重體腺 的英文怎麼說
中文拼音 [zhòngtǐxiàn]
重體腺
英文
pituitarygland-
Results maidang rutong granules can promote the dilation and hyperplasia of acinus cavity and conduit in mammary gland, reduce the mammary interlobular fat connective tissue, significantly increase pituitary acidophil number and serum prolactin level, increase the milk volume of lactation rats and their offspring ' s body weight
結果麥當乳通顆粒可促進乳腺腺泡腔及導管擴大增生,減少乳腺小葉間脂肪結締組織,明顯增加垂體嗜酸性細胞數量和血清泌乳素水平,從而顯著增加母大鼠的泌乳量,並顯著提高其所喂養的仔鼠體重。Adrenal function studies in low birth weight infants
低出生體重兒腎上腺皮質功能的研究If this energy is left unused, the adrenalin will continue coursing through your veins, diverting energy away from vital bodily functions
如果這些能量沒有消耗完,腎上腺素將會繼續流向血管,身體重要機能所需的能量都被轉移了。Hcg test strip hcg human chorines gonadotropin begins to appear in female body after conception. it is important for female to test hcg earliest
女性在懷孕以後體內會開始分泌絨毛膜促性腺激素,早期檢測該激素,對女性具有非常重要的指導意義。The diagnostic value of the chest roentgeno gram and physical findings for the constrictive pericarditis are addressed
對于緊縮性心包膜炎我們提出胸部放射腺攝影及身體檢查發現為重要之診斷輔助。The cause that causes dark skiing ulcer has a lot of, have endocrine, food, genetic factor, the one mite bug that returning bug having mite also is the main reason that causes dark skiing ulcer lives inside wool bursa and sebaceous glands, it absorbs the nutrition of wool bursa and sebaceous glands cell, discrepancy skin carries a lot of bacteria, it secretes the dead damage body of excretive material and mite bug to be able to cause the skin organize inflammation to cause dark skiing ulcer
引起暗瘡的原因有很多,有內分泌、飲食、遺傳的因素,還有蟎蟲也是引起暗瘡的重要原因之一蟎蟲生活在毛囊和皮脂腺內,它吸收毛囊和皮脂腺細胞的營養,出入皮膚帶入很多細菌,它分泌排泄的物質和蟎蟲的死亡殘體都會造成皮膚組織發炎引起暗瘡。Secretion derangement - unliquefaction sperm the prostate is mainly exocrine gland, the prostatic fluid it secretes is important part of the sperm, not only provides menstruum circumstance for the sperm fluid, but also ensures all kinds of elements for sperm movement. here we should especially mention the gene fluidized sperm
前列腺主要是個外分泌腺體,它分泌的前列腺液是構成精液的重要部分,不僅為精子提供了適合生存的溶媒環境,還保證了精子活動所需要的各種要素,其中特別應提到的是控制精液流體狀態的因子。Preparation and identification of recombinant adenoviral vectors containing human wild type spk and its mutant gene
攜帶人鞘氨醇激酶及突變體基因重組腺病毒載體的制備及表達Construction of recombinant adeno - associated virus vector expressing glial cell line - derived neurotrophic factor labeled by green fluorescent protein
綠色熒光蛋白標記的大鼠膠質細胞源性神經營養因子重組腺病毒載體的構建及其表達3. using clamp technique, ex vivo gene transfer into liver graft was performed during cold preservation via perfusion of the portal vein with 5ml ringer ' s solution containing replication - defective adenovirus vector adhuctla4 - ig
供肝冷保存時,採用血管夾技術lamptechnique )經門靜脈灌注攜帶融合基因hllctla4dg的重組腺病毒,于術后3天、 7天能定性檢測到hllctla4ig在受體外劃血卜1 。Adenovirus - mediated gene transfer of acidic fibroblast growth factor induces angiogenesis in vitro
重組腺病毒體外誘導血管新生的實驗研究Construction of the recombinant adenovirus vector carrying antisense multidrug resistance gene
靶向肝癌細胞的重組腺相關病毒載體的構建Construction of recombinant adeno - associated virus vectors carrying double gene of antisense multidrug resistance - associated protein and antisense multidrug resistance
1雙耐藥基因的重組腺相關病毒載體的構建與鑒定Expressive efficiency of recombinant adenovirus vector of human osteoprotegerin gene in bone marrow stroma cell in rats
人骨保護素基因重組腺病毒載體在大鼠骨髓基質細胞中的表達效率Using ex vivo gene transfer technique, exogenous gene was introduced to the liver graft during cold preservation and express locally in the graft. the effect of inhibition of rejection and inducing liver graft tolerance was observed. through this study, the possibility of achieving graft tolerance by gene transfer without routine immunosuppressive drugs was explored
我們採用adeasy腺病毒載體系統,自行構建攜帶huctla4 - ig的重組腺病毒,通過先體外后體內( exvivo )基因轉移技術,于供肝冷保存時,將該治療基因導入大鼠移植肝,使其于移植肝局部表達,觀察其抑制排斥反應,誘導大鼠移植肝免疫耐受的作用。The mechanism is that the introduced complementary oligonucleotides can bind to the corresponding mrna or double - stranded dna in genome and form partial double - stranded molecules or triple - stranded nucleic acid molecules by sequence - specific and nonsequence - specific antisense action, thus the target gene will be orientationally blocked and expression of the target inhibited so that therapeutic effect could be attained. in this study, we designed a fragment of human c ii ta cdna in antisense orientation using mrna of c ii ta as template. the primers were designed based on 94 - 500 nucleotides segment in 5 " end of ciita gene so that the interested gene contained 407 base pairs which included two aug codons in 1 16 and 188 nucleotides as well as the splicing site between the first and the second exons
本研究設計以c tamrna為模板的反義cdna片段,從c ta基因5 』端第94位到500位核苷酸段設計引物,目的片段407bp ,覆蓋第116和188位兩個aug密碼子,也包含了第一外顯子和第二外顯子間的剪接位點:用常規分子生物學方法構建了反義片段的腺病毒表達載體( padeasy - 1系統) ;腺病毒載體經hek293細胞包裝產生含反義片段的重組腺病毒,用氯化銫密度梯度離心法獲得純化的高滴度腺病毒;進行體外基因轉移,分別用反義片段真核表達載體轉染p388d1細胞和用重組腺病毒感染hela細胞,觀察導入的c ta基因反義rna抑制細胞內組成型或誘導型c ta基因表達的作用,從而達到調控mhc -類分子表達的目的。No recipient of group a ( without any treatment, n = 5 ) or group b ( treated with adgfp, n = 4 ) died within three weeks after transplantation and severe acute rejection ( massive periportal infiltrate, endothelilitis, damage to biliary epithelium and severe tissue destruction ) was confirmed by pathological examination of the graft. in contrast, all recipients of group c ( treated with adhuctla4 - ig, n = 5 ) achieved lohg - term liver allograft survival ( > l50d )
35 ,屍0刀5八而灌注攜帶融合基因a個ig的重組腺病毒組組, fi ? 5 )受體鼠均能獲得長期生存( 150天) ; a組與c組間、 b組與c組間,生存期均有顯著性差異』 ( p 0刀1人a組與b組,在術后8天行移植肝活檢,病理學檢查證實:移植肝均發生嚴重的細胞性排斥。Experimental study on effect of recombinant adenovirus vector carrying apopotin gene on hepatoma cells
重組腺病毒載體攜帶凋亡素基因對肝癌細胞的作用Construction of a recombined adenovirus vector carrying hbv - s gene and its expression of hbsag in dendritic cell
重組腺病毒載體的構建及在樹突狀細胞的表達Construction of the recombinant adenovirus vector carrying antisense multidrug resistance - associated protein
攜帶反義多藥耐藥相關蛋白的重組腺病毒載體的構建分享友人