肝組織樣的 的英文怎麼說

中文拼音 [gānzhīyàngde]
肝組織樣的 英文
hepatoid
  • : 名詞(人和高等動物的消化器官之一) liver
  • : 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
  • : Ⅰ名詞1. (形狀) appearance; shape 2. (樣品) sample; model; pattern Ⅱ量詞(表示事物的種類) kind; type
  • : 4次方是 The fourth power of 2 is direction
  • 組織 : 1 (組織系統) organization; organized system 2 (組成) organize; form 3 [紡織] weave 4 [醫學] [...
  1. Collection and preservation of samples : as soon as the three vital signs disappeared, the dogs were anatomized, and the heart, liver, kidney, spleen, lung, brain, muscle in the injection location and no injection location, the heart blood, urine, bile, cerebrospinal fluid ( csf ) in the lateral ventricle and spinal subarachnoid space, spinal cord ( medulla oblongata, cervical cord, the upper beast spinal cord, breast spinal cord and waist spinal cord ) were taken out, some of which were preserved at - 20 for qualitative and quantitative analysis, and the others were fixed with 4 % formaldehyde for the pathology observation

    3 、品採集:當心電、血壓和呼吸全部消失時,迅速解剖動物,採取心臟、臟、腎臟、脾臟、肺臟、大腦、注射部位肌肉、注射部位20cm以外肌肉、心血、尿液、膽汁、側山西醫科大學碩士學位論文腦室腦脊液、脊髓腔腦脊液和不同節段脊髓(包括延髓、頸髓、上胸部脊髓、胸部脊髓和腰部脊髓)等,冷凍保存。 4 、病理觀察:採取心臟、臟、 』腎臟、脾臟、肺臟、大腦、脊髓等, 4 %甲醛固定,石蠟包埋,切片, he染色,光鏡觀察。
  2. Deficiency of apoe may promote to produce and develop atherosclerotic lessions. the apoe gene - targeted mice will result in marked regression of both early and advanced atherosclerotic lesions by injected apoe recombinant protein, or by transfected adviral vector with apoe cdna to express human apoe transgene in liver, or by transplantation of bone marrow with normal rat apoe gene. this demonstrates that apoe gene and its expressing product can inhibit progression of atherogenesis. apoe3 has a more effective prevention from as than apoe2 and apoe4

    Apoe缺失可促進動脈粥硬化發生發展,給apoe基因敲除鼠反復注射apoe重蛋白、在中用腺病毒載體表達apoe蛋白、移植帶有正常apoe基因小鼠骨髓,都能使apoe基因敲除鼠動脈粥硬化得到回復,表明apoe基因及其表達產物對動脈粥硬化發生具有抑制作用, apoe _ 3對動脈硬化阻抑作用要比apoe _ 2和apoe _ 4都明顯。
  3. Hla - g1, which is a newly defined non - classical hla class i molecule, plays an important role in mediating immunotolerance and protecting embryo and even some kinds of tumors from nk cells attacking. the full - length coding sequences containing cdna of hla - g1 were cloned from placenta, monocytes and liver cancer tissue of chinese donors. sequence analysis reveals that it is a highly conserved human gene with only two amino acid mutation sites compared to foreign nationality. its truncated form was overexpressed in

    從中國人外周血單個核細胞胎盤品中克隆了包含完整hla - g1讀框cdna與國外同行獲得該基因及其蛋白質序列比較分析表明,該基因雖然有著細微種族特異性,但高度保守並獲得了它截斷型重蛋白,根據蛋白一級結構和同源比較方法,模建了它及其與特異性受體kir2dl4形成復合體空間結構模擬,預測了它們之間相互作用特徵。
  4. The incidence of postembolization syndrome ( pes ) was determined as well as objective tumor response rates by the world health organization ( who ), response evaluation criteria in solid tumors ( recist ), and european association for the study of the liver ( easl ) criteria

    栓塞形成后癥狀( pes )發生率和客觀腫瘤應答率一,由世界衛生( who )標準,實體瘤應答評價標準( recist )和歐洲臟研究協會( easl )標準來決定。
  5. The clsp gene is located approximately 3 kb and 90 kb centromeric to the clr and cls gene, respectively, and their genes form a short cluster in a region of about 115kb in 12pl3. the cluster gene arrangement and the sequence similarities of the cub and trypsin - like serine protease domain of clsp with other complement component 1 subcomponents supported a common evolutionary history by consecutive gene dup

    利用pcr檢測了clspmrna在人正常分佈,結果發現,人clspmrna廣泛表達於人正常中,如在胎盤、臟、腎臟、胰腺中表達量較高,在肺、脾、前列腺、卵巢、結腸、外周血有中度表達,而在心臟、骨骼肌、胸腺、翠
  6. Objective to establish a complex pcr method and to investigate the genetic polymorphism and population difference of three loci on y - chromosome, so as to provide a database for forensic medicine casework. methods edta - blood specimens were collected from 163 unrelated males in han population in taiyuan. different tissues of one corpse were analyzed including blood, muscle, liver and kidney

    方法( 1 )本採集:隨機抽取163名太原地區漢族無親緣關系男性個體靜脈血, edta抗凝,進行dys390 、 dys391和dys393基因座等位基因及單倍型頻率分佈調查;採集同一屍體血液、肌肉、臟、腎進行同一性檢測;採集20例兩代家系血進行突變觀察;取20例女性個體血進行男性特異性檢驗。
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