腎小體 的英文怎麼說

In the renin - angiotensin - aldosterone system, the juxtaglomerular apparatus helps regulate volume and pressure

在腎素-血管緊張素-醛固酮系統中，腎小球旁體幫助調節血容量和壓力。

Activation of rat liver microsomal glutathione s - transferase by chlorambucil and cyclophosphamide in vitro

高糖對人腎小球系膜細胞過氧化物酶體增殖物激活受體家族表達的影響

Specification for human nephron renal corpuscle model

腎腎單位腎小體放大模型技術條件

Glomerular changes are both frequent and severe.

腎小體的病變是常見而嚴重的。

Monocytes, neutrophils, and lymphocytes are present in same glomeruli.

一些腎小體中，可能存在單核細胞，嗜中性白細胞的淋巴細胞。

Seen here within the glomeruli are crescents composed of proliferating epithelial cells

腎小球內由增生的壁層上皮細胞組成的新月體。

A case suffering from diabetes and lymphocytosis complicated with immunotactoid glomerulopathy

淋巴細胞增生癥伴糖尿病合併免疫類晶體腎小球病一例

It has been proposed that these fragments represent lysosomal products regurgitated to the tubular lumen4

因此有人提出這些碎片是返流入腎小管管腔的溶酶體產物。

Flesh anhydride and urea nitrogen are the child of protein metabolization, by nephritic eduction body outside, the chroma in its blood can regard reason as the index of function of kidney spherule filtration

肌酐及尿素氮為蛋白質代謝的產物，由腎臟排出體外，故其血中濃度可作為腎小球濾過功能的指標。

The steady dead generation and time that was caused by the isolated virus was certain by chicken embryo which was inoculated on seven or nine days. the histopathological changs of the infectious stunting syndrom were studied by the way of ordinary paraffin section and he dying. the experimental result were as follows : the test proved that the changes of the chicken embryo were different in different stage. the chicken embryo dead in a week after it inoculated. the body was dropsy and hemorrhage. dead before it hatched out, the embyo body were dropsy, pale and slime. the liver was yellow and swolled, gallbladder ( vesica fellea ) was filled with bile. bursa and glandula thymus analosis. the kindey dropsy. bowel lamina were humble, dilatation. gas and yellow foam were filled the bowel. histopathological changes were that, in early stage, obvious changes of liver and kindey were dropsy, hemorrhage and necrosis. two types eosinophilic intranuclear inclusion bodies including large round and little granular were present in cells of the above organs. the obvious changes of bursa were dropsy, adverse folliiculated growth and little lymphocytes proliferating, 19 - 21 days chicken embryo, one or two big empty vacuoles were prensent in cells of liver and kindey. the number of the folliculi was growing, the vacuoles between cells were larger

膽囊充盈、其內充滿稀薄的膽汁；法氏囊、胸腺萎縮，腸道擴張、腸壁菲薄、內充滿氣體及黃色泡沫狀物；腎臟腫大。病理組織學變化方面，早期肝臟、腎臟、腸主要以出血、水腫和壞死為主，且肝細胞核及腎小管的上皮細胞核內均發現有核內包涵體，包涵體呈嗜酸性，為大型圓形包涵體或不規則的顆粒狀；法氏囊則以水腫、濾泡發育不良、小型淋巴細胞數量增多為主。 19 21日齡雞胚肝細胞、腎小管上皮細胞的胞漿內出現1 2各大的空泡，法氏囊濾泡數目增多細胞間有較大空隙。

Renin, a proteolytic enzyme formed in the granules of the juxtaglomerular apparatus cells, catalyzes conversion of the protein angiotensinogen to angiotensin i, a decapeptide

腎素是腎小球旁體細胞顆粒內形成的一種蛋白水解酶，催化蛋白血管緊張素原轉換為血管緊張素，即十肽。

Renin secretion is controlled by at least four mechanisms that are not mutually exclusive : a renal vascular receptor responds to changes in tension in the afferent arteriolar wall ; a macula densa receptor detects changes in the delivery rate or concentration of nacl in the distal tubule ; circulating angiotensin has a negative feedback effect on renin secretion ; and the sympathetic nervous system stimulates renin secretion via the renal nerve mediated by receptors

腎素的分泌至少受四種互不排斥的機制控制：腎血管受體對向心小動脈壁張力變化的反應；緻密斑受體發現遠端腎小管內氯化鈉傳遞速率或濃度的變化；循環的血管緊張素對腎素的分泌的負反饋效應；和交感神經系統經由受體介導的腎神經刺激分泌腎素。

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，重點報道了組織器官的原位再生復制的臨床程序，報道了組織潛能再生細胞的發現和存在，以及該細胞的增殖分化和形成組織器官的變化規律.以燒傷后皮膚組織器官的原位再生復制為模型，研究出了體外組織潛能再生細胞復制組織器官的培養方法;以體外組織器官的復制為模型，建立了尋找原位組織器官再生復制所需生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組織功能單位為組織器官，從而建立了原位組織器官再生復制的組織學基礎.為了驗證組織潛能再生細胞的再生潛能，建立了皮膚器官原位再生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組織器官的原位和體外復制模型，以多組織器官的成功復制確定潛能再生細胞的作用，確定生命研究再生物質的重要性，確定組織器官原位再生復制的可行性，確定了組織器官原位再生復制的生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，以近二百幅多個組織器官原位和體外再生復制的實體圖片，展示了潛能再生細胞復制的組織器官和大器官司實體;展示了細胞再生復制器官的全過程.真實的報告了組織器官原位再生復制的成果.所公布的主要成果為:皮膚器官的原位再生復制;胃腸黏膜組織器官的原位和體外再生復制;毛囊組織器官的原位和體外再生復制;神經組織器官的原位復制;胰腺組織器官的體外復制;骨髓組織的體外復制;腎小球小管組織器官的體外復制;心肌的體外復制等.為了讓更多的人學會和掌握組織器官原位再生復制技術，本報告首次公布實施技術的重要環節和技術流程;首次公布了生命再生物質的框架和組成.作者自費研究成果對人類生命科學的一大貢獻

Effect of saikosaponin d on rats glomerular mesangial cell proliferation and extracellular matrix hyperplasia in vitro

柴胡皂苷d對體外培養的大鼠腎小球系膜細胞增殖和細胞外基質分泌的影響

Zu ning, dong xi, fu guixiang and et al effect of saikosaponin d on rats glomerular mesangial cell proliferation and extracellular matrix hyperplasia in vitro

柴胡皂苷d對體外培養的大鼠腎小球系膜細胞增殖和細胞外基質分泌的影響

Methods wt5bzrats mcs were cultivated and identified

方法體外培養鑒定大鼠腎小球mc 。

The term gcd has been loosely used in the literature and many conditions with only occasional cortical cysts e. g. trisomy 13 - 15 and zellweger ' s syndrome, have been included < 2 >

「腎小球囊性腎病」已經被廣泛的使用在文獻和偶爾出現在皮質囊腫的病例中，這些病例包括13 15三體和腦肝腎綜合征< 2 > 。

Sympathetic innervation of the juxtaglomerular apparatus in the kidney releases renin ; angiotensin stimulates autonomic centers in the brain to increase sympathetic discharge

腎臟腎小球旁體的交感神經支配釋放腎素；血管緊張素刺激大腦自主中樞，增加交感沖動發放。

Detection of urinary mcp - 1, - catenin and ck19 molecules in patients with renal diseases and their correlations with crescents in glomeruli

腎臟病患者尿液中三種分子的檢測及其與腎小球新月體病變的關系

( 3 ) there was only ldh5 in the livers of al l groups of microtus fortis. the ldh4 and ldh5 were absent in the kidneys of the small voles from heilongjiang, but five kinds of ldh isozymes were all found in the kidneys of the other three groups

（ 3 ）四類東方田鼠的肝臟中都只含ldh5 ；腎臟中，除黑龍江小體型東方田鼠缺乏ldh4和ldh5外，其餘三類東方田鼠都含五種ldh同工酶。