生后腎組織 的英文怎麼說

中文拼音 [shēnghòushènzhī]
生后腎組織 英文
metanephrogenic tissue
  • : Ⅰ動詞1 (生育; 生殖) give birth to; bear 2 (出生) be born 3 (生長) grow 4 (生存; 活) live;...
  • : 名詞[生理學] (腎臟) kidney
  • : Ⅰ名詞1 (由不多的人員組成的單位) group 2 (姓氏) a surname Ⅱ動詞(組織) organize; form Ⅲ量詞(...
  • : 動詞(編織) knit; weave
  • 組織 : 1 (組織系統) organization; organized system 2 (組成) organize; form 3 [紡織] weave 4 [醫學] [...
  1. Using cd, cu, zn and cr as experimental toxicants and crucian as experimental creature, we employed the environmental biotechniques ( flame atomic absorption spectrophotometry, the method of improved pyrogallol autoxidation and electron microscopy ) to study the acute toxicity and secure concentrations of heavy metals to crucian ; the accumulation and distribution of mixed heavy metals to fingling crucian ; the activities of superoxide dismutase ( sod ) of gill and liver tissues and the hispathological and ultrastructural change of superfine structure of liver and kidney of crucian after cadmium exposure. through which, we intended to fully and systemically study the toxic influence of heavy metals to fish, and preliminarily discuss the influence of heavy metals pollution to the diversified level of fish such as individual, organ, tissue, cell and molecule. thus we tried to provide scientific evidence to establish preventative management measures, avoid and relieve the harm of heavy metals pollution to aquicolous ecosystem in time

    以這幾種重金屬作為實驗毒物,以鯽魚為實驗動物,應用環境物技術、火焰原子吸收分光光度法、鄰苯三酚自氧化法、透射電鏡等技術研究了重金屬cu 、 zn 、 cd和cr對鯽魚的急性毒性及其安全濃度評價、混合重金屬在鯽魚幼體內的積累和分佈、 cd對鯽魚鰓和肝臟中sod活性的影響、 cd對鯽魚肝細胞和細胞超微結構的影響等,全面和系統地研究了水環境中重金屬暴露對魚類的毒性影響,初步探討了重金屬污染對魚類的個體? ?器官? ?? ?細胞? ?分子等各水平層次的影響,為制定漁業產上預防性的管理措施提供科學依據,及時避免或減輕重金屬污染對水態系統造成的損害。
  2. It is a rare spindle cell neoplasm that was initially reported in the pleura, mediastinum, and lungs. recently, many extrathoracic locations, including kidney and retroperitoneal soft tissue, hae been described

    纖維瘤為很罕見紡錘狀細胞腫瘤,常見于胸膜、縱隔和肺。近來發現該瘤也可發於胸部以外的部位,如臟、腹膜等。
  3. In this report, we mainly covered the following aspects of " tissue organ regeneration and replication in situ " : 1 ) procedures of tissue organd regeneration and replication and replication in clnical practice ; 2 ) the discover and existence of potentiald regenerative cell ( prc ) ; 3 ) the proliferation, differentiation and regeneration law of potential law of potential regenerative cells ; 4 ) study procedure on tissue organ regeneration and replication from prcs in vitro based on the model of full skin organ regeneration in situ after extensive in vitro, set up the method and technology of searching life regenerative substance required in tissue organ regeneration and replication in situ. in this study, first, the whole human body is divided into 206 function units, which are the " tissue organ " in regeneration study. then the histology foundation of tissue organ regeneration and replication in situ is set up. in ordre to prove the existence of the potential regenerative cells and their potential baility and function, we established clinical tracking rechnique of skin organ regeneration in situ ; meanwhile, several tissue organ regeneration and replication in vitro models which represent different kinds of runctions were sucessfully set up, with all these techniques and models, we confirmed : 1 ) the existence, function and ability of pptemtoa regenerative cells ; 2 ) the importance of life regenerative substance ; 3 ) the feasibility of tissue organ regeneration and replication in situ ; 4 ) the big value of tissue organ regeneration and replication in situ in life science and medicine progerss. we also showed the possible foreground of capture cancer with this method and technologh. in this report, nearly 200 photographs of several tissue organ regeneration and replication in situ or in vitro demonstrated the whole process of tissue organ and big organ entities regeneration and replication from cells. the results of tissue organ regeneration and replication in situ mainly include : 1 ) whole skin organ regeneration and replication in situ ; 2 ) gastrointestinal mucosa tissue organ regeneration in vitro ; 3 ) hair follicle tissue organ regeneration in situ or in vitro ; 4 ) never tissue organ regeneration in situ ; 5 ) pancreas tissue organ regeneration and replication in vitro ; 5 ) marrow tissue regeneration in vitro ; 6 ) renal glomerulus and tubule tissue organ tugeneraation in vitro ; 7 ) heart muscle regeneration in vitro, etcl. in order to let more and more people know and understand this technology of tissue organd regeneration and replication in situ, herein, for the first time, we publicize the key points of actualizing this technology. also, we publicized the technology procedures and the frame constitute of life substances. we bilieve this is a big contribution to human science

    本研究報告,重點報道了器官的原位再復制的臨床程序,報道了潛能再細胞的發現和存在,以及該細胞的增殖分化和形成器官的變化規律.以燒傷皮膚器官的原位再復制為模型,研究出了體外潛能再細胞復制器官的培養方法;以體外器官的復制為模型,建立了尋找原位器官再復制所需命物質的方法和技術.本研究,首先按人體的器官功能,分解為206個功能單位,確立了所復制的人體器官中的功能單位為器官,從而建立了原位器官再復制的學基礎.為了驗證潛能再細胞的再潛能,建立了皮膚器官原位再的實體臨床跟蹤技術,同時又建立了能代表有關器官功能類別的代表器官的原位和體外復制模型,以多器官的成功復制確定潛能再細胞的作用,確定命研究再物質的重要性,確定器官原位再復制的可行性,確定了器官原位再復制的命科學研究和醫學進步的重大應用價值,同時展示了用此方法和技術攻克癌癥的前景.本研究報告,以近二百幅多個器官原位和體外再復制的實體圖片,展示了潛能再細胞復制的器官和大器官司實體;展示了細胞再復制器官的全過程.真實的報告了器官原位再復制的成果.所公布的主要成果為:皮膚器官的原位再復制;胃腸黏膜器官的原位和體外再復制;毛囊器官的原位和體外再復制;神經器官的原位復制;胰腺器官的體外復制;骨髓的體外復制;小球小管器官的體外復制;心肌的體外復制等.為了讓更多的人學會和掌握器官原位再復制技術,本報告首次公布實施技術的重要環節和技術流程;首次公布了命再物質的框架和成.作者自費研究成果對人類命科學的一大貢獻
  4. Levels of fasting blood glucose and 24h urinary microcontent of albumin 24 h malb were determined dynamically ; the serum glycosyl hemoglobin hba1c was determined after the last medication ; the ultrastructural changes of kidney were observed by transmission electron microscope ; the expressions of collagen, fibronctin, laminin ln, and the ecm metabolism influencing factors, including mmp2, tissue inhibitor of metalloproteinase timp2, transfer growth factor 1 tgf 1 in renal tissue were detected by immunohistological chemistry and image collecting analytical system

    動態檢測各大鼠空腹血糖fbg 24h尿微量白蛋白24h malb ,末次給藥測定大鼠血漿糖化血紅蛋白hba1c透射電鏡觀察各大鼠臟超微結構改變,應用免疫化技術及圖像採集分析系統測定各大鼠中型膠原c纖維連接蛋白fn層粘連蛋白ln的表達,測定影響ecm代謝的基質金屬蛋白酶2 mmp2基質金屬蛋白酶抑制劑2 timp2及轉化長因子1 tgf 1的表達。
  5. Abstract : purpose : to investigate the diagnosis, treatments and prognosis of adrenal cortical carcinoma in children. methods : data of 2 cases of adrenal cortical carcinoma in chidren were analyzed retrospectively about their diagnosis and treatments. results : 2 cases of adrenal cortical carcinoma were treated surgically : 1 case had cushing syndrom, 1 case presented a soft tissue tumor of leg without adrenal symptom. conclusions : it may be grown up immediately and spreadout directly in adrenal cortical carcinoma of children. in adrenal cortical carcinoma of non - symptom, it s symptom concealed, early diagnosis and immediate treatments may play a decisive role to the prognosis of adrenal cortical carcinoma

    文摘:目的:探討兒童上腺皮質癌的臨床特徵及其診斷、治療和預.方法:對2例兒童上腺皮質癌患者均行手術治療,並對其發病及診治過程進行分析.結果: 2例上腺皮質癌中, 1例為柯興綜合征表現, 1例為無功能性、小腿軟腫塊表現.結論:兒童上腺皮質癌長迅速,可直接播散.無功能性上腺皮質癌癥狀隱蔽,早期診斷、及時治療對改善預後起決定性作用
  6. The biological characteristics and toxicity of russula subnigricans hongo was studied for the first time from ecology and morphologic characteristics and histology, the orthogonal experiment of the optimum culture condition, the analysis of components, apoptosis of the cells from little white rat liver and kidney induced by extract of russula subnigricans hongo, to the histopathologic changes observation of little white rat liver and kidney through ecological observation, light microscopy and scanning electron microscopy, reversed - phase high performance liquid chromatography, agarose gel electrophoresis, transmission electron micioscopy. the result showed as below : based on ecological observation of russula subnigricans hongo, its ecological environment was investigated in order to simulate its ecological environment when they are cultivated

    利用菌種分離技術、光鏡技術、電鏡技術、高效液相色譜技術、毒理實驗技術、電泳方法等對亞稀褶黑菇( russulasubnigricanshongo )的物學特性和毒性機理進行了研究,主要包括以下內容:亞稀褶黑菇的態學和學研究、菌種分離培養、掃描電鏡觀察、成分分析、粗毒液誘導小自鼠肝細胞凋亡,小白鼠中毒細胞透射電鏡觀察,研究結果如下: 1
  7. Observation of chicken phenotype and rt - pcr results of tyrp1 expression in 8 day, 16 day embryos and 2 day hatched chicken also showed that melanin accumulation was appeared after detection of tyrp1 in silky. meanwhile, tyrpi expression was only detected in eyes of white leghorn ( except for kidney ), the only tissue where melanin exists

    Rt - pcr檢測白萊航和烏骨雞的8天、 16天胚胎和出2天各的tyrp1表達,結合對表型的觀察發現,烏骨雞各中黑色素的沉積隨tyrp1的表達出現,而白萊航(除臟外)只在有黑色素沉積的眼睛中表達tyrp1 ,其他既無tyrp1的表達也無黑色素沉積。
  8. It is clearly demonstrated that this method is useful for direct identification and cloning of genes encoding cellular drug - binding proteins without purification. this excellent feature of drug - western method allows more rapid and convenient identification of cellular drug - binding proteins than the other methods described before. translationally controlled tumor protein ( tctp ) was first identified as a tumor protein in ascitic tumor and erythroleukemia in mouse

    翻譯控制腫瘤蛋白最初在小鼠腫瘤細胞中被發現,是一個受翻譯過程所阻遏並與腫瘤長相關的蛋白質,隨在酵母及植物和除細胞外的各種動物正常細胞中被發現。
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