遺傳原因 的英文怎麼說

中文拼音 [yízhuànyuányīn]
遺傳原因 英文
hereditary cause
  • 遺 : 遺動詞[書面語] （贈與） offer as a gift; make a present of sth : 遺之千金 present sb with a gener...
  • 傳 : 傳名詞1 （解釋經文的著作） commentaries on classics 2 （傳記） biography 3 （敘述歷史故事的作品）...
  • 原 : Ⅰ形容詞1 （最初的; 原來的） primary; original; former 2 （沒有加工的） unprocessed; raw Ⅱ動詞（原...
  • 因 : Ⅰ動詞[書面語] （沿襲） follow; carry on Ⅱ介詞1 [書面語] （憑借; 根據） on the basis of; in accord...
  • 遺傳 : [生物學] heredity; hereditary; inheritance; inherit
  1. This paper introduced the application of biotechnology in rice genetics and breeding, including tissue culture, cell mutants selection, protoplast fusion, apomixis, molecular mark assisted breeding and genic transformation

    簡要綜述了生物技術在水稻遺傳育種中的應用，主要包括組織培養、細胞突變體的篩選、原生質體融合、無融合生殖以及分子標記輔助育種和轉基因技術等方面。
  2. Traditional chinese medicine says the causes of oral ulcer that are always associated with lower immunity, endocrine disorders, hereditary factors, overstrain and fatigue are complicated. find out the causes and the right remedy can be prescribed for the illness

    病因較復雜，與自身免疫機能低下內分泌功能紊亂遺傳因素精神過度緊張疲勞等有關，只要查明原因，對癥下藥就有一定的療效。
  3. We concluded that ( 1 ) motion asymmetry correlates closely with early - onset eye disorders that hinder the normal development of binocular vision ; ( 2 ) motion asymmetry correlates less with pure amblyopia ; ( 3 ) motion asymmetry is not unique to infantile esotropia syndrome ; ( 4 ) persisted motion asymmetry in adult is acquired rather than gene - determined ; ( 5 ) motion asymmetry may not be the cause of strabismus ; ( 6 ) motion asymmetry my not be secondary to disorganized nondecussated optic pathway and ( 7 ) motion asymmetry is an overall immaturity of sensory - motor pathway

    我們的結論是： （ 1 ）任何早發性眼科疾病，假如阻礙了正常的雙眼視覺發育，則造成不對稱的運動覺； （ 2 ）運動覺不對稱並不直接和弱視本身相關聯； （ 3 ）運動覺不對稱並非幼兒型內斜視專有的特徵； （ 4 ）成人的運動覺若不對稱，是視覺發育過程中受到阻礙造成，而非遺傳而來的； （ 5 ）運動覺不對稱並非斜視的原因； （ 6 ）運動覺不對稱的原因並非來自視覺神經路徑上太多的非交叉視覺神經； （ 7 ）運動覺不對稱是向感覺到運動總體視路徑發育不全所造成的結果。
  4. 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。
  5. Some of these events may appear to recapitulate features of primitive genomes, providing indirect clues as to how early genetic systems could have functioned

    隔代遺傳中的一些事件可能會再次反映出原始基因組的特徵，從而為早期遺傳學系統是如何擁有功能提供間接的線索。
  6. Hemochromatosis can be primary ( the cause is probably an autosomal recessive genetic disease ) or secondary ( excess iron intake or absorption, liver disease, or numerous transfusions )

    血色素沉著癥或可以是原發的（病因大概為常染色體隱性遺傳病） ，也可以是繼發的（過多的鐵攝取或吸收、肝臟疾病、大量輸血） 。
  7. If have congenital drawback, be atavistic mostly, should grandson generation is shown, but drug is used when you narrate may fetal development or traumatic cause, belong to acquired reason, that won ' t arrive hereditarily next generation

    如有先天性缺陷大都是隔代遺傳，要孫輩顯現出來，但你述可能胎兒發育時用藥或外傷引起，屬後天原因，那就不會遺傳到下一代！
  8. This article reviews the clinical manifestations, mutation feature, gene location and phenotype of different ischemic cerebrovascular disease caused by monogenic disorders, including coagulation disorders, erythrocytic disorders, inherited small vessel disease, metabolic disorders, connective tissue diseases, vasculopathies and disorders of unknown etiology

    本文主要闡述了單基因遺傳障礙引起的缺血性腦血管病，包括凝血障礙、血細胞病、遺傳性小血管病、代謝障礙、結締組織病、大動脈病及不明原因引起缺血性腦血管病的臨床特徵、突變特點、基因定位及表型等遺傳學研究進展。
  9. Individuals from sub - saharan africa and australian aborigines might have similar skin pigmentation ( because of adapting to strong sun ), but genetically they are quite dissimilar

    非洲次撒哈拉地區居民與澳洲原住民，皮膚色素的分佈也許相同（因為適應強烈的日曬） ，但是論遺傳組成，他們極不相似。
  10. The reasults are summed up as following : 1 the study on chromosomes and mitoses of bmn cells the cell line, bmn, is a silkworm cell line widely used in silkworm molecular genetics, cell engineering, gene engineering and baculovirus expression system but whose genetics and cytobiology studies are nearly untouched. the chromosomes and mitoses of the bmn cells are researched by the air - drying method and culturing cells on cover glasses

    同時，還通過原代培養實驗對新的家蠶胚胎細胞系的建立進行了探索和嘗試，並對家蠶胚胎原代培養過程中出現的細胞和組織類型進行了觀察、探討與研究。 1bmn細胞有絲分裂及染色體研究bmn細胞是家蠶分子遺傳學，細胞工程、基因工程和桿狀病毒表達系統中廣泛應用的家蠶細胞，但其遺傳學和細胞生物學背景知之甚少。
  11. Neither the bank, its associates, nor any of their directors, officers or employees, shall be liable to the customer for any expenses, loss or damage suffered by or occasioned to the customer by reason of any action taken or omitted to be taken by any one or all of the bank, its associates, their directors, officers, employees or agents pursuant to these conditions or in connection therewith other than as a result of the fraud, wilful default or negligence of the bank, its associates, their directors, officers, employees or agents ; the bank s failure in good faith to honour any stop - payment instructions given by the customer ; the presentation to the bank of any cheque or other payment order which is post - dated ; the bank failing to honour any draft drawn on it by the customer, but the bank shall immediately return such draft to the customer through the normal channels giving the reason for the dishonour ; any loss, damage, destruction or misdelivery of or to the securities howsoever caused unless the same shall result from the negligence of, or theft by, the bank or its associates or any of their directors, officers or employees, in which event the extent of the liability of the bank shall be limited to the market value of such securities at the date of discovery of the loss and even if the bank has been advised of the possibility of such loss or damage ; unauthorised use or forging of any authorised signature as a result of the negligence, wilful default or fraud of the customer ; subject to condition 5. 5, any act or omission, or insolvency of, any person not associated with the bank including, without limitation, a third party nominee or depositary ; viii the collection or deposit or crediting to the custodian accounts of invalid, fraudulent or forged securities or any entry in the custodian accounts which may be made in connection therewith ; any malfunction of, or error in the transmission of information caused by, any electrical or mechanical machine or system or any interception of communication facilities, abnormal operating conditions, labour difficulties, acts of god, or any similar or dissimilar causes beyond the reasonable control of the bank and notwithstanding paragraph, the error, failure, negligence, act or omission of any other person, system, institution or payment infrastructure

    本行其聯系人士其各董事高級人員或雇員均毋須向客戶因以下理由而使客戶蒙受或產生之任何開支損失或虧損負責： i本行其聯系人士其董事高級人員雇員或代理人根據此等條件採取或遺漏採取有關之行動，但由於本行其聯系人士其董事高級人員雇員或代理人之欺詐行為故意失責或疏忽所造成者除外ii本行本真誠地未能依約替客戶執行止付指示iii向本行提交任何遠期支票或其他付款指示iv本行未能兌現由客戶開出之匯票，但本行將立即透過正常渠道將該匯票退回客戶，並解釋拒付之理由v無論如何導致之任何證券之損失損毀毀壞或錯誤交付除非上述各項乃因本行或其聯系人士或其任何董事高級人員或雇員之疏忽或盜竊所引致，而在該等情況下，本行的責任將只限於在發現損失當日該等證券之市值，以及即使本行已獲知該等賠償之可能性vi因客戶之疏忽故意失責或欺詐行為而導致的任何偽造授權簽名或不獲授權使用該簽名vii在第5 . 5 a條之規限下，與本行無關者之任何行動或遺漏或無償債能力包括但不限於第三者代名人或寄存處viii代收或存入或貸存於保管人賬戶的無效偽造或假冒證券或在保管人賬戶記入可能與此有關之賬項ix任何電子機械或系統失靈或因該等機件或系統產生的資料傳送錯誤或任何通訊設施之終斷不正常操作情況勞工問題天災或非本行所能合理控制之任何類似或非類似原因及x盡管有第ix項，任何其他人系統機構或付款設施的錯誤故障疏忽行動或遺漏。
  12. In gene technology, there are some other problems of whether gene diagnosis are confidential, how to abort fetus with genetic diseases, and whether gene treatment results in virus infection and activates protocarcinogenic gene

    基因技術中基因診斷存在診斷是否保密、有遺傳疾病的胎兒如何進行人工流產；基因治療存在感染病毒和激活原癌基因問題。
  13. This paper reviews known and suspected causes of stillbirth including genetic abnormalities, infection, fetal - maternal hemorrhage, and a variety of medical conditions in the mother

    這篇文章回顧了已知的和懷疑的造成死胎的原因，包括遺傳學的異常，感染，胎兒-母親出血和母親的醫療條件不同。
  14. The obtained results do not support a major gene for body mass index in chinese, the discrepancies between our study and previous studies may result from ethnic difference between chinese and other populations ; the general model provides the best fit to the data, while the environmental model is the second parsimonious model, perhaps due to complex mode of body mass index inheritance ; a moderate heritability estimate is found for body mass index ( h2 = 0. 313 ), lower than that of other populations, this is presumably due to the fact that aside from the influence of genetic bases, body mass index is strongly influenced by environmental factors and that there is a low proportion of obese individuals in samples ( only 4. 1 % individuals have body mass index > 30 )

    分離分析的結果表明， （ 1 ）體重指數不存在主基因分離，不同於在其他非中國人群中檢測的結果，說明存在種群差異性； （ 2 ）一般模型提供了最合適模型，環境模型是次之的嚴格模型，可能由於體重指數遺傳模式的復雜性所致； （ 3 ）中國人群中體重指數具有適中的遺傳率（ h ~ 2 = 0 . 313 ） ，低於其他人群中的結果，這是由於體重指數除了受遺傳因素影響外還受環境因素影響及樣本中低比例的肥胖個體（ 4 . 1的個體bmi 30 ）的原因。
  15. The hwtx - i gene was chemically synthesized according to its known cdna sequence, the gene was inserted into vector ppic9k which contained aoxj promotor and the sequence of a secreting signal peptide - a - factor, the cloning ppic9k / hwtx - i was constructed and confirmed by two - step pcr and dna sequence analysis, then it was transformed into host strain gs115, a his + muts cell line was screened and multicopy transformants were screened by various g418 concentrations, the multicopy transformant was named gh1. gh1 was cultivated in flasks. after 6 days of induction by 0. 5 % methanol, the supernatant was checked by 16. 5 % tricine - sds page, which showed there was a band in the position of 3. 5 - 6. 1kd, then it was isolated and desalted by ultrofiltration followed by ion exchange of cm column, after reverse phase hplc of ci8 and vacuum drying, the purified rhwtx - 1 was obtained which was proved to be correct recombinant hwtx - i by tricine sds - page, maldi - tof mass spectrometry, amino acid composition analysis, the n - terminal amino acid sequence and its biological activity, the final field of the purified rhwtx - i was about 80mg / l, accounting for 23. 6 % of it total secretory proteins

    將帶有hwtx -基因的ppic9k經blgii線性化后，轉化酵母宿主菌gs115原生質體后經篩選陽性克隆並經表型鑒定為his ~ + mut ~ s酵母菌，進一步用遺傳毒素g418篩選多拷貝的轉化菌株，命名為gh1 ；將gh1甲醇酵母菌用0 . 5的甲醇誘導表達，發酵上清經90飽和度的（ nh _ 4 ） _ 2so _ 4沉澱， yw - 3 （ mwc03000 ）的超濾膜超濾，再經cm陽離子交換， c _ （ 18 ）反相hplc純化得到分子量為4kd左右的組分，其中4289 . 05的組分經質譜鑒定，氨基酸組成分析和序列測定為正確的表達產物，生物學活性表明其活性為天然毒素活性70 % ，表達量為80mg / l 。
  16. The third cause appears to be genetics

    第三種改變眼睛顏色的原因是遺傳基因。
  17. Apart from the reason of heredity, the dark and yellow skins are caused by the abnormal metabolism of the cutin on the epidermis and incomplete cleansing of oil and dirt

    黯淡無光、偏晦黃色肌膚，除了遺傳原因外，常常是由於表皮的角質層無法正常代謝、油脂、污垢無法徹底清除而導致的。
  18. Only about 1 - 2 % of cases are genetic

    只有的病例是和遺傳原因有關。
  19. What then makes people left - handed if it is not simply genetic

    那麼什麼是人慣用左手如果它不是簡單的遺傳原因？
  20. Children and young adults who have inherited high cholesterol may reduce their risk of clogged arteries by taking vitamins c and e, researchers have reported

    研究人員表示：那些因為遺傳原因引起的體內膽固醇過高的兒童或是年輕人，可以通過服用維生素c或者是e來降低膽固醇，減少血脈堵塞的風險。
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