纖維上皮病 的英文怎麼說

中文拼音 [xiānwéishàngbìng]
纖維上皮病 英文
fibroepithelioma
  • : 纖形容詞(細小) fine; minute
  • : Ⅰ動詞1 (連接) tie up; hold together; link 2 (保持; 保全) maintain; safeguard; preserve; keep ...
  • : 上名詞[語言學] (指上聲) falling-rising tone
  • : Ⅰ名詞1 (人或物體表面的一層組織) skin 2 (皮革) leather; hide 3 (毛皮) fur 4 (包在外面的一層...
  • : Ⅰ名詞1 (疾病; 失去健康的狀態) illness; sickness; disease; malum; nosema; malady; morbus; vitium...
  • 纖維 : fibre; staple; filamentary
  1. Typical pathological changes is leprosy granulation swollen namely leprosy is nodal, by composition of place of afterbirth of large and small of connective tissue of embedded leprosy bacili, there is epithelial appearance cell, oar cell to reach fiber cell all round

    典型變是麻風肉芽腫即麻風結節,由內含麻風桿菌結締組織巨細胞所組成,四周有樣細胞、漿細胞及成細胞。
  2. Purpose ependyma is lined in lumen surface of brain ' s ventricles which is composed of single ciliated cuboidal epithelium and a major component of brain csf barrier ( bcb ) and blood csf barrier ( blcb ). it plays an important role in production of csf, signal traiisttiission, maintainance of homeostasis within the brain, and so on, and a focus of developing pathway both for administration of some drugs into the brain and treatment of brain ' s diseases. ependyma may be specified in some sites perhaps owing to functional need and modified its structures of cells and tissue, which has been called circumventricular organs ( cvos ) since 50 of 20 century

    目的室管膜是襯覆在腦室內面的單層毛立方,是腦-腦脊液屏障,血-腦脊液屏障的主要組成部分,在腦脊液的產生,腦內信息的轉導,護腦的微環境等方面具有重要的作用,也是腦內給藥和腦疾治療新途徑開發關注的焦點之一;室管膜在一些部位可能是由於功能的需要其細胞和組織結構發生了特化,在二十世紀五十年代人們將這些特化的室管膜稱為室周器官。
  3. In a series of 30 cases of retinitis pigmentosa, pigment epithelial alterations included mottling of the macula in 8 eyes ( 13. 3 % ), bull ' s - eye pattern in 24 eyes ( 40 % ) and atrophy or hypopigmentation in 56 eyes ( 93. 3 % ) ; macular edema with retinal thickening was present in 30 eyes ( 50 % ), cystoid macular edema in 18 eyes ( 30 % ) ; broadening or loss of foveal reflex was present in 60 eyes ( 100 % ), preretinal membrane noticed in 58 eyes ( 96. 7 % ) and macular hemorrhage in one eye ( 1. 7 % )

    摘要對網膜色素變性癥的例30例60眼探討其黃斑部灶的情形,網膜色素層變化中的雜色斑點變見於8眼,頻率為13 . 3 % ,牛眼樣灶見於24眼( 40 % ) ,網膜脫色素灶為56眼( 93 . 3 % ) ;黃斑部浮腫之網膜增厚為30眼( 50 % ) ,類囊胞浮腫為18眼( 30 % ) ;其它變化包括中心窩反射消失或增寬為60眼( 100 % ) ,網膜前膜為58眼( 96 . 7 % ) ,黃斑部出血和疑似網膜下新生血管各為1眼( 1 . 7 % ) 。
  4. " the concept is that systemic sclerosis, which is a severe disease characterized by systemic fibrosis, is at the beginning mainly a vascular disease, and we hypothesize that using major vascular drugs ( calcium channel blockers, endothelin antagonists, prostacyclins, phosphodiesterase inhibitors, etc. ) from the beginning and at appropriate dosage may interfere with the fibrotic process which seems secondary, " dr

    「從概念講,系統性硬化是一種以系統性的化變性為特徵的嚴重疾,早期主要表現在血管性的變,因此我們推測早期、適量地應用主要作用於血管的藥物(如鈣離子阻斷劑,內素拮抗劑,前列環素,磷酸二酯酶抑制劑等)可能可以干預似乎是繼發發生的化過程。 」
  5. " the concept is that systemic sclerosis, which is a seere disease characterized by systemic fibrosis, is at the beginning mainly a ascular disease, and we hypothesize that using major ascular drugs ( calcium channel blockers, endothelin antagonists, prostacyclins, phosphodiesterase inhibitors, etc. ) from the beginning and at appropriate dosage may interfere with the fibrotic process which seems secondary, " dr

    「從概念講,系統性硬化是一種以系統性的化變性為特徵的嚴重疾,早期主要表現在血管性的變,因此我們推測早期、適量地應用主要作用於血管的藥物(如鈣離子阻斷劑,內素拮抗劑,前列環素,磷酸二酯酶抑制劑等)可能可以干預似乎是繼發發生的化過程。 」
  6. The research team of prof chan hsiao chang, director of the epithelial cell biology research centre, in collaboration with zhejiang academy of medical sciences, demonstrated that cystic fibrosis transmembrane conductance regulator cftr is involved in transporting bicarbonate into sperm, and thus, is vital to sperm fertilizing capacity and male fertility. cftr is an anion channel, mutations of which cause cystic fibrosis, a disease characterized by defective cl - and hco3 - transport with clinical manifestations in a number of organ systems

    由陳小章教授領導的香港中文大學細胞生物學研究中心的研究人員,與浙江醫學科學院合作,證實囊性化跨膜電導調節器( cftr )負責輸送碳酸氫根進入精子,對精子授精能力及男性生育能力非常重要; cftr是一個陰離子通道,其基因突變會導致囊性化,因為氯離子和碳酸氫根( hco3 - )分泌缺陷,引發一系列器官徵。
  7. The newly identified gene, nyd - sp27 has structural similarity to an isoform of phospholipase c. nyd - sp27 was expressed endogenously in human pancreatic - duct cells and upregulated in cystic fibrosis. researchers has proved that suppression of the gene resulted in augmentation of phospholipase - c - coupled calcium - ion release and protein kinase c activity, improvement in the amount of mutated cftr reaching the plasma membrane, and thus restoration of pancreatic anion secretion

    Nyd - sp27內源性表達在人體的胰腺導管細胞,並在囊性化時表達增高,顯示該基因可能與變有關。研究人員發現通過抑制該基因在人體囊性化胰腺導管細胞中的表達,可以糾正缺陷的胰腺陰離子分泌。
  8. In subjects with idiopathic pulmonary fibrosis, gsh deficiency in the elf has been observed ( 6 )

    (研究6 )檢驗自發性肺患發現其肺液里缺乏谷胱甘肽。
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