用的研究
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    The Study of UV-induced DNA Damage and Repair Mechanism and Antagonism Effects of Antioxidants in Human Lens Epithelial Cells
    紫外线诱导的人LEC DNA损伤修复机制及抗氧化剂的拮抗作用的实验研究
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    Coloning, Expression and Cytotoxicity to Human Lens Epithelial Cells of Targeting Toxin DT_(389)-hbFGF
    靶向毒素DT_(389)-hbFGF的克隆表达及对人晶状体上皮细胞毒性研究
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    The Protective Effects and Mechanisms of Erythropoietin on the Injured Retinal Ganglion Cells Induced by Ischemia
    促红细胞生成素对缺血导致视网膜神经节细胞损伤的保护作用及其机制
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  cells
Xi defined a partition ofWf into canonical right cells and the right order ≤R on the set of cells.
      
This paper shows how the Kazhdan-Lusztig theory of cells can be directly applied to establish the quasi-heredity ofq-Schur algebras.
      
Coordinates on Schubert cells, Kostant's harmonic forms, and the Bruhat Poisson structure onG/B
      
Also, we discuss possible connections to the positive and cluster geometry of G/B+ × G/B-, which would generalize results of Fomin and Zelevinsky on double Bruhat cells and Marsh and Rietsch on double Schubert cells.
      
Alpha2-Adrenergic Receptors in Intestinal Epithelial Cells: Mechanisms of Signaling, Role, and Regulation
      
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Histopathologic examination of the epidermis showed,in cases of intra-dermal epithelioma,eccrine poroma,clear cell acanthoma and epidermodyspla-sia verruciformis,clumps of heteromorphic epidermal cells with specific features.The authors pointed out that in some of these cases, the clinical signs are not remarkable, however,the histopathological changes are quite distinct between eccrine poroma and eccrine poroepithelioma,or between epidermodys-plasia verruciformis and verruca planus.The authors stated...

Histopathologic examination of the epidermis showed,in cases of intra-dermal epithelioma,eccrine poroma,clear cell acanthoma and epidermodyspla-sia verruciformis,clumps of heteromorphic epidermal cells with specific features.The authors pointed out that in some of these cases, the clinical signs are not remarkable, however,the histopathological changes are quite distinct between eccrine poroma and eccrine poroepithelioma,or between epidermodys-plasia verruciformis and verruca planus.The authors stated that they firstly described the presence of grouped va-cuolar degeneration in epidermis in cases of epidermodysplasia verruciformis.

在皮肤组织病理检查中,常可在表皮中观察到与周围正常细胞不同的特殊细胞团.作者根据所见病例,介绍了表皮内上皮瘤、汗管口瘤、透明细胞棘细胞瘤及疣状表皮发育不良症等有上述病变的几种少见皮肤病。它们在临床上几无特异变化,主要靠病理诊断。作者还介绍了汗管口瘤与汗管口上皮瘤、疣状表皮发育不良症与扁平疣的病理鉴别诊断,首次报告了疣状表皮发育不良症的表皮中,空泡变性呈团块状存在,并描述其变化特点.

Xeroderma pigmentosum (XP) is anexceedingly rare disease, which isautosomal recessive genetically, chron-ically progressive and multisystemicwith the skin as the major targetorgan. The eyes are often involved.The characteristics of XP, just asGrindon described, are "a rare, chron-ic, fatal disease, beginning in infan-cy, characterized by freckking,atrophic stops, telangiectasis andkeratosis, and later by the developmentof carcinomata and sarcomata." Thesesigns usually occur at a very early age.The Desanctis-Cacchione...

Xeroderma pigmentosum (XP) is anexceedingly rare disease, which isautosomal recessive genetically, chron-ically progressive and multisystemicwith the skin as the major targetorgan. The eyes are often involved.The characteristics of XP, just asGrindon described, are "a rare, chron-ic, fatal disease, beginning in infan-cy, characterized by freckking,atrophic stops, telangiectasis andkeratosis, and later by the developmentof carcinomata and sarcomata." Thesesigns usually occur at a very early age.The Desanctis-Cacchione syndrome isthe most severe form of XP. In additionto the skin lesions, the syndromeconsists of microcephaly with mentaldeficiency premature closure of thesutures retarded growth and sexualdevelopment choreoathetosis, cerebellarataxia eventual quadriparesis withshortening of the achilles tendons andsometimes sensorineural deafness. In this paper seven patients withXP seen in last 20 years in GeneralHospital, Sichuan Medical College arepresented. Three were in-patients andfour out-patients. Besides the skinlesions in exposed regions, ocularaffections were seen in all the patients,especially on the skin of eyelids. Theyappeared often early and were severe.The conjunctiva and orbits might besimultaneously involved. Biopsy wasperformed on six patients and malign-ancies were confirmed in five. Theyall were proved to be either basal cellcarcinoma or squamous cell carcinoma,except one case of orbital malignantmelanoma. The onset of XP occurs most com-monly in early childhood. Five patientshad their onsets before the age of 3. Inthis series the youngest one had the ill-ness at the age of 6 months. The oldestcase had his onset at the age of 13,and he got cancer at 16. The patientdied 17 years after the discovery ofthe malignancy. The relatively lateonset and long survival of the patientmight be due to the optimal remedieshe had received. This was a ratherrare case in XP. The occurrence of this disease iscommonly seen in summer and spring.In this series four occurred in summertwo in spring, and one obscure. Skinlesions have a predilection for theexposed parts of the body in typicalcases.But one patient in this series hadcutaneous changes all over the bodyincluding freckles and white flecks onthe skin of the buttocks, scrotum penisand inner and outer surface of thethighs. Seven patients in this series camefrom 5 families. The development ofXP is closely related to heredity,especially consanguineous marriage of parents or grand-parents. In 2 of thefamilies, the patients' parents weremarried in sibship, and in one of therest 3 families there were 2 or 3 mem-bers suffering from XP simultaneously.Cases 4 and 5 were sib brother andsib sister and in their family 4 of 5siblings had similar clinical manifes-tations. Case 5 was an advanced patientclinically but biopsies of skin of theforearm and bulbar conjunctiva failedto reveal malignant change. Nothingabnormal was discovered by karyotypeexamination in 3 cases. In 1968, JE Cleaver demonstratedthat the main biochemical defect wasthe failure of excision-repair of ultra-violet (UV) damage of DNA in fibro-blasts in the skin of patient with XP.This aberration was believed to beassociated with the UV-endonucleasethat initiates excision. Subsequentstudies suggested that XP might involveenzymatic defects in more than onesystem. Lynch reported an eight-yearfollow up a pair of 16 year-old identi-cal twin brothers. Histological findingsfrom skin biopsy of each twin werefound consistent with XP. But theyhad been assiduously protected fromsolar radiation since birth. They didnot develop any evidence of skincancer. The prognosis of this disease isbad. All the patients have a tend todevelop canceration at the advancedstage. Lynch indicated that malignantskin tumors, most commonly basal andsquamous cell carcinomas, occurred inparticular all of the patients at a veryearly age. Malignant melanoma occurredin at least 3% of these patients. Pa-tients with XP usually died within thefirst two decades of their lives due tometastasis from the malignant skintumors In this series, 5 patients with XPdeve

本文报告7例着色性干皮病,该病除皮肤损害外,均合并有眼部病变。6例经病理检查证实有癌变者5例,其中以基底细胞癌和鳞状上皮癌为多,仅1例为眼眶恶性黑色素瘤。作者对本病的好发部位、发病年龄和季节进行了分析,并着重对本病的发病机理、遗传因素以及癌变和预防措施等问题,进行了简要的讨论。

Guinea Pig spiral organs damaged by exposure of the animal to 125 dB whitenoise for 2 hours were studied under scanning electron-microscope.Pronounceddegenerative changes were found only in specimens taken a month after exposure.However,in the specimens taken immediately after exposure slight early changes,such-as scattering, lying prostrate,or loss of hairs of the hair cells,could be clearlyobserved which were difficult to be identified with phase-contrast microscope inthe usual surface-preparation.

用扫描电镜观察了强声致伤后豚鼠耳蜗螺旋器的形态变化。强声为125dB SPL 连续2小时的白噪声。在暴露后一月制作的标本上观察到豚鼠耳螺旋器的损伤情况比暴露后即时制作的标本重,但在后者已可清楚地观察到听毛散乱、倒伏和脱落等早期变化,而这些早期变化用一般铺片技术检查是不容易发现的。

 
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