自律細胞 的英文怎麼說

中文拼音 [bāo]
自律細胞 英文
rhythmic cell
  • : Ⅰ代詞(自己) self; oneself; one s own Ⅱ副詞(自然;當然) certainly; of course; naturally; willin...
  • : Ⅰ名1 (法律; 規則) law; rule; statute; regulation 2 (律詩的簡稱) short for lüshi 3 (姓氏) a ...
  • : 形容詞1 (條狀物橫剖面小) thin; slender 2 (顆粒小) in small particles; fine 3 (音量小) thin ...
  • : Ⅰ名詞1 (胞衣) afterbirth2 (同一個國家或民族的人) fellow countryman; compatriot Ⅱ形容詞(同胞...
  • 自律 : [哲學] autonomy自律性 autorhythmicity; automaticity
  • 細胞 : cell; sytes; bioplast; cella; [口語] gene; [生物學] cellule; cellule cellulli cellulo ; cello ; k...
  1. Characters controlled by the dna of extranuclear organelles are not inherited according to mendelian laws and are transmitted only through the female line, since only the female gametes have an appreciable amount of cytoplasm

    由於質大多來母體所產生的配子,所以由核外的器的dna所控制的遺傳性狀一般只隨母系而遺傳,也不符合孟德爾定
  2. Conclusions ( 1 ) subacute senile mouse model can be used in immunosenesence reseach. ( 2 ) cd 137 may be an marker of aging. ( 3 ) the protection to aicd of cd137 decreased, indicate the function of cd137 was unusual. ( 4 ) the effect of d - galactose can modelling the different stage of aging. ( 5 ) the decrease of cd 137 expression on t cell from subacute senile mouse model and the aging mouse were due to the declining of their mrna. ( 6 ) the expression of cd 137 on t cells from from subacute senile mouse model and the aging mouse have a time dependently derease and the peak of cd 137 expression appeared earlier while the aging keep going on

    結論( 1 ) d -半乳糖致亞急性衰老小鼠模型tcd137分子表達變化規然衰老小鼠相似,造模兩個月後的大劑量組小鼠即可用於衰老個體cd137分子的相關研究。 ( 2 )模型小鼠cd137分子表達隨衰老的發生發展呈規性變化,提示該分子可能為t衰老的分子標志。 ( 3 )即使在衰老狀態下,機體對cd137分于的表達依然具有調控作用,提示兔疫系統的代償能力仍然存在。
  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的發現和存在,以及該的增殖分化和形成組織器官的變化規.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,展示了潛能再生復制的組織器官和大器官司實體;展示了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.作者費研究成果對人類生命科學的一大貢獻
  4. One of the characteristic features in myocardium cells is its autorhythmicity

    性是心肌的基本功能之一。
  5. Myocardial bioelectric phenomena and their mechanism, the characters of excitation transmission in heart ; the periodicity changes and their characters of myocardial excitability, autorhythmicity and pacemaker of heart ; pumping function of heart and evaluation ; the concept, mechanism and influencing factors of arterial blood pressure ; carotid sinus and aortic arch baroreceptor reflex

    心肌(工作自律細胞)的生物電現象及其形成的機制,心內興奮傳播的特點;心肌興奮性的周期性變化及其特點,性和心臟的起搏點;心臟的泵血功能及其評價;動脈血壓的概念、形成機制、影響因素;頸動脈竇和主動脈弓壓力感受性反射。
  6. The cardiac impulse originates in a relatively small group of primary pacemaker cells. typical primary pacemaker cells have the highest intrinsic frequency in firing. following its firing, there is a slow depolarization called pacemaker potential

    位於右心房竇房結內的起搏具有最高的固有發放節,每次發放后即出現一個緩慢的動去極化過程,心率主要取決于起搏去極化的斜率。
  7. ( 4 ) the myocardium cell group on embryonic body fibroblast feeder was cultured successfully. the myocardium tissue grew gradually, its contraction changed with temperature and morphology changed with time, and not all myocardium tissue could contract

    ( 4 )小鼠胚體成纖維可以與心肌團共培養,並出現性收縮,團逐漸增長,其收縮情況隨溫度變化而變化,隨時間變化其形態學發生變化,而且並非所有心肌團都能收縮。
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