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   细胞 在 眼科与耳鼻咽喉科 分类中 的翻译结果: 查询用时:0.503秒
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细胞
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  cellular
    CELLULAR IMMUNITY IN PATIENTS WITH VOGT-KOYANAGI-HARADA SYNDROME
    Vogt-Koyanagi-Harada综合征患者的细胞免疫功能测定
短句来源
    Experimental Study of Cellular Response on the Surface of Implanted
    后房型人工晶体植入术后晶体表面细胞反应的实验研究
短句来源
    The study of cellular DNA content and PCNA expression of vesicular nucleus cell carcinoma of the nasopharynx
    鼻咽泡状核细胞癌DNA含量与PCNA计数的研究
短句来源
    Flow Cytometric Analysis of Cellular DNA Content of Paraffin-embedded Tissue of Nasopharyngeal Carcinoma (NPC)
    流式细胞仪与鼻咽癌石蜡包埋组织DNA含量分析
短句来源
    Methods: Ovalbumirl(OVA) absorbed to aluminum hydroxide was used to construct the allergic rhinitis model(group C),and nebulized IFN-r 12 ug was inhaled once daily on day 23 to day 30.The nasal lavage fluid was collected on day 31,and the cellular constituents,levels of IL-4,IL-5 and IgE were determined.
    方法:采用卵清蛋白(OVA)、氢氧化铝建立大鼠AR模型。 IFN-r鼻腔吸入组(C组)与模型建立第23~30天,每日1次鼻腔吸入IFN-r 12μg,第31天取鼻腔灌洗液测定细胞成分,白介素(IL)-4,IL-5浓度,取血测定血浆IgE水平。
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  “细胞”译为未确定词的双语例句
    An in Vitro Mitotic Stimulating Experimental Study of Human Nerve Growth Factor Gene Transfected Cat Corneal Endothelia
    人β-神经生长因子基因转染体外培养猫角膜内皮细胞促进其分裂再生的实验研究
短句来源
    Purified Primary Culture of Human Retinal Microvessel Endothelium and Pericytes with Magnetic Beads and Effects of Inflammation and Hypoxia on Its Expression of PDGF-B/PDGFR-β and Ang-1/Tie-2
    免疫磁珠法原代纯化培养人视网膜微血管内皮细胞与周细胞及炎症与缺氧对其PDGF-B/PDGFR-β和Ang-1/Tie2表达的影响
短句来源
    The Influence of Cochlea Injury on Cochlear Neucleus of Chinchilla
    卡铂损伤灰鼠耳蜗内毛细胞对其耳蜗核神经元的影响
短句来源
    The Immunologic Studies of Experimental Heterogous Lamellar Keratoplasty
    实验性异种板层角膜移植的免疫学研究——特异性体液免疫及非特异性细胞免疫测定
短句来源
    Endothelial Healing in Cat Corneal Alkali Burn
    碱烧伤角膜内皮细胞层的创伤修复——创伤闭合的动力学观察
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  cellular
After 24h incubation, cellular DNA was isolated and analyzed for BP-derived DNA adducts by 32P-postlabeling technique.
      
Evolution complexity of the elementary cellular automaton of rule 22
      
Cellular automata are the discrete dynamical systems of simple construction but with complex and varied behaviors.
      
In this paper, the elementary cellular automaton of rule 22 is studied by the tools of formal language theory and symbolic dynamics.
      
Complexity analysis of time series generated by elementary cellular automata
      
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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 that they...

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。

23 cases with tympanic membrane perforation were successfully treated with heterogenous tissue grafting.In six cases, the underlay grafting method was used, and the outlay method was in 6 cases. After operation, all perforations were nicely healed up.The graft tissue used is the waste product in manufacturing cat-gut unqualified for regular suturing.Segments of this cat-gut purified and chromified, whitish in colour, and tape-like in shape were used.Each segment measured 1 or 1.5 cm in width proved a little...

23 cases with tympanic membrane perforation were successfully treated with heterogenous tissue grafting.In six cases, the underlay grafting method was used, and the outlay method was in 6 cases. After operation, all perforations were nicely healed up.The graft tissue used is the waste product in manufacturing cat-gut unqualified for regular suturing.Segments of this cat-gut purified and chromified, whitish in colour, and tape-like in shape were used.Each segment measured 1 or 1.5 cm in width proved a little too thin, and should be double-folded or triple-folded.A segment of cat-gut sectioned and examined under the microscope, was found to contain nothing else than plenty of collagen fibers .Cat-gut could be kept in 75% alcohol under room temperature.From our limited experience, it seems to be a very -useful grafting material in ear surgery and worthy of further trial and observation. To our knowledge no similar report has been noticed in current medical literatures.

本文报告采用异种组织进行鼓膜修补术,获得成功。所用移植组织为羊肠线生产时的废料,经净化及铬化,色白,如带状,宽1~1.5cm,较菲薄,可用75%酒精浸泡,保存于室温中。经切片检查,仅见许多胶原纤维,无其他组织细胞。进行鼓膜穿孔修补术时,应将其双叠或二叠后植入较好。曾试用于23例患鼓膜穿孔者(内植法17例,外植法6例),术后穿孔均已愈合,听力亦有提高。初步认为这种异种组织为很有价值的移植材料,拟作进一步研究、观察。据作者所知,这种方法以往文献中尚未见报告。

 
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